Identification and characterization of a novel protein ISOC2 that interacts with p16INK4a

被引:17
作者
Huang, Xiaoyi
Shi, Zhongcheng
Wang, Wei
Bai, Jing
Chen, Zhenghua
Xu, Jiujin
Zhang, Dekai
Fu, Songbin
机构
[1] Harbin Med Coll, Dept Med Genet, Harbin 150081, Peoples R China
[2] Gansu Yasheng Salt Ind Grp Co Ltd, Post Doctoral Stn Beijing Branch, Beijing, Peoples R China
[3] Chinese Acad Sci, Inst Genet & Dev Biol, Beijing, Peoples R China
[4] Texas A&M Univ, Syst Hlth Sci Ctr, Inst Biosci & Technol, Ctr Extracellular Matrix Biol, Houston, TX 77030 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ISOC2; p16(INK4a); yeast two hybrid; protein-protein interaction; tumor suppressor gene;
D O I
10.1016/j.bbrc.2007.06.181
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
p16(INK4a), is a multiple tumor suppressor, playing an important role in proliferation and tumorigenesis. To screen the p16(INK4a) -associated proteins, we performed a yeast two-hybrid assay and identified a novel protein isochorismatase domain containing 2 (ISOC2). ISOC2 conserves in different species, and encodes 205 and 210 amino acids in human and mouse, respectively. The expression of ISOC2 in mouse is universal but predominantly in uterus, stomach, and urinary tract system. Interaction between ISOC2 and p16(INK4a) was verified using in vitro pull-down assays and in vivo co-immunoprecipitation. Confocal microscopy studies using green and cyan fluorescent fusion proteins determined that ISOC2 co-localizes with p16(INK4a). Over-expressed ISOC2 is able to inhibit p16(INK4a) in dose-dependent manner. Our data indicated that ISOC2 is a novel functional protein, which is able to bind and co-localize with a tumor suppressor INK4, INK4, gene p16(INK4a). Over-expressed ISOC2 inhibits the expression of p16(INK4a), suggesting that this novel gene may play a role during the INK4a tumor development by interacting with p16(INK4a). (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:287 / 293
页数:7
相关论文
共 29 条
[1]   The tumor suppressor p16Ink4a regulates T lymphocyte survival [J].
Bianchi, T. ;
Rufer, N. ;
MacDonald, H. R. ;
Migliaccio, M. .
ONCOGENE, 2006, 25 (29) :4110-4115
[2]   Ink4a and Arf differentially affect cell proliferation and neural stem cell self-renewal in Bmi1-deficient mice [J].
Bruggeman, SWM ;
Valk-Lingbeek, ME ;
van der Stoop, PPM ;
Jacobs, JJL ;
Kieboom, K ;
Tanger, E ;
Hulsman, D ;
Leung, C ;
Arsenijevic, Y ;
Marino, S ;
van Lohuizen, M .
GENES & DEVELOPMENT, 2005, 19 (12) :1438-1443
[3]   Pak4 induces premature senescence via a pathway requiring p16INK4/P19ARF and mitogen-activated protein kinase signaling [J].
Cammarano, MS ;
Nekrasova, T ;
Noel, B ;
Minden, A .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (21) :9532-9542
[4]   The p16INK4a tumour suppressor protein inhibits αvβ3 integrin-mediated cell spreading on vitronectin by blocking PKC-dependent localization of αvβ3 to focal contacts [J].
Fåhraeus, R ;
Lane, DP .
EMBO JOURNAL, 1999, 18 (08) :2106-2118
[5]   A NOVEL GENETIC SYSTEM TO DETECT PROTEIN PROTEIN INTERACTIONS [J].
FIELDS, S ;
SONG, OK .
NATURE, 1989, 340 (6230) :245-246
[6]   Direct interaction and cooperative role of tumor suppressor p16 with band 3 (AE1) [J].
Fu, GH ;
Wang, Y ;
Xi, YH ;
Shen, WW ;
Pan, XY ;
Shen, WZ ;
Jiang, XS ;
Chen, GQ .
FEBS LETTERS, 2005, 579 (10) :2105-2110
[7]   Identification of a gene expression signature associated with recurrent disease in squamous cell carcinoma of the head and neck [J].
Ginos, MA ;
Page, GP ;
Michalowicz, BS ;
Patel, KJ ;
Volker, SE ;
Pambuccian, SE ;
Ondrey, FG ;
Adams, GL ;
Gaffney, PM .
CANCER RESEARCH, 2004, 64 (01) :55-63
[8]   PPARα inhibits vascular smooth muscle cell proliferation underlying intimal hyperplasia by inducing the tumor suppressor p16INK4a [J].
Gizard, F ;
Amant, C ;
Barbier, O ;
Bellosta, S ;
Robillard, R ;
Percevault, F ;
Sevestre, H ;
Krimpenfort, P ;
Corsini, A ;
Rochette, J ;
Glineur, C ;
Fruchart, JC ;
Torpier, G ;
Staels, B .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (11) :3228-3238
[9]   Frequent p16INK4a inactivation is an early and frequent event of intraductal papillary neoplasm of the liver arising in hepatolithiasis [J].
Ishikawa, A ;
Sasaki, M ;
Sato, Y ;
Ohira, S ;
Chen, IF ;
Huang, SF ;
Oda, K ;
Nimura, Y ;
Nakanuma, Y .
HUMAN PATHOLOGY, 2004, 35 (12) :1505-1514
[10]   Control of the replicative life span of human fibroblasts by p16 and the polycomb protein Bmi-1 [J].
Itahana, K ;
Zou, Y ;
Itahana, Y ;
Martinez, JL ;
Beausejour, C ;
Jacobs, JJL ;
van Lohuizen, M ;
Band, V ;
Campisi, J ;
Dimri, GP .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (01) :389-401