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Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster

Wild populations of the model organism Drosophila melanogaster experience highly heterogeneous environments over broad geographical ranges as well as over seasonal and annual timescales. Diapause is a primary adaptation to environmental heterogeneity, and in D. melanogaster the propensity to enter d...

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Autores principales: Zhao, Xiaqing, Bergland, Alan O., Behrman, Emily L., Gregory, Brian D., Petrov, Dmitri A., Schmidt, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009998/
https://www.ncbi.nlm.nih.gov/pubmed/26568616
http://dx.doi.org/10.1093/molbev/msv263
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author Zhao, Xiaqing
Bergland, Alan O.
Behrman, Emily L.
Gregory, Brian D.
Petrov, Dmitri A.
Schmidt, Paul S.
author_facet Zhao, Xiaqing
Bergland, Alan O.
Behrman, Emily L.
Gregory, Brian D.
Petrov, Dmitri A.
Schmidt, Paul S.
author_sort Zhao, Xiaqing
collection PubMed
description Wild populations of the model organism Drosophila melanogaster experience highly heterogeneous environments over broad geographical ranges as well as over seasonal and annual timescales. Diapause is a primary adaptation to environmental heterogeneity, and in D. melanogaster the propensity to enter diapause varies predictably with latitude and season. Here we performed global transcriptomic profiling of naturally occurring variation in diapause expression elicited by short day photoperiod and moderately low temperature in two tissue types associated with neuroendocrine and endocrine signaling, heads, and ovaries. We show that diapause in D. melanogaster is an actively regulated phenotype at the transcriptional level, suggesting that diapause is not a simple physiological or reproductive quiescence. Differentially expressed genes and pathways are highly distinct in heads and ovaries, demonstrating that the diapause response is not uniform throughout the soma and suggesting that it may be comprised of functional modules associated with specific tissues. Genes downregulated in heads of diapausing flies are significantly enriched for clinally varying single nucleotide polymorphism (SNPs) and seasonally oscillating SNPs, consistent with the hypothesis that diapause is a driving phenotype of climatic adaptation. We also show that chromosome location-based coregulation of gene expression is present in the transcriptional regulation of diapause. Taken together, these results demonstrate that diapause is a complex phenotype actively regulated in multiple tissues, and support the hypothesis that natural variation in diapause propensity underlies adaptation to spatially and temporally varying selective pressures.
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spelling pubmed-50099982017-03-01 Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster Zhao, Xiaqing Bergland, Alan O. Behrman, Emily L. Gregory, Brian D. Petrov, Dmitri A. Schmidt, Paul S. Mol Biol Evol Discoveries Wild populations of the model organism Drosophila melanogaster experience highly heterogeneous environments over broad geographical ranges as well as over seasonal and annual timescales. Diapause is a primary adaptation to environmental heterogeneity, and in D. melanogaster the propensity to enter diapause varies predictably with latitude and season. Here we performed global transcriptomic profiling of naturally occurring variation in diapause expression elicited by short day photoperiod and moderately low temperature in two tissue types associated with neuroendocrine and endocrine signaling, heads, and ovaries. We show that diapause in D. melanogaster is an actively regulated phenotype at the transcriptional level, suggesting that diapause is not a simple physiological or reproductive quiescence. Differentially expressed genes and pathways are highly distinct in heads and ovaries, demonstrating that the diapause response is not uniform throughout the soma and suggesting that it may be comprised of functional modules associated with specific tissues. Genes downregulated in heads of diapausing flies are significantly enriched for clinally varying single nucleotide polymorphism (SNPs) and seasonally oscillating SNPs, consistent with the hypothesis that diapause is a driving phenotype of climatic adaptation. We also show that chromosome location-based coregulation of gene expression is present in the transcriptional regulation of diapause. Taken together, these results demonstrate that diapause is a complex phenotype actively regulated in multiple tissues, and support the hypothesis that natural variation in diapause propensity underlies adaptation to spatially and temporally varying selective pressures. Oxford University Press 2016-03 2015-11-13 /pmc/articles/PMC5009998/ /pubmed/26568616 http://dx.doi.org/10.1093/molbev/msv263 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
spellingShingle Discoveries
Zhao, Xiaqing
Bergland, Alan O.
Behrman, Emily L.
Gregory, Brian D.
Petrov, Dmitri A.
Schmidt, Paul S.
Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster
title Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster
title_full Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster
title_fullStr Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster
title_full_unstemmed Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster
title_short Global Transcriptional Profiling of Diapause and Climatic Adaptation in Drosophila melanogaster
title_sort global transcriptional profiling of diapause and climatic adaptation in drosophila melanogaster
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009998/
https://www.ncbi.nlm.nih.gov/pubmed/26568616
http://dx.doi.org/10.1093/molbev/msv263
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