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聚C结合蛋白1在神经元细胞中细胞定位的分子基础。

Molecular basis of cellular localization of poly C binding protein 1 in neuronal cells.

作者信息

Berry Andrea M, Flock Kelly E, Loh Horace H, Ko Jane L

机构信息

Department of Biology, Seton Hall University, 208 McNulty Hall, 400 South Orange Avenue, South Orange, NJ 07079, USA.

出版信息

Biochem Biophys Res Commun. 2006 Nov 3;349(4):1378-86. doi: 10.1016/j.bbrc.2006.09.012. Epub 2006 Sep 12.

Abstract

Poly C binding protein 1 (PCBP) is involved in the transcriptional regulation of neuronal mu-opioid receptor gene. In this study, we examined the molecular basis of PCBP cellular/nuclear localization in neuronal cells using EGFP fusion protein. PCBP, containing three KH domains and a variable domain, distributed in cytoplasm and nucleus with a preferential nuclear expression. Domain-deletional analyses suggested the requirement of variable and KH3 domains for strong PCBP nuclear expression. Within the nucleus, a low nucleolar PCBP expression was observed, and PCBP variable domain contributed to this restricted nucleolar expression. Furthermore, the punctate nuclear pattern of PCBP was correlated to its single-stranded (ss) DNA binding ability, with both requiring cooperativity of at least three sequential domains. Collectively, certain PCBP domains thus govern its nuclear distribution and transcriptional regulatory activity in the nucleus of neurons, whereas the low nucleolar expression implicates the disengagement of PCBP in the ribosomal RNA synthesis.

摘要

多聚胞嘧啶结合蛋白1(PCBP)参与神经元μ-阿片受体基因的转录调控。在本研究中,我们使用EGFP融合蛋白研究了PCBP在神经元细胞中细胞/核定位的分子基础。PCBP含有三个KH结构域和一个可变结构域,分布于细胞质和细胞核中,且优先在细胞核中表达。结构域缺失分析表明,可变结构域和KH3结构域对于PCBP在细胞核中的强表达是必需的。在细胞核内,观察到PCBP在核仁中的表达较低,且PCBP可变结构域导致了这种核仁表达受限。此外,PCBP的点状核模式与其单链(ss)DNA结合能力相关,两者都需要至少三个连续结构域的协同作用。总的来说,某些PCBP结构域因此决定了其在神经元细胞核中的核分布和转录调控活性,而核仁中低表达暗示PCBP在核糖体RNA合成中不参与。

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Molecular basis of cellular localization of poly C binding protein 1 in neuronal cells.聚C结合蛋白1在神经元细胞中细胞定位的分子基础。
Biochem Biophys Res Commun. 2006 Nov 3;349(4):1378-86. doi: 10.1016/j.bbrc.2006.09.012. Epub 2006 Sep 12.

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