This includes detailed description of the Cell Cycle and Cell Cycle regulation. Courtesy: Campbell Biology Book, And Dr, Rosemary Redfield Lectures, University of British Columbia.
The document summarizes Mendel's laws of inheritance based on his experiments with pea plants. It discusses Mendel's discovery of the laws of dominance, segregation, and independent assortment through monohybrid and dihybrid crosses. The law of dominance states that one trait will mask the other in hybrid offspring. The law of segregation explains that alleles separate during gamete formation so each gamete contains one allele. The law of independent assortment says that allele pairs assort independently, resulting in multiple allele combinations in offspring. Mendel's laws explained inheritance of traits for the first time.
1. Chromosomes contain DNA and package it into a smaller size. In eukaryotes, DNA is contained in linear chromosomes while prokaryotes have circular chromosomes.
2. Humans have 23 chromosome pairs including one sex chromosome pair that determines gender. Genes are located on chromosomes and can exist in different alleles that determine traits.
3. The genotype is an individual's combination of alleles, which determines their phenotype or physical traits. Dominant alleles will be expressed over recessive alleles. Many factors can influence the relationship between genotype and phenotype.
Replication is the process by which DNA duplicates itself for transmission to daughter cells. It ensures exact transmission of genetic information from one cell generation to the next. Replication involves semi-conservative synthesis of new DNA strands based on existing DNA templates. It requires specific enzymes and occurs through initiation, elongation, and termination steps. Initiation begins at an origin of replication and results in unwinding and denaturation of the DNA helix. Elongation then extends the new strands bidirectionally until replication forks from adjacent origins meet and terminate the process.
The document summarizes key aspects of the cell cycle and cell division. It discusses the phases of the cell cycle including interphase and mitosis. It describes chromosome structure and duplication. It explains the process of mitosis and cytokinesis. It also discusses regulation of the cell cycle through checkpoints at the G1/S and G2/M transitions to ensure DNA integrity before cell division.
It is the presentation on the MEIOSIS phase of the Cell division.
It includes all the details and definitions that are related to the topic of meiosis with the labelled diagrams.
If you have any query or a question, you may ask in the comment box.
thanks.
Mitosis is the process of nuclear division in eukaryotic cells. It is divided into four main stages: prophase, metaphase, anaphase and telophase. During prophase, the nuclear envelope and nucleolus disappear. In metaphase, chromosomes align along the metaphase plate. In anaphase, chromatids separate and move towards opposite poles. Finally, in telophase, nuclear envelopes form around the separated chromosomes and cytokinesis occurs to divide the cytoplasm. Mitosis plays an important role in growth, development, and repair of multicellular organisms.
This document discusses types of chromosomes and karyotypes. There are four basic types of chromosomes: telocentric, acrocentric, sub-metacentric, and metacentric. A karyotype is a pictorial arrangement of chromosomes according to their size and shape. It involves preparing photographs of chromosomes during cell division and arranging them in order. Karyotypes can be used to detect chromosomal abnormalities and determine genetic risks.
The document summarizes Mendel's laws of inheritance based on his experiments with pea plants. It discusses Mendel's discovery of the laws of dominance, segregation, and independent assortment through monohybrid and dihybrid crosses. The law of dominance states that one trait will mask the other in hybrid offspring. The law of segregation explains that alleles separate during gamete formation so each gamete contains one allele. The law of independent assortment says that allele pairs assort independently, resulting in multiple allele combinations in offspring. Mendel's laws explained inheritance of traits for the first time.
1. Chromosomes contain DNA and package it into a smaller size. In eukaryotes, DNA is contained in linear chromosomes while prokaryotes have circular chromosomes.
2. Humans have 23 chromosome pairs including one sex chromosome pair that determines gender. Genes are located on chromosomes and can exist in different alleles that determine traits.
3. The genotype is an individual's combination of alleles, which determines their phenotype or physical traits. Dominant alleles will be expressed over recessive alleles. Many factors can influence the relationship between genotype and phenotype.
Replication is the process by which DNA duplicates itself for transmission to daughter cells. It ensures exact transmission of genetic information from one cell generation to the next. Replication involves semi-conservative synthesis of new DNA strands based on existing DNA templates. It requires specific enzymes and occurs through initiation, elongation, and termination steps. Initiation begins at an origin of replication and results in unwinding and denaturation of the DNA helix. Elongation then extends the new strands bidirectionally until replication forks from adjacent origins meet and terminate the process.
The document summarizes key aspects of the cell cycle and cell division. It discusses the phases of the cell cycle including interphase and mitosis. It describes chromosome structure and duplication. It explains the process of mitosis and cytokinesis. It also discusses regulation of the cell cycle through checkpoints at the G1/S and G2/M transitions to ensure DNA integrity before cell division.
It is the presentation on the MEIOSIS phase of the Cell division.
It includes all the details and definitions that are related to the topic of meiosis with the labelled diagrams.
If you have any query or a question, you may ask in the comment box.
thanks.
Mitosis is the process of nuclear division in eukaryotic cells. It is divided into four main stages: prophase, metaphase, anaphase and telophase. During prophase, the nuclear envelope and nucleolus disappear. In metaphase, chromosomes align along the metaphase plate. In anaphase, chromatids separate and move towards opposite poles. Finally, in telophase, nuclear envelopes form around the separated chromosomes and cytokinesis occurs to divide the cytoplasm. Mitosis plays an important role in growth, development, and repair of multicellular organisms.
This document discusses types of chromosomes and karyotypes. There are four basic types of chromosomes: telocentric, acrocentric, sub-metacentric, and metacentric. A karyotype is a pictorial arrangement of chromosomes according to their size and shape. It involves preparing photographs of chromosomes during cell division and arranging them in order. Karyotypes can be used to detect chromosomal abnormalities and determine genetic risks.
DNA sequencing is the process of determining the order of nucleotides in DNA. There are several methods of DNA sequencing including conventional, cycle sequencing, automated sequencing, and pyrosequencing. Conventional methods include chemical degradation and chain termination. Chemical degradation uses base-specific chemical reactions to cleave DNA fragments for sequencing. Chain termination uses DNA polymerase and dideoxynucleotides to terminate DNA strand extension for sequencing. Cycle sequencing applies the chain termination method to PCR for linear amplification of sequencing products. Automated sequencing uses fluorescence labeling for high-throughput sequencing. Pyrosequencing sequences DNA by detecting pyrophosphate release during polymerase nucleotide incorporation without electrophoresis.
1) Mendel conducted breeding experiments with pea plants over 10 years to study inheritance of traits from parents to offspring.
2) He found that some traits are dominant and others recessive, with dominant traits masking recessive traits in the first filial generation.
3) Mendel also discovered that traits are inherited independently according to his Law of Independent Assortment.
This document provides information on the structure of DNA. It describes that DNA is found in the nucleus of eukaryotic cells and in mitochondria and chloroplasts. DNA is made up of genes located on chromosomes, which are made of DNA and proteins. The structure of DNA is a double helix with nitrogen bases sticking out from the sides and pairing with each other through hydrogen bonds between adenine and thymine and guanine and cytosine. The sides of the ladder-like structure are made up of alternating sugar and phosphate groups.
Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.
General and molecular genetics.
cDNA Library ,Introduction,Discovery of cDNA library,Preparation ,construction,Enzymes used in cDNA library,uses ,advantages and disadvantages of cDNA library.
This document summarizes the process of meiosis. It begins by defining meiosis as the type of cell division that occurs in sex cells and results in four daughter cells each with half the number of chromosomes as the parent cell. It then describes the two divisions of meiosis - meiosis I and meiosis II. The rest of the document delves into the specific stages of meiosis I (prophase I, metaphase I, anaphase I, telophase I) and meiosis II. It also explains how genetic recombination occurs through crossing over in prophase I. Finally, it provides overviews of spermatogenesis and oogenesis, the processes by which sperm and eggs are formed through meiosis in
The document provides an overview of meiosis cell division. It defines meiosis as a type of cell division that produces gametes with half the normal number of chromosomes. Meiosis occurs in two stages, Meiosis I and Meiosis II, and has four phases - prophase, metaphase, anaphase and telophase. In meiosis I, homologous chromosomes pair and may exchange genetic material through crossing over, resulting in genetic variation. This reduces the chromosome number from diploid to haploid. Meiosis II then divides the haploid cells into four haploid daughter cells.
DNA can be damaged by physical, chemical, and environmental agents through various types of alterations including single or double base changes, breaks in the DNA chain, or cross-linkages between bases. The cell has multiple DNA repair mechanisms to correct damage including base excision repair, nucleotide excision repair, mismatch repair, and double-strand break repair. Base excision repair removes single damaged bases while nucleotide excision repair removes larger segments of damaged DNA. Mismatch repair corrects errors that occur during DNA replication. Double-strand break repair repairs more severe breaks in both strands of the DNA that can lead to chromosomal abnormalities. Defects in DNA repair pathways can result in increased cancer risks.
The document summarizes the structure and development of dicot and monocot embryos. It states that in dicots, the embryo typically has two cotyledons, an embryonic shoot apex (plumule), and an embryonic root apex (radicle). It describes the asymmetrical cell divisions that form a proembryo and later a globular proembryo in dicots. In monocots, the embryo has a single large cotyledon called a scutellum with lateral plumule and radicle protected by coleoptile and coleorhiza. It notes the first oblique cell division in monocots also forms a proembryo that develops organs through further cell divisions
This document describes the structure and development of the anther and pollen grain. It contains the following key points:
1. The anther has four microsporangia surrounded by four layers - epidermis, endothecium, middle layers, and tapetum. The tapetum nourishes developing pollen grains.
2. Microsporogenesis occurs as microspore mother cells in the sporogenous tissue undergo meiosis to form microspore tetrads.
3. Mature pollen grains contain a vegetative cell and generative cell. The generative cell can divide to form two sperm cells ready for fertilization.
The document summarizes DNA replication through three key points:
1. DNA replication is semi-conservative, where each parent strand serves as a template for a new complementary strand, resulting in two new double helices that are each half original and half new DNA.
2. Replication occurs through the unwinding of the DNA double helix by helicase, with the parent strands acting as templates for DNA polymerase to add complementary nucleotides to each new strand.
3. The lagging strand is synthesized discontinuously in short segments called Okazaki fragments that are later joined together, while the leading strand is synthesized continuously in the 5’ to 3’ direction as the replication fork progresses.
The document discusses different forms of DNA structure that can be adopted based on environmental conditions. The main forms discussed are B-DNA, A-DNA, Z-DNA, C-DNA, D-DNA and E-DNA. B-DNA is the most common form, having a right-handed double helix structure with 10 base pairs per turn. A-DNA and Z-DNA are also double helical but have different structural characteristics than B-DNA such as base pair spacing and groove size. The various forms arise in response to changes in humidity, ionic conditions and DNA sequence composition.
The document discusses regulation of the cell cycle. It explains that the cell cycle is regulated through checkpoints and cyclin-dependent protein kinases (Cdks) and cyclins. There are three main checkpoints - at the ends of G1 and G2 phases, and during metaphase. These checkpoints ensure DNA integrity and replication, and proper chromosome attachment before progression to the next phase. Cdks drive progression when activated by binding with cyclins, which are synthesized and degraded throughout the cycle in response to cellular signals.
The lecture describes the mechanism of Photoperiodism and Vernalization in in-depth details w.r.t Arabidopsis thaliana. Queries are always welcome.... Dr. Nitin Wahi (wahink@gmail.com).
DNA contains the instructions for development, life, and reproduction. It is a double-stranded helix made of nucleotides. Each nucleotide contains a phosphate, sugar (deoxyribose in DNA), and one of four nitrogenous bases: adenine, cytosine, guanine, or thymine. The strands are held together by hydrogen bonds between complementary base pairs, with adenine bonding to thymine and cytosine bonding to guanine. DNA stores genetic information, directs protein synthesis, determines genetic coding, and is responsible for heredity and cell functions.
The nuclear pore complex regulates the passage of molecules between the nucleus and cytoplasm. It is comprised of several subunits that form a channel with a central pore. Surrounding the pore is a nonmembranous annulus with spoke-like structures. The pore wall contains columnar and lumenal subunits anchored by transmembrane proteins. Tiny fibrils extend from both sides in basket-like configurations, with different protein compositions on each side. Nuclear pores allow entry and exit of proteins and molecules to perform functions inside and outside the nucleus.
1) Griffith discovered a "transforming principle" that allowed non-virulent bacteria to become virulent after exposure to heat-killed virulent bacteria.
2) Avery, MacLeod, and McCarty determined that the transforming principle was DNA through experiments treating components with DNAses, RNAses, and proteases.
3) Hershey and Chase provided definitive evidence that DNA is the genetic material through experiments using bacteriophages containing radioactive DNA or protein to infect bacteria, showing that only DNA was transferred.
DNA repair is a collection of processes cells use to identify and correct damage to DNA. Failure to repair damaged DNA leads to mutations, which are permanent changes in the DNA sequence. There are several types of DNA damage including mismatches, modified DNA bases, and single or double strand breaks. Cells use multiple repair pathways like direct reversal, base excision repair, nucleotide excision repair, recombination repair, and translesion DNA synthesis to fix different types of DNA damage. Homologous recombination repairs double strand breaks by exchanging DNA between similar molecules, while site-specific and transposon recombination involve movement of DNA between defined sequences.
Cell division is the process by which a parent cell divides into two or more daughter cells. There are two main types of cell division: mitosis and meiosis. Mitosis produces two identical daughter cells during growth and repair of the body. It ensures the genetic makeup remains the same. Meiosis produces gametes with half the number of chromosomes and involves two cell divisions. It results in genetic diversity that is important for sexual reproduction.
The cell cycle consists of interphase and the mitosis phase. Interphase includes G1, S, and G2 phases where the cell grows and duplicates its DNA. Mitosis is divided into prophase, metaphase, anaphase, and telophase where the chromosomes and cell contents are separated into two daughter cells. Meiosis includes two cell divisions to produce four haploid cells from one diploid cell. Meiosis I separates homologous chromosomes and meiosis II separates sister chromatids.
DNA sequencing is the process of determining the order of nucleotides in DNA. There are several methods of DNA sequencing including conventional, cycle sequencing, automated sequencing, and pyrosequencing. Conventional methods include chemical degradation and chain termination. Chemical degradation uses base-specific chemical reactions to cleave DNA fragments for sequencing. Chain termination uses DNA polymerase and dideoxynucleotides to terminate DNA strand extension for sequencing. Cycle sequencing applies the chain termination method to PCR for linear amplification of sequencing products. Automated sequencing uses fluorescence labeling for high-throughput sequencing. Pyrosequencing sequences DNA by detecting pyrophosphate release during polymerase nucleotide incorporation without electrophoresis.
1) Mendel conducted breeding experiments with pea plants over 10 years to study inheritance of traits from parents to offspring.
2) He found that some traits are dominant and others recessive, with dominant traits masking recessive traits in the first filial generation.
3) Mendel also discovered that traits are inherited independently according to his Law of Independent Assortment.
This document provides information on the structure of DNA. It describes that DNA is found in the nucleus of eukaryotic cells and in mitochondria and chloroplasts. DNA is made up of genes located on chromosomes, which are made of DNA and proteins. The structure of DNA is a double helix with nitrogen bases sticking out from the sides and pairing with each other through hydrogen bonds between adenine and thymine and guanine and cytosine. The sides of the ladder-like structure are made up of alternating sugar and phosphate groups.
Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.
General and molecular genetics.
cDNA Library ,Introduction,Discovery of cDNA library,Preparation ,construction,Enzymes used in cDNA library,uses ,advantages and disadvantages of cDNA library.
This document summarizes the process of meiosis. It begins by defining meiosis as the type of cell division that occurs in sex cells and results in four daughter cells each with half the number of chromosomes as the parent cell. It then describes the two divisions of meiosis - meiosis I and meiosis II. The rest of the document delves into the specific stages of meiosis I (prophase I, metaphase I, anaphase I, telophase I) and meiosis II. It also explains how genetic recombination occurs through crossing over in prophase I. Finally, it provides overviews of spermatogenesis and oogenesis, the processes by which sperm and eggs are formed through meiosis in
The document provides an overview of meiosis cell division. It defines meiosis as a type of cell division that produces gametes with half the normal number of chromosomes. Meiosis occurs in two stages, Meiosis I and Meiosis II, and has four phases - prophase, metaphase, anaphase and telophase. In meiosis I, homologous chromosomes pair and may exchange genetic material through crossing over, resulting in genetic variation. This reduces the chromosome number from diploid to haploid. Meiosis II then divides the haploid cells into four haploid daughter cells.
DNA can be damaged by physical, chemical, and environmental agents through various types of alterations including single or double base changes, breaks in the DNA chain, or cross-linkages between bases. The cell has multiple DNA repair mechanisms to correct damage including base excision repair, nucleotide excision repair, mismatch repair, and double-strand break repair. Base excision repair removes single damaged bases while nucleotide excision repair removes larger segments of damaged DNA. Mismatch repair corrects errors that occur during DNA replication. Double-strand break repair repairs more severe breaks in both strands of the DNA that can lead to chromosomal abnormalities. Defects in DNA repair pathways can result in increased cancer risks.
The document summarizes the structure and development of dicot and monocot embryos. It states that in dicots, the embryo typically has two cotyledons, an embryonic shoot apex (plumule), and an embryonic root apex (radicle). It describes the asymmetrical cell divisions that form a proembryo and later a globular proembryo in dicots. In monocots, the embryo has a single large cotyledon called a scutellum with lateral plumule and radicle protected by coleoptile and coleorhiza. It notes the first oblique cell division in monocots also forms a proembryo that develops organs through further cell divisions
This document describes the structure and development of the anther and pollen grain. It contains the following key points:
1. The anther has four microsporangia surrounded by four layers - epidermis, endothecium, middle layers, and tapetum. The tapetum nourishes developing pollen grains.
2. Microsporogenesis occurs as microspore mother cells in the sporogenous tissue undergo meiosis to form microspore tetrads.
3. Mature pollen grains contain a vegetative cell and generative cell. The generative cell can divide to form two sperm cells ready for fertilization.
The document summarizes DNA replication through three key points:
1. DNA replication is semi-conservative, where each parent strand serves as a template for a new complementary strand, resulting in two new double helices that are each half original and half new DNA.
2. Replication occurs through the unwinding of the DNA double helix by helicase, with the parent strands acting as templates for DNA polymerase to add complementary nucleotides to each new strand.
3. The lagging strand is synthesized discontinuously in short segments called Okazaki fragments that are later joined together, while the leading strand is synthesized continuously in the 5’ to 3’ direction as the replication fork progresses.
The document discusses different forms of DNA structure that can be adopted based on environmental conditions. The main forms discussed are B-DNA, A-DNA, Z-DNA, C-DNA, D-DNA and E-DNA. B-DNA is the most common form, having a right-handed double helix structure with 10 base pairs per turn. A-DNA and Z-DNA are also double helical but have different structural characteristics than B-DNA such as base pair spacing and groove size. The various forms arise in response to changes in humidity, ionic conditions and DNA sequence composition.
The document discusses regulation of the cell cycle. It explains that the cell cycle is regulated through checkpoints and cyclin-dependent protein kinases (Cdks) and cyclins. There are three main checkpoints - at the ends of G1 and G2 phases, and during metaphase. These checkpoints ensure DNA integrity and replication, and proper chromosome attachment before progression to the next phase. Cdks drive progression when activated by binding with cyclins, which are synthesized and degraded throughout the cycle in response to cellular signals.
The lecture describes the mechanism of Photoperiodism and Vernalization in in-depth details w.r.t Arabidopsis thaliana. Queries are always welcome.... Dr. Nitin Wahi (wahink@gmail.com).
DNA contains the instructions for development, life, and reproduction. It is a double-stranded helix made of nucleotides. Each nucleotide contains a phosphate, sugar (deoxyribose in DNA), and one of four nitrogenous bases: adenine, cytosine, guanine, or thymine. The strands are held together by hydrogen bonds between complementary base pairs, with adenine bonding to thymine and cytosine bonding to guanine. DNA stores genetic information, directs protein synthesis, determines genetic coding, and is responsible for heredity and cell functions.
The nuclear pore complex regulates the passage of molecules between the nucleus and cytoplasm. It is comprised of several subunits that form a channel with a central pore. Surrounding the pore is a nonmembranous annulus with spoke-like structures. The pore wall contains columnar and lumenal subunits anchored by transmembrane proteins. Tiny fibrils extend from both sides in basket-like configurations, with different protein compositions on each side. Nuclear pores allow entry and exit of proteins and molecules to perform functions inside and outside the nucleus.
1) Griffith discovered a "transforming principle" that allowed non-virulent bacteria to become virulent after exposure to heat-killed virulent bacteria.
2) Avery, MacLeod, and McCarty determined that the transforming principle was DNA through experiments treating components with DNAses, RNAses, and proteases.
3) Hershey and Chase provided definitive evidence that DNA is the genetic material through experiments using bacteriophages containing radioactive DNA or protein to infect bacteria, showing that only DNA was transferred.
DNA repair is a collection of processes cells use to identify and correct damage to DNA. Failure to repair damaged DNA leads to mutations, which are permanent changes in the DNA sequence. There are several types of DNA damage including mismatches, modified DNA bases, and single or double strand breaks. Cells use multiple repair pathways like direct reversal, base excision repair, nucleotide excision repair, recombination repair, and translesion DNA synthesis to fix different types of DNA damage. Homologous recombination repairs double strand breaks by exchanging DNA between similar molecules, while site-specific and transposon recombination involve movement of DNA between defined sequences.
Cell division is the process by which a parent cell divides into two or more daughter cells. There are two main types of cell division: mitosis and meiosis. Mitosis produces two identical daughter cells during growth and repair of the body. It ensures the genetic makeup remains the same. Meiosis produces gametes with half the number of chromosomes and involves two cell divisions. It results in genetic diversity that is important for sexual reproduction.
The cell cycle consists of interphase and the mitosis phase. Interphase includes G1, S, and G2 phases where the cell grows and duplicates its DNA. Mitosis is divided into prophase, metaphase, anaphase, and telophase where the chromosomes and cell contents are separated into two daughter cells. Meiosis includes two cell divisions to produce four haploid cells from one diploid cell. Meiosis I separates homologous chromosomes and meiosis II separates sister chromatids.
The document discusses the processes of mitosis and meiosis. It explains that mitosis is how eukaryotic cells divide to produce identical daughter cells through nuclear division. Meiosis involves two cell divisions that result in four haploid cells each with half the number of chromosomes as the original cell. The stages of mitosis include prophase, metaphase, anaphase and telophase. Similarly, meiosis has two divisions - meiosis I and meiosis II - which each consist of prophase, metaphase, anaphase and telophase stages. The document provides detailed explanations of each stage of mitosis and meiosis.
Chapter 5 cell division SPM Biology Form 4Yee Sing Ong
Mitosis and meiosis both involve cell division, but have key differences:
Mitosis produces two identical diploid daughter cells through one nuclear division, while meiosis produces four non-identical haploid gametes through two nuclear divisions. Meiosis involves homologous chromosome pairing and crossing over during prophase I, which introduces genetic variation. The first meiotic division reduces the chromosome number by half to produce haploid cells, and the second division separates sister chromatids. Meiosis is essential for sexual reproduction to generate egg and sperm cells.
JNL College ( Pallavi for Botany B.Sc Part I) Topic-Cell Division.pdfRajneeshTiwari27
The document summarizes the processes of mitosis and meiosis. It explains that mitosis produces two identical daughter cells through replication of genetic material and division, while meiosis produces four genetically distinct gametes through two cell divisions. It also describes the key stages and substages of each process, including prophase, metaphase, anaphase, and telophase for both mitosis and meiosis I. Additionally, it notes that meiosis involves a S phase followed by two cell divisions while mitosis involves one cell division.
Meiosis is a two-step process of cell division that results in four daughter cells each with half the number of chromosomes as the original parent cell. It occurs only in sex cells. In meiosis I, homologous chromosomes separate and are distributed into two daughter cells. Meiosis II then separates the sister chromatids, resulting in a total of four haploid daughter cells. The purpose of meiosis is to produce gametes for sexual reproduction.
The cell cycle consists of interphase and mitosis. Interphase includes G1, S, and G2 phases where the cell grows and duplicates its DNA. Mitosis separates the duplicated chromosomes into two identical daughter cells through prophase, metaphase, anaphase and telophase. Meiosis produces gametes through two cell divisions. Meiosis I separates homologous chromosomes and Meiosis II separates sister chromatids, resulting in four haploid cells.
Cell division occurs through mitosis and meiosis. Mitosis produces two identical daughter cells and is used for cell growth and repair. Meiosis produces four haploid cells through two cell divisions and is involved in sexual reproduction to create sex cells. The key differences are that mitosis maintains chromosome number while meiosis reduces it, and meiosis involves homologous chromosome pairing and genetic recombination during prophase I.
Cell division occurs through mitosis and meiosis. Mitosis produces two identical daughter cells from one parent cell during growth and repair. Meiosis reduces the chromosome number by half and produces genetic variation through independent assortment and crossing over during gamete formation for sexual reproduction. The cell cycle is tightly regulated and consists of interphase, mitosis, and cytokinesis. Errors in meiosis can result in genetic disorders.
The study of the cell cycle focuses on mechanisms that regulate the timing and frequency of DNA duplication and cell division. As a biological concept, the cell cycle is defined as the period between successive divisions of a cell. During this period, the contents of the cell must be accurately replicated.
The cell cycle is regulated by cyclins and cyclin-dependent kinases.
How long is one cell cycle?
Depends. Eg. Skin cells every 24 hours. Some bacteria every 2 hours. Some cells every 3 months. Cancer cells very short. Nerve cells never.
Programmed cell death:
Each cell type will only do so many cell cycles then die. (Apoptosis)
Cell division occurs through either mitosis or meiosis. Mitosis produces two identical daughter cells during somatic cell division. It has four phases: prophase, metaphase, anaphase and telophase. Meiosis produces gametes through two cell divisions that result in four haploid cells each with one copy of each chromosome. Meiosis has two rounds: meiosis I which separates homologous chromosomes, and meiosis II which separates sister chromatids. Both ensure genetic variation between offspring.
The document summarizes the cell cycle and different types of cell division. It discusses the stages of interphase (G1, S, G2 phases), mitosis and its four phases (prophase, metaphase, anaphase, telophase), and cytokinesis. It also describes the two types of cell division - mitosis which produces identical daughter cells and meiosis which reduces the chromosome number by half to produce gametes. Meiosis involves two cell divisions, Meiosis I and Meiosis II, with chromosome segregation occurring once in each division.
This document provides information about cell division through mitosis and meiosis. It discusses the three main types of cell division - binary fission in prokaryotes, mitosis in eukaryotes for growth and repair, and meiosis in eukaryotes for sexual reproduction. The stages of mitosis (prophase, metaphase, anaphase, telophase) and meiosis I and II are described in detail. The cell cycle is also summarized, including the interphase and mitotic phases.
Here are the key points about meiosis:
1. Mitosis produces genetically identical diploid body cells.
2. Meiosis produces genetically unique haploid gametes (sperm and egg cells) with half the number of chromosomes as body cells.
3. Humans have 23 chromosomes in their haploid gametes.
4. Meiosis involves two cell divisions (Meiosis I and Meiosis II) which results in four haploid cells from one original diploid cell.
5. Chromosomes are replicated once before meiosis, not between the two meiotic divisions.
6. Cells become genetically different during meiosis due to independent assortment of homologous chromosomes and crossing over.
Here are the key points about meiosis:
1. Mitosis produces genetically identical diploid body cells.
2. Meiosis produces genetically unique haploid gametes (sperm and egg cells) with half the number of chromosomes as body cells.
3. Humans have 23 chromosomes in their haploid gametes.
4. Meiosis involves two cell divisions (Meiosis I and Meiosis II) which results in four haploid daughter cells from one original diploid cell.
5. Chromosomes are replicated once before meiosis, not between the two meiotic divisions.
6. Cells become genetically different during meiosis due to independent assortment of homologous chromosomes and crossing over.
Cell division occurs through binary fission in prokaryotes, where the genetic material duplicates and the cell splits into two identical daughter cells. Eukaryotes undergo the more complex processes of mitosis and meiosis. Mitosis produces two identical daughter cells during normal cell growth and replacement. Meiosis results in four haploid cells through two cell divisions, reducing the chromosome number by half and allowing for genetic variation in sexual reproduction.
Mitosis and meiosis are the two main types of cell division. Mitosis produces two identical daughter cells through symmetric division, while meiosis produces four haploid gametes through two rounds of division. During mitosis, DNA replication occurs, followed by nuclear and cell division to produce two identical daughter cells with the same number of chromosomes. Meiosis involves one round of DNA replication followed by two nuclear divisions. The first division separates homologous chromosomes, reducing ploidy by half. The second division separates sister chromatids to produce four haploid gametes. This allows for genetic diversity through independent assortment and crossing over during the first meiotic division.
ntry points of glucogenicamino acids after transamination
are indicated by arrows extended from circles
the key gluconeogenicenzymes are enclosed in double
bordered boxes. oated fashion. They are interdependent; each forms a strand in the web of life. Parasitology is
the science that deals with organisms living in the human body (the host) and the medical significance of
this host-parasite relationship.
ASSOCIATION BETWEEN PARASITE AND HOST
A parasite is a living organism, which takes its nourishment and other needs from ahost; the host is an
organism which supports the parasite. The hosts vary depending on whether they harbor the various
stages in parasitic development
DIFFERENT KINDS OF PARASITES
Ectoparasite – a parasitic organism that lives on the outer surface of its host, e.g. lice, ticks, mites etc.
Endoparasites parasites that live inside the body of their host, e.g. Entamoeba histolytica.
Obligate Parasite- This parasite is completely dependent on the host during a segment or all of its life
cycle, e.g. Plasmodium spp.
Facultative parasite – an organism that exhibits both parasitic and non-parasitic modes of living and
hence does not absolutely depend on the parasitic way of life but is capable of adapting to it if paced on
a host. E.g. Naegleria fowleri
Accidental parasite – when a parasite attacks an unnatural host and survives. E.g. Hymenolepis diminuta
(rat tapeworm).
Erratic parasite - is one that wanders in to an organ in which it is not usually found. E.g. Entamoeba
histolytica in the liver or lung of humans.
Most of the parasites which live in/on the body of the host do not cause disease (non-pathogenic
parasites). In Medical parasitology we focus on most of the disease causing (pathogenic) parasites.
However, understanding parasites which do not ordinariy produce disease in heathy
(immunocompetent) individuals but do cause illness in individuals with impaired defense mechanism
(opportunistic parasites) is becoming of paramount importance because of the increasing prevaence of
HIV/AIDS in our country.
DIFFERENT KINDS OF HOSTS
Definitive host – a host that harbors a parasite in the adult stage or where the parasite undergoes a
sexual method of reproduction.
Intermediate host - harbors the arval stages of the parasite or an asexual cycle of development takes
pace. In some cases, larval development is completed in two different intermediate hosts, referred to
as first and second intermediate hosts.
Paratenic host – a host that serves as a temporary refuge and vehicle for reaching an obligatory host,
usually the definitive host, i.e. it is not necessary for the completion of the parasites life cycle.
Reservoir host – a host that makes the parasite available for the transmission to another host and is
usually not affected by the infection.
Natural host a host that is naturally infected with certain species of parasite.
Accidental host – a host that is under normal circumstances not infected with th
Mitosis and meiosis are the two types of cell division. Mitosis produces two identical daughter cells through replication of chromosomes followed by their equal distribution into the two daughter cells. This allows growth and repair of somatic cells. Meiosis produces gametes through two rounds of division. The first division separates homologous chromosomes, reducing the chromosome number by half. The second division separates sister chromatids to generate four haploid gametes. This genetic diversity through independent assortment of homologous chromosomes and random fertilization provides the basis for sexual reproduction and evolution. Loss of cell cycle control through oncogene activation or tumor suppressor inactivation can lead to uncontrolled cell division and cancer.
Cell division occurs through mitosis and meiosis. Mitosis produces two identical daughter cells and is important for growth and repair. It has four phases: prophase, metaphase, anaphase and telophase. Meiosis reduces the chromosome number by half and produces genetic variation important for sexual reproduction. Meiosis has two divisions and involves homologous chromosome pairing, crossing over and separation into four haploid cells. The key difference is that mitosis maintains ploidy levels while meiosis reduces them, resulting in genetic variation.
Introduction to Protein Families and DatabasesRohit Satyam
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Bermuda Triangle and Its associated SecretsRohit Satyam
Bermuda Triangle has seen a lot of disappearances of Ships, air crafts, and who knows much more. The presentation focuses on exploring the science and possible reasons behind such disappearances.
Interviews are hard to get through. You often need to be smart enough to influence those on the other side of the table. There is no prescribed format of the DO'S and DONT'S but keeping in mind certain points might surely increase your probability of getting selected.
This slide covers briefly how intracellular and extracellular bacteria elicits an immune response, how bacteria evade from the immune system, what complement system is, opsonization, neutralisation, septic shock, sepsis, superantigens, phagocytosis, interleukins, Toll-like receptors, a list of diseases caused by bacterias and their names etc.
This presentation is about the advances in Renewable Resources of energy. This includes the innovations in the field of Solar Energy, Wind Energy, Water Energy and Success Stories and Ongoing work worldwide. This is what I call a Technovation.
Imagine that you have been told you have an illness that cannot be cured or what if your body has been irreversibly paralysed. There is no hope. But there is a science that could change that. It’s Called Stem Cell Research and it’s an important step in the medical revolution. But it comes with controversies as it uses Human Embryos’ as Raw Material.
But something astounding happened in the year 2006 that removed the usage of surplus embryos from the equation altogether. It’s about a brand new technology that can turn back the clock on your body cells. This is cutting edge of science where new developments are happing all the time. The iPSCs could be the potential medicine of 21st century. So what are stem cells? Why do they Matter? What are iPSCs and how it changed the biological rules?
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
Authoring a personal GPT for your research and practice: How we created the Q...Leonel Morgado
Thematic analysis in qualitative research is a time-consuming and systematic task, typically done using teams. Team members must ground their activities on common understandings of the major concepts underlying the thematic analysis, and define criteria for its development. However, conceptual misunderstandings, equivocations, and lack of adherence to criteria are challenges to the quality and speed of this process. Given the distributed and uncertain nature of this process, we wondered if the tasks in thematic analysis could be supported by readily available artificial intelligence chatbots. Our early efforts point to potential benefits: not just saving time in the coding process but better adherence to criteria and grounding, by increasing triangulation between humans and artificial intelligence. This tutorial will provide a description and demonstration of the process we followed, as two academic researchers, to develop a custom ChatGPT to assist with qualitative coding in the thematic data analysis process of immersive learning accounts in a survey of the academic literature: QUAL-E Immersive Learning Thematic Analysis Helper. In the hands-on time, participants will try out QUAL-E and develop their ideas for their own qualitative coding ChatGPT. Participants that have the paid ChatGPT Plus subscription can create a draft of their assistants. The organizers will provide course materials and slide deck that participants will be able to utilize to continue development of their custom GPT. The paid subscription to ChatGPT Plus is not required to participate in this workshop, just for trying out personal GPTs during it.
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
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The pygmy halfbeak Dermogenys colletei, is known for its viviparous nature, this presents an intriguing case of relatively low fecundity, raising questions about potential compensatory reproductive strategies employed by this species. Our study delves into the examination of fecundity and the Gonadosomatic Index (GSI) in the Pygmy Halfbeak, D. colletei (Meisner, 2001), an intriguing viviparous fish indigenous to Sarawak, Borneo. We hypothesize that the Pygmy halfbeak, D. colletei, may exhibit unique reproductive adaptations to offset its low fecundity, thus enhancing its survival and fitness. To address this, we conducted a comprehensive study utilizing 28 mature female specimens of D. colletei, carefully measuring fecundity and GSI to shed light on the reproductive adaptations of this species. Our findings reveal that D. colletei indeed exhibits low fecundity, with a mean of 16.76 ± 2.01, and a mean GSI of 12.83 ± 1.27, providing crucial insights into the reproductive mechanisms at play in this species. These results underscore the existence of unique reproductive strategies in D. colletei, enabling its adaptation and persistence in Borneo's diverse aquatic ecosystems, and call for further ecological research to elucidate these mechanisms. This study lends to a better understanding of viviparous fish in Borneo and contributes to the broader field of aquatic ecology, enhancing our knowledge of species adaptations to unique ecological challenges.
The technology uses reclaimed CO₂ as the dyeing medium in a closed loop process. When pressurized, CO₂ becomes supercritical (SC-CO₂). In this state CO₂ has a very high solvent power, allowing the dye to dissolve easily.
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As the population is increasing and will reach about 9 billion upto 2050. Also due to climate change, it is difficult to meet the food requirement of such a large population. Facing the challenges presented by resource shortages, climate
change, and increasing global population, crop yield and quality need to be improved in a sustainable way over the coming decades. Genetic improvement by breeding is the best way to increase crop productivity. With the rapid progression of functional
genomics, an increasing number of crop genomes have been sequenced and dozens of genes influencing key agronomic traits have been identified. However, current genome sequence information has not been adequately exploited for understanding
the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
high-throughput phenotyping has become the major bottleneck restricting crop breeding. Plant phenomics has been defined as the high-throughput, accurate acquisition and analysis of multi-dimensional phenotypes
during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/
When I was asked to give a companion lecture in support of ‘The Philosophy of Science’ (https://shorturl.at/4pUXz) I decided not to walk through the detail of the many methodologies in order of use. Instead, I chose to employ a long standing, and ongoing, scientific development as an exemplar. And so, I chose the ever evolving story of Thermodynamics as a scientific investigation at its best.
Conducted over a period of >200 years, Thermodynamics R&D, and application, benefitted from the highest levels of professionalism, collaboration, and technical thoroughness. New layers of application, methodology, and practice were made possible by the progressive advance of technology. In turn, this has seen measurement and modelling accuracy continually improved at a micro and macro level.
Perhaps most importantly, Thermodynamics rapidly became a primary tool in the advance of applied science/engineering/technology, spanning micro-tech, to aerospace and cosmology. I can think of no better a story to illustrate the breadth of scientific methodologies and applications at their best.
2. Table Of Contents:
1. Introduction to types
2. Mitosis
3. Meiosis
4. Difference b/w Mitosis And Meiosis
By: Rohit Satyam
BT 2nd Yr
3. Two Basic Process In Cell
Reproduction
1. Cell-Growth: Period of synthesis and
duplication of various components
of cell.
2. Cell-Division: Adult cell divides into
two daughter.
5. Cell Cycle
Definition: All those changes which occur
during cell growth and cell division are
collectively called Cell Cycle.
Two Parts of Cell Cycle:
1.Interphase
2. M-Phase
8. Interphase
• Also known as RESTING PHASE(no visible changes occur)/
Metabolically active phase/ preparatory phase/ energy
phase.
• Three sub phases are:
1. G1/ Gap-I/ Post mitotic/ Pre-synthetic/ First growth
phase:
• Pooling of Amino Acid & Nucleotides for protein and
Nucleic Acid synthesis respectively.
• Energy molecules and enzyme synthesis
• Carbohydrates, Lipids and Protein Synthesis
• Chromosome are Fully Extended
9. 2. S/ Synthetic phase:
• DNA replicates semiconservately forming two sister chromatids
joined at centromere/ primary constriction.
•Histone synthesis
NOTE: In this phase the DNA amount doubles(4N) But the
chromosomes number remain same
3. G2/ Gap-2/ Post Synthetic/ Pre mitotic phase/ second
growth phase: Increase in Nuclear Volume
•Synthesis of:
1. Spindle Proteins 2. Three types of RNA molecules
3. ATP molecules 4. Mitochondria Duplication
5. Damaged DNA is Repaired
10. M-Phase/ Mitotic Phase/ D-phase
• It involves the separation of SISTER CHROMATIDS & their
redistribution into daughter cells.
• Orderly distribution of cell organelles
• It consists of two stages:
1. Karyokinesis: (Karyon: Nucleus And Kinesis: movement): It
involves division of nucleus for which nucleus develops a
constriction in centre and becomes dumbell-shaped.
Constriction divides the parent nucleus into two daughter
nucleus.
2. Cytokinesis: ( kytos= cell): Division of cytoplasm. A
constriction in Plasma membrane develops a constriction
and deepens centripetally and finally divides into two cells.
11. Terminology
1. Homologous Chromosomes: The cell has
two sets of each chromosome; one of the pair
is derived from the mother and the other from
the father. The maternal and paternal
chromosomes in a homologous pair have the
same genes at the same loci, but possibly
different alleles.
2. Kinetochores: On the surface of each
centromere, there are two disc like areas where
the spindle fibres attaches. They are k/a
Kinetochores.
12.
13.
14.
15.
16. Pair of homologous
chromosomes in
diploid parent cell
Duplicated pair
of homologous
chromosomes
Chromosomes
duplicate
Sister
chromatids
Diploid cell with
duplicated
chromosomes
Homologous
chromosomes separate
Haploid cells with
duplicated chromosomes
Sister chromatids
separate
Haploid cells with unduplicated chromosomes
Interphase
Meiosis I
Meiosis II
2
1
17. Mitosis
•It is also called Somatic Cell Division or
Equational Division.
•In this, mature somatic cell divides in such a way
that chromosome number is kept constant in
daughter cell equal to parent cell, so that
daughter cell are quantitatively & qualitatively
similar to Parent Cell, so it is called Equational
Division.
18. •Mitosis produces two
genetically identical
cells.
•Mitosis is referred to in
the following stages:
prophase, metaphase,
anaphase, and telophase.
Mitosis
19. •In prophase, the cell begins the
process of division.
•The chromosomes condense.
Prophase
20.
21. Prophase
• Nuclear envelope disappears.
•Centrioles migrate to opposite poles of the cell.
•Asters and spindle fibers form.
23. Metaphase
• The chromosomes line
up at the equator of the
cell (metaphase plate),
with the centrioles at
opposite ends and the
spindle fibers attached
to the centromeres.
Centriole
Centriole
Spindle
fibers
Metaphase
plate
24.
25.
26.
27.
28. Anaphase
• In anaphase, the
centromeres divide.
• At this point, each
chromosome goes from
having 2 sister
chromatids to being 2
separate chromosomes
29. The spindle fibers contract and
the chromosomes are pulledto
opposite poles.
30. Telophase
• In telophase the nucleus
actually divides.
• The chromosomes are at
the poles of the cell.
• The nuclear envelope re-
forms around the two
sets of chromosomes.
31. Cytokinesis
• The division of the
cytoplasm.
• In animal cells, a
Cleavage Furrow
forms and separates
Daughter Cells
Cleavagefurrowin a dividingfrogcell.
33. ANIMAL VS. PLANT MITOSIS
• ANIMAL CELL
– Centriole and
aster present
– Daughter cells
separated by
cleavage furrow
• PLANT CELL
– No visible
centriole or aster
– Daughter cells
separated by cell
plate
34. The Stages of Meiosis
• After chromosomes duplicate, two divisions
follow
– Meiosis I (reductional division): homologs pair
up and separate, resulting in two haploid
daughter cells with replicated chromosomes
– Meiosis II (equational division) sister chromatids
separate
• The result is four haploid daughter cells with
unreplicated chromosomes
35. Meiosis
It is called REDUCTIONAL DIVISION
because it involves formation of 4
daughter cells which have half
chromosome number to those in their
parental cell.
38. •Meiosis I is preceded by interphase,
when the chromosomes are duplicated to
form sister chromatids
•The sister chromatids are genetically
identical and joined at the centromere
•The single centrosome replicates,
forming two centrosomes
39. Division in meiosis I occurs in
four phases
–Prophase I
–Metaphase I
–Anaphase I
–Telophase I and
cytokinesis
40. Prophase I
•Prophase I typically occupies more
than 90% of the time required for
meiosis
•Chromosomes begin to condense
•In synapsis, homologous
chromosomes loosely pair up, aligned
gene by gene
41. Sister chromatids
of one duplicated
chromosome
Key
Maternal set of
chromosomes (n 3)
Paternal set of
chromosomes (n 3)
Key
2n 6
Centromere
Two nonsister
chromatids in
a homologous pair
Pair of homologous
chromosomes
(one from each set)
42.
43.
44.
45.
46.
47.
48.
49.
50.
51.
52.
53.
54. 1. Leptotene/ Leptonema (leptos= Thin tene= Thread)
• Also called THIN THREADED STAGE
• Volume of nucleas increases.
• Formation of Aster
• Condensation of nuclear chromatin by dehydration and
spiralization .
2. Zygotene/ Zygonema:
• Pairing( k/a Synapsis or Syndesis) of homologous chromosomes
to form Bivalents. It occurs due to forces of attraction between
alleles on Homologous Chromosomes
• Pairing of Homologous chromosomes in Zipper Fashion
No of Bivalents= ½ of total no of chromosomes in a diploid cell.
• Further condensation of chromosomes and moving away of asters.
• Under EM, a filamentous ladder-like nucleoproteinous complex
called Synaptonemal Complex is observed.
55.
56. 3. Pachytene/ Pachynema/ Thick Thread stage:
• Further condensation of chromosome. Sister chromatids
are clearly visible and are joined at centromere and is called
Dyad. Each bivalent has 2 dyad and is called a tetrad(i.e. 4
chromatids).
• Recombination sometimes takes place wherein exchange of
genes or crossing over b/w two non sister chromatids of
Homologous Chromosomes occurs at the points called
Recombination Nodules. This is enzimetically controlled
process and is regulated by recombinase enzyme.
• Moving away of Asters.
57. Crossing Over
• Crossing over produces recombinant
chromosomes, which combine DNA
inherited from each parent
• Crossing over begins very early in
prophase I, as homologous chromosomes
pair up gene by gene
58. •In crossing over, homologous
portions of two nonsister chromatids
trade places
•Crossing over contributes to genetic
variation by combining DNA from two
parents into a single chromosome
59. 4. Diplotene/ Diplonema:
• Nuclear membrane disappears and Nucleoli start
disappearing.
• Desynapsis- Is separation of Homologous
Chromosomes begins due to dissolution of
synaptonemal complex.
• Chismata are Visible & Terminilization.
5. Diakinesis
• Terminilization Completed. But still Homologous
chromosomes are attached at the ends.
•Formation of Spindle & Complete disappearance of
spindles.
60.
61. Metaphase I
• In metaphase I, tetrads line up at the
metaphase plate, with one chromosome
facing each pole
• Microtubules from one pole are attached
to the kinetochore of one chromosome of
each tetrad
• Microtubules from the other pole are
attached to the kinetochore of the other
chromosome
64. Anaphase I
•In anaphase I, pairs of homologous
chromosomes separate
•One chromosome moves toward each pole,
guided by the spindle apparatus
•Sister chromatids remain attached at the
centromere and move as one unit toward the
pole
65. Telophase I and Cytokinesis
•In the beginning of telophase I, each
half of the cell has a haploid set of
chromosomes; each chromosome still
consists of two sister chromatids
•Cytokinesis usually occurs
simultaneously, forming two haploid
daughter cells
66. •In animal cells, a cleavage furrow forms;
in plant cells, a cell plate forms.
•No chromosome replication occurs
between the end of meiosis I and the
beginning of meiosis II because the
chromosomes are already replicated.
67. Prophase I Metaphase I Anaphase I Telophase I and
Cytokinesis
Centrosome
(with centriole pair)
Sister
chromatids
Chiasmata
Spindle
Homologous
chromosomes
Fragments
of nuclear
envelope
Duplicated homologous
chromosomes (red and blue)
pair and exchange segments;
2n 6 in this example.
Centromere
(with kinetochore)
Metaphase
plate
Microtubule
attached to
kinetochore
Chromosomes line up
by homologous pairs.
Sister chromatids
remain attached
Homologous
chromosomes
separate
Each pair of homologous
chromosomes separates.
Cleavage
furrow
Two haploid
cells form; each
chromosome
still consists
of two sister
chromatids.
68. Meiosis II
Division in meiosis II also occurs in four
phases
•Prophase II
•Metaphase II
•Anaphase II
•Telophase II and cytokinesis
•Meiosis II is very similar to mitosis
69. Prophase II
•In prophase II, a spindle
apparatus forms
•In late prophase II, chromosomes
(each still composed of two
chromatids) move toward the
metaphase plate
70. Metaphase II
•In metaphase II, the sister chromatids
are arranged at the metaphase plate
•Because of crossing over in meiosis I,
the two sister chromatids of each
chromosome are no longer genetically
identical
•The kinetochores of sister chromatids
attach to microtubules extending from
opposite poles
71. Anaphase II
•In anaphase II, the sister
chromatids separate.
•The sister chromatids of each
chromosome now move as two
newly individual chromosomes
toward opposite poles.
72. Telophase II and Cytokinesis
•In telophase II, the chromosomes
arrive at opposite poles.
•Nuclei form, and the chromosomes
begin decondensing.
73. •Cytokinesis separates the cytoplasm.
•At the end of meiosis, there are four
daughter cells, each with a haploid set
of unreplicated chromosomes.
•Each daughter cell is genetically distinct
from the others and from the parent cell.
74.
75. Prophase II Metaphase II Anaphase II
Telophase II and
Cytokinesis
Sister chromatids
separate
Haploid daughter
cells forming
During another round of cell division, the sister chromatids finally separate;
four haploid daughter cells result, containing unduplicated chromosomes.
76. MEIOSIS I: Separates homologous chromosomes
Prophase I Metaphase I Anaphase I
Telophase I and
Cytokinesis
Centrosome
(with centriole pair)
Sister
chromatids
Chiasmata
Spindle
Homologous
chromosomes
Fragments
of nuclear
envelope
Duplicated homologous
chromosomes (red and blue)
pair and exchange segments;
2n 6 in this example.
Centromere
(with kinetochore)
Metaphase
plate
Microtubule
attached to
kinetochore
Chromosomes line up
by homologous pairs.
Sister chromatids
remain attached
Homologous
chromosomes
separate
Each pair of homologous
chromosomes separates.
Cleavage
furrow
Two haploid cells
form; each chromosome
still consists of two
sister chromatids.
MEIOSIS I: Separates sister chromatids
Prophase II Metaphase II Anaphase II
Telophase II and
Cytokinesis
Sister chromatids
separate
Haploid daughter
cells forming
During another round of cell division, the sister chromatids finally separate;
four haploid daughter cells result, containing unduplicated chromosomes.
77.
78. Figure 13.11-5
Prophase I
of meiosis
Nonsister chromatids
held together
during synapsis
Pair of homologs
Chiasma
Centromere
TEM
Anaphase I
Anaphase II
Daughter
cells
Recombinant chromosomes
79. • Three events are unique to meiosis, and all
three occur in meiosis l
• Synapsis and crossing over in prophase I:
Homologous chromosomes physically
connect and exchange genetic information
• At the metaphase plate, there are paired
homologous chromosomes (tetrads), instead
of individual replicated chromosomes
• At anaphase I, it is homologous
chromosomes, instead of sister chromatids,
that separate
80. Figure 13.9
Prophase
Duplicated
chromosome
MITOSIS
Chromosome
duplication
Parent cell
2n 6
Metaphase
Anaphase
Telophase
2n 2n
Daughter cells
of mitosis
MEIOSIS
MEIOSIS I
MEIOSIS II
Prophase I
Metaphase I
Anaphase I
Telophase I
Haploid
n 3
Chiasma
Chromosome
duplication Homologous
chromosome pair
Daughter
cells of
meiosis I
Daughter cells of meiosis II
n n n n
SUMMARY
Property Mitosis Meiosis
DNA
replication
Number of
divisions
Synapsis of
homologous
chromosomes
Number of
daughter cells
and genetic
composition
Role in the
animal body
Occurs during interphase before
mitosis begins
One, including prophase, metaphase,
anaphase, and telophase
Does not occur
Two, each diploid (2n) and genetically
identical to the parent cell
Enables multicellular adult to arise from
zygote; produces cells for growth, repair,
Occurs during interphase before meiosis I begins
Two, each including prophase, metaphase, anaphase,
and telophase
Occurs during prophase I along with crossing over
between nonsister chromatids; resulting chiasmata
hold pairs together due to sister chromatid cohesion
Four, each haploid (n), containing half as many
chromosomes as the parent cell; genetically different
from the parent cell and from each other
Produces gametes; reduces number of chromosomes
by half and introduces genetic variability among the
Editor's Notes
The synaptonemal complex is a protein structure that forms between homologous chromosomes (two pairs of sister chromatids) during meiosis and is thought to mediate chromosome pairing, synapsis, and recombination. It is now evident that the synaptonemal complex is not required for genetic recombination[citation needed]. Research has shown that not only does it form after genetic recombination but mutant yeast cells unable to assemble a synaptonemal complex can still engage in the exchange of genetic information.[citation needed] It is currently thought that the SC functions primarily as a scaffold to allow interacting chromatids to complete their crossover activities. The synaptonemal complex is a tripartite structure consisting of two parallel lateral regions and a central element.