Of the four eukaryotic structural maintenance of chromosomes (SMC) proteins, the yeast SMC1 and SMC3 proteins were recently shown to be required for mitotic and meiotic sister chromatid cohesion and DNA recombination. Very little is known on the role of mammalian SMC proteins in meiosis, and no cell- or tissue-specific variant of SMC proteins has been reported. This proposal focuses on the cellular, molecular, and organismal analysis of a novel, meiosis-specific SMC protein identified by us, named SMC1beta. SMC1beta is homologous to somatic SMC1 and considered a meiosis-specific isoform. We propose that SMC1beta plays an essential role in mammalian meiosis. This role should be in meiotic sister chromatid cohesion and DNA recombination, and should require interactions with other meiotic proteins, and meiosis-specific protein-DNA structures.
Our aim i s to determine the developmental stage-specificity of SMC1beta expression in spermatogenesis, to identify and characterize proteins that specifically interact with SMC1beta and to decipher the interaction of SMC1beta with meiotic chromatin. Indications exist for a novel SMC1beta/SMC3 complex, and for a function of SMC1beta in prophase I and in later stages of meiosis. The in vivo function of SMC1beta will be studied by deleting the gene in mice. We expect a meiosis-specific phenotype in the animals. A prominent feature of SMC1beta is a basic C-terminal 28 amino acids sequence. We predict that this unique C-terminal motif contributes to the protein specific molecular and cellular features, which we will analyze. Our work will also establish the novel concept of cell-type specific SMC protein variants. Since we consider SMC1beta a key protein for mammalian meiosis, our results will be important not only for better understanding mammalian SMC protein biology, but also for understanding meiotic chromatin and DNA dynamics, and thus for human reproductive biology and health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM062517-03
Application #
6636578
Study Section
Reproductive Biology Study Section (REB)
Program Officer
Carter, Anthony D
Project Start
2001-06-01
Project End
2006-05-31
Budget Start
2003-06-01
Budget End
2004-05-31
Support Year
3
Fiscal Year
2003
Total Cost
$296,625
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
078861598
City
New York
State
NY
Country
United States
Zip Code
10029
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Revenkova, Ekaterina; Herrmann, Kathleen; Adelfalk, Caroline et al. (2010) Oocyte cohesin expression restricted to predictyate stages provides full fertility and prevents aneuploidy. Curr Biol 20:1529-33
Adelfalk, Caroline; Janschek, Johannes; Revenkova, Ekaterina et al. (2009) Cohesin SMC1beta protects telomeres in meiocytes. J Cell Biol 187:185-99
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Kouznetsova, Anna; Novak, Ivana; Jessberger, Rolf et al. (2005) SYCP2 and SYCP3 are required for cohesin core integrity at diplotene but not for centromere cohesion at the first meiotic division. J Cell Sci 118:2271-8
Jessberger, Rolf (2005) How to divorce engaged chromosomes? Mol Cell Biol 25:18-22
Firooznia, Adriana; Revenkova, Ekaterina; Jessberger, Rolf (2005) From the XXVII North American Testis Workshop: the function of SMC and other cohesin proteins in meiosis. J Androl 26:1-10

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