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Molecular mapping of the mouse ob mutation

  • J. M. Friedman
  • , R. L. Leibel
  • , D. S. Siegel
  • , J. Walsh
  • , N. Bahary
  • Rockefeller University

Research output: Contribution to journal › Article › peer-review

167 Scopus citations

Abstract

The mouse ob mutation has been mapped relative to a series of RFLPs among the progeny of three separate mouse crosses: an intraspecific backcross, an intraspecific intercross, and an interspecific intercross. Genotypic assignment at the ob locus was made by making use of measurements of body mass index and the plasma concentrations of glucose and insulin. These data have suggested that the development of diabetes in these animals is a consequence of unlinked polygenes. There was also evidence that unlinked Mus spretus alleles can diminish the obesity of ob obmice. From these data we have mapped several markers on chromosome 6 with the following order: cen-Cola-2-Met-ob-Cpa-Tcrb. The homologs of markers that flank ob map to human chromosome 7q, suggesting that if there is a human homologue of ob, it maps to 7q31.

Original languageEnglish
Pages (from-to)1054-1062
Number of pages9
JournalGenomics
Volume11
Issue number4
DOIs
StatePublished - Dec 1991

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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