昼夜节律钟对光周期的转录组可塑性:雄性褪黑激素作用小鼠的研究

IF 2.9 3区 生物学 Q2 BIOLOGY
Journal of Biological Rhythms Pub Date : 2024-10-01 Epub Date: 2024-08-02 DOI:10.1177/07487304241265439
Olivia H Cox, Manuel A Gianonni-Guzmán, Jean-Philippe Cartailler, Matthew A Cottam, Douglas G McMahon
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引用次数: 0

摘要

季节性昼长或昼夜节律光周期是一种普遍存在的环境信号,对生理和行为产生深远影响。在哺乳动物中,中央昼夜节律钟位于下丘脑的簇上核(SCN)中,它接收视网膜输入,并使生物体的生理和行为与当时的光周期同步,或称 "同步"。诱导过程会诱导 SCN 产生持续的可塑性,但人们对 SCN 可塑性的分子机制尚不完全清楚。不同光周期的诱导持续改变了SCN时钟及其驱动节律的时间、波形、周期和光重置特性。为了阐明光周期可塑性分子机制的新候选基因,我们对在长光周期(光:暗[LD] 16:8)和短光周期(光:暗 8:16)下饲养的小鼠整个SCN进行了RNA测序。在光周期较长的小鼠中检测到的节律基因较少,一般来说,基因表达节律的时间提前了4-6小时。时钟相关基因 "天时 "以及与光反应、神经肽、γ-氨基丁酸(GABA)、离子通道和血清素有关的 SCN 基因的表达发生了明显变化。特别引人注目的是神经肽信号基因 Prokr2 和 Cck 的表达差异,以及 3 个 SCN 光反应基因 Dusp4、Rasd1 和 Gem 表达的趋同调控。Dusp4和Rasd1的转录调控以及Gem的相位调控是SCN光反应可塑性的令人信服的候选分子机制,它们通过调控SCN神经元中关键的NMDAR-MAPK/ERK-CREB/CRE光信号通路来实现。对Prokr2和Cck的调控可能对光周期调节过程中SCN神经网络的重构起到关键作用。我们的研究结果表明,SCN光反应和神经肽信号基因组是阐明光周期可塑性新机制的丰富底物。数据也可在 http://circadianphotoperiodseq.com/ 上获得,用户可以查看这些光周期条件下基因的表达和节律特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transcriptomic Plasticity of the Circadian Clock in Response to Photoperiod: A Study in Male Melatonin-Competent Mice.

Seasonal daylength, or circadian photoperiod, is a pervasive environmental signal that profoundly influences physiology and behavior. In mammals, the central circadian clock resides in the suprachiasmatic nuclei (SCN) of the hypothalamus where it receives retinal input and synchronizes, or entrains, organismal physiology and behavior to the prevailing light cycle. The process of entrainment induces sustained plasticity in the SCN, but the molecular mechanisms underlying SCN plasticity are incompletely understood. Entrainment to different photoperiods persistently alters the timing, waveform, period, and light resetting properties of the SCN clock and its driven rhythms. To elucidate novel candidate genes for molecular mechanisms of photoperiod plasticity, we performed RNA sequencing on whole SCN dissected from mice raised in long (light:dark [LD] 16:8) and short (LD 8:16) photoperiods. Fewer rhythmic genes were detected in mice subjected to long photoperiod, and in general, the timing of gene expression rhythms was advanced 4-6 h. However, a few genes showed significant delays, including Gem. There were significant changes in the expression of the clock-associated gene Timeless and in SCN genes related to light responses, neuropeptides, gamma aminobutyric acid (GABA), ion channels, and serotonin. Particularly striking were differences in the expression of the neuropeptide signaling genes Prokr2 and Cck, as well as convergent regulation of the expression of 3 SCN light response genes, Dusp4, Rasd1, and Gem. Transcriptional modulation of Dusp4 and Rasd1 and phase regulation of Gem are compelling candidate molecular mechanisms for plasticity in the SCN light response through their modulation of the critical NMDAR-MAPK/ERK-CREB/CRE light signaling pathway in SCN neurons. Modulation of Prokr2 and Cck may critically support SCN neural network reconfiguration during photoperiodic entrainment. Our findings identify the SCN light response and neuropeptide signaling gene sets as rich substrates for elucidating novel mechanisms of photoperiod plasticity. Data are also available at http://circadianphotoperiodseq.com/, where users can view the expression and rhythmic properties of genes across these photoperiod conditions.

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来源期刊
CiteScore
6.10
自引率
8.60%
发文量
48
审稿时长
>12 weeks
期刊介绍: Journal of Biological Rhythms is the official journal of the Society for Research on Biological Rhythms and offers peer-reviewed original research in all aspects of biological rhythms, using genetic, biochemical, physiological, behavioral, epidemiological & modeling approaches, as well as clinical trials. Emphasis is on circadian and seasonal rhythms, but timely reviews and research on other periodicities are also considered. The journal is a member of the Committee on Publication Ethics (COPE).
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