Mammalian Genome

, Volume 4, Issue 9, pp 481–484

Urogenital syndrome (us): a developmental mutation on Chromosome 2 of the mouse

  • Priscilla W. Lane
  • Connie S. Birkenmeier
Original Contributions

DOI: 10.1007/BF00364781

Cite this article as:
Lane, P.W. & Birkenmeier, C.S. Mammalian Genome (1993) 4: 481. doi:10.1007/BF00364781

Abstract

Urogenital syndrome (us) is a recessive mutation in mice characterized primarily by abnormalities of the axial skeleton and urogenital organs. We established linkage of us with the centromeric end of Chromosome (Chr) 2, using the Robertsonian Chr Rb(2.8)2Lub. Analysis of progeny from crosses using the Chr 2 markers Danforth's short tail (Sd) and ulnaless (Ul) positioned us near two loci that have recently been mapped by RFLPs, nonerythroid α-spectrin (Spna-2) and the paired-box-containing-gene-8 (Pax-8). The position of us relative to these loci was established by analysis of progeny from interspecific backcrosses between the us strains and Mus spretus. The estimated map distances and most likely gene order are centromere-Pax-8-2.1±1.2-us-0.7±0.7-Spna-2; however, the reverse order cannot be ruled out. Our data make it unlikely that us is a mutation in either Spna-2 or Pax-8. Spna-2 is close enough to us, however, to be a useful marker for positional cloning of the us gene. The human mutation Nail-patella-syndrome (NPS1) maps to the region of human Chr 9 (9q34) that is homologous to the us region of mouse Chr 2. Phenotypic similarities between the two syndromes suggest the possibility that they are caused by mutations at homologous loci.

Copyright information

© Springer-Verlag New York Inc 1993

Authors and Affiliations

  • Priscilla W. Lane
    • 1
  • Connie S. Birkenmeier
    • 1
  1. 1.The Jackson Laboratory600 Main StreetBar HarborUSA

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