C VALUE, C VALUE PARADOX , COT CURVE ANALYSIS.pptxMurugaveni B
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This document discusses the C-value, C-value paradox, and COT curve analysis. It defines the C-value as the total amount of DNA in a genome. It explains that the C-value paradox arose because early research assumed complexity increased with DNA amount, but some organisms like salamanders have more DNA than humans despite lower complexity. The document outlines the COT curve technique which analyzes renaturation kinetics to measure genome complexity based on repetitive sequences. It applies COT curve analysis to understand genome size, sequence complexity, and the proportion of single-copy versus repetitive DNA.
This Presentation will be helpful to undergraduate and postgraduate students of biology and biotechnology in understanding the significance of COT curves in determination of gene and genome complexity amoug various organisms
This document summarizes key aspects of eukaryotic genome organization. It discusses how eukaryotic genomes contain both unique and repetitive sequences. Repetitive sequences are present in hundreds or thousands of copies and do not code for proteins. The complexity of eukaryotic genomes can be studied using denaturation and renaturation analysis of DNA. This technique separates DNA into single strands and then analyzes how quickly different sequences reassociate upon cooling. Faster renaturation indicates repetitive sequences while slower renaturation indicates unique sequences. Eukaryotic genomes contain much higher percentages of repetitive DNA compared to prokaryotes.
Gene cloning involves copying a gene and inserting it into a self-replicating vector to produce multiple copies of the gene. PCR (polymerase chain reaction) is a technique used to amplify specific genes. Both gene cloning and PCR are important for obtaining pure samples of genes and amplifying them for various applications like sequencing, expression of proteins, and genetic engineering.
The document discusses DNA fingerprinting, nucleic acid hybridization, and rRNA sequence analysis. It defines DNA fingerprinting as a technique used to identify individuals by extracting and identifying their unique DNA base pair pattern. Nucleic acid hybridization is described as the process of forming a double stranded nucleic acid from joining two complementary single strands of DNA or RNA. rRNA sequence analysis is used to construct phylogenetic trees of life based on comparing 16s rRNA sequences between organisms.
Genome organization of prokaryotes and eukaryotesSuganyaPaulraj
油
1. Prokaryotic genetic material is usually a single, circular chromosome located in the nucleoid region. Eukaryotic genetic material is contained within the nucleus in the form of linear chromosomes composed of DNA and proteins.
2. Chromosomes contain genes and vary in number between species. Eukaryotic chromosomes are packaged with histone proteins into chromatin and can exist in condensed or uncondensed states.
3. Genetic material exists in different structural and functional states between prokaryotes and eukaryotes.
DNA organization or Genetic makeup in Prokaryotic and Eukaryotic SystemsBir Bahadur Thapa
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DNA organization or Genetic makeup in Prokaryotic and Eukaryotic Systems!! It is prepared under the syllabus of Tribhuwan University, Nepal, MSc. 3rd Semester as a lecture class!!
The document summarizes key aspects of biotechnology and the human genome project. It discusses that the human genome project achieved sequencing the human genome between 1990-2003. It found around 25,000 genes and that non-coding 'junk' DNA plays an important role. It also summarizes sequencing progress on chromosomes Y, X and 1. It discusses uses of genetic engineering like producing insulin in bacteria and other proteins. It outlines techniques like restriction endonucleases, PCR, DNA profiling, gel electrophoresis and cloning.
genome structure and repetitive sequence.pdfNetHelix
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Welcome to our channel, where science meets discovery! In today's enlightening video, we unravel the mysteries of life at its most fundamental level - the chromosomes.
Join us on an exhilarating journey deep within the human cell as we explore the intricate architecture and organization of these tiny yet immensely powerful structures.
Don't forget to subscribe to the channel and hit the notification bell to stay updated with all the latest and exciting content. Thank you for your continuous support and for watching us.
Bacterial genomes provide insights into bacterial function, origins, and diversity. They range in size from 0.6 to over 10 megabase pairs. Analysis of bacterial genomes reveals gene content and organization, as well as base pair composition trends. Bacterial chromosomes are typically circular and condensed via supercoiling, though some bacteria have linear or multiple chromosomes. Genome analysis techniques like GC skew help locate origins of replication.
The document discusses genomic concepts including:
- Genomics is the study of genomes including large chromosomal segments containing many genes. Functional genomics aims to deduce information about DNA function.
- The human genome contains 3.2 billion base pairs with about 3% coding for proteins. Genome size is measured in picograms or base pair number and complexity is distinct from length.
- Chromosomal organization differs between prokaryotes and eukaryotes. Eukaryotes possess multiple linear chromosomes packed into complexes while prokaryotes have single circular chromosomes.
- Much non-coding DNA in large genomes includes introns, regulatory elements, repeats and intergenic sequences. Nucleic acid thermodynamics
Molecular biological techniques utilize DNA, RNA, and enzymes that interact with nucleic acids to understand biology at a molecular level. Molecular pathology applies these techniques to detect and predict disease states by examining things like inherited diseases, infectious diseases, cancers, and genetic variations. Key techniques discussed include DNA hybridization, restriction enzymes, polymerase chain reaction, and analyzing single nucleotide polymorphisms.
UNIQUE AND REPETITIVE DNA.a derailed presentationkingmaxton8
油
The document discusses unique and repetitive DNA sequences found in eukaryotic genomes. It defines unique DNA as sequences present in a single copy that encode for proteins. Repetitive DNA makes up a large portion of eukaryotic genomes and includes highly repetitive sequences like satellite DNA near centromeres, and moderately repetitive sequences dispersed throughout genomes like transposons. The repetitive elements are further classified based on length and copy number as tandem repeats including satellites, minisatellites and microsatellites.
1. DNA is packaged into nucleosomes by winding around histone proteins. This beads-on-a-string structure further condenses into the 30nm chromatin fiber.
2. Chromatin fiber is packaged into either loosely packed euchromatin, which contains actively transcribed genes, or tightly packed heterochromatin, which contains mostly repetitive sequences.
3. During cell division, chromatin maximally condenses into chromosomes, with two arms separated by a centromere and capped by telomeres at either end. This allows for orderly separation of genetic material during cell division.
The document discusses different types of genomes, including viral, bacterial, plant, and animal genomes. It provides details on the structure and size of these genomes. Some key points include:
- A genome is the complete set of DNA or RNA in an organism, including all its genes. It provides all the information needed to build and maintain the organism.
- Viral genomes can be single or double-stranded DNA or RNA and range in size from 2kb to 2500kb. Bacterial genomes are generally smaller than eukaryotic genomes, ranging from 130kb to 14Mbp.
- Plant genomes can vary greatly in size from 15Mbp in green algae to much larger and complex genomes in
This document provides information on genetics and DNA. It discusses that DNA is found coiled in chromatin in the nucleus of cells. During cell division, chromatin coils tightly to form chromosomes which are duplicated so each new cell contains a full set. DNA is made of nucleotides containing a sugar, phosphate, and one of four nitrogenous bases. The bases bond with each other to form the sides of the DNA double helix structure. Experiments by Griffith, Hershey and Chase provided evidence that DNA is the genetic material. Watson and Crick used evidence from Franklin and others to develop the first model of the DNA double helix structure. DNA holds the instructions for development and reproduction and can replicate itself through semiconservative replication.
This document provides information on genetics and DNA. It discusses that DNA is found coiled in chromatin in the nucleus of cells. During cell division, chromatin coils tightly to form chromosomes which are duplicated so each new cell contains a full set. DNA is made of nucleotides containing a sugar, phosphate, and one of four nitrogenous bases. The bases bond with each other to form the DNA double helix structure. Experiments by Griffith, Hershey and Chase provided evidence that DNA is the genetic material. Watson and Crick deduced the DNA structure is a double helix with specific base pairing between A-T and G-C. DNA holds the code for inheritance and protein production. It can replicate through semiconservative replication to make
The document describes Cot curve analysis, a technique used to determine DNA sequence complexity in genomes. DNA is denatured by heating and allowed to renature at different time points. The percentage of single-stranded DNA is plotted against Cot value, the product of DNA concentration and renaturation time. Species with more complex genomes have higher Cot1/2 values as complementary sequences take longer to encounter each other. Eukaryotic genomes contain repetitive sequences that affect the Cot curve shape, with highly repetitive sequences renaturing fastest and single-copy sequences slowest.
The document discusses several key topics related to DNA structure and function:
DNA replication ensures each cell has an exact copy of the DNA before cell division. Errors are constantly checked and repaired to maintain high fidelity. DNA is also rearranged through processes like recombination. The tightly regulated enzymes that perform these metabolic processes were demonstrated by the Meselson-Stahl experiment to replicate DNA using a semiconservative mechanism. DNA is organized through various levels of compaction into condensed chromosomes. This dynamic structure, along with features like centromeres and telomeres, helps regulate DNA accessibility and proper segregation during cell division.
This document summarizes key concepts about DNA as the genetic material. It describes that DNA is found within chromosomes in the nucleus, and that chromosomes contain many genes. Genes code for proteins and functions. The entire human genome contains instructions for making cells. DNA is made up of nucleotides with a phosphate group, sugar, and nitrogenous base. The structure of DNA was discovered to be a double helix. DNA packages into nucleosomes within chromatin and is tightly packed in heterochromatin. A series of experiments by Griffith, Avery, Hershey and Chase provided evidence that DNA is the genetic material that can be transformed and passed from parents to offspring.
The document discusses various topics related to genetics and biotechnology including genetic engineering, polymerase chain reaction (PCR), DNA profiling, and genetically modified foods. It provides definitions and explanations of key terms and processes such as how PCR is used to amplify DNA, the steps involved in PCR including denaturation, annealing and elongation, and how gel electrophoresis can be used to analyze PCR products. It also summarizes techniques like DNA profiling that are used for forensic investigations and paternity testing.
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The document summarizes key aspects of biotechnology and the human genome project. It discusses that the human genome project achieved sequencing the human genome between 1990-2003. It found around 25,000 genes and that non-coding 'junk' DNA plays an important role. It also summarizes sequencing progress on chromosomes Y, X and 1. It discusses uses of genetic engineering like producing insulin in bacteria and other proteins. It outlines techniques like restriction endonucleases, PCR, DNA profiling, gel electrophoresis and cloning.
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Welcome to our channel, where science meets discovery! In today's enlightening video, we unravel the mysteries of life at its most fundamental level - the chromosomes.
Join us on an exhilarating journey deep within the human cell as we explore the intricate architecture and organization of these tiny yet immensely powerful structures.
Don't forget to subscribe to the channel and hit the notification bell to stay updated with all the latest and exciting content. Thank you for your continuous support and for watching us.
Bacterial genomes provide insights into bacterial function, origins, and diversity. They range in size from 0.6 to over 10 megabase pairs. Analysis of bacterial genomes reveals gene content and organization, as well as base pair composition trends. Bacterial chromosomes are typically circular and condensed via supercoiling, though some bacteria have linear or multiple chromosomes. Genome analysis techniques like GC skew help locate origins of replication.
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- The human genome contains 3.2 billion base pairs with about 3% coding for proteins. Genome size is measured in picograms or base pair number and complexity is distinct from length.
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The document discusses unique and repetitive DNA sequences found in eukaryotic genomes. It defines unique DNA as sequences present in a single copy that encode for proteins. Repetitive DNA makes up a large portion of eukaryotic genomes and includes highly repetitive sequences like satellite DNA near centromeres, and moderately repetitive sequences dispersed throughout genomes like transposons. The repetitive elements are further classified based on length and copy number as tandem repeats including satellites, minisatellites and microsatellites.
1. DNA is packaged into nucleosomes by winding around histone proteins. This beads-on-a-string structure further condenses into the 30nm chromatin fiber.
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The document discusses different types of genomes, including viral, bacterial, plant, and animal genomes. It provides details on the structure and size of these genomes. Some key points include:
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2. GENOME:
Genome is the some total of all genetic material
of an organism.
Haploid set of genome present in the cell of an
organism.
Human beings have 3 billion base pairs in their
haploid cells and 6 billion base pairs in their
diploid cells
An organisms may have either DNA or RNA as
their genetic material.
4. It was said that as complexity increases, the c-value ( amount of
DNA) increases from simpler to complex forms.
For e.g; human beings are the high complex organisms and
bacteria,viruses,mycoplasma,algae,fungi are lower organisms which
are simpler forms.
This means that the amount of DNA increases from simpler to
complex forms.
There is a linear relationship between genome size and organism
complexity.
5. WHAT IS THE C VALUE PARADOX?
This term is given by C. A. Thomas in 1971, when repeated sequences
of DNA were discovered, explaining in every case no relationship
between genome size and complexity of organisms.
The DNA content of an organisms genome is related to the
morphological complexity of eukaryotes but it is observed that it is
different in higher eukaryotes.
In higher eukaryotes there is no correlation between complexity and
genomic size; this is called the C value paradox. Genome size is the
total amount of DNA contained within the copy of a single genome.
It is measured in terms of picograms and base pairs.
6. Morphologically similar organisms appear to have different amounts
of DNA in their genome.
Living organisms are classified into two categories: eukaryotes, which
are complex organisms with organized nuclei, and prokaryotes, which
are simpler organisms without organized nuclei.
It was commonly believed that the complexity of an organism was
reflected in its DNA content, with eukaryotes having a higher
percentage of DNA than prokaryotes.
However, recent findings have shown that this is not always the case,
and there are many exceptions to this rule. Therefore, it is incorrect
to assume that the amount of DNA in an organism is always
proportional to its complexity.
7. In other words, we can say simpler the organism smaller the genome,
complex the organism larger the genome.
The complexity of an organism can be predicted by knowing the size
of the genome and the size of the genome can be predicted by the
complexity of an organism.
The eukaryotic genome consists of two parts, coding DNA and non
Coding DNA. Coding DNA is a protein synthesizing DNA and non-
coding DNA is present in multiple copies.
The human genome consists of 2% of Coding DNA and 98% non
Coding DNA.
9. EXAMPLE;
1. Salamanders have 40 times more DNA in comparison to humans,
whereas humans are more complex organisms compared to
salamanders.
2. Housefly and Drosophila both are in the same group but the
housefly C value is higher than Drosophila.
REASON FOR C VALUE PARADOX;
The reason for this is the presence of repetitive DNA, which means
the sequence of DNA which repeats in the genome many times.
10. C VALUE ENIGMA:
C value enigma represents an updated term of the C value paradox, It
was given by Dr. T. Ryan Gregory in 2001.
C value enigma relates to variation in the amount of non Coding DNA
found within the genomes of different eukaryotes.
The variation of non-coding DNA varies from species to species.
C Value enigma explains properly the reason for the C value paradox
and defines what types of non-coding DNA are found in the
eukaryotic genome and its function and what proportions they are
present.
11. COT CURVE ANALYSIS:
It is a technique for measuring the complexity (size) of DNA or genome.
The technique was developed by Roy Britten and Eric Davidson in 1960.
The technique is based on the principle of DNA renaturation kinetics.
Principle: The rate of renaturation is directly proportional to the number of
times the sequences are present in the genome.
Given enough time all DNA that is denatured will reassociate or reanneal in
a given DNA sample.
The more the repetitive sequence the less will be the time taken for
renaturation.
12. PROCEDURE:
The process involves denaturation of DNA
by heating and allowed to reanneal by
cooling.
The renaturation of DNA is assessed
stereoscopically.
Large DNA molecules take longer time to
reanneal.
13. WHAT IS COT VALUE?
The renaturation depends on the following factors DNA
concentration, reassociation temperature, cation concentration and
viscosity.
Cot=DNA Concentration (moles/L) X renaturation time in seconds X
buffer factor (that accounts for the effects of cations on the speed of
renaturation).
Cot:Co=Concentration of DNA and t= time taken for renaturation Low
cot value indicates more number of repetitive sequences
High cot value indicates more number of unique sequences or less
number of repetitive sequences.
For example: Bacteria- 99.7% Single Copy
14. HOW TO CALCULATE COT VALUE?
Cot=DNA Concentration (moles/L) X renaturation time in seconds X
buffer factor (that accounts for the effects of cations on the speed of
renaturation).
Nucleotide concentration = 0.050 M
Renaturation time = 344 sec
Buffer factor, 0.5 M SPB = 5.820
Cot value = 0.050X 344 X 5.820=100.000
16. APPLICATION OF COT CURVE ANALYSIS:
Understanding genome size and
complexity.
Understanding complexity of
sequences.
Understanding relative proportion of
single copy and repetitive sequences.
17. REFERENCES:
1. 4th edition biochemistry Donald Voet &
Judith G. Voet.
2. Lehninger, 4th edition, Principal of
biochemistry, David L. Nelson & Michael.