Literature DB >> 9660953

Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog.

D L Pittman1, J Cobb, K J Schimenti, L A Wilson, D M Cooper, E Brignull, M A Handel, J C Schimenti.   

Abstract

DMC1 is a meiosis-specific gene first discovered in yeast that encodes a protein with homology to RecA and may be component of recombination nodules. Yeast dmc1 mutants are defective in crossing over and synaptonemal complex (SC) formation, and arrest in late prophase of meiosis I. We have generated a null mutation in the Dmc1 gene in mice and show that homozygous mutant males and females are sterile with arrest of gametogenesis in the first meiotic prophase. Chromosomes in mutant spermatocytes fail to synapse, despite the formation of axial elements that are the precursor to the SC. The strong similarity of phenotypes in Dmc1-deficient mice and yeast suggests that meiotic mechanisms have been highly conserved through evolution.

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Year:  1998        PMID: 9660953     DOI: 10.1016/s1097-2765(00)80069-6

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  229 in total

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4.  Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis.

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Journal:  Genetics       Date:  2000-10       Impact factor: 4.562

5.  Meiotic errors activate checkpoints that improve gamete quality without triggering apoptosis in male germ cells.

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6.  Genetic and cytological characterization of the RecA-homologous proteins Rad51 and Dmc1 of Schizosaccharomyces pombe.

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Review 8.  Germ cell differentiation from pluripotent cells.

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9.  Proteasome activator PA200 is required for normal spermatogenesis.

Authors:  Bernard Khor; Andrea L Bredemeyer; Ching-Yu Huang; Isaiah R Turnbull; Ryan Evans; Leonard B Maggi; J Michael White; Laura M Walker; Kay Carnes; Rex A Hess; Barry P Sleckman
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

10.  An essential role of DmRad51/SpnA in DNA repair and meiotic checkpoint control.

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