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
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