The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation
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 ba...
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Veröffentlicht in: | Genomics (San Diego, Calif.) Calif.), 1990-11, Vol.8 (3), p.586-590 |
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Zusammenfassung: | 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
-
dw
1
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. |
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ISSN: | 0888-7543 1089-8646 |
DOI: | 10.1016/0888-7543(90)90050-5 |