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首页> 外文期刊>Neuron >Analysis of clock proteins in mouse SCN demonstrates phylogenetic divergence of the circadian clockwork and resetting mechanisms.
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Analysis of clock proteins in mouse SCN demonstrates phylogenetic divergence of the circadian clockwork and resetting mechanisms.

机译:小鼠SCN中时钟蛋白的分析表明,昼夜节律和复位机制的系统发育差异。

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摘要

The circadian clock in the suprachiasmatic nuclei (SCN) is comprised of a cell-autonomous, autoregulatory transcriptional/translational feedback loop. Its molecular components include three period and two cryptochrome genes. We describe circadian patterns of expression of mPER2 and mPER3 in the mouse SCN that are synchronous to those for mPER1, mCRY1, and mCRY2. Coimmunoprecipitation experiments demonstrate in vivo associations of the SCN mPER proteins with each other and with the mCRY proteins, and of mCRY proteins with mTIM, but no mPER/mTIM interactions. Examination of the effects of weak and strong resetting light pulses on SCN clock proteins highlights a central role for mPER1 in photic entrainment, with no acute light effects on either the mCRY or mTIM proteins. These clock protein interactions and photic responses in mice are divergent from those described in Drosophila.
机译:视交叉上核(SCN)中的昼夜节律时钟由细胞自主的,自动调节的转录/翻译反馈环组成。它的分子成分包括三个周期和两个隐色基因。我们描述了小鼠SCN中与mPER1,mCRY1和mCRY2同步的昼夜节律性表达的mPER2和mPER3。免疫共沉淀实验证明了SCN mPER蛋白彼此之间以及与mCRY蛋白的体内关联,以及mCRY蛋白与mTIM的体内关联,但没有mPER / mTIM相互作用。对弱和强复位光脉冲对SCN时钟蛋白的影响进行的研究突出了mPER1在光气夹带中的核心作用,而对mCRY或mTIM蛋白均无急性光影响。小鼠中的这些时钟蛋白相互作用和光响应与果蝇中描述的不同。

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