DNA replication is the process by which a cell makes an identical copy of its DNA before cell division. It occurs during the S phase of interphase and involves unwinding the DNA double helix, synthesizing new strands complementarily using existing strands as templates, and sealing the newly synthesized DNA. Key enzymes involved include DNA helicase, DNA polymerase, DNA primase, and DNA ligase. DNA polymerase adds nucleotides to the leading strand continuously but must add fragments called Okazaki fragments discontinuously to the lagging strand due to the anti-parallel nature of DNA replication.
DNA replication is the process by which a cell makes an identical copy of its DNA when it divides. It involves unwinding the DNA double helix, synthesizing new strands while using the original strands as templates, and joining the new strands. Key proteins involved include DNA helicase, DNA polymerase, DNA primase, and DNA ligase. Errors during replication can lead to mutations in the DNA sequence.
This document contains instructions for homework assignment #2 in a genetics course. It includes questions about gene expression, mutation, protein function, recombination, and cancer genetics. Students are asked to answer questions about promoter sequences, start/stop codons, amino acid changes, Holliday junction formation, cancer hotspots, and pedigrees. Diagrams illustrate chromosome structure, gene fusions, and potential recombination outcomes.
This document contains instructions and questions for a genetics homework assignment. It asks the student to:
1) Draw the structure of two base-paired dinucleotides and indicate relevant atoms and bonds.
2) Identify which of several pairs of mutations would have a greater consequence to a gene's function and explain why.
3) Analyze domain structures and mutations in a gene responsible for hearing and memory and explain the resulting phenotypes.
4) Describe the consequences of various mutations in a gene on transcript and protein production.
5) Briefly explain how a gene family can arise.
6) Discuss how the idea that ATP is not limiting in eukaryotic cells relates to the presence of intr
This document contains instructions for homework assignment #2 in a genetics course. It includes questions about gene expression, mutation, protein function, recombination, and cancer genetics. Students are asked to answer questions about DNA sequences, genetic code, chromosome structure, and mechanisms like transcription, translation, and recombination through diagrams and short explanations.
This document provides details and questions for a homework assignment on genetics concepts. It includes 8 questions covering topics like gene expression, DNA and protein structures, mitotic and meiotic recombination, pedigrees, and mutational consequences. The instructor provides explanations and asks students to answer questions in short responses or by drawing out processes. The goal is for students to integrate and apply their understanding of core genetics topics.
This summarizes a genetics homework assignment involving:
1) Drawing the structure of hydrogen-bonded DNA strands showing C-G and G-C base pairs.
2) Identifying which of two mutations would have a greater impact on gene function.
3) Analyzing a gene with three domains involved in two functions, and mutations within it.
4) Predicting effects of mutations in a gene regulated by p53 on transcript and protein production.
5) Briefly explaining how a gene family can arise from two similar genes.
6) Discussing how abundant ATP relates to the presence of introns in eukaryotic genes.
DNA replication begins with DNA helicase unwinding the double helix at the origin of replication. The leading strand is synthesized continuously while the lagging strand is synthesized discontinuously in fragments called Okazaki fragments. DNA primase adds an RNA primer and DNA polymerase extends each primer into DNA. DNA ligase joins the Okazaki fragments together to form a complete lagging strand.
DNA replication involves DNA helicase unwinding the DNA double helix. DNA polymerase then synthesizes a complementary strand to each original strand. On the leading strand DNA polymerase synthesizes continuously, while on the lagging strand it synthesizes in fragments called Okazaki fragments, which are later joined together. DNA polymerase needs an RNA primer to begin synthesizing each Okazaki fragment, which is later replaced with DNA by DNA polymerase 1. This process continues until the entire DNA double helix is replicated.
DNA replication is the process by which a cell makes an identical copy of its DNA when it divides. It involves unwinding the DNA double helix, synthesizing new strands while using the original strands as templates, and joining the new strands. Key proteins involved include DNA helicase, DNA polymerase, DNA primase, and DNA ligase. Errors during replication can lead to mutations in the DNA sequence.
This document contains instructions for homework assignment #2 in a genetics course. It includes questions about gene expression, mutation, protein function, recombination, and cancer genetics. Students are asked to answer questions about promoter sequences, start/stop codons, amino acid changes, Holliday junction formation, cancer hotspots, and pedigrees. Diagrams illustrate chromosome structure, gene fusions, and potential recombination outcomes.
This document contains instructions and questions for a genetics homework assignment. It asks the student to:
1) Draw the structure of two base-paired dinucleotides and indicate relevant atoms and bonds.
2) Identify which of several pairs of mutations would have a greater consequence to a gene's function and explain why.
3) Analyze domain structures and mutations in a gene responsible for hearing and memory and explain the resulting phenotypes.
4) Describe the consequences of various mutations in a gene on transcript and protein production.
5) Briefly explain how a gene family can arise.
6) Discuss how the idea that ATP is not limiting in eukaryotic cells relates to the presence of intr
This document contains instructions for homework assignment #2 in a genetics course. It includes questions about gene expression, mutation, protein function, recombination, and cancer genetics. Students are asked to answer questions about DNA sequences, genetic code, chromosome structure, and mechanisms like transcription, translation, and recombination through diagrams and short explanations.
This document provides details and questions for a homework assignment on genetics concepts. It includes 8 questions covering topics like gene expression, DNA and protein structures, mitotic and meiotic recombination, pedigrees, and mutational consequences. The instructor provides explanations and asks students to answer questions in short responses or by drawing out processes. The goal is for students to integrate and apply their understanding of core genetics topics.
This summarizes a genetics homework assignment involving:
1) Drawing the structure of hydrogen-bonded DNA strands showing C-G and G-C base pairs.
2) Identifying which of two mutations would have a greater impact on gene function.
3) Analyzing a gene with three domains involved in two functions, and mutations within it.
4) Predicting effects of mutations in a gene regulated by p53 on transcript and protein production.
5) Briefly explaining how a gene family can arise from two similar genes.
6) Discussing how abundant ATP relates to the presence of introns in eukaryotic genes.
DNA replication begins with DNA helicase unwinding the double helix at the origin of replication. The leading strand is synthesized continuously while the lagging strand is synthesized discontinuously in fragments called Okazaki fragments. DNA primase adds an RNA primer and DNA polymerase extends each primer into DNA. DNA ligase joins the Okazaki fragments together to form a complete lagging strand.
DNA replication involves DNA helicase unwinding the DNA double helix. DNA polymerase then synthesizes a complementary strand to each original strand. On the leading strand DNA polymerase synthesizes continuously, while on the lagging strand it synthesizes in fragments called Okazaki fragments, which are later joined together. DNA polymerase needs an RNA primer to begin synthesizing each Okazaki fragment, which is later replaced with DNA by DNA polymerase 1. This process continues until the entire DNA double helix is replicated.
Gene Cloning Very Detailed Antibiotic Resistanceallyjer
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DNA replication involves converting a single DNA helix into two identical copies through a semi-conservative process. Helicase splits and unwinds the DNA strands. Nucleotides are then added in the 5' to 3' direction by DNA polymerase III to the new strands based on base pairing rules, with A joining to T and C joining to G. The leading strand is synthesized continuously while the lagging strand is formed in fragments called Okazaki fragments that are later joined by DNA ligase.
The document describes the process of DNA replication. It begins with DNA unwinding at the origin of replication site, where helicase enzymes cause the double helix to separate. Free nucleotides then base pair with the exposed, complementary bases on each single strand. DNA polymerase joins the nucleotides to form new polynucleotide chains. Finally, the two new DNA molecules each contain one original and one new strand, and the double helix reforms.
This document summarizes a lesson on DNA replication. It begins with introducing the topic and dividing students into groups to complete different activities related to DNA replication. It then reviews the key terms and defines the three main steps of DNA replication: unzipping, base pairing, and joining. The importance of DNA replication is explained as ensuring that all body cells carry the same genetic material and instructions are copied exactly for the next generation. Students are assessed through a quiz asking them to list the steps of DNA replication and complete DNA replication activities. They are assigned to study the next topics of DNA transcription and translation.
The document describes the central dogma of molecular biology:
DNA is transcribed into RNA, which is then translated into proteins. DNA contains the genetic code in nucleotides that make up genes. RNA polymerase transcribes DNA into messenger RNA (mRNA) in the nucleus. mRNA is then translated by ribosomes in the cytoplasm into proteins based on the RNA code using transfer RNA (tRNA) and amino acids. The process of protein synthesis involves transcription of DNA to mRNA and then translation of mRNA to proteins.
DNA replication is the process by which DNA makes a copy of itself during cell division. In molecular biology, DNA replication is the biological process of producing two identical replicas of DNA from one original DNA molecule. DNA replication occurs in all living organisms acting as the basis for biological inheritance.
Step 1: Replication Fork Formation. Before DNA can be replicated, the double stranded molecule must be โunzippedโ into two single strands. ...
Step 2: Primer Binding. The leading strand is the simplest to replicate. ...
Step 3: Elongation. ...
Step 4: Termination.
DNA replication begins at origins of replication where the double helix unwinds. DNA helicase unwinds and unzips the DNA strands. DNA polymerase III then reads the strands in a 3' to 5' direction and synthesizes new strands in a 5' to 3' direction, matching the base pairs. DNA polymerase I changes any RNA primers to DNA at Okazaki fragments. This process produces two identical copies of the original DNA.
The document explains how to use a codon table to translate mRNA sequences into amino acid sequences during protein synthesis. It details the process of transcription of DNA to mRNA, translation of mRNA in the ribosome using tRNA molecules, and how to use the codon table to determine which amino acid corresponds to an mRNA codon. The overall purpose is to explain how codons are used to determine the amino acid sequence of proteins from genetic information in DNA.
The document summarizes the central dogma of molecular biology: DNA is transcribed into RNA, which is then translated into protein. It describes the processes of DNA replication, transcription of DNA to mRNA, and translation of mRNA to proteins using tRNAs and ribosomes. Mutations are explained as changes to the DNA sequence that can alter protein production through frameshift or substitution errors. Recent research has found transcriptional exclusion of mutated alleles at the single-cell level.
The central dogma of molecular biology describes the flow of genetic information within biological systems. It states that DNA is transcribed into RNA, and RNA is translated into protein. While information flows from DNA to RNA to protein, it cannot flow in the reverse direction from protein back to nucleic acids. There are some exceptions, such as reverse transcription in retroviruses and RNA replication in certain viruses. The central dogma establishes the principle that genetic information can be converted between DNA and RNA.
DNA replication in eukaryotes proceeds in a coordinated process of initiation, elongation, and termination. Initiation begins at specific origin of replication sequences and involves the assembly of pre-replication complexes. During elongation, helicases unwind the DNA strands exposing templates for DNA polymerase enzymes to synthesize new daughter strands. Termination occurs when the polymerases reach the end regions called telomeres, which are then extended by the enzyme telomerase to allow replication to continue.
Ch 7 dna structure and function blank sp 2018C Ebeling
ย
This document provides an overview of DNA structure and gene function. It begins with learning objectives related to DNA, RNA, proteins, transcription, translation, and mutations. Key concepts covered include the central dogma, components of DNA, roles of DNA, RNA and proteins, transcription and its steps, mRNA processing, translation and its steps, the genetic code, and types of mutations. Diagrams illustrate these concepts and examples are given throughout.
Sadeeqsheshe the central dogma of molecular biologySadeeq Sheshe
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The document describes the central dogma of molecular biology, which states that DNA is replicated, then transcribed into RNA, and RNA is translated into protein. It provides details on DNA replication, transcription, and translation. DNA replication involves DNA polymerase copying DNA in the 5'-3' direction. Transcription involves RNA polymerase transcribing DNA into RNA. Translation occurs on ribosomes and involves mRNA being read in triplets to produce a polypeptide chain. The processes are generally conserved between prokaryotes and eukaryotes but have structural and mechanistic differences.
1. DNA replication is the process by which daughter DNA molecules are synthesized from a parental DNA template. It ensures the genetic information is transferred to the next generation with high fidelity.
2. Replication occurs semi-conservatively such that each new double helix contains one strand from the original parent DNA and one newly synthesized strand. It also occurs bidirectionally from an origin of replication.
3. DNA polymerases are the key enzymes that catalyze DNA synthesis. Other important enzymes and proteins include primase, helicase, topoisomerase, ligase, and single-stranded DNA binding proteins. Together they facilitate the initiation, elongation and termination of DNA replication.
The document outlines the three major stages of transcription and translation: 1) replication, where DNA is copied during cell division; 2) transcription, where part of a DNA strand is copied into mRNA; and 3) translation, where the mRNA is used by the ribosome to produce a polypeptide based on the mRNA codons. During translation, tRNAs bring amino acids to the ribosome which link them together based on the mRNA codons to form a protein.
DNA replication is the process where a DNA molecule makes an identical copy of itself. There are three proposed models of replication: conservative, dispersive, and semi-conservative. The widely accepted semi-conservative model involves unwinding the DNA double helix, attaching primers to each strand, and synthesizing new complementary strands in the 5' to 3' direction along each template strand. This results in two double-stranded DNA molecules each with one original strand and one new strand.
There are three main levels of control to ensure DNA replication is initiated only once per cell cycle in bacteria:
1. ATP hydrolysis by beta-clamp protein
2. Sequestration of hemimethylated DNA by SeqA protein
3. Titration of DnaA protein levels through its regulatory locus
In eukaryotes, licensing factors like ORC, Cdc6, Cdt1 and MCM proteins bind to origins of replication and license them for a single round of replication. After replication begins, these factors dissociate from origins preventing re-replication. Geminin protein also prevents re-licensing of newly synthesized DNA in G2 phase.
DNA polymerase proofreads
DNA replication occurs through a semiconservative process where each parental DNA strand serves as a template for the synthesis of a new complementary strand. This results in two daughter molecules each composed of one original parental strand and one newly synthesized strand. In eukaryotes, replication occurs during S phase of the cell cycle. The major enzymes involved are DNA polymerases, helicases, and ligases which unwind, copy, and join the strands respectively. Errors are corrected by proofreading and repair mechanisms to maintain genomic integrity.
The document describes the process of DNA replication. It explains that the enzyme helicase unzips the DNA double helix by splitting the hydrogen bonds between the bases. DNA polymerase then adds complementary bases to each strand, creating two identical copies. The leading strand adds bases continuously from 5' to 3'. The lagging strand adds bases in fragments from 3' to 5' using an RNA primer and DNA polymerase to join the fragments.
Tyler Young raised a medaka fish named Jeffery from an embryo. He observed and documented Jeffery's development over 9 days, from stage 2 to stage 36 when he hatched. Tyler provided daily care and changed Jeffery's water until he was ready to be released into a community tank with other fish. Though sad to see Jeffery go, Tyler knew it was better for him to swim freely with other medakas.
Joey is a chick being documented from its first day of development through hatching. Over the course of 8 days, the author records Joey progressing through various embryonic development stages from 29 hours old in stage 18 to finally hatching on day 8. Brief notes are made about Joey's heartbeat, growth, and current developmental stage each day.
DNA replication involves unwinding the DNA double helix using the enzyme helicase. On the leading strand, DNA polymerase III continuously adds nucleotides to form the leading strand. On the lagging strand, which is discontinuous, RNA primers are added by primase and DNA polymerase II builds Okazaki fragments by adding nucleotides between primers. The primers are later removed and replaced with DNA to form a continuous DNA strand.
Dexter narrates his experience hatching from an egg over the course of 7 days. He describes each developmental stage, including his organs becoming visible and his heartbeat increasing in rate. On the seventh day, he finally hatches from the egg and is able to freely swim in his petri dish. Dexter survived with just having his water changed daily. He acknowledges having a rough start but credits Shaylyn and Jenna for taking good care of him.
Gene Cloning Very Detailed Antibiotic Resistanceallyjer
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DNA replication involves converting a single DNA helix into two identical copies through a semi-conservative process. Helicase splits and unwinds the DNA strands. Nucleotides are then added in the 5' to 3' direction by DNA polymerase III to the new strands based on base pairing rules, with A joining to T and C joining to G. The leading strand is synthesized continuously while the lagging strand is formed in fragments called Okazaki fragments that are later joined by DNA ligase.
The document describes the process of DNA replication. It begins with DNA unwinding at the origin of replication site, where helicase enzymes cause the double helix to separate. Free nucleotides then base pair with the exposed, complementary bases on each single strand. DNA polymerase joins the nucleotides to form new polynucleotide chains. Finally, the two new DNA molecules each contain one original and one new strand, and the double helix reforms.
This document summarizes a lesson on DNA replication. It begins with introducing the topic and dividing students into groups to complete different activities related to DNA replication. It then reviews the key terms and defines the three main steps of DNA replication: unzipping, base pairing, and joining. The importance of DNA replication is explained as ensuring that all body cells carry the same genetic material and instructions are copied exactly for the next generation. Students are assessed through a quiz asking them to list the steps of DNA replication and complete DNA replication activities. They are assigned to study the next topics of DNA transcription and translation.
The document describes the central dogma of molecular biology:
DNA is transcribed into RNA, which is then translated into proteins. DNA contains the genetic code in nucleotides that make up genes. RNA polymerase transcribes DNA into messenger RNA (mRNA) in the nucleus. mRNA is then translated by ribosomes in the cytoplasm into proteins based on the RNA code using transfer RNA (tRNA) and amino acids. The process of protein synthesis involves transcription of DNA to mRNA and then translation of mRNA to proteins.
DNA replication is the process by which DNA makes a copy of itself during cell division. In molecular biology, DNA replication is the biological process of producing two identical replicas of DNA from one original DNA molecule. DNA replication occurs in all living organisms acting as the basis for biological inheritance.
Step 1: Replication Fork Formation. Before DNA can be replicated, the double stranded molecule must be โunzippedโ into two single strands. ...
Step 2: Primer Binding. The leading strand is the simplest to replicate. ...
Step 3: Elongation. ...
Step 4: Termination.
DNA replication begins at origins of replication where the double helix unwinds. DNA helicase unwinds and unzips the DNA strands. DNA polymerase III then reads the strands in a 3' to 5' direction and synthesizes new strands in a 5' to 3' direction, matching the base pairs. DNA polymerase I changes any RNA primers to DNA at Okazaki fragments. This process produces two identical copies of the original DNA.
The document explains how to use a codon table to translate mRNA sequences into amino acid sequences during protein synthesis. It details the process of transcription of DNA to mRNA, translation of mRNA in the ribosome using tRNA molecules, and how to use the codon table to determine which amino acid corresponds to an mRNA codon. The overall purpose is to explain how codons are used to determine the amino acid sequence of proteins from genetic information in DNA.
The document summarizes the central dogma of molecular biology: DNA is transcribed into RNA, which is then translated into protein. It describes the processes of DNA replication, transcription of DNA to mRNA, and translation of mRNA to proteins using tRNAs and ribosomes. Mutations are explained as changes to the DNA sequence that can alter protein production through frameshift or substitution errors. Recent research has found transcriptional exclusion of mutated alleles at the single-cell level.
The central dogma of molecular biology describes the flow of genetic information within biological systems. It states that DNA is transcribed into RNA, and RNA is translated into protein. While information flows from DNA to RNA to protein, it cannot flow in the reverse direction from protein back to nucleic acids. There are some exceptions, such as reverse transcription in retroviruses and RNA replication in certain viruses. The central dogma establishes the principle that genetic information can be converted between DNA and RNA.
DNA replication in eukaryotes proceeds in a coordinated process of initiation, elongation, and termination. Initiation begins at specific origin of replication sequences and involves the assembly of pre-replication complexes. During elongation, helicases unwind the DNA strands exposing templates for DNA polymerase enzymes to synthesize new daughter strands. Termination occurs when the polymerases reach the end regions called telomeres, which are then extended by the enzyme telomerase to allow replication to continue.
Ch 7 dna structure and function blank sp 2018C Ebeling
ย
This document provides an overview of DNA structure and gene function. It begins with learning objectives related to DNA, RNA, proteins, transcription, translation, and mutations. Key concepts covered include the central dogma, components of DNA, roles of DNA, RNA and proteins, transcription and its steps, mRNA processing, translation and its steps, the genetic code, and types of mutations. Diagrams illustrate these concepts and examples are given throughout.
Sadeeqsheshe the central dogma of molecular biologySadeeq Sheshe
ย
The document describes the central dogma of molecular biology, which states that DNA is replicated, then transcribed into RNA, and RNA is translated into protein. It provides details on DNA replication, transcription, and translation. DNA replication involves DNA polymerase copying DNA in the 5'-3' direction. Transcription involves RNA polymerase transcribing DNA into RNA. Translation occurs on ribosomes and involves mRNA being read in triplets to produce a polypeptide chain. The processes are generally conserved between prokaryotes and eukaryotes but have structural and mechanistic differences.
1. DNA replication is the process by which daughter DNA molecules are synthesized from a parental DNA template. It ensures the genetic information is transferred to the next generation with high fidelity.
2. Replication occurs semi-conservatively such that each new double helix contains one strand from the original parent DNA and one newly synthesized strand. It also occurs bidirectionally from an origin of replication.
3. DNA polymerases are the key enzymes that catalyze DNA synthesis. Other important enzymes and proteins include primase, helicase, topoisomerase, ligase, and single-stranded DNA binding proteins. Together they facilitate the initiation, elongation and termination of DNA replication.
The document outlines the three major stages of transcription and translation: 1) replication, where DNA is copied during cell division; 2) transcription, where part of a DNA strand is copied into mRNA; and 3) translation, where the mRNA is used by the ribosome to produce a polypeptide based on the mRNA codons. During translation, tRNAs bring amino acids to the ribosome which link them together based on the mRNA codons to form a protein.
DNA replication is the process where a DNA molecule makes an identical copy of itself. There are three proposed models of replication: conservative, dispersive, and semi-conservative. The widely accepted semi-conservative model involves unwinding the DNA double helix, attaching primers to each strand, and synthesizing new complementary strands in the 5' to 3' direction along each template strand. This results in two double-stranded DNA molecules each with one original strand and one new strand.
There are three main levels of control to ensure DNA replication is initiated only once per cell cycle in bacteria:
1. ATP hydrolysis by beta-clamp protein
2. Sequestration of hemimethylated DNA by SeqA protein
3. Titration of DnaA protein levels through its regulatory locus
In eukaryotes, licensing factors like ORC, Cdc6, Cdt1 and MCM proteins bind to origins of replication and license them for a single round of replication. After replication begins, these factors dissociate from origins preventing re-replication. Geminin protein also prevents re-licensing of newly synthesized DNA in G2 phase.
DNA polymerase proofreads
DNA replication occurs through a semiconservative process where each parental DNA strand serves as a template for the synthesis of a new complementary strand. This results in two daughter molecules each composed of one original parental strand and one newly synthesized strand. In eukaryotes, replication occurs during S phase of the cell cycle. The major enzymes involved are DNA polymerases, helicases, and ligases which unwind, copy, and join the strands respectively. Errors are corrected by proofreading and repair mechanisms to maintain genomic integrity.
The document describes the process of DNA replication. It explains that the enzyme helicase unzips the DNA double helix by splitting the hydrogen bonds between the bases. DNA polymerase then adds complementary bases to each strand, creating two identical copies. The leading strand adds bases continuously from 5' to 3'. The lagging strand adds bases in fragments from 3' to 5' using an RNA primer and DNA polymerase to join the fragments.
Tyler Young raised a medaka fish named Jeffery from an embryo. He observed and documented Jeffery's development over 9 days, from stage 2 to stage 36 when he hatched. Tyler provided daily care and changed Jeffery's water until he was ready to be released into a community tank with other fish. Though sad to see Jeffery go, Tyler knew it was better for him to swim freely with other medakas.
Joey is a chick being documented from its first day of development through hatching. Over the course of 8 days, the author records Joey progressing through various embryonic development stages from 29 hours old in stage 18 to finally hatching on day 8. Brief notes are made about Joey's heartbeat, growth, and current developmental stage each day.
DNA replication involves unwinding the DNA double helix using the enzyme helicase. On the leading strand, DNA polymerase III continuously adds nucleotides to form the leading strand. On the lagging strand, which is discontinuous, RNA primers are added by primase and DNA polymerase II builds Okazaki fragments by adding nucleotides between primers. The primers are later removed and replaced with DNA to form a continuous DNA strand.
Dexter narrates his experience hatching from an egg over the course of 7 days. He describes each developmental stage, including his organs becoming visible and his heartbeat increasing in rate. On the seventh day, he finally hatches from the egg and is able to freely swim in his petri dish. Dexter survived with just having his water changed daily. He acknowledges having a rough start but credits Shaylyn and Jenna for taking good care of him.
The document summarizes the early development of a Japanese Medaka egg named Jamaal over the course of 8 days from fertilization to hatching as observed by two biology students. It describes the physical changes and developmental stages Jamaal goes through each day, including the formation of organs and structures. By day 8, Jamaal has hatched from the egg and is released to swim with other fish, concluding his time under the care and observation of his student parents.
The document describes the process of protein synthesis, which has two main steps: transcription and translation. During transcription, RNA polymerase binds to DNA and builds an mRNA strand using the coding region as a template, before the mRNA strand exits the nucleus. Translation then occurs on ribosomes, where tRNAs bring amino acids to the mRNA start codon and assemble a protein based on the mRNA sequence until reaching the stop codon.
- The document is a journal written from the perspective of a fish egg describing its development from fertilization through hatching over 10 days in a classroom biology lab.
- The egg provides daily updates on its physical changes like developing organs and eyes and increasing heart rate as it grows, as well as its excitement to hatch.
- On day 10, the egg hatches and can swim, then learns it was part of a project that interested students in observing the growth of fish eggs.
The document describes the process of protein synthesis through transcription and translation. It shows RNA polymerase binding to DNA and transcribing mRNA using the DNA as a template. The mRNA then exits the nucleus through the nuclear pore and binds to a ribosome in the cytoplasm where translation occurs. Amino acids are joined together based on the mRNA codons to form a protein.
DNA replication occurs through a semi-conservative process where the parental double helix unwinds and each strand serves as a template to produce two new DNA molecules, each with one original and one new strand. Replication begins at multiple origins of replication and proceeds bidirectionally. Enzymes such as helicase unwind the DNA and single-strand binding proteins stabilize the separated strands. DNA polymerase adds complementary nucleotides to the 3' ends of the new strands which grow toward each other, producing daughter strands. The leading strand is continuous while the lagging strand is synthesized discontinuously in short Okazaki fragments later joined by DNA ligase.
Joey is a medaka fish egg that is observed and documented over 8 days as it develops and hatches. On the first day at stage 18, Joey is a small egg that has been alive for 26 hours. By day 2 at stage 23, Joey has a faint heartbeat visible under the microscope after 46 hours. On day 3 at stage 29, Joey's retinas and thick pectoral fins are clearly seen and its heart is visible in photos. Joey continues developing organs and features until hatching on day 8 at stage 36 as a free swimming fish.
Fish is a medaka egg that has begun its journey from Japan to America. Over the course of 10 days, Fish develops various features like an oil globule, eyes, a tail, and filaments. Fish's heart also begins beating at 128 beats per minute. On day 10, Fish finally hatches out of its egg. Fish hopes to one day return to Japan and encourage other fish to make the same journey.
This document summarizes the development of a medaka fish embryo named Nemo over the course of 12 days from its earliest stages as a single cell through hatching as a free-swimming fish. Some key events include the formation of eyes by day 2, increased growth and tail formation by day 5, resemblance to a reptile by day 6, and finally hatching from its egg on day 9 as a fully developed fish. The text describes Nemo's development stage-by-stage with labeled diagrams and notes on physical changes and behaviors.
The document describes an edible cell model created by students to represent the main structures of the cell. Various candies and icings were used to represent the cell wall, cell membrane, nucleus, mitochondria, chloroplast, Golgi body, smooth endoplasmic reticulum, rough endoplasmic reticulum, ribosomes, vacuoles, nuclear membrane, cytoplasm, lysosomes, cytoskeleton, nucleolus, and chromatin. A description is provided for each cellular component and what food item was used to model it.
DNA replication involves unwinding the DNA double helix by helicase to separate the strands. Polymerase III then adds complementary nucleotides to each free 3' end of the parental strands in the 5' to 3' direction to synthesize new daughter strands. The leading strand is synthesized continuously in the 5' to 3' direction, while the lagging strand is synthesized in short fragments that are later joined together.
DNA replication is the process where DNA copies itself for cell division. It involves unwinding the double helix, synthesizing a complementary strand for each, and resulting in two identical DNA molecules. The leading strand is replicated continuously while the lagging strand requires RNA primers and Okazaki fragments. Enzymes such as helicase, primase, DNA polymerase, and ligase facilitate the process to ensure accurate copying and transmission of genetic information to new cells.
DNA replication involves unwinding the DNA double helix using the enzyme helicase. On the leading strand, DNA polymerase III continuously adds nucleotides to form the leading strand. On the lagging strand, which is discontinuous, RNA primers are added by primase and DNA polymerase II builds Okazaki fragments by adding nucleotides between primers. The primers are later removed and replaced with DNA to form a continuous DNA strand.
Protein synthesis Horner Jacob (cooler than Michael Lin)punxsyscience
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This document summarizes the process of protein synthesis from transcription of DNA in the nucleus to translation of mRNA in the cytoplasm. It shows RNA polymerase transcribing DNA to form mRNA, which exits the nucleus through the nuclear pore. The mRNA then binds to a ribosome in the cytoplasm where translation occurs. The ribosome binds mRNA and tRNA to synthesize proteins by linking amino acids specified by mRNA codons. tRNA brings complementary bases to form codon-anticodon base pairs, leaving behind amino acids to form polypeptide chains that eventually fold into functional protein structures.
The document describes the process of protein synthesis. DNA in the nucleus is transcribed into mRNA by RNA polymerase. The mRNA strand exits the nucleus and binds to a ribosome in the cytoplasm. tRNA molecules matching the mRNA codons bring amino acids to the ribosome. The amino acids are linked together through peptide bonds to form a protein chain that eventually folds into a functional three-dimensional structure.
DNA replication involves unwinding the DNA double helix using the enzyme helicase. On the leading strand, DNA polymerase III continuously adds nucleotides to form the leading strand. On the lagging strand, which is discontinuous, RNA primers are added by primase and DNA polymerase II builds the strand through Okazaki fragments. DNA polymerase I then removes the RNA primers and fills in the remaining gaps.
DNA replication involves DNA helicase unwinding the DNA double helix. DNA polymerase then synthesizes a complementary strand to each original strand. On the leading strand DNA polymerase synthesizes continuously, while on the lagging strand it synthesizes in fragments called Okazaki fragments, which are later joined together. DNA polymerase needs an RNA primer to begin synthesizing each Okazaki fragment, which is later replaced with DNA by DNA polymerase 1. This process continues until the entire DNA double helix is replicated.
DNA replication involves unwinding the double helix, separating the strands, and using DNA polymerase to add complementary nucleotides to each strand. The leading strand is continuously synthesized from 5' to 3', while the lagging strand is synthesized in fragments called Okazaki fragments that are later joined by DNA ligase. DNA must replicate to produce new cells for growth and repair. Mutations can occur if the wrong nucleotide base pairs are formed during replication.
DNA replication is the process by which a single DNA helix is converted into two identical copies. It is described as semi-conservative replication. The helicase enzyme unwinds and splits the double-stranded DNA helix. Nucleotides are then added in the 5' to 3' direction to form new strands using DNA polymerase III. This results in two DNA molecules each with one original and one newly synthesized strand.
DNA replication is the process of copying a double-stranded DNA molecule in order to pass genetic material to daughter cells. It begins at an origin site where an enzyme called helicase unzips the DNA strands. DNA polymerase III then adds nucleotides that match the template strands, using A-T and G-C base pairing. Since it can only add to the 3' end, an RNA primer is needed for polymerase to begin nucleotide chains on the lagging strand, which is synthesized in Okazaki segments moving away from the replication fork.
DNA helicase begins unwinding the DNA molecule at an AT bond in the origin of replication. It splits the double bonds between the bases, leaving two single strands. The leading strand is then replicated continuously in the 5' to 3' direction. The lagging strand must be replicated in short fragments called Okazaki fragments because DNA polymerase can only add bases in the 5' to 3' direction. DNA primase temporarily makes the lagging strand 5' to 3' to allow replication of Okazaki fragments.
The document summarizes the process of DNA replication. It explains that DNA is made of two strands bound together by hydrogen bonds between complementary nucleotide base pairs (A-T, C-G). DNA helicase unwinds the double helix, RNA polymerase helps synthesize new strands, and DNA polymerase adds complementary nucleotides to each new strand by finding the matching bases. Okazaki fragments are produced on the lagging strand and later joined by DNA ligase. The process faithfully duplicates DNA so that each new cell produced through cell division contains a full set of genes.
The document describes the process of DNA replication. It involves unwinding of the DNA double helix by helicase, followed by DNA polymerase adding nucleotides to both strands in the 5' to 3' direction. RNA primers are required for lagging strand synthesis. DNA polymerase I replaces RNA with DNA and ligates Okazaki fragments. Once completed, two identical copies of the original DNA are produced.
DNA replication is the process where DNA copies itself for cell division. It involves unwinding the double helix, synthesizing a complementary strand for each, and then rewinding into two identical double helix DNA molecules. Several enzymes are involved including helicase, polymerase, primase, ligase, and telomerase. DNA replication must be highly accurate to maintain the integrity of genetic information as cells continue to divide.
The document outlines the process of DNA replication. It begins with helicase splitting the DNA double helix into single strands. RNA primase adds RNA primers to the lagging strand for DNA polymerase to begin DNA synthesis. DNA polymerase adds nucleotides to both strands in the 5' to 3' direction. Okazaki fragments are formed on the lagging strand and later joined by DNA ligase. The process continues until both strands have been replicated.
DNA replication is the process by which DNA copies itself. It involves unwinding the DNA double helix into single strands, using DNA polymerase to add complementary nucleotides to each strand to create two new double helices identical to the original. The leading strand is replicated continuously while the lagging strand is replicated in short sections that are later joined together. Enzymes such as DNA polymerase, DNA ligase, and topoisomerase precisely copy DNA to enable inheritance of genetic traits.
DNA replication is the process by which DNA copies itself during cell division. It occurs in three main stages: first, DNA helicase unwinds the double helix at the origin of replication; then, RNA primase constructs an RNA primer to mark the starting point for DNA polymerase to synthesize new strands of DNA by adding nucleotides; and finally, DNA ligase seals the DNA strands by forming phosphodiester bonds between nucleotides. DNA replication ensures each new cell formed during cell division contains an identical copy of the DNA code.
The document discusses the history and structure of DNA. Some key points include:
- DNA was identified as the genetic material through experiments by Griffith, Hershey and Chase.
- The structure of DNA was discovered in the 1950s by Watson and Crick using data from Rosalind Franklin. They identified DNA's double helix structure.
- DNA is made up of nucleotides containing phosphate, sugar (deoxyribose) and one of four nitrogenous bases (A, T, C, G). The bases bond together in a complementary, antiparallel fashion between strands.
1) The document reviews biological compounds including carbohydrates, lipids, proteins, and nucleic acids.
2) It describes the structures of proteins including primary, secondary, tertiary, and quaternary structure.
3) Nucleic acids are composed of nucleotides that are made up of phosphate groups, sugars (ribose or deoxyribose), and nitrogenous bases. DNA and RNA differ in their sugar and base components.
DNA replication is semi-conservative and involves many enzymes. It begins at a replication origin where the DNA unwinds. RNA primers are added and DNA polymerase adds nucleotides to the 3' end of the primers to synthesize new DNA strands. The leading strand is synthesized continuously while the lagging strand is synthesized in fragments that are later joined. Transcription and translation then convert gene information into proteins.
DNA replication involves unwinding the DNA double helix by helicase. This exposes the nucleotides which serve as templates for DNA polymerase to synthesize new strands that are complementary to the templates. DNA primase attaches RNA primers that DNA polymerase uses to initiate DNA synthesis in the 5' to 3' direction, while reading the template in the 3' to 5' direction. DNA ligase seals the fragments to form intact double-stranded DNA molecules.
DNA contains genetic instructions used by organisms. It is a double-stranded molecule that replicates through unwinding by helicase. The leading strand replicates continuously while the lagging strand replicates discontinuously in fragments called Okazaki fragments. DNA replication ensures genetic material is passed from parent to daughter cells.
DNA replication begins with DNA helicase unwinding the DNA double helix and breaking the hydrogen bonds between complementary DNA bases. Single-stranded binding proteins bind to the separated strands to prevent them from rewinding. DNA polymerase III then reads one strand of DNA in the 3' to 5' direction and synthesizes the new complementary strand in the 5' to 3' direction, pairing nucleotides based on base pairing rules. DNA primase adds short RNA primers to initiate synthesis of Okazaki fragments on the lagging strand.
It is a short and concise slide about DNA replication and Repair. It is prepared keeping in mind for Undergraduates level but PG also might find it handy.
The document discusses the history and process of DNA replication. It describes how DNA was determined to be the genetic material and the discovery of its double helix structure by Watson and Crick using Rosalind Franklin's X-ray diffraction images. DNA replication begins at origins of replication and proceeds bidirectionally. The leading strand is synthesized continuously while the lagging strand is synthesized discontinuously in short segments that are later joined by ligase. Each new DNA molecule contains one original parental strand and one newly synthesized strand.
DNA replication occurs semi-conservatively, with each parental strand serving as a template for synthesis of a new complementary strand. This results in two identical DNA molecules, each with one original parental strand and one newly synthesized strand. Replication is initiated at the origin of replication and proceeds bidirectionally around the circular bacterial chromosome. Enzymes such as helicase unwind the parental DNA, topoisomerases relieve supercoiling, and DNA polymerase adds complementary nucleotides using the parental strands as templates.
Gregor Mendel was an Austrian monk who is considered the father of genetics. He conducted experiments with pea plants in which he studied 7 different traits. Through his experiments, Mendel discovered the principles of heredity, including that traits are passed from parents to offspring through discrete units called genes, and that some genes are dominant while others are recessive. When Mendel crossed plants with different traits, he found that the offspring expressed the traits of only one parent, not a blend, and that recessive traits could reappear in later generations. This led Mendel to propose that genes segregate and assort independently during the formation of gametes.
The document describes the process of protein synthesis. It explains that RNA polymerase first breaks the hydrogen bonds of DNA to copy it and make an mRNA strand. The mRNA strand then leaves the nucleus through the nuclear pore into the cytoplasm. In the cytoplasm, the mRNA binds to a ribosome where tRNA reads its bases and adds complementary amino acids to form a polypeptide chain.
Transcription occurs in the cell nucleus where DNA is unzipped and RNA polymerase adds complementary RNA nucleotides to the DNA template strand, forming mRNA. The mRNA is processed - a cap and tail are added and introns are removed. The completed mRNA contains codons of three nucleotides that code for amino acids. Translation occurs in the cytoplasm where the mRNA binds to ribosomes and tRNA molecules with matching anticodons deliver amino acids specified by mRNA codons, assembling the polypeptide chain specified by the mRNA.
This flip book depicts the process of protein synthesis, showing how DNA is transcribed into mRNA, which is then translated by ribosomes into a polypeptide chain. The flip book steps through transcription, where RNA polymerase copies DNA into mRNA, then translation, where the mRNA passes through the ribosome and interacts with tRNA and rRNA to add amino acids in the correct order specified by codons until a full protein is synthesized.
This document is a flip book that summarizes the process of protein synthesis. It shows how DNA is transcribed into mRNA by RNA polymerase in the nucleus. The mRNA is then transported out of the nucleus through the nuclear pore and binds to the ribosome in the cytoplasm. The ribosome reads the mRNA codons and binds transfer RNA (tRNA) with complementary anticodons. The tRNA brings amino acids to form peptide bonds and a polypeptide chain, which eventually folds into a functional protein.
This flip book depicts the process of protein synthesis, showing how DNA is transcribed into mRNA, which is then translated by ribosomes into a polypeptide chain. The flip book steps through transcription, where RNA polymerase copies DNA into mRNA, then translation, where the mRNA passes through the ribosome and interacts with tRNA and rRNA to add amino acids in the correct order specified by codons until a full protein is synthesized.
The document describes the process of transcription and translation in a cell. RNA polymerase unwinds DNA and creates an mRNA strand in the nucleus. The mRNA strand then moves to the cytoplasm through the nuclear pore. In the cytoplasm, the mRNA strand binds to a ribosome where tRNA brings amino acids to add to a growing polypeptide chain based on the mRNA codons. The polypeptide chain then folds into the final 3D protein structure.
The document describes the process of protein synthesis, which occurs in two steps: transcription and translation. In transcription, DNA is unwound and an mRNA strand is created using nucleotides. In translation, the mRNA strand is sent to the cytoplasm where it binds to a ribosome. tRNA molecules then bind to the ribosome and add amino acids specified by the mRNA code, forming a peptide bond between amino acids and creating a protein chain.
The document describes the process of protein synthesis, which occurs in two steps: transcription and translation. In transcription, DNA is unwound and an mRNA strand is created using nucleotides. The mRNA strand is then released and the DNA strands rebind. In translation, the mRNA moves to the cytoplasm and binds to ribosomes. tRNA molecules bind to the ribosome according to the mRNA code, and each tRNA connects to a specific amino acid. Translation begins as tRNA molecules form base pairs with the mRNA, and peptide bonds form between the amino acids, creating a protein.
The document describes the process of protein synthesis, which occurs in two main steps - transcription and translation. Transcription takes place in the nucleus and involves RNA polymerase copying genetic information from DNA to mRNA. Translation occurs in the cytoplasm at ribosomes, where the mRNA code is used to assemble amino acids in the correct order to produce a protein. The start codon on mRNA pairs with a complementary tRNA to initiate translation.
DNA replication begins at the origin of replication where DNA helicase unwinds and unzips the double helix. DNA polymerase reads the bases on one strand and adds complementary bases to the other strand. The leading strand is replicated continuously while the lagging strand is replicated discontinuously in fragments called Okazaki fragments. DNA primase adds primers to fill in the lagging strand, and DNA ligase seals the fragments together with phosphodiester bonds.
This protein synthesis flip book illustrates the process of transcription and translation. It shows DNA being transcribed into mRNA by RNA polymerase in the nucleus. The mRNA is then transported to the cytoplasm where it passes through ribosomes. During this process, transfer RNA (tRNA) molecules match to the mRNA codons and add amino acids to form a polypeptide chain through peptide bonds. Eventually a full protein is synthesized from the mRNA instructions.
The document outlines the process of protein synthesis which has two main parts - transcription and translation. In transcription, mRNA strands are created in the nucleus from a DNA template with the help of RNA polymerase. The mRNA then exits the nucleus through nuclear pores. In translation, which occurs in the cytoplasm, ribosomes read the mRNA to produce a protein. Transfer RNA molecules match their anticodons to mRNA codons and bring corresponding amino acids. The amino acids are linked together by peptide bonds to form a polypeptide chain, which becomes a protein when translation is complete.
Protein synthesis flipbook @yoloswagginator24punxsyscience
ย
The document summarizes the process of protein synthesis. It describes how RNA polymerase unwinds DNA and copies it to mRNA. The mRNA strand then exits the nucleus through the nuclear pore and moves to ribosomes. At the ribosomes, the mRNA is read and translated to form a polypeptide chain of amino acids.
The document outlines the process of protein synthesis which has two main parts - transcription and translation. In transcription, mRNA strands are created in the nucleus from a DNA template with the help of RNA polymerase. The mRNA then exits the nucleus through nuclear pores. In translation, which occurs in the cytoplasm, ribosomes read the mRNA to produce a protein. Transfer RNA molecules match their anticodons to mRNA codons and bring corresponding amino acids. The amino acids are linked together by peptide bonds to form a polypeptide chain, which becomes a protein when translation is complete.
The document shows the process of protein synthesis:
1) In the nucleus, RNA polymerase unzips DNA and copies its sequence into a messenger RNA (mRNA) strand.
2) The mRNA exits the nucleus through the nuclear pore and enters the cytoplasm.
3) In the cytoplasm, the mRNA binds to a ribosome which reads its sequence in groups of three bases (codons).
4) Transfer RNA (tRNA) molecules matching these codons bring specific amino acids to the ribosome.
5) The amino acids are linked together to form a polypeptide chain, which later folds into a functional protein.
The document is a flip book that summarizes the key steps of protein synthesis: 1) DNA is unwound in the cell nucleus and an mRNA strand is produced, 2) the mRNA strand moves from the nucleus to the cytoplasm where ribosomes are located, 3) ribosomes read the mRNA strand and amino acids are attached through peptide bonds to form a protein, which then folds into its tertiary structure.
The document summarizes the process of protein synthesis. DNA in the nucleus is transcribed into mRNA by RNA polymerase. The mRNA then exits the nucleus and binds to a ribosome in the cytoplasm. The ribosome reads the mRNA and uses transfer RNA molecules to add amino acids to form a protein chain. The protein folds into its final shape.
The document discusses protein synthesis in cells. It explains that RNA polymerase in the cell nucleus reads DNA and synthesizes mRNA. The mRNA then exits the nucleus through nuclear pores and binds to ribosomes. At the ribosomes, tRNA matches codons on the mRNA and releases amino acids, forming peptide bonds between amino acids to create a polypeptide chain. When the ribosome reaches a stop codon, the polypeptide releases and folds into its tertiary structure to become a functional protein.
The process of transcription begins in the cell nucleus, where RNA polymerase breaks apart DNA and uses it as a template to create mRNA strands. During this process, thymine is replaced with uracil to form RNA. The mRNA strand then exits the nucleus through a nuclear pore. Translation occurs in the cytoplasm, where the mRNA is read by ribosomes in groups of three codons. Transfer RNA molecules bring amino acids to the ribosome based on codon-anticodon base pairing. As the ribosome moves along the mRNA, the growing polypeptide chain is released once a stop codon is reached.
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A business may deal with both sales and purchases occasionally. They buy things from vendors and then sell them to their customers. Such dealings can be confusing at times. Because multiple clients may inquire about the same product at the same time, after purchasing those products, customers must be assigned to them. Odoo has a tool called Reception Report that can be used to complete this assignment. By enabling this, a reception report comes automatically after confirming a receipt, from which we can assign products to orders.
Level 3 NCEA - NZ: A Nation In the Making 1872 - 1900 SML.pptHenry Hollis
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The History of NZ 1870-1900.
Making of a Nation.
From the NZ Wars to Liberals,
Richard Seddon, George Grey,
Social Laboratory, New Zealand,
Confiscations, Kotahitanga, Kingitanga, Parliament, Suffrage, Repudiation, Economic Change, Agriculture, Gold Mining, Timber, Flax, Sheep, Dairying,
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Whether you're new to SEO or looking to refine your existing strategies, this webinar will provide you with actionable insights and practical tips to elevate your nonprofit's online presence.
This presentation was provided by Racquel Jemison, Ph.D., Christina MacLaughlin, Ph.D., and Paulomi Majumder. Ph.D., all of the American Chemical Society, for the second session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session Two: 'Expanding Pathways to Publishing Careers,' was held June 13, 2024.
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This document provides an overview of wound healing, its functions, stages, mechanisms, factors affecting it, and complications.
A wound is a break in the integrity of the skin or tissues, which may be associated with disruption of the structure and function.
Healing is the bodyโs response to injury in an attempt to restore normal structure and functions.
Healing can occur in two ways: Regeneration and Repair
There are 4 phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. This document also describes the mechanism of wound healing. Factors that affect healing include infection, uncontrolled diabetes, poor nutrition, age, anemia, the presence of foreign bodies, etc.
Complications of wound healing like infection, hyperpigmentation of scar, contractures, and keloid formation.
How Barcodes Can Be Leveraged Within Odoo 17Celine George
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THE SACRIFICE HOW PRO-PALESTINE PROTESTS STUDENTS ARE SACRIFICING TO CHANGE T...indexPub
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The recent surge in pro-Palestine student activism has prompted significant responses from universities, ranging from negotiations and divestment commitments to increased transparency about investments in companies supporting the war on Gaza. This activism has led to the cessation of student encampments but also highlighted the substantial sacrifices made by students, including academic disruptions and personal risks. The primary drivers of these protests are poor university administration, lack of transparency, and inadequate communication between officials and students. This study examines the profound emotional, psychological, and professional impacts on students engaged in pro-Palestine protests, focusing on Generation Z's (Gen-Z) activism dynamics. This paper explores the significant sacrifices made by these students and even the professors supporting the pro-Palestine movement, with a focus on recent global movements. Through an in-depth analysis of printed and electronic media, the study examines the impacts of these sacrifices on the academic and personal lives of those involved. The paper highlights examples from various universities, demonstrating student activism's long-term and short-term effects, including disciplinary actions, social backlash, and career implications. The researchers also explore the broader implications of student sacrifices. The findings reveal that these sacrifices are driven by a profound commitment to justice and human rights, and are influenced by the increasing availability of information, peer interactions, and personal convictions. The study also discusses the broader implications of this activism, comparing it to historical precedents and assessing its potential to influence policy and public opinion. The emotional and psychological toll on student activists is significant, but their sense of purpose and community support mitigates some of these challenges. However, the researchers call for acknowledging the broader Impact of these sacrifices on the future global movement of FreePalestine.
2. DNA Replication occurs before a cell
splits apart. The replication process
takes place during mitosis. To be more
specific, it takes place in a step of
mitosis called interphase. Interphase
has different steps also. DNA
replication takes place during the S
phase of interphase.
3. DNA replication is a process that is
very essential in every cell. If DNA
replication did not occur, cells
wouldnโt function properly. DNA
replication occurs so that when cells
divide, the new cells have the same
DNA as the cell they were made
from.
4. As you know, DNA is made up of two
strands. During DNA replication, an
enzyme called DNA helicase
โunzipsโ these two strands. These
two strands have different names,
which are the lagging and leading
strand.
5. The leading strand is synthesized
continuously in the 5 prime to 3
prime direction, while the lagging
strand is synthesized discontinuously
in the 5 prime to 3 prime direction.
6. DNA polymerase III adds nucleotides
to the end of a growing DNA strand.
DNA primase is an enzyme that
marks a starting point on the lagging
strand. DNA polymerase I removes
the starting point from the lagging
strand and replaces it with DNA.
7. DNA ligase joins Okazaki fragments,
which are short, newly synthesized
DNA fragments that are formed on
the lagging strand. DNA ligase also
seals repairs, and seals
recombination fragments. That is
how DNA replication occurs.
8. So you can get a better
understanding, the following slides
will demonstrate the entire DNA
replication process.
25. DNAA
5โ
T
Polymerase
III C
C
T
A
T
RNA Primer 3
A
G
DNA polymerase III is able to add
nucleotides continuously to the leading
strand of DNA. Meanwhile, the lagging
strand goes through many different
steps to add the nucleotides.
C
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G
A
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RNA
G
RNA Primer
Primase
C
Leading
Strand
Lagging
Strand
A
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C
3โ
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5
32. T
T
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This enzyme
converts the
RNA into DNA
and
synthesizes
the lagging
strand in the
5โ to 3โ
direction.
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RNA Primer
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A
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5โ
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33. T
T
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This enzyme
converts the
RNA into DNA
and
synthesizes
the lagging
strand in the
5โ to 3โ
direction.
G
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DNA
G
Polymerase
A
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RNA Primer
T
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A
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DNA T
Polymerase
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RNAI Primer
C
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36. T
T
3โ
A
C
5โ
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RNA Primer
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DNA
G
3โ Polymerase
3โ
RNA Primer
C
A
This enzyme converts
the RNA into DNA and
synthesizes the
lagging strand in the
5โ to 3โ direction.
5โ
C
T
G
C
5
39. 5โ
A
T
T
G
C
5โ
DNA
polymerase
I has
synthesized
as far as it
could. Now
itโs time for
the next
enzyme
RNA I T
Primer
A
G
T
C
G
C
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A
A
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3โ
3
A
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3โ
G
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DNA
C
3โ
RNA Primer
C
A
5โ
C
5
40. 5โ
A
T
T
G
C
5โ
DNA
polymerase
I has
synthesized
as far as it
could. Now
itโs time for
the next
enzyme
G
T
C
G
C
G
T
A
A
T
G
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A
A
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C
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3โ
3
A
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3โ
RNA I T
Primer
A
G
G
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DNA
C
3โ
RNA Primer
C
A
5โ
C
5
54. T
T
3โ Now, the 5โ
next
A
C
5โ
A
G
C
G
T
T
A
C
G
C
enzyme,
which we
had
already
seen
beforeโฆ
A
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A
A
T
A
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G
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G
G
C
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A
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3โ
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3โ
RNA Primer
C
A
5โ
C
3
77. T
T
A
C
5โ
A
G
C
G
5โ
And then itโs
leaves again
after
finishing its
job..
T
T
3โ
A
A
C
G
C
G
T
A
T
T
A
T
A
C
G
C
G
C
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A
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C
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A
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3โ
A
G
C
G
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C
3
Meanwhileโฆ
G
T
5โ
3โ
DNA
Polymer
C
A
I
G
RNA Primer 5
C
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93. A
T
T
A
C
G
3โ The DNA 5โ
T
ligase has yet
one last bond
to form!
T
A
C
G
G
C
G
T
A
T
A
A
T
A
T
C
G
C
G
G
C
G
C
T
A
T
A
G
C
G
C
A
T
A
T
C
5โ
A
G
C
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C
C
3โ
5โ
3โ
G
G
DNA
Ligase
C
3
5
100. T
T
A
C
5โ
A
G
C
G
3โ
5โ
Now we are
left with two
identical
strands of DNA.
A
T
T
A
C
G
C
G
T
T
A
A
T
A
T
C
G
C
G
G
C
G
C
T
A
T
A
G
C
G
C
A
T
A
T
C
3โ
A
G
C
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C
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3
5โ
3โ
5
101. Keep in mind that the
DNA molecules are in a
twisted shape.
108. They become permanent mutations
after the next cell division. This is
because once these mistakes have
been established, the cell no longer
recognizes them as errors.
109. Special Vocabulary:
โข Telomeres- Telomeres are structures found at the end
of chromosomes.
โข Okazaki fragments- Okazaki fragments are short,
newly formed DNA segments.
โข DNA ligase- DNA ligase forms a phosphodiester bond,
joining the Okazaki fragments into a
continuous strand of DNA.
110. Special Vocabulary:
โข Telomerase- Telomerase is an enzyme that is
especially found in cancer cells. This
enzyme adds nucleotides to telomeres.
โข Cancer- Cancer is a disorder when some of the bodyโs
cells lose the ability to control growth.
โข Transplanted cells- Transplanted cells are injected
into your body to replace
damaged or diseased cells.
111. Special Vocabulary:
โข Cloning- Cloning is making genetically identical cells
that were produced from a single cell.
โข Aging- Aging is the process of growing older.