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浦肯野细胞信使核糖核酸在树突中的3'非翻译区依赖性定位。

3'UTR-dependent localization of a Purkinje cell messenger RNA in dendrites.

作者信息

Zhang Rui, Zhang Xulun, Bian Feng, Pu Xin-an, Schilling Karl, Oberdick John

机构信息

Center for Molecular Neurobiology and Department of Neuroscience, The Ohio State University, 206 Rightmire Hall, 1060 Carmack Road, Columbus, OH 43210, USA.

出版信息

Cerebellum. 2008;7(3):482-93. doi: 10.1007/s12311-008-0051-y.

Abstract

Pcp2(L7) is a Purkinje cell-specific GoLoco domain protein that modulates activation of Galphai/o proteins by G protein-coupled receptors. A likely downstream effector of this pathway is the P-type Ca(2+) channel, and thereby, the intrinsic electrophysiology of Purkinje cells could be modulated by Pcp2(L7). It has long been known that the Pcp2(L7) mRNA is abundantly localized in dendrites, suggesting the possibility of distal synthesis and local changes in levels of the protein. As a first step to uncover the trafficking and translational mechanisms for this mRNA, we have begun identifying the cis-acting sequences important for its localization in dendrites. Using expression of modified transgenes in vivo, we show that the 3'UTR, only 65 bases long, is necessary in this process.

摘要

Pcp2(L7)是一种浦肯野细胞特异性的GoLoco结构域蛋白,它通过G蛋白偶联受体调节Galphai/o蛋白的激活。该信号通路一个可能的下游效应器是P型Ca(2+)通道,因此,浦肯野细胞的内在电生理可能受到Pcp2(L7)的调节。长期以来已知Pcp2(L7)mRNA大量定位于树突中,这提示了该蛋白进行远端合成以及局部水平变化的可能性。作为揭示该mRNA转运和翻译机制的第一步,我们已开始鉴定对其在树突中定位至关重要的顺式作用序列。通过在体内表达修饰的转基因,我们发现仅65个碱基长的3'UTR在此过程中是必需的。

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