Related Experiment Video
Updated: May 5, 2026

11:27
Studying DNA Looping by Single-Molecule FRET
Published on: June 28, 2014
14.8K
Distributions of dimeric tandem repeats in non-coding and coding DNA sequences.
N V Dokholyan1, S V Buldyrev, S Havlin
1Center for Polymer Studies, Boston University, Boston, MA 02215, USA. dokh@wild.harvard.edu
Journal of Theoretical Biology
|February 10, 2000
Summary
DNA tandem repeat length distributions differ between coding and non-coding regions. Coding DNA shows exponential distributions, while non-coding DNA exhibits power-law tails, suggesting varying evolutionary pressures and mutation tolerance across species.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Tandem repeats are repetitive DNA sequences.
- Their length distributions can reveal insights into DNA evolution and function.
- Previous studies have explored repeat distributions, but a comprehensive analysis across diverse taxa and DNA types is needed.
Purpose of the Study:
- To analyze the length distribution functions of all 16 possible dimeric tandem repeats.
- To compare these distributions across coding and non-coding DNA in diverse species.
- To investigate the evolutionary and mutational factors shaping these distributions.
Main Methods:
- Analysis of DNA sequences from human, mouse, Caenorhabditis elegans, and yeast genomes.
- Statistical modeling of dimeric tandem repeat length distributions.
- Comparative genomics across different taxonomic partitions.
Main Results:
- All 16 dimeric tandem repeat distributions in coding DNA are exponential.
- Most dimeric repeat distributions in non-coding DNA show long tails fitting a power-law function.
- Distribution shapes vary significantly across species and dimer types, indicating a lack of universality.
Conclusions:
- Exponential distributions in coding DNA suggest strong evolutionary pressure against repeat expansion.
- Power-law tails in non-coding DNA may result from higher mutation tolerance and diverse mutational mechanisms.
- The non-universal nature of these distributions highlights species-specific genomic characteristics.
More Related Videos
Related Concept Videos
Gene Families
8.0K
Gene families consist of groups of genes proposed to have originated from a common ancestor. Typically these arise through events in which a gene or genes are mistakenly duplicated during cell division. Unlike their parent genes (which are subject to selection pressure to maintain function), these gene copies do not need to preserve their sequences and may evolve at a relatively faster rate.
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
Occasionally these regions can be adapted to take on new roles within the organism, becoming novel genes...
8.0K
Polytene Chromosomes
9.3K
Polytene chromosomes are giant interphase chromosomes with several DNA strands placed side by side. They were discovered in the year 1881 by Balbiani in salivary glands, intestine, muscles, malpighian tubules, and hypoderm of larvae Chironomus plumosus. Hence, these are also called "Salivary gland chromosomes." These are found in insects of the order Diptera and Collembola; in certain organs of mammals; and synergids, antipodes of flowering plants. Polytene chromosomes are also...
9.3K
Cooperative Binding of Transcription Regulators
6.0K
Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome. Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form...
6.0K
Gene Duplication and Divergence
6.8K
The seminal work of Ohno in 1970 popularized the idea of gene duplication and divergence. DNA sequence comparison studies reveal that a large portion of the genes in bacteria, archaebacteria, and eukaryotes was generated by gene duplication and divergence, indicating its critical role in evolution.
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are...
The duplicated copies of the gene are called Paralogs. Paralogs with similar sequences and functions form a gene family. Across several species, a large number of gene families are...
6.8K
Comparing Copy Number Variations and SNPs
11.6K
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%...
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%...
11.6K
Sanger Sequencing
800.8K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
800.8K

