Affiliation:
1. Department of Genetics, Cell, and Developmental Biology, University of Minnesota, Minneapolis, Minnesota 55455
Abstract
ABSTRACT
Proteins containing the DM domain, a zinc finger-like DNA binding motif, have been implicated in sexual differentiation in diverse metazoan organisms. Of seven mammalian DM domain genes, only
Dmrt1
and
Dmrt2
have been functionally analyzed. Here, we report expression analysis and targeted disruption of
Dmrt4
(also called
DmrtA1
) in the mouse.
Dmrt4
is widely expressed during embryonic and postnatal development. However, we find that mice homozygous for a putative null mutation in
Dmrt4
develop essentially normally, undergo full sexual differentiation in both sexes, and are fertile. We observed two potential mutant phenotypes in
Dmrt4
mutant mice. First, ovaries of most mutant females have polyovular follicles, suggesting a role in folliculogenesis. Second, 25% of mutant males consistently exhibited copulatory behavior toward other males. We also tested potential redundancy between
Dmrt4
and two other gonadally expressed DM domain genes,
Dmrt1
and
Dmrt7
. We observed no enhancement of gonadal phenotypes in the double mutants, suggesting that these genes function independently in gonadal development.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
54 articles.
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