Department of Neuroscience, Sackler Program in Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts 02111.
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115.
Genetics. 2018 Mar;208(3):1195-1207. doi: 10.1534/genetics.117.300342.
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.
我们描述了一个基于全基因组 microRNA(miRNA)的筛选,以鉴定大脑神经胶质细胞功能,这些功能对于昼夜节律行为是必需的。为了鉴定调节昼夜节律的神经胶质 miRNA,我们采用了一组“miR-海绵”,以特异性地抑制 miRNA 的功能。我们的初步筛选鉴定出 20 种调节昼夜节律行为的神经胶质 miRNA。我们详细研究了两种 miRNA,miR-263b 和 miR-274,发现它们都在成年星形胶质细胞中发挥作用,以调节行为。在成年期特异性抑制 miR-263b 或 miR-274 会急性损害昼夜节律性运动活动节律,而对神经胶质或时钟神经元细胞活力没有影响。为了鉴定 miR-263b 和 miR-274 的潜在 RNA 靶标,我们采用 RNA 干扰为基础的方法,筛选了 35 个预测的 miRNA 靶标。两种假定的 miR-274 靶标 CG4328 和 MESK2 的神经胶质敲低导致节律性显著降低。miR-274 靶标的同源性与哺乳动物对应物相似,提示可能与神经胶质调节节律性相关的机制。