Homologous recombination is required during meiosis to promote accurate segregation of homologous chromosomes at the first meiotic division. Several proteins have been identified that are required for MEIOTIC RECOMBINATION in the yeast Saccharomyces, but the specific role of these proteins in recombination is largely unknown. The long term goals of this work are to determine the molecular mechanism of meiotic recombination and the way in which meiotic cells ensure that recombination is complete before undergoing division. This study focuses on one meiotic protein, Dmc1, that is required for meiotic recombination. Thy homology of Dmc1 to the E. coli RecA protein suggests Dmc1 plays a pivotal role in recombination. RecA is required for recombination and REPAIR OF DNA DAMAGE in E. coli. Purified RecA promotes the central reaction in recombination: the formation of homologous joints between two DNA molecules. Dmc1 protein will be purified and characterized to determine what activities it shares with RecA. The formation of recombination products requires numerous enzymatic activities in addition to those displayed by RecA. Some or all of the proteins required for meiotic recombination may form a multiprotein complex. There is existing cytological evidence that large complexes form during meiotic recombination. In addition, two recombination proteins that are related to Dmc1, have been shown to bind other recombination proteins. Fluorescence microscopy, immunoassay, and genetic selection will be used to identify proteins that form complexes with Dmc1 during recombination. Time-course and mutational analyses will be used to characterize the pathway of recombination complex assembly. Dmc1 also plays a role in the control of the meiotic CELL CYCLE. Mutants cells that lack Dmc1 arrest in meiosis. The mechanisms that causes cell cycle arrest in the absence of Dmc1 will be characterized genetically by isolation of genetic suppressor that fail to arrest. These experiments will yield results relevant to the etiology of birth defects and cancer and may also suggest ways to improve cancer therapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM050936-02
Application #
2189151
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1994-04-01
Project End
1999-03-31
Budget Start
1995-04-01
Budget End
1996-03-31
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Chicago
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Chan, Yuen-Ling; Zhang, Annie; Weissman, Benjamin P et al. (2018) RPA resolves conflicting activities of accessory proteins during reconstitution of Dmc1-mediated meiotic recombination. Nucleic Acids Res :
Gataulin, Daniil V; Carey, Jeffrey N; Li, Junya et al. (2018) The ATPase activity of E. coli RecA prevents accumulation of toxic complexes formed by erroneous binding to undamaged double stranded DNA. Nucleic Acids Res 46:9510-9523
Chan, Yuen-Ling; Bishop, Douglas K (2018) Purification of Saccharomyces cerevisiae Homologous Recombination Proteins Dmc1 and Rdh54/Tid1 and a Fluorescent D-Loop Assay. Methods Enzymol 600:307-320
Grubb, Jennifer; Brown, M Scott; Bishop, Douglas K (2015) Surface Spreading and Immunostaining of Yeast Chromosomes. J Vis Exp :e53081
Mason, Jennifer M; Dusad, Kritika; Wright, William Douglass et al. (2015) RAD54 family translocases counter genotoxic effects of RAD51 in human tumor cells. Nucleic Acids Res 43:3180-96
Shinohara, Miki; Hayashihara, Kayoko; Grubb, Jennifer T et al. (2015) DNA damage response clamp 9-1-1 promotes assembly of ZMM proteins for formation of crossovers and synaptonemal complex. J Cell Sci 128:1494-506
Brown, M Scott; Grubb, Jennifer; Zhang, Annie et al. (2015) Small Rad51 and Dmc1 Complexes Often Co-occupy Both Ends of a Meiotic DNA Double Strand Break. PLoS Genet 11:e1005653
Joshi, Neeraj; Brown, M Scott; Bishop, Douglas K et al. (2015) Gradual implementation of the meiotic recombination program via checkpoint pathways controlled by global DSB levels. Mol Cell 57:797-811
Chan, Yuen-Ling; Brown, M Scott; Qin, Daoming et al. (2014) The third exon of the budding yeast meiotic recombination gene HOP2 is required for calcium-dependent and recombinase Dmc1-specific stimulation of homologous strand assimilation. J Biol Chem 289:18076-86
Lao, Jessica P; Cloud, Veronica; Huang, Chu-Chun et al. (2013) Meiotic crossover control by concerted action of Rad51-Dmc1 in homolog template bias and robust homeostatic regulation. PLoS Genet 9:e1003978

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