During evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes

Abstract Background The present availability of full genome sequences of a broad range of animal species across the whole range of evolutionary history enables one to ask questions as to the distribution of genes across the chromosomes. Do newly recruited genes, as new clades emerge, distribute at r...

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Autores principales: Wilfred D. Stein, Moshe B. Hoshen
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Lenguaje:EN
Publicado: BMC 2021
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Acceso en línea:https://doaj.org/article/57830cb866eb446b8aed688b5222ae85
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spelling oai:doaj.org-article:57830cb866eb446b8aed688b5222ae852021-11-08T10:57:31ZDuring evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes10.1186/s12864-021-08066-31471-2164https://doaj.org/article/57830cb866eb446b8aed688b5222ae852021-11-01T00:00:00Zhttps://doi.org/10.1186/s12864-021-08066-3https://doaj.org/toc/1471-2164Abstract Background The present availability of full genome sequences of a broad range of animal species across the whole range of evolutionary history enables one to ask questions as to the distribution of genes across the chromosomes. Do newly recruited genes, as new clades emerge, distribute at random or at non-random locations? Results We extracted values for the ages of the human genes and for their current chromosome locations, from published sources. A quantitative analysis showed that the distribution of newly-added genes among and within the chromosomes appears to be increasingly non-random if one observes animals along the evolutionary series from the precursors of the tetrapoda through to the great apes, whereas the oldest genes are randomly distributed. Conclusions Randomization will result from chromosome evolution, but less and less time is available for this process as evolution proceeds. Much of the bunching of recently-added genes arises from new gene formation as paralogues in gene families, near the location of genes that were recruited in the preceding phylostratum. As examples we cite the KRTAP, ZNF, OR and some minor gene families. We show that bunching can also result from the evolution of the chromosomes themselves when, as for the KRTAP genes, blocks of genes that had previously been on disparate chromosomes become linked together.Wilfred D. SteinMoshe B. HoshenBMCarticleChromosomesGene distributionNewly-recruited genesParaloguesPhylostratigraphyGene agesBiotechnologyTP248.13-248.65GeneticsQH426-470ENBMC Genomics, Vol 22, Iss 1, Pp 1-17 (2021)
institution DOAJ
collection DOAJ
language EN
topic Chromosomes
Gene distribution
Newly-recruited genes
Paralogues
Phylostratigraphy
Gene ages
Biotechnology
TP248.13-248.65
Genetics
QH426-470
spellingShingle Chromosomes
Gene distribution
Newly-recruited genes
Paralogues
Phylostratigraphy
Gene ages
Biotechnology
TP248.13-248.65
Genetics
QH426-470
Wilfred D. Stein
Moshe B. Hoshen
During evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes
description Abstract Background The present availability of full genome sequences of a broad range of animal species across the whole range of evolutionary history enables one to ask questions as to the distribution of genes across the chromosomes. Do newly recruited genes, as new clades emerge, distribute at random or at non-random locations? Results We extracted values for the ages of the human genes and for their current chromosome locations, from published sources. A quantitative analysis showed that the distribution of newly-added genes among and within the chromosomes appears to be increasingly non-random if one observes animals along the evolutionary series from the precursors of the tetrapoda through to the great apes, whereas the oldest genes are randomly distributed. Conclusions Randomization will result from chromosome evolution, but less and less time is available for this process as evolution proceeds. Much of the bunching of recently-added genes arises from new gene formation as paralogues in gene families, near the location of genes that were recruited in the preceding phylostratum. As examples we cite the KRTAP, ZNF, OR and some minor gene families. We show that bunching can also result from the evolution of the chromosomes themselves when, as for the KRTAP genes, blocks of genes that had previously been on disparate chromosomes become linked together.
format article
author Wilfred D. Stein
Moshe B. Hoshen
author_facet Wilfred D. Stein
Moshe B. Hoshen
author_sort Wilfred D. Stein
title During evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes
title_short During evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes
title_full During evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes
title_fullStr During evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes
title_full_unstemmed During evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes
title_sort during evolution from the earliest tetrapoda, newly-recruited genes are increasingly paralogues of existing genes and distribute non-randomly among the chromosomes
publisher BMC
publishDate 2021
url https://doaj.org/article/57830cb866eb446b8aed688b5222ae85
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