MCC, a cytoplasmic protein that blocks cell cycle progression from the G(0)/G(1) to S phase

被引:35
作者
Matsumine, A
Senda, T
Baeg, GH
Roy, BC
Nakamura, Y
Noda, M
Toyoshima, K
Akiyama, T
机构
[1] OSAKA UNIV, SCH MED, DEPT ANAT, OSAKA 565, JAPAN
[2] OSAKA UNIV, INST MICROBIAL DIS, DEPT ONCOGENE RES, OSAKA 565, JAPAN
[3] UNIV TOKYO, INST MED SCI, MOLEC MED LAB, TOKYO 108, JAPAN
[4] KYOTO UNIV, FAC MED, DEPT MOLEC ONCOL, KYOTO 606, JAPAN
关键词
D O I
10.1074/jbc.271.17.10341
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
The MCC gene was isolated from the human chromosome 5q21 by positional cloning and was found to be mutated in several colorectal tumors. In this study, we prepared specific antibodies and detected the MCC gene product as a cytoplasmic 100-kDa phosphoprotein in mouse NIH3T3 cells. Immunoelectron microscopic analysis showed that the MCC protein is associated with the plasma membrane and membrane organelles in mouse intestinal epithelial cells and neuronal cells. The amount of the MCC protein remained constant during the cell cycle progression of NIH3T3 cells, while its phosphorylation state changed markedly in a cell cycle-dependent manner, being weakly phosphorylated in the G(0)/G(1) and highly phosphorylated during the G(1) to S transition. Overexpression of the MCC protein blocked the serum-induced cell cycle transition from the G(1) to S phase, whereas a mutant MCC, initially identified in a colorectal tumor, did not exhibit this activity. These results suggest that the MCC protein may play a role in the signaling pathway negatively regulating cell cycle progression.
引用
收藏
页码:10341 / 10346
页数:6
相关论文
共 46 条
[11]   IDENTIFICATION AND CHARACTERIZATION OF THE FAMILIAL ADENOMATOUS POLYPOSIS-COLI GENE [J].
GRODEN, J ;
THLIVERIS, A ;
SAMOWITZ, W ;
CARLSON, M ;
GELBERT, L ;
ALBERTSEN, H ;
JOSLYN, G ;
STEVENS, J ;
SPIRIO, L ;
ROBERTSON, M ;
SARGEANT, L ;
KRAPCHO, K ;
WOLFF, E ;
BURT, R ;
HUGHES, JP ;
WARRINGTON, J ;
MCPHERSON, J ;
WASMUTH, J ;
LEPASLIER, D ;
ABDERRAHIM, H ;
COHEN, D ;
LEPPERT, M ;
WHITE, R .
CELL, 1991, 66 (03) :589-600
[12]   INHIBITION OF CDK2 ACTIVITY IN-VIVO BY AN ASSOCIATED 20K REGULATORY SUBUNIT [J].
GU, Y ;
TURCK, CW ;
MORGAN, DO .
NATURE, 1993, 366 (6456) :707-710
[13]   WT1-MEDIATED GROWTH SUPPRESSION OF WILMS-TUMOR CELLS EXPRESSING A WT1 SPLICING VARIANT [J].
HABER, DA ;
PARK, S ;
MAHESWARAN, S ;
ENGLERT, C ;
RE, GG ;
HAZENMARTIN, DJ ;
SENS, DA ;
GARVIN, AJ .
SCIENCE, 1993, 262 (5142) :2057-2059
[14]  
HARPER JW, 1993, CELL, V75, P805
[15]   REGULATION OF RETINOBLASTOMA PROTEIN FUNCTIONS BY ECTOPIC EXPRESSION OF HUMAN CYCLINS [J].
HINDS, PW ;
MITTNACHT, S ;
DULIC, V ;
ARNOLD, A ;
REED, SI ;
WEINBERG, RA .
CELL, 1992, 70 (06) :993-1006
[16]   SUPPRESSION OF THE NEOPLASTIC PHENOTYPE BY REPLACEMENT OF THE RB GENE IN HUMAN CANCER-CELLS [J].
HUANG, HJS ;
YEE, JK ;
SHEW, JY ;
CHEN, PL ;
BOOKSTEIN, R ;
FRIEDMANN, T ;
LEE, EYHP ;
LEE, WH .
SCIENCE, 1988, 242 (4885) :1563-1566
[17]  
HUANG Y, 1992, CANCER RES, V52, P6525
[18]   IDENTIFICATION OF DELETION MUTATIONS AND 3 NEW GENES AT THE FAMILIAL POLYPOSIS LOCUS [J].
JOSLYN, G ;
CARLSON, M ;
THLIVERIS, A ;
ALBERTSEN, H ;
GELBERT, L ;
SAMOWITZ, W ;
GRODEN, J ;
STEVENS, J ;
SPIRIO, L ;
ROBERTSON, M ;
SARGEANT, L ;
KRAPCHO, K ;
WOLFF, E ;
BURT, R ;
HUGHES, JP ;
WARRINGTON, J ;
MCPHERSON, J ;
WASMUTH, J ;
LEPASLIER, D ;
ABDERRAHIM, H ;
COHEN, D ;
LEPPERT, M ;
WHITE, R .
CELL, 1991, 66 (03) :601-613
[19]   DIMER FORMATION BY AN N-TERMINAL COILED-COIL IN THE APC PROTEIN [J].
JOSLYN, G ;
RICHARDSON, DS ;
WHITE, R ;
ALBER, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) :11109-11113
[20]   THE TGF-BETA SUPERFAMILY - NEW MEMBERS, NEW RECEPTORS, AND NEW GENETIC TESTS OF FUNCTION IN DIFFERENT ORGANISMS [J].
KINGSLEY, DM .
GENES & DEVELOPMENT, 1994, 8 (02) :133-146