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核机制介导大鼠视交叉上核中血管加压素mRNA表达的节律性变化。

Nuclear mechanisms mediate rhythmic changes in vasopressin mRNA expression in the rat suprachiasmatic nucleus.

作者信息

Carter D A, Murphy D

机构信息

Neuropeptide Laboratory, National University of Singapore.

出版信息

Brain Res Mol Brain Res. 1992 Feb;12(4):315-21. doi: 10.1016/0169-328x(92)90133-v.

Abstract

Vasopressin (VP) gene expression in the rat suprachiasmatic nucleus (SCN) is subject to a cyclical mode of regulation which is indicative of a close association with the circadian clock intrinsic to this area of the hypothalamus. Previous studies show that both the amount and size (due to differential polyadenylation) of VP mRNA are reduced during the dark phase of the daily cycle. We have now identified the cellular site wherein these changes are mediated. By transcriptional run-on analysis of nuclei isolated at different time points from the SCN we have shown that an attenuation of transcriptional activity can account for the dark-phase reduction in VP mRNA levels; by comparison with other genes expressed in this tissue, a significant, VP gene-specific reduction was observed which resulted in dark-phase transcriptional activity at 30% of light-phase activity (P less than 0.005). A similar diurnal variation was not found in the supraoptic nucleus. In addition, by Northern analysis of sub-cellular RNA pools, we have demonstrated that the smaller, dark-phase-specific VP RNA species is located, in abundance, within the nuclear fraction. These results provide clear evidence that the cyclical changes in SCN VP mRNA expression are primarily regulated within the nucleus, indicating that any potential regulation in the cytoplasm is of secondary importance. Further analysis of the molecular components which mediate the cyclical changes in transcriptional activity of the VP gene may identify fundamental aspects of neuronal timing mechanisms.

摘要

大鼠视交叉上核(SCN)中血管加压素(VP)基因的表达受到周期性调控模式的影响,这表明它与下丘脑该区域固有的昼夜节律时钟密切相关。先前的研究表明,在每日周期的黑暗阶段,VP mRNA的量和大小(由于不同的多聚腺苷酸化)都会减少。我们现在已经确定了介导这些变化的细胞位点。通过对在不同时间点从SCN分离的细胞核进行转录延伸分析,我们发现转录活性的减弱可以解释黑暗阶段VP mRNA水平的降低;与该组织中表达的其他基因相比,观察到VP基因特异性的显著降低,导致黑暗阶段的转录活性为光照阶段活性的30%(P小于0.005)。在视上核中未发现类似的昼夜变化。此外,通过对亚细胞RNA池的Northern分析,我们证明较小的、黑暗阶段特异性的VP RNA种类大量存在于核部分中。这些结果提供了明确的证据,表明SCN中VP mRNA表达的周期性变化主要在细胞核内受到调控,这表明细胞质中的任何潜在调控都是次要的。对介导VP基因转录活性周期性变化的分子成分的进一步分析可能会揭示神经元计时机制的基本方面。

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