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Quantitative trait loci that modify the severity of spotting in piebald mice.
Author(s) -
William J. Pavan,
Susanna Mac,
Ming Cheng,
S M Tilghman
Publication year - 1995
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.5.1.29
Subject(s) - biology , spotting , quantitative trait locus , genetics , coat , backcrossing , white (mutation) , phenotype , allele , inbred strain , gene mapping , neural crest , gene , chromosome , paleontology , physics , optics
Mice homozygous for the recessive mutation piebald (s) exhibit a white-spotted coat caused by the defective development of neural crest-derived melanocytes. The severity of white spotting varies greatly, depending on the genetic background on which s is expressed. A backcross between two inbred strains of s/s mice that exhibit large differences in the degree of spotting was used to identify six genetic modifiers of piebald spotting on chromosomes 2, 5, 7, 8, 10, and 13. The loci differed in their spatial contribution to spotting on the dorsal versus ventral surfaces of mice; nonadditive interactions were observed between loci on chromosomes 2 and 5. This study underscores the power of using genetic analyses to identify and analyze loci involved in modifying the severity of phenotypic traits in mice.

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