@article{168436,
  keywords = {Animals, Nucleic Acid Conformation, DNA, Protein Structure, Tertiary, Humans, Mutation, Cell Line, Protein Binding, Cell Proliferation, Blotting, Western, Microscopy, Fluorescence, Mutagenesis, Site-Directed, Flow Cytometry, DNA-Binding Proteins, Mice, Cell Division, Cells, Cultured, Plasmids, Enzyme Inhibitors, Apoptosis, Proto-Oncogene Proteins, Cell Separation, G2 Phase, Annexin A5},
  author = {Ping La and Albert Silva and Zhaoyuan Hou and Haoren Wang and Robert Schnepp and Nieng Yan and Yigong Shi and Xianxin Hua},
  title = {Direct binding of DNA by tumor suppressor menin},
  abstract = {<p>Menin is a tumor suppressor that is mutated in patients with multiple endocrine neoplasia type I (MEN1), an inherited tumor-prone syndrome. Because there is no obvious conserved structural domain in menin that suggests a biochemical function, little is known as to how menin suppresses tumorigenesis. Although menin interacts with a variety of nuclear proteins including transcription factors, it is unknown whether menin itself can directly bind DNA. Here we show that menin directly binds to double-stranded DNA. It also binds a variety of DNA structures, including Y-structures, branched structures, and 4-way junction structures. The COOH terminus of menin mediates binding to DNA, but MEN1 disease-derived mutations in the COOH terminus abolish the ability of menin to bind DNA. Importantly, these MEN1 disease-related menin mutants also fail to repress cell proliferation as well as cell cycle progression at the G2/M phase. Furthermore, detailed mutagenesis studies indicate that positively charged residues in two nuclear localization signals mediate direct DNA binding as well as repression of cell proliferation. Collectively, these results demonstrate, for the first time, a novel biochemical activity of menin, binding to DNA, and link its DNA binding to the regulation of cell proliferation.</p>
},
  year = {2004},
  journal = {J Biol Chem},
  volume = {279},
  pages = {49045-54},
  month = {11/2004},
  issn = {0021-9258},
  doi = {10.1074/jbc.M409358200},
  language = {eng},
}