Cargando…
Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster
Circadian rhythms influence physiological processes from sleep–wake cycles to body temperature and are controlled by highly conserved cycling molecules. Although the mechanistic basis of the circadian clock has been known for decades, the extent to which circadian rhythms vary in nature and the unde...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326971/ https://www.ncbi.nlm.nih.gov/pubmed/30341464 http://dx.doi.org/10.1007/s10519-018-9932-0 |
_version_ | 1783386382079623168 |
---|---|
author | Harbison, Susan T. Kumar, Shailesh Huang, Wen McCoy, Lenovia J. Smith, Kirklin R. Mackay, Trudy F. C. |
author_facet | Harbison, Susan T. Kumar, Shailesh Huang, Wen McCoy, Lenovia J. Smith, Kirklin R. Mackay, Trudy F. C. |
author_sort | Harbison, Susan T. |
collection | PubMed |
description | Circadian rhythms influence physiological processes from sleep–wake cycles to body temperature and are controlled by highly conserved cycling molecules. Although the mechanistic basis of the circadian clock has been known for decades, the extent to which circadian rhythms vary in nature and the underlying genetic basis for that variation is not well understood. We measured circadian period (Ʈ) and rhythmicity index in the Drosophila Genetic Reference Panel (DGRP) and observed extensive genetic variation in both. Seven DGRP lines had sexually dimorphic arrhythmicity and one line had an exceptionally long Ʈ. Genome-wide analyses identified 584 polymorphisms in 268 genes. We observed differences among transcripts for nine genes predicted to interact among themselves and canonical clock genes in the long period line and a control. Mutations/RNAi knockdown targeting these genes also affected circadian behavior. Our observations reveal that complex genetic interactions influence high levels of variation in circadian phenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10519-018-9932-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6326971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-63269712019-01-25 Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster Harbison, Susan T. Kumar, Shailesh Huang, Wen McCoy, Lenovia J. Smith, Kirklin R. Mackay, Trudy F. C. Behav Genet Original Research Circadian rhythms influence physiological processes from sleep–wake cycles to body temperature and are controlled by highly conserved cycling molecules. Although the mechanistic basis of the circadian clock has been known for decades, the extent to which circadian rhythms vary in nature and the underlying genetic basis for that variation is not well understood. We measured circadian period (Ʈ) and rhythmicity index in the Drosophila Genetic Reference Panel (DGRP) and observed extensive genetic variation in both. Seven DGRP lines had sexually dimorphic arrhythmicity and one line had an exceptionally long Ʈ. Genome-wide analyses identified 584 polymorphisms in 268 genes. We observed differences among transcripts for nine genes predicted to interact among themselves and canonical clock genes in the long period line and a control. Mutations/RNAi knockdown targeting these genes also affected circadian behavior. Our observations reveal that complex genetic interactions influence high levels of variation in circadian phenotypes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10519-018-9932-0) contains supplementary material, which is available to authorized users. Springer US 2018-10-19 2019 /pmc/articles/PMC6326971/ /pubmed/30341464 http://dx.doi.org/10.1007/s10519-018-9932-0 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Harbison, Susan T. Kumar, Shailesh Huang, Wen McCoy, Lenovia J. Smith, Kirklin R. Mackay, Trudy F. C. Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster |
title | Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster |
title_full | Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster |
title_fullStr | Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster |
title_full_unstemmed | Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster |
title_short | Genome-Wide Association Study of Circadian Behavior in Drosophila melanogaster |
title_sort | genome-wide association study of circadian behavior in drosophila melanogaster |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6326971/ https://www.ncbi.nlm.nih.gov/pubmed/30341464 http://dx.doi.org/10.1007/s10519-018-9932-0 |
work_keys_str_mv | AT harbisonsusant genomewideassociationstudyofcircadianbehaviorindrosophilamelanogaster AT kumarshailesh genomewideassociationstudyofcircadianbehaviorindrosophilamelanogaster AT huangwen genomewideassociationstudyofcircadianbehaviorindrosophilamelanogaster AT mccoylenoviaj genomewideassociationstudyofcircadianbehaviorindrosophilamelanogaster AT smithkirklinr genomewideassociationstudyofcircadianbehaviorindrosophilamelanogaster AT mackaytrudyfc genomewideassociationstudyofcircadianbehaviorindrosophilamelanogaster |