Literature DB >> 12682919

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

Katsuya Hirano1, Ying Zeng, Mayumi Hirano, Junji Nishimura, Hideo Kanaide.   

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. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12682919     DOI: 10.1002/jcb.10499

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  3 in total

1.  Molecular analysis of the p27/kip1 gene in breast cancer.

Authors:  Hatice Tigli; Nur Buyru; Nejat Dalay
Journal:  Mol Diagn       Date:  2005

2.  14-3-3 suppresses the nuclear localization of threonine 157-phosphorylated p27(Kip1).

Authors:  Toshihiro Sekimoto; Masahiro Fukumoto; Yoshihiro Yoneda
Journal:  EMBO J       Date:  2004-04-01       Impact factor: 11.598

3.  Transforming growth factor-beta induces Cdk2 relocalization to the cytoplasm coincident with dephosphorylation of retinoblastoma tumor suppressor protein.

Authors:  Kimberly A Brown; Richard L Roberts; Carlos L Arteaga; Brian K Law
Journal:  Breast Cancer Res       Date:  2004-02-04       Impact factor: 6.466

  3 in total

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