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在 Ran(+/-)成纤维细胞中,Ran 表达减少会增加细胞因子刺激的 AP-1 亚基 c-Fos 和 c-Jun 的核内丰度。

Reduced Ran expression in Ran(+/-) fibroblasts increases cytokine-stimulated nuclear abundance of the AP-1 subunits c-Fos and c-Jun.

机构信息

Laboratory of Immunology, Centre hospitalier de l'Université de Montréal (CRCHUM)-Hôpital Notre-Dame, Montreal, Quebec, Canada.

出版信息

FEBS Lett. 2010 Nov 19;584(22):4623-6. doi: 10.1016/j.febslet.2010.10.030. Epub 2010 Oct 21.

DOI:10.1016/j.febslet.2010.10.030
PMID:20965183
Abstract

Ran (Ras-related nuclear protein), a Ras family GTPase, is involved in multiple cellular functions, including the regulation of DNA replication, cell cycle progression, nuclear structure formation, RNA processing-exportation, and nuclear protein importation. Ran(+/-) embryonic stem (ES) cells were produced in an attempt to generate Ran null mutant mice. Even after an extremely large number of blastocyst injections, no Ran(+/-) chimeric mice could be generated. Ran(+/-) ES cell-derived fibroblasts showed reduced Ran protein expression, and manifested augmented nuclear abundance of AP-1 factors (c-Jun and c-Fos) upon cytokine stimulation. Our experiments demonstrated that intracellular Ran protein levels controlled the nuclear presence of certain transcription factors, such as c-Fos and c-Jun.

摘要

Ran(Ras-related nuclear protein)是 Ras 家族 GTPase 的一种,参与多种细胞功能,包括 DNA 复制、细胞周期进程、核结构形成、RNA 加工-输出以及核蛋白输入的调节。Ran(+/-)胚胎干细胞(ES 细胞)的产生是为了试图生成 Ran 缺失突变体小鼠。即使经过大量的囊胚注射,也无法生成 Ran(+/-)嵌合小鼠。Ran(+/-)ES 细胞衍生的成纤维细胞显示出 Ran 蛋白表达减少,并且在细胞因子刺激下,AP-1 因子(c-Jun 和 c-Fos)的核内丰度增加。我们的实验表明,细胞内 Ran 蛋白水平控制着某些转录因子(如 c-Fos 和 c-Jun)在核内的存在。

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