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miR-276a 调控日常睡眠的机制。

Regulatory mechanism of daily sleep by miR-276a.

机构信息

Department of Entomology, MOA Key Lab of Pest Monitoring and Green Management, College of Plant Protection, China Agricultural University, Beijing, China.

College of Life Science, Hebei University, Baoding, China.

出版信息

FASEB J. 2021 Jan;35(1):e21222. doi: 10.1096/fj.202001220R.

Abstract

MiRNAs have attracted more attention in recent years as regulators of sleep and circadian rhythms after their roles in circadian rhythm and sleep were discovered. In this study, we explored the roles of the miR-276a on daily sleep in Drosophila melanogaster, and found a regulatory cycle for the miR-276a pathway, in which miR-276a, regulated by the core CLOCK/CYCLE (CLK/CYC) transcription factor upstream, regulates sleep via suppressing targets TIM and NPFR1. (a) Loss of miR-276a function makes the flies sleep more during both daytime and nighttime, while flies with gain of miR-276a function sleep less; (b) MiR-276a is widely expressed in the mushroom body (MB), the pars intercerebralis (PI) and some clock neurons lateral dorsal neurons (LNds), in which tim neurons is important for sleep regulation; (c) MiR-276a promoter is identified to locate in the 8th fragment (aFrag8) of the pre-miR-276a, and this fragment is directly activated and regulated by CLK/CYC; (4) MiR-276a is rhythmically oscillating in heads of the wild-type w , but this oscillation disappears in the loss of function mutant clk ; (5) The neuropeptide F receptor 1 (npfr1) was found to be a downstream target of miR-276a. These results clarify that the miR-276a is a very important factor for sleep regulation.

摘要

近年来,miRNAs 作为睡眠和昼夜节律的调节剂引起了更多的关注,因为它们在昼夜节律和睡眠中的作用被发现。在这项研究中,我们探讨了 miR-276a 在黑腹果蝇昼夜睡眠中的作用,发现了 miR-276a 通路的一个调节循环,其中 miR-276a 受核心 CLOCK/CYCLE (CLK/CYC) 转录因子上游的调节,通过抑制 TIM 和 NPFR1 来调节睡眠。(a) miR-276a 功能丧失使果蝇在白天和夜间都睡得更多,而 miR-276a 功能获得的果蝇则睡得更少;(b) miR-276a 在蘑菇体 (MB)、脑间部 (PI) 和一些时钟神经元 lateral dorsal neurons (LNds) 中广泛表达,其中 tim 神经元对睡眠调节很重要;(c) 鉴定出 miR-276a 启动子位于 pre-miR-276a 的第 8 个片段 (aFrag8) 中,该片段直接被 CLK/CYC 激活和调节;(4) miR-276a 在 w 型野生型头部呈节律性振荡,但这种振荡在 clk 功能丧失突变体中消失;(5) 发现神经肽 F 受体 1 (npfr1) 是 miR-276a 的下游靶标。这些结果阐明了 miR-276a 是睡眠调节的一个非常重要的因素。

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