Interaction of MCM7 and RACK1 for Activation of MCM7 and Cell Growth

• Published in: The American journal of pathology Vol. 182; no. 3; pp. 796 - 805
• Main Authors: Zhang, Xi-Yue, Tang, Lang-Zhu, Ren, Bao-Guo, Yu, Yan P, Nelson, Joel, Michalopoulos, George, Luo, Jian-Hua
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.03.2013; American Society for Investigative Pathology
• Subjects: Cell Cycle Proteins - metabolism; Cell Line, Tumor; Cell Proliferation; Cell Transformation, Neoplastic; Chromatin - metabolism; DNA - biosynthesis; DNA-Binding Proteins - metabolism; Enzyme Activation; GTP-Binding Proteins - metabolism; Humans; Minichromosome Maintenance Complex Component 7; Models, Biological; Neoplasm Proteins - metabolism; Nuclear Proteins - metabolism; Pathology; Protein Binding; Protein Kinase C - metabolism; Receptors for Activated C Kinase; Receptors, Cell Surface - metabolism; Regular; S Phase
• ISSN: 0002-9440; 1525-2191
• DOI: 10.1016/j.ajpath.2012.11.020

MCM7 is one of the pivotal DNA replication licensing factors in controlling DNA synthesis and cell entry into S phase. Its expression and DNA copy number are some of the most predictive factors for the growth and behavior of human malignancies. In this study, we identified that MCM7 interacts with the receptor for activated protein kinase C 1 (RACK1), a protein kinase C (PKC) adaptor, in vivo and in vitro . The RACK1 binding motif in MCM7 is located at the amino acid 221-248. Knocking down RACK1 significantly reduced MCM7 chromatin association, DNA synthesis, and cell cycle entry into S phase. Activation of PKC by 12-O-tetradecanoylphorbol-13-acetate dramatically decreased MCM7 DNA replication licensing and induced cell growth arrest. Activation of PKC induced redistribution of RACK1 from nucleus to cytoplasm and decreased RACK1-chromatin association. The MCM7 mutant that does not bind RACK1 has no DNA replication licensing or oncogenic transformation activity. As a result, this study demonstrates a novel signaling mechanism that critically controls DNA synthesis and cell cycle progression.