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Nucleotide diversity inflation as a genome- wide response to experimental lifespan extension in Drosophila melanogaster

Michalak, Pawel ; Kang, Lin ; Sarup, Pernille M ; Schou, Mads F LU and Loeschcke, Volker (2017) In BMC Genomics 18.
Abstract
Background: Evolutionary theory predicts that antagonistically selected alleles, such as those with divergent pleiotropic effects in early and late life, may often reach intermediate population frequencies due to balancing selection, an elusive process when sought out empirically. Alternatively, genetic diversity may increase as a result of positive frequency-dependent selection and genetic purging in bottlenecked populations.
Results: While experimental evolution systems with directional phenotypic selection typically result in at least local heterozygosity loss, we report that selection for increased lifespan in Drosophila melanogaster leads to an extensive
genome-wide increase of nucleotide diversity in the selected lines... (More)
Background: Evolutionary theory predicts that antagonistically selected alleles, such as those with divergent pleiotropic effects in early and late life, may often reach intermediate population frequencies due to balancing selection, an elusive process when sought out empirically. Alternatively, genetic diversity may increase as a result of positive frequency-dependent selection and genetic purging in bottlenecked populations.
Results: While experimental evolution systems with directional phenotypic selection typically result in at least local heterozygosity loss, we report that selection for increased lifespan in Drosophila melanogaster leads to an extensive
genome-wide increase of nucleotide diversity in the selected lines compared to replicate control lines, pronounced in regions with no or low recombination, such as chromosome 4 and centromere neighborhoods. These changes,
particularly in coding sequences, are most consistent with the operation of balancing selection and the antagonistic pleiotropy theory of aging and life history traits that tend to be intercorrelated. Genes involved in antioxidant defenses, along with multiple lncRNAs, were among those most affected by balancing selection. Despite the overwhelming genetic diversification and the paucity of selective sweep regions, two genes with functions important for central nervous system and memory, Ptp10D and Ank2, evolved under positive selection in the longevity lines.
Conclusions: Overall, the ‘evolve-and-resequence’ experimental approach proves successful in providing unique insights into the complex evolutionary dynamics of genomic regions responsible for longevity. (Less)
Please use this url to cite or link to this publication:
author
; ; ; and
publishing date
type
Contribution to journal
publication status
published
subject
in
BMC Genomics
volume
18
article number
18:84
pages
11 pages
publisher
BioMed Central (BMC)
external identifiers
  • pmid:28088192
  • scopus:85009373415
ISSN
1471-2164
DOI
10.1186/s12864-017-3485-0
language
English
LU publication?
no
id
97c5bf73-ae97-45b1-94a1-5bedb2f1ef43
alternative location
http://dx.doi.org/10.1186/s12864-017-3485-0
date added to LUP
2017-12-18 09:40:58
date last changed
2022-04-01 21:26:41
@article{97c5bf73-ae97-45b1-94a1-5bedb2f1ef43,
  abstract     = {{Background: Evolutionary theory predicts that antagonistically selected alleles, such as those with divergent pleiotropic effects in early and late life, may often reach intermediate population frequencies due to balancing selection, an elusive process when sought out empirically. Alternatively, genetic diversity may increase as a result of positive frequency-dependent selection and genetic purging in bottlenecked populations.<br/>Results: While experimental evolution systems with directional phenotypic selection typically result in at least local heterozygosity loss, we report that selection for increased lifespan in Drosophila melanogaster leads to an extensive<br/>genome-wide increase of nucleotide diversity in the selected lines compared to replicate control lines, pronounced in regions with no or low recombination, such as chromosome 4 and centromere neighborhoods. These changes,<br/>particularly in coding sequences, are most consistent with the operation of balancing selection and the antagonistic pleiotropy theory of aging and life history traits that tend to be intercorrelated. Genes involved in antioxidant defenses, along with multiple lncRNAs, were among those most affected by balancing selection. Despite the overwhelming genetic diversification and the paucity of selective sweep regions, two genes with functions important for central nervous system and memory, Ptp10D and Ank2, evolved under positive selection in the longevity lines.<br/>Conclusions: Overall, the ‘evolve-and-resequence’ experimental approach proves successful in providing unique insights into the complex evolutionary dynamics of genomic regions responsible for longevity.}},
  author       = {{Michalak, Pawel and Kang, Lin and Sarup, Pernille M and Schou, Mads F and Loeschcke, Volker}},
  issn         = {{1471-2164}},
  language     = {{eng}},
  publisher    = {{BioMed Central (BMC)}},
  series       = {{BMC Genomics}},
  title        = {{Nucleotide diversity inflation as a genome- wide response to experimental lifespan extension in Drosophila melanogaster}},
  url          = {{http://dx.doi.org/10.1186/s12864-017-3485-0}},
  doi          = {{10.1186/s12864-017-3485-0}},
  volume       = {{18}},
  year         = {{2017}},
}