Silky-feather has been selected and fixed in some breeds due to its unique appearance. This phenotype is caused by a single recessive gene (hookless, h). Here we map the silky-feather locus to chromosome 3 by linkage analysis and subsequently fine-map it to an 18.9 kb interval using the identical by descent (IBD) method. Further analysis reveals that a C to G transversion located upstream of the prenyl (decaprenyl) diphosphate synthase, subunit 2 (PDSS2) gene is causing silky-feather. All silky-feather birds are homozygous for the G allele. The silky-feather mutation significantly decreases the expression of PDSS2 during feather development in vivo. Consistent with the regulatory effect, the C to G transversion is shown to remarkably reduce PDSS2 promoter activity in vitro. We report a new example of feather structure variation associated with a spontaneous mutation and provide new insight into the PDSS2 function.
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http://dx.doi.org/10.1371/journal.pgen.1004576 | DOI Listing |
PLoS Genet
August 2014
State Key Laboratory for Agrobiotechnology, China Agricultural University, Beijing, China; National Engineering Laboratory for Animal Breeding, China Agricultural University, Beijing, China; College of Animal Science and Technology, Yunnan Agricultural University, Kunming, Yunnan, China.
Silky-feather has been selected and fixed in some breeds due to its unique appearance. This phenotype is caused by a single recessive gene (hookless, h). Here we map the silky-feather locus to chromosome 3 by linkage analysis and subsequently fine-map it to an 18.
View Article and Find Full Text PDFTwenty-two progeny in a single backcross family of a species hybrid between the dwarf turtle dove and the ring-neck dove exhibited strong association in a repulsion phase of linkage between the silky feather trait and the species-specific hu-8 blood character. This family constituted a test cross for six characters: sex, peanut reactivity, silky feathering, and the three independent species-specific blood characters, hu-1, hu-4, and hu-8.
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