|Associate Professor||Asako FURUKORI|
|Assistant Professor||Mika HIGASHIDE|
Homologous recombination, an exchange between DNA strands, plays a role in the maintenance of genome stability and the production of genome diversity. While, in mitosis, it is required for the repair of DNA damage, it is for the segregation of homologous chromosome at meiotic division I. Meiotic recombination is coupled with chromosome morphogenesis and is under a strict control. Malfunction of the recombination leads cancer and infertility in human. In order to reveal molecular mechanism of the recombination, we have been analyzing genes and proteins involved in the process using molecular, genetical and biochemical methods.
Current Research Programs
- In vivo and in vivo analysis of recombination reactions
- Analysis of proteins working with RecA homologues in recombination
- Analysis of the roles of chromatin modification in meiotic recombination
- Mechanisms of choice of DSB repair pathways
- Analysis of recombination in human cells
- In vivo assembly and disassembly of Rad51 and Rad52 complexes during double-strand break repair. Miyazaki, T., Bressan, D. A., Shinohara, M., Haber, J. E., Shinohara, A. (2004) EMBO J. 23, 939-949.
- A protein complex containing Mei5 and Sae3 promotes the assembly of the meiosis-specific RecA homolog Dmc1. Hayase, A., Takagi, M., Miyazaki, T., Oshiumi, H., Shinohara, M., Shinohara, A. (2004) Cell 119, 927-940.
- Isolation and characterization of novel xrs2 mutations in Saccharomyce cerevisiae. Shima K., Suzuki M., Shinohara, M. (2005) Genetics 170, 71-85.