Journal of Biological Chemistry
Volume 271, Issue 17, 26 April 1996, Pages 10341-10346
Journal home page for Journal of Biological Chemistry

Cell Biology and Metabolism
MCC, a Cytoplasmic Protein That Blocks Cell Cycle Progression from the G0/G1 to S Phase (∗)

https://doi.org/10.1074/jbc.271.17.10341Get rights and content
Under a Creative Commons license
open access

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 G0/G1 and highly phosphorylated during the G1 to S transition. Overexpression of the MCC protein blocked the serum-induced cell cycle transition from the G1 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.

Cited by (0)

This work was supported by grants-in-aid for scientific research on priority areas from the Ministry of Education, Science, Culture and Sports. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore by hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

§

Present address: Dept. of Anatomy, School of Medicine, Nagoya University, Nagoya 466, Japan.

Present address: The Center for Adult Diseases, Osaka 537, Japan.