Faculty Research 1990 - 1999

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

Document Type

Article

Publication Date

1998

Keywords

Animal, Chromosomes/physiology, DNA-Binding Proteins/analysis/genetics, Female, Fluorescent Antibody Technique Germ-Line Mutation, Infertility/genetics, Male, Meiosis/physiology, Mice, Mice, Knockout, Oocytes/chemistry/physiology, Prophase/physiology, Rec A Protein/genetics, Recombinant Proteins/analysis/genetics, Recombination, Genetic/physiology, Spermatozoa/chemistry/physiology

First Page

697

Last Page

705

JAX Source

Mol Cell 1998 Apr;1(5):697-705

Grant

GM45415/GM/NIGMS, HD31376/HD/NICHD, CA34196/CA/NCI

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.

Share

COinS