期刊
GENETICS
卷 208, 期 3, 页码 1195-1207出版社
GENETICS SOCIETY AMERICA
DOI: 10.1534/genetics.117.300342
关键词
glial biology; astrocyte; circadian behavior; microRNA
资金
- National Institutes of Health [R01 NS065900, R01 MH099554, R01 NS069695, T32 NS061764, P30 NS047243]
- MRC [G0902418] Funding Source: UKRI
- Medical Research Council [G0902418] Funding Source: researchfish
We describe a genome-wide microRNA (miRNA)-based screen to identify brain glial cell functions required for circadian behavior. To identify glial miRNAs that regulate circadian rhythmicity, we employed a collection of miR-sponges to inhibit miRNA function in a glia-specific manner. Our initial screen identified 20 glial miRNAs that regulate circadian behavior. We studied two miRNAs, miR-263b and miR-274, in detail and found that both function in adult astrocytes to regulate behavior. Astrocyte-specific inhibition of miR-263b or miR-274 in adults acutely impairs circadian locomotor activity rhythms with no effect on glial or clock neuronal cell viability. To identify potential RNA targets of miR-263b and miR-274, we screened 35 predicted miRNA targets, employing RNA interference-based approaches. Glial knockdown of two putative miR-274 targets, CG4328 and MESK2, resulted in significantly decreased rhythmicity. Homology of the miR-274 targets to mammalian counterparts suggests mechanisms that might be relevant for the glial regulation of rhythmicity.
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