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Feminization of complex traits in Drosophila melanogaster via female-limited X chromosome evolution

Lund-Hansen, Katrine K. LU orcid ; Abbott, Jessica K. LU orcid and Morrow, Edward H. (2020) In Evolution 74(12). p.2703-2713
Abstract

A handful of studies have investigated sexually antagonistic constraints on achieving sex-specific fitness optima, although exclusively through male-genome-limited evolution experiments. In this article, we established a female-limited X chromosome evolution experiment, where we used an X chromosome balancer to enforce the inheritance of the X through the matriline, thus removing exposure to male selective constraints. This approach eliminates the effects of sexually antagonistic selection on the X chromosome, permitting evolution toward a single sex-specific optimum. After multiple generations of selection, we found strong evidence that body size and development time had moved toward a female-specific optimum, whereas reproductive... (More)

A handful of studies have investigated sexually antagonistic constraints on achieving sex-specific fitness optima, although exclusively through male-genome-limited evolution experiments. In this article, we established a female-limited X chromosome evolution experiment, where we used an X chromosome balancer to enforce the inheritance of the X through the matriline, thus removing exposure to male selective constraints. This approach eliminates the effects of sexually antagonistic selection on the X chromosome, permitting evolution toward a single sex-specific optimum. After multiple generations of selection, we found strong evidence that body size and development time had moved toward a female-specific optimum, whereas reproductive fitness and locomotion activity remained unchanged. The changes in body size and development time are consistent with previous results, and suggest that the X chromosome is enriched for sexually antagonistic genetic variation controlling these particular traits. The lack of change in reproductive fitness and locomotion activity could be due to a number of mutually nonexclusive explanations, including a lack of sexually antagonistic variance on the X chromosome for those traits or confounding effects of the use of the balancer chromosome. This study is the first to employ female-genome-limited selection and adds to the understanding of the complexity of sexually antagonistic genetic variation.

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author
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publishing date
type
Contribution to journal
publication status
published
subject
keywords
Drosophila melanogaster, experimental evolution, intralocus sexual conflict, sex chromosomes, sexual antagonism
in
Evolution
volume
74
issue
12
pages
11 pages
publisher
Wiley-Blackwell
external identifiers
  • scopus:85085885011
  • pmid:32438467
ISSN
0014-3820
DOI
10.1111/evo.14021
language
English
LU publication?
yes
id
e4a2a2f4-931e-4b88-b12a-2285979cacb4
date added to LUP
2020-07-03 11:50:17
date last changed
2024-06-26 18:15:38
@article{e4a2a2f4-931e-4b88-b12a-2285979cacb4,
  abstract     = {{<p>A handful of studies have investigated sexually antagonistic constraints on achieving sex-specific fitness optima, although exclusively through male-genome-limited evolution experiments. In this article, we established a female-limited X chromosome evolution experiment, where we used an X chromosome balancer to enforce the inheritance of the X through the matriline, thus removing exposure to male selective constraints. This approach eliminates the effects of sexually antagonistic selection on the X chromosome, permitting evolution toward a single sex-specific optimum. After multiple generations of selection, we found strong evidence that body size and development time had moved toward a female-specific optimum, whereas reproductive fitness and locomotion activity remained unchanged. The changes in body size and development time are consistent with previous results, and suggest that the X chromosome is enriched for sexually antagonistic genetic variation controlling these particular traits. The lack of change in reproductive fitness and locomotion activity could be due to a number of mutually nonexclusive explanations, including a lack of sexually antagonistic variance on the X chromosome for those traits or confounding effects of the use of the balancer chromosome. This study is the first to employ female-genome-limited selection and adds to the understanding of the complexity of sexually antagonistic genetic variation.</p>}},
  author       = {{Lund-Hansen, Katrine K. and Abbott, Jessica K. and Morrow, Edward H.}},
  issn         = {{0014-3820}},
  keywords     = {{Drosophila melanogaster; experimental evolution; intralocus sexual conflict; sex chromosomes; sexual antagonism}},
  language     = {{eng}},
  number       = {{12}},
  pages        = {{2703--2713}},
  publisher    = {{Wiley-Blackwell}},
  series       = {{Evolution}},
  title        = {{Feminization of complex traits in Drosophila melanogaster via female-limited X chromosome evolution}},
  url          = {{http://dx.doi.org/10.1111/evo.14021}},
  doi          = {{10.1111/evo.14021}},
  volume       = {{74}},
  year         = {{2020}},
}