4.0 Article

A transgenic insertion causing cryptorchidism in mice

Journal

GENESIS
Volume 30, Issue 1, Pages 26-35

Publisher

WILEY
DOI: 10.1002/gene.1029

Keywords

cryptorchidism; infertility; insertional mutation

Funding

  1. NICHD NIH HHS [R01 HD037067-01A1, R01 HD037067] Funding Source: Medline

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A distinctive feature of gonadal maturation in mammals is the movement to an extraabdominal location. Testicular descent is a complex, multistage process whereby the embryonic gonads migrate from their initial abdominal position to the scrotum. Failure in this process results in cryptorchidism, a frequent congenital birth defect in humans. We report here a new mouse transgenic insertional mutation, cryptorchidism with white spotting (crsp), Males homozygous for crsp exhibit a high intraabdominal position of the testes, associated with complete sterility, Heterozygous males have a wildtype phenotype, and homozygous females are fertile. Surgically descended testes in crsp/crsp males show normal spermatogenesis, Using FISH and genetic analyses, the transgenic insert causing the crsp mutation has been mapped to the distal part of mouse chromosome 5. Transgene integration resulted in a 550-kb deletion located upstream of the Brca2 gene. A candidate gene encoding a novel G protein-coupled receptor (Great) with an expression pattern suggesting involvement in testicular descent has been identified. genesis 30:26-35, 2001. (C) 2001 Wiley-Liss, Inc.

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