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p27Kip1的抗降解异构体p27Kip1R的核定位及生长抑制的序列要求

Sequence requirement for nuclear localization and growth inhibition of p27Kip1R, a degradation-resistant isoform of p27Kip1.

作者信息

Hirano Katsuya, Zeng Ying, Hirano Mayumi, Nishimura Junji, Kanaide Hideo

机构信息

Division of Molecular Cardiology, Research Institute of Angiocardiology, Graduate School of Medical Sciences, Kyushu University 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

J Cell Biochem. 2003 May 1;89(1):191-202. doi: 10.1002/jcb.10499.

Abstract

p27(Kip1R) is an isoform of p27(Kip1), having a distinct C-terminus. The sequences of p27(Kip1R) required for nuclear localization and growth inhibition were determined in HeLa cells using a green fluorescence protein (GFP) as a reporter molecule. Region 153-168 and residues K168 and I169 were determined to play a critical role in the nuclear localization of p27(Kip1R). Aliphatic amino acid was found to be a substitute for the basic residue in the typical nuclear localization signal, while its functional substitution was incomplete, thereby causing a significant cytoplasmic retention of p27(Kip1R). p27(Kip1R) is thus the first example of an atypical bipartite nuclear localization signal with aliphatic amino acid as a functional residue. Despite cytoplasmic retention, p27(Kip1R) inhibited the cell growth as well as p27(Kip1), while GFP alone had no effect. The mutants lacking an N-terminus containing the binding regions for cyclins and cyclin-dependent kinases also showed a significant degree of nuclear localization, but failed to inhibit cell growth. The growth inhibition by p27(Kip1R) as well as p27(Kip1) was thus suggested to originate in the common N-terminal region.

摘要

p27(Kip1R)是p27(Kip1)的一种异构体,具有独特的C末端。在HeLa细胞中,以绿色荧光蛋白(GFP)作为报告分子,确定了p27(Kip1R)核定位和生长抑制所需的序列。已确定153 - 168区域以及K168和I169残基在p27(Kip1R)的核定位中起关键作用。发现脂肪族氨基酸可替代典型核定位信号中的碱性残基,但其功能替代并不完全,从而导致p27(Kip1R)在细胞质中大量滞留。因此,p27(Kip1R)是以脂肪族氨基酸作为功能残基的非典型双分型核定位信号的首个实例。尽管存在细胞质滞留,p27(Kip1R)与p27(Kip1)一样能抑制细胞生长,而单独的GFP则无此作用。缺乏包含细胞周期蛋白和细胞周期蛋白依赖性激酶结合区域的N末端的突变体也显示出显著程度的核定位,但未能抑制细胞生长。因此,p27(Kip1R)以及p27(Kip1)的生长抑制作用被认为起源于共同的N末端区域。

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