The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation

Sally A. Camper, Thomas L. Saunders, Ronald W. Katz, Roger H. Reeves

Research output: Contribution to journalArticlepeer-review

178 Scopus citations

Abstract

Two nonallelic mouse mutations with severe dwarf phenotypes are characterized by a lack of growth hormone, prolactin, and thyroid stimulating hormone. The cells that normally synthesize these pituitary hormones express a common transcription factor called GHF-1 or Pit-1. Using an intersubspecific backcross, we have demonstrated tight linkage of the Pit-1 and Snell dwarf (dw) genes on mouse chromosome 16. No recombination was observed between Pit-1 and dw in 110 individuals examined. Southern blot analysis of genomic DNA reveals that the Pit-1 gene is rearranged in C3H HeJ- dw1 dw mice but not in coisogenic +/+ animals, providing molecular evidence that a lesion in the Pit-1 gene results in the Snell dwarf phenotype. Demonstration of low levels of Pit-1 expression in Ames dwarf (df) mice implies that both Pit-1 and df expression may be required for pituitary differentiation.

Original languageEnglish (US)
Pages (from-to)586-590
Number of pages5
JournalGenomics
Volume8
Issue number3
DOIs
StatePublished - Nov 1990

ASJC Scopus subject areas

  • Genetics

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