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      Evidence that natural selection maintains genetic variation for sleep in Drosophila melanogaster

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          Abstract

          Background

          Drosophila melanogaster often shows correlations between latitude and phenotypic or genetic variation on different continents, which suggests local adaptation with respect to a heterogeneous environment. Previous phenotypic analyses of latitudinal clines have investigated mainly physiological, morphological, or life-history traits. Here, we studied latitudinal variation in sleep in D. melanogaster populations from North and Central America. In parallel, we used RNA-seq to identify interpopulation gene expression differences.

          Results

          We found that in D. melanogaster the average nighttime sleep bout duration exhibits a latitudinal cline such that sleep bouts of equatorial populations are roughly twice as long as those of temperate populations. Interestingly, this pattern of latitudinal variation is not observed for any daytime measure of activity or sleep. We also found evidence for geographic variation for sunrise anticipation. Our RNA-seq experiment carried out on heads from a low and high latitude population identified a large number of gene expression differences, most of which were time dependent. Differentially expressed genes were enriched in circadian regulated genes and enriched in genes potentially under spatially varying selection.

          Conclusion

          Our results are consistent with a mechanistic and selective decoupling of nighttime and daytime activity. Furthermore, the present study suggests that natural selection plays a major role in generating transcriptomic variation associated with circadian behaviors. Finally, we identified genomic variants plausibly causally associated with the observed behavioral and transcriptomic variation.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12862-015-0316-2) contains supplementary material, which is available to authorized users.

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          Most cited references40

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Coupled oscillators control morning and evening locomotor behaviour of Drosophila.

            Daily rhythms of physiology and behaviour are precisely timed by an endogenous circadian clock. These include separate bouts of morning and evening activity, characteristic of Drosophila melanogaster and many other taxa, including mammals. Whereas multiple oscillators have long been proposed to orchestrate such complex behavioural programmes, their nature and interplay have remained elusive. By using cell-specific ablation, we show that the timing of morning and evening activity in Drosophila derives from two distinct groups of circadian neurons: morning activity from the ventral lateral neurons that express the neuropeptide PDF, and evening activity from another group of cells, including the dorsal lateral neurons. Although the two oscillators can function autonomously, cell-specific rescue experiments with circadian clock mutants indicate that they are functionally coupled.
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              Morning and evening peaks of activity rely on different clock neurons of the Drosophila brain.

              In Drosophila, a 'clock' situated in the brain controls circadian rhythms of locomotor activity. This clock relies on several groups of neurons that express the Period (PER) protein, including the ventral lateral neurons (LN(v)s), which express the Pigment-dispersing factor (PDF) neuropeptide, and the PDF-negative dorsal lateral neurons (LN(d)s). In normal cycles of day and night, adult flies exhibit morning and evening peaks of activity; however, the contribution of the different clock neurons to the rest-activity pattern remains unknown. Here, we have used targeted expression of PER to restore the clock function of specific subsets of lateral neurons in arrhythmic per(0) mutant flies. We show that PER expression restricted to the LN(v)s only restores the morning activity, whereas expression of PER in both the LN(v)s and LN(d)s also restores the evening activity. This provides the first neuronal bases for 'morning' and 'evening' oscillators in the Drosophila brain. Furthermore, we show that the LN(v)s alone can generate 24 h activity rhythms in constant darkness, indicating that the morning oscillator is sufficient to drive the circadian system.
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                Author and article information

                Contributors
                nhsvetec@ucdavis.edu
                lizzhao@ucdavis.edu
                psaelao@ucdavis.edu
                jcchiu@ucdavis.edu
                djbegun@ucdavis.edu
                Journal
                BMC Evol Biol
                BMC Evol. Biol
                BMC Evolutionary Biology
                BioMed Central (London )
                1471-2148
                13 March 2015
                13 March 2015
                2015
                : 15
                : 41
                Affiliations
                [ ]Department of Evolution and Ecology, University of California, 3352 Storer Hall, One Shields Ave., Davis, CA 95618 USA
                [ ]Department of Entomology and Nematology, University of California, Davis, CA USA
                Article
                316
                10.1186/s12862-015-0316-2
                4374177
                25776330
                19d3877f-b228-4428-9088-cce9b5549f26
                © Svetec et al.; licensee BioMed Central. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 21 November 2014
                : 24 February 2015
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2015

                Evolutionary Biology
                drosophila melanogaster,latitudinal cline,spatially varying selection,locomotor activity,sleep,circadian rhythms,gene expression,rna-seq

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