Mehthylases are those enzymes which catalyze the transference of only a methyl group (-CH3) from a donor to the target molecule.
Since we are talking about DNA Methylases these are those enzymes in which the target or recipient molecule happens to be a DNA or Nucleotide in a DNA sequence.
A class of enzymes that alter the supercoiling of double-stranded DNA. (In supercoiling the DNA molecule coils up like a telephone cord, which shortens the molecule.) The topoisomerases act by transiently cutting one or both strands of the DNA.
The regulation of DNA supercoiling is essential to DNA transcription and replication, the DNA helix must unwind to permit the proper function of the enzymatic machinery involved in these processes.
BAC & YAC are artificially prepared chromosomes to clone DNA sequences.yeast artificial chromosome is capable of carrying upto 1000 kbp of inserted DNA sequence
BAC & YAC are artificially prepared chromosomes to clone DNA sequences.yeast artificial chromosome is capable of carrying upto 1000 kbp of inserted DNA sequence
Sanger sequencing is one of the DNA sequencing methods used to identify and determine the sequence (Nucleotide) of DNA .This is an enzymatic method of sequencing developed by Fred Sanger.
Sanger sequencing is one of the DNA sequencing methods used to identify and determine the sequence (Nucleotide) of DNA .This is an enzymatic method of sequencing developed by Fred Sanger.
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 most essential part for biological inheritance.
As a periodontist, it is of utmost importance to understand the genetic basis of inheritance in periodontal diseases be able to relate to the various polymorphisms associated with periodontal diseases. This ppt presents the basics of genetics from the point of view of future understanding of polymorphisms related to periodontal diseases.
Identify each of the enzymes involved in DNA replication and whether.pdfarjuncollection
Identify each of the enzymes involved in DNA replication and whether they are used during
synthesis of the leading strand, lagging strand, or both
Solution
ANS:
REPLICATION:
Replication is a process of duplication of DNA .the replication had specific time in S
phase. All the cellular molecules had timing programed inside the cells, the time depends on
species. Replication occur during the S phase of eukaryotic cell cycle.it is highly accurate
process and involved the faithful transmission of the genetically information from parental DNA
to two daughter DNA duplexes.
Replication involves the polymerization of precursor of d NTPs (d ATP, d GTP, d CTP, d TTP).
B. ENZYMOLOGY IN REPLICATION:
Replication is a complex process the various enzymes/proteins are involved in this.
1. DNA polymerase:
It can polymerized the d NTP’s directed by template strand of DNA so called DNA
DEPENDENT DNA POLYMARASE.
In eukaryotes 5 different DNA polymerase are there (Pol Alfa, Pol Beta, Pol Gama, Pol Delta
and Pol Epsilon).
DNA Pol Alfa can initiate replication in both leading and lagging strands, it dual activity so often
called as Pol Alfa/ primase enzyme.
DNA pol Delta is a major replication enzyme involved in the replication of both leading and
lagging strands.
2. DNA A protein: also called initiation protein, it involved in recognition & binding to origin.
3. DNA HELICASE: 1st component in replisoma, it possess an ATPase activity, it separates the
2 parental strands of DNA, It always binds to lagging strand.
4. PRIMASE: Involved in synthesis of RNA primer, always binds to helicase results the
formation of primosome.
5. SSB protein: It prevents reannealing of DNA, it removes the secondary structure prevent in
DNA.
6. DNA Topoisomerase 1: Relaxes tension due to un coiling of dna.it binds downstream of
replication fork.
7. DNA Gyrase: It binds up stream of replication fork and introduces Negative supercoiling.
8. DNA LIGASE: It covalently seals the nick between the adjacent okazaki fragments.
9. Termination protein: Also called TUS protein, binds the TER sites results termination.
10. DNA Topoisomerase 4: Involved in decapitation of the 2 circular daughter DNA duplexes
obtained after replication.
Synthesis of the leading strand and lagging strand:
Semi –conservative mechanism:
In this the 2 strands of DNA separated from each other and each strand act as template for
synthesis of anew complimentary strand ,such daughter duplex contain 1 parental and 1 newly
synthesize strand.
Replication always began from fixed point called origin.as unwinding DNA produced a Y
shaped junction called REPLICATIONPORK. That represents origin of replication.
As the replication pork moved in one direction the DNA copies continuously in both strands.
Then the replication missionary should be able to synthesize in both 5\'-3\' and 3\'-5\' direction.
But the DNA polymerase involved in replication can added a new nucleotide only to 3\'end of
growingchain.so DNA always synthesized in 5\'-3\' .
Please find the answers and explanations belowPart 1 (TrueFalse).pdfaparnatiwari291
Please find the answers and explanations below:
Part 1 (True/False)
1. Replication and transcription proceed in 5\' to 3\' direction: TRUE (Both DNA replication and
transcription of mRNA proceed in 5\' to 3\' direcition. This is because the firstly, the DNA
polymerase retains only 5\' to 3\' directionality and thus, replication begins only in this direction.
.Secondarily, there must be sequence similarity between the DNA and the RNA transcribed from
it thus the orientation of transcription is necessarily 5\' to 3\' in nature)
2. All cells have telomerase activity : FALSE (Telomerase or terminal transferase is an enzyme
which is required for maintenance of terminal positions of chromosomes by self-replication and
prevents shortening of chromosomes. It also prevents sticking of chromosomes together and thus
clumping of chromosomes. Telomerase acitivty is absent in majority of somatic cells in the
body.)
3. Only mRNA is transcribed: TRUE (Only the mRNA which carries the necessary information
for translation is transcribed from the DNA template. The tRNA is utilized to transfer the
transcribed information and rRNA is utilized to generate the polypeptide on the ribosomal
surface during translation)
4. Promoter regions are upstream from the gene: TRUE (A gene promoter is the region of DNA
located upstream the gene to be transcribed and carries the consensus sequence which could be
recognized by RNA polymerase for its binding and carrying on transcription)
5. A single tRNA can carry several different amino acids: FALSE (The tRNA is specific for only
one kind of amino acid which it could carry. It is a highly stringent and specific nature of this
biomolecule which determines the specificness for the amino acid which will be synthesized
from the codon)
Part 2
Please find the definitions below:
1. Semi-conservative replication: The mode of replication of double stranded DNA in which a
daughter DNA molecules carries a strand from parent DNA and the complementary strand is
synthesized de novo is called semi-conservative replication.
2. Okazaki fragments: Okazaki fragments are short stretches of DNA synthesized
discountinuously on the lagging strand on the open frame of the parent DNA. These stretches of
DNA are finally conjoined together to form a continous strand of newly synthesized DNA.
3. Consensus sequence: Consensus sequences are those genetically conserved sequences of DNA
which remain similar (upto 99%) within organisms of same or different species and are actively
engaged in crucial functions such as promoter region binding, transcription sites for transcription
factors, enzymatic genes etc. Any change or deterioration in these consesus sequence might be
highly deletrious for the cells.
4. Codon: A codon can be defined as a triplet set of nucleotides which come in a specific order
and encode for a specific type of amino acid upon translation. For example, the codon AAA
encodes for amino acid lysine. Exceptionally, codons UAA, UAG and UGA do not .
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
This pdf is about the Schizophrenia.
For more details visit on YouTube; @SELF-EXPLANATORY;
https://www.youtube.com/channel/UCAiarMZDNhe1A3Rnpr_WkzA/videos
Thanks...!
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...
Dna methylases & topoisomerases
1. Presentation on DNA Methylases &
Topoisomerases
Submitted To – Dr. Munish Sharma
Submitted By – Abhishek Kumar (CUHP19BOT01)
2. DNA Methylases
Mehthylases are those enzymes which catalyze the transference
of only a methyl group (-CH3) from a donor to the target molecule.
Since we are talking about DNA Methylases these are those
enzymes in which the target or recipient molecule happens to be a
DNA or Nucleotide in a DNA sequence.
Methylation normally occurs on Cytosine & Adenine residue in
DNA sequences.
The process of transfer of methyl group to its substrate is called
Methylation.
3. There is a molecule known as S – Adenosyl Mehionine known as
SAM. This is a molecule which happens to be a universal donor
for all types of DNA Methyl transferases.
DNA methyl transferase (DNMT) mediates transference of a
methyl group from the donor to the target nucleotide, at the
same time the donor gets converted from S-Adenosyl
Methionine to S – Adenosyl Homocystine.
4. DNA Methylation regulates genes or silence genes without
changing DNA sequences, as a part of epigenetic regulation.
In Bacterial system, methylation play a major role in
preventing their genome from degradation by restriction
enzymes.
Some common examples of methyltransferases are – DNA
Adenyl Methyltransferase (DAM) , O-methyltransferase etc.
5. Classification of Methyltransferases
Three different patterns of DNA Methylation has been observed so
far. The targets of methylation include –
Fifth position carbon of Cytosine (m5C), fourth position nitrogen
of cytosine (m4C) and sixth position nitrogen of Adenine (m6A)
7. TOPOISOMERASES
A class of enzymes that alter the supercoiling of double-
stranded DNA. (In supercoiling the DNA molecule coils up like a
telephone cord, which shortens the molecule.) The
topoisomerases act by transiently cutting one or both strands of
the DNA.
The regulation of DNA supercoiling is essential to DNA
transcription and replication, the DNA helix must unwind to permit
the proper function of the enzymatic machinery involved in these
processes.
Topoisomerases serve to maintain both the transcription and
replication of DNA.
8. Role of Topoisomerases
The winding problem of DNA arises due to the
intertwined nature of its double-helical structure.
During DNA replication and transcription, DNA
becomes overwound ahead of a replication fork.
If left unabated, this torsion would eventually
stop the ability of RNA & DNA polymerase
involved in these processes to continue down the
DNA strand.
Topoisomerases bind to either single-stranded
or double-stranded DNA and cut the phosphate
backbone of the DNA.
This intermediate break allows the DNA to be
9. Types of Topoisomerase
Topoisomerases I : breaks only one strand
Topoisomerases II : breaks both strands
10. Type I topoisomerases are enzymes that cut one of the
two strands of double-stranded DNA, relax the strand, and
reanneal the strand.
11. Type II topoisomerases cut both strands of the DNA helix
simultaneously. They use the hydrolysis of ATP. These
enzymes change the linking number of circular DNA by ±2