Fine structure mapping and deletion analysis of the murine piebald locus

D. L. Metallinos, A. J. Oppenheimer, E. M. Rinchik, L. B. Russell, W. Dietrich, S. M. Tilghman

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27 Scopus citations

Abstract

piebald (s) is a recessive mutation that affects the development of two cell types of neural crest origin: the melanocytes, responsible for pigment synthesis in the skin, and enteric ganglia, which innervate the lower bowel. As a result, mice carrying piebald mutations exhibit white spotting in the coat and aganglionic megacolon. Previously the gene had been localized to the distal half of mouse chromosome 14. To determine its precise location relative to molecular markers, an intersubspecific backcross was generated. Two anchor loci of chromosome 14, slaty and hypogonadal, in addition to simple sequence length repeat markers, were used to localize s to a 2-cM interval defined by the markers D14Mit38 and D14Mit42. The molecular markers were also used to characterize nine induced s alleles. Three of these mutations exhibited no deletions or rearrangements of the flanking markers, whereas the other six had two or more of these markers deleted. The extent of the deletions was found to be consistent with the severity of the homozygous phenotype. The location of deletion breakpoints in the induced alleles, coupled with the recombination breakpoints in the backcross progeny, provide useful molecular landmarks to define the location of the piebald gene.

Original languageEnglish (US)
Pages (from-to)217-223
Number of pages7
JournalGenetics
Volume136
Issue number1
StatePublished - 1994

All Science Journal Classification (ASJC) codes

  • Genetics

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    Metallinos, D. L., Oppenheimer, A. J., Rinchik, E. M., Russell, L. B., Dietrich, W., & Tilghman, S. M. (1994). Fine structure mapping and deletion analysis of the murine piebald locus. Genetics, 136(1), 217-223.