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Related Concept Videos

The Nucleosome01:19

The Nucleosome

Human DNA is almost two meters long. However, it is compressed inside a tiny nucleus measuring only a few microns in diameter. To make this degree of compaction possible, DNA is organized into several sequential levels so that it can fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
In a chromosome, DNA is wound twice around a protein complex called a histone octamer core, which consists of 8 histone proteins. This...
The Nucleosome02:33

The Nucleosome

DNA in a human cell is almost 2m long and it is packed inside a tiny nucleus that is only a few microns in diameter. The level of compaction of DNA inside the nucleus is astonishing. It is organized into several sequentially higher levels of compaction to fit into such a tiny space. The most compact form of DNA is a chromosome that can be seen under a microscope in a dividing cell.
DNA is wound twice around a protein complex called histone core, that consist of 8 histone proteins. This complex...
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
Nucleic Acids and Nucleotides01:20

Nucleic Acids and Nucleotides

Nucleic acids are the most important macromolecules for the continuity of life. They carry the cell's genetic blueprint and have instructions for its functioning. The two main types of nucleic acids are deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
Deoxyribonucleic Acid (DNA)
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DNA as a Genetic Template02:05

DNA as a Genetic Template

Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...

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Electrophoretic Analysis of Replication Through Structure-Prone DNA Repeats Within the SV40-Based Human Episome
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Electrophoretic Analysis of Replication Through Structure-Prone DNA Repeats Within the SV40-Based Human Episome

Published on: September 13, 2024

Genome nucleotide composition shapes variation in simple sequence repeats.

Xiangjun Tian1, Joan E Strassmann, David C Queller

  • 1Department of Ecology and Evolutionary Biology, Rice University, USA.

Molecular Biology and Evolution
|October 15, 2010
PubMed
Summary
This summary is machine-generated.

Genome nucleotide composition significantly influences the abundance and types of simple sequence repeats (SSRs), also known as microsatellites. Higher AT or GC content correlates with increased SSRs, with a dip around 50% AT content.

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Area of Science:

  • Genomics
  • Molecular Biology
  • Bioinformatics

Background:

  • Simple sequence repeats (SSRs), or microsatellites, are prevalent in genomes but exhibit significant interspecies variation in abundance.
  • The underlying drivers of this variation, particularly the role of genome nucleotide composition, remain incompletely understood.

Purpose of the Study:

  • To investigate the relationship between genome AT/GC content and the abundance and characteristics of simple sequence repeats (SSRs).
  • To test the hypothesis that genomes with extreme AT or GC bias generate more SSRs due to replication slippage.

Main Methods:

  • Identification of perfect tandem repeats (1-6 bp iterations) across 25 diverse protist genomes.
  • Statistical analysis, including quadratic regressions, to correlate SSR density, frequency, and motif composition with genome-wide AT/GC content.

Main Results:

  • SSR density and frequency show a strong quadratic correlation with genome AT content, with minima near 50% AT and increasing abundance towards both extremes.
  • The composition of SSR motifs (AT-rich vs. GC-rich) is significantly correlated with genome nucleotide bias.
  • Amino acid homopolymer repeats also exhibit a quadratic relationship with AT content.

Conclusions:

  • Genome nucleotide composition is a major determinant of SSR abundance and motif makeup, explaining up to half of the observed variance.
  • The findings support the hypothesis that replication slippage mechanisms are influenced by local nucleotide composition, impacting SSR formation.