Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster.
The genomic causes of inbreeding depression are poorly known. Several studies have found widespread transcriptomic alterations in inbred organisms, but it remains unclear which of these alterations are causes of the depression and which are mere responses to the ensuing physiological stress induced...
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doaj-edae2d279c274bf6a22b92f73fb009052020-11-24T22:00:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0187e7006710.1371/journal.pone.0070067Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster.Carlos GarciaVictoria AvilaHumberto QuesadaArmando CaballeroThe genomic causes of inbreeding depression are poorly known. Several studies have found widespread transcriptomic alterations in inbred organisms, but it remains unclear which of these alterations are causes of the depression and which are mere responses to the ensuing physiological stress induced by increased homozygosity due to inbreeding. Attempting to differentiate causes from responses, we made a c-DNA microarray analysis of inbreeding depression in Drosophila melanogaster. The rationale of the experiment was that, while depression is a general phenomenon involving reductions in fitness in different inbred lines, its first genetic causes would be different for each inbred line, as they are expected to be caused by the fixation of rare deleterious genes. We took four sets of inbred sublines, each set descending from a different founding pair obtained from a large outbred stock, and compared the expression of the three most depressed sublines and the three least depressed sublines from each set. Many changes in expression were common to all sets, but fourteen genes, grouped in four expression clusters, showed strong set-specific changes, and were therefore possible candidates to be sources of the inbreeding depression observed.http://europepmc.org/articles/PMC3726430?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Carlos Garcia Victoria Avila Humberto Quesada Armando Caballero |
spellingShingle |
Carlos Garcia Victoria Avila Humberto Quesada Armando Caballero Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster. PLoS ONE |
author_facet |
Carlos Garcia Victoria Avila Humberto Quesada Armando Caballero |
author_sort |
Carlos Garcia |
title |
Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster. |
title_short |
Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster. |
title_full |
Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster. |
title_fullStr |
Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster. |
title_full_unstemmed |
Candidate transcriptomic sources of inbreeding depression in Drosophila melanogaster. |
title_sort |
candidate transcriptomic sources of inbreeding depression in drosophila melanogaster. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
The genomic causes of inbreeding depression are poorly known. Several studies have found widespread transcriptomic alterations in inbred organisms, but it remains unclear which of these alterations are causes of the depression and which are mere responses to the ensuing physiological stress induced by increased homozygosity due to inbreeding. Attempting to differentiate causes from responses, we made a c-DNA microarray analysis of inbreeding depression in Drosophila melanogaster. The rationale of the experiment was that, while depression is a general phenomenon involving reductions in fitness in different inbred lines, its first genetic causes would be different for each inbred line, as they are expected to be caused by the fixation of rare deleterious genes. We took four sets of inbred sublines, each set descending from a different founding pair obtained from a large outbred stock, and compared the expression of the three most depressed sublines and the three least depressed sublines from each set. Many changes in expression were common to all sets, but fourteen genes, grouped in four expression clusters, showed strong set-specific changes, and were therefore possible candidates to be sources of the inbreeding depression observed. |
url |
http://europepmc.org/articles/PMC3726430?pdf=render |
work_keys_str_mv |
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