Literature DB >> 26003631

Adaptive potential of genomic structural variation in human and mammalian evolution.

David W Radke, Charles Lee.   

Abstract

Because phenotypic innovations must be genetically heritable for biological evolution to proceed, it is natural to consider new mutation events as well as standing genetic variation as sources for their birth. Previous research has identified a number of single-nucleotide polymorphisms that underlie a subset of adaptive traits in organisms. However, another well-known class of variation, genomic structural variation, could have even greater potential to produce adaptive phenotypes, due to the variety of possible types of alterations (deletions, insertions, duplications, among others) at different genomic positions and with variable lengths. It is from these dramatic genomic alterations, and selection on their phenotypic consequences, that adaptations leading to biological diversification could be derived. In this review, using studies in humans and other mammals, we highlight examples of how phenotypic variation from structural variants might become adaptive in populations and potentially enable biological diversification. Phenotypic change arising from structural variants will be described according to their immediate effect on organismal metabolic processes, immunological response and physical features. Study of population dynamics of segregating structural variation can therefore provide a window into understanding current and historical biological diversification.
© The Author 2015. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  adaptive variant; copy number variation; evolution; genomic structural variation; nonpathogenic phenotype; segregating polymorphisms

Mesh:

Year:  2015        PMID: 26003631      PMCID: PMC6278953          DOI: 10.1093/bfgp/elv019

Source DB:  PubMed          Journal:  Brief Funct Genomics        ISSN: 2041-2649            Impact factor:   4.241


  126 in total

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Authors:  J Ren; H Mao; Z Zhang; S Xiao; N Ding; L Huang
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6.  Copy number variation influences gene expression and metabolic traits in mice.

Authors:  Luz D Orozco; Shawn J Cokus; Anatole Ghazalpour; Leslie Ingram-Drake; Susanna Wang; Atila van Nas; Nam Che; Jesus A Araujo; Matteo Pellegrini; Aldons J Lusis
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7.  CCL3L1 copy number variation and susceptibility to HIV-1 infection: a meta-analysis.

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8.  Large multiallelic copy number variations in humans.

Authors:  Robert E Handsaker; Vanessa Van Doren; Jennifer R Berman; Giulio Genovese; Seva Kashin; Linda M Boettger; Steven A McCarroll
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Journal:  PLoS Genet       Date:  2013-01-17       Impact factor: 5.917

10.  Impact of constitutional copy number variants on biological pathway evolution.

Authors:  Maria Poptsova; Samprit Banerjee; Omer Gokcumen; Mark A Rubin; Francesca Demichelis
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3.  Absolute quantification reveals the stable transmission of a high copy number variant linked to autoinflammatory disease.

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4.  Analysis of Copy Number Variation in the Abp Gene Regions of Two House Mouse Subspecies Suggests Divergence during the Gene Family Expansions.

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7.  Similarity-Based Analysis of Allele Frequency Distribution among Multiple Populations Identifies Adaptive Genomic Structural Variants.

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Review 8.  The Role of Structural Variation in Adaptation and Evolution of Yeast and Other Fungi.

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  8 in total

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