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Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics

Mammalian genomes are replete with millions of polymorphic sites, among which those genetic variants that are colocated on the same chromosome and exist close to one another form blocks of closely linked mutations known as haplotypes. The linkage within haplotypes is constantly disrupted due to meio...

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Autores principales: Qiu, Shuhao, McSweeny, Andrew, Choulet, Samuel, Saha-Mandal, Arnab, Fedorova, Larisa, Fedorov, Alexei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007542/
https://www.ncbi.nlm.nih.gov/pubmed/24723728
http://dx.doi.org/10.1093/gbe/evu075
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author Qiu, Shuhao
McSweeny, Andrew
Choulet, Samuel
Saha-Mandal, Arnab
Fedorova, Larisa
Fedorov, Alexei
author_facet Qiu, Shuhao
McSweeny, Andrew
Choulet, Samuel
Saha-Mandal, Arnab
Fedorova, Larisa
Fedorov, Alexei
author_sort Qiu, Shuhao
collection PubMed
description Mammalian genomes are replete with millions of polymorphic sites, among which those genetic variants that are colocated on the same chromosome and exist close to one another form blocks of closely linked mutations known as haplotypes. The linkage within haplotypes is constantly disrupted due to meiotic recombination events. Whole ensembles of such numerous haplotypes are subjected to evolutionary pressure, where mutations influence each other and should be considered as a whole entity—a gigantic matrix, unique for each individual genome. This idea was implemented into a computational approach, named Genome Evolution by Matrix Algorithms (GEMA) to model genomic changes taking into account all mutations in a population. GEMA has been tested for modeling of entire human chromosomes. The program can precisely mimic real biological processes that have influence on genome evolution such as: 1) Authentic arrangements of genes and functional genomic elements, 2) frequencies of various types of mutations in different nucleotide contexts, and 3) nonrandom distribution of meiotic recombination events along chromosomes. Computer modeling with GEMA has demonstrated that the number of meiotic recombination events per gamete is among the most crucial factors influencing population fitness. In humans, these recombinations create a gamete genome consisting on an average of 48 pieces of corresponding parental chromosomes. Such highly mosaic gamete structure allows preserving fitness of population under the intense influx of novel mutations (40 per individual) even when the number of mutations with deleterious effects is up to ten times more abundant than those with beneficial effects.
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spelling pubmed-40075422014-05-02 Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics Qiu, Shuhao McSweeny, Andrew Choulet, Samuel Saha-Mandal, Arnab Fedorova, Larisa Fedorov, Alexei Genome Biol Evol Research Article Mammalian genomes are replete with millions of polymorphic sites, among which those genetic variants that are colocated on the same chromosome and exist close to one another form blocks of closely linked mutations known as haplotypes. The linkage within haplotypes is constantly disrupted due to meiotic recombination events. Whole ensembles of such numerous haplotypes are subjected to evolutionary pressure, where mutations influence each other and should be considered as a whole entity—a gigantic matrix, unique for each individual genome. This idea was implemented into a computational approach, named Genome Evolution by Matrix Algorithms (GEMA) to model genomic changes taking into account all mutations in a population. GEMA has been tested for modeling of entire human chromosomes. The program can precisely mimic real biological processes that have influence on genome evolution such as: 1) Authentic arrangements of genes and functional genomic elements, 2) frequencies of various types of mutations in different nucleotide contexts, and 3) nonrandom distribution of meiotic recombination events along chromosomes. Computer modeling with GEMA has demonstrated that the number of meiotic recombination events per gamete is among the most crucial factors influencing population fitness. In humans, these recombinations create a gamete genome consisting on an average of 48 pieces of corresponding parental chromosomes. Such highly mosaic gamete structure allows preserving fitness of population under the intense influx of novel mutations (40 per individual) even when the number of mutations with deleterious effects is up to ten times more abundant than those with beneficial effects. Oxford University Press 2014-04-10 /pmc/articles/PMC4007542/ /pubmed/24723728 http://dx.doi.org/10.1093/gbe/evu075 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Qiu, Shuhao
McSweeny, Andrew
Choulet, Samuel
Saha-Mandal, Arnab
Fedorova, Larisa
Fedorov, Alexei
Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics
title Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics
title_full Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics
title_fullStr Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics
title_full_unstemmed Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics
title_short Genome Evolution by Matrix Algorithms: Cellular Automata Approach to Population Genetics
title_sort genome evolution by matrix algorithms: cellular automata approach to population genetics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007542/
https://www.ncbi.nlm.nih.gov/pubmed/24723728
http://dx.doi.org/10.1093/gbe/evu075
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