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Quantitative genomics of starvation stress resistance in Drosophila

BACKGROUND: A major challenge of modern biology is to understand the networks of interacting genes regulating complex traits, and the subset of these genes that affect naturally occurring quantitative genetic variation. Previously, we used P-element mutagenesis and quantitative trait locus (QTL) map...

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Autores principales: Harbison, Susan T, Chang, Sherman, Kamdar, Kim P, Mackay, Trudy FC
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1088964/
https://www.ncbi.nlm.nih.gov/pubmed/15833123
http://dx.doi.org/10.1186/gb-2005-6-4-r36
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author Harbison, Susan T
Chang, Sherman
Kamdar, Kim P
Mackay, Trudy FC
author_facet Harbison, Susan T
Chang, Sherman
Kamdar, Kim P
Mackay, Trudy FC
author_sort Harbison, Susan T
collection PubMed
description BACKGROUND: A major challenge of modern biology is to understand the networks of interacting genes regulating complex traits, and the subset of these genes that affect naturally occurring quantitative genetic variation. Previously, we used P-element mutagenesis and quantitative trait locus (QTL) mapping in Drosophila to identify candidate genes affecting resistance to starvation stress, and variation in resistance to starvation stress between the Oregon-R (Ore) and 2b strains. Here, we tested the efficacy of whole-genome transcriptional profiling for identifying genes affecting starvation stress resistance. RESULTS: We evaluated whole-genome transcript abundance for males and females of Ore, 2b, and four recombinant inbred lines derived from them, under control and starved conditions. There were significant differences in transcript abundance between the sexes for nearly 50% of the genome, while the transcriptional response to starvation stress involved approximately 25% of the genome. Nearly 50% of P-element insertions in 160 genes with altered transcript abundance during starvation stress had mutational effects on starvation tolerance. Approximately 5% of the genome exhibited genetic variation in transcript abundance, which was largely attributable to regulation by unlinked genes. Genes exhibiting variation in transcript abundance among lines did not cluster within starvation resistance QTLs, and none of the candidate genes affecting variation in starvation resistance between Ore and 2b exhibited significant differences in transcript abundance between lines. CONCLUSIONS: Expression profiling is a powerful method for identifying networks of pleiotropic genes regulating complex traits, but the relationship between variation in transcript abundance among lines used to map QTLs and genes affecting variation in quantitative traits is complicated.
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spelling pubmed-10889642005-05-05 Quantitative genomics of starvation stress resistance in Drosophila Harbison, Susan T Chang, Sherman Kamdar, Kim P Mackay, Trudy FC Genome Biol Research BACKGROUND: A major challenge of modern biology is to understand the networks of interacting genes regulating complex traits, and the subset of these genes that affect naturally occurring quantitative genetic variation. Previously, we used P-element mutagenesis and quantitative trait locus (QTL) mapping in Drosophila to identify candidate genes affecting resistance to starvation stress, and variation in resistance to starvation stress between the Oregon-R (Ore) and 2b strains. Here, we tested the efficacy of whole-genome transcriptional profiling for identifying genes affecting starvation stress resistance. RESULTS: We evaluated whole-genome transcript abundance for males and females of Ore, 2b, and four recombinant inbred lines derived from them, under control and starved conditions. There were significant differences in transcript abundance between the sexes for nearly 50% of the genome, while the transcriptional response to starvation stress involved approximately 25% of the genome. Nearly 50% of P-element insertions in 160 genes with altered transcript abundance during starvation stress had mutational effects on starvation tolerance. Approximately 5% of the genome exhibited genetic variation in transcript abundance, which was largely attributable to regulation by unlinked genes. Genes exhibiting variation in transcript abundance among lines did not cluster within starvation resistance QTLs, and none of the candidate genes affecting variation in starvation resistance between Ore and 2b exhibited significant differences in transcript abundance between lines. CONCLUSIONS: Expression profiling is a powerful method for identifying networks of pleiotropic genes regulating complex traits, but the relationship between variation in transcript abundance among lines used to map QTLs and genes affecting variation in quantitative traits is complicated. BioMed Central 2005 2005-03-24 /pmc/articles/PMC1088964/ /pubmed/15833123 http://dx.doi.org/10.1186/gb-2005-6-4-r36 Text en Copyright © 2005 Harbison et al.; licensee BioMed Central Ltd.
spellingShingle Research
Harbison, Susan T
Chang, Sherman
Kamdar, Kim P
Mackay, Trudy FC
Quantitative genomics of starvation stress resistance in Drosophila
title Quantitative genomics of starvation stress resistance in Drosophila
title_full Quantitative genomics of starvation stress resistance in Drosophila
title_fullStr Quantitative genomics of starvation stress resistance in Drosophila
title_full_unstemmed Quantitative genomics of starvation stress resistance in Drosophila
title_short Quantitative genomics of starvation stress resistance in Drosophila
title_sort quantitative genomics of starvation stress resistance in drosophila
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1088964/
https://www.ncbi.nlm.nih.gov/pubmed/15833123
http://dx.doi.org/10.1186/gb-2005-6-4-r36
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