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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Main Authors: Carlos Garcia, Victoria Avila, Humberto Quesada, Armando Caballero
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3726430?pdf=render
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spelling 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
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AT humbertoquesada candidatetranscriptomicsourcesofinbreedingdepressionindrosophilamelanogaster
AT armandocaballero candidatetranscriptomicsourcesofinbreedingdepressionindrosophilamelanogaster
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