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1.
Science ; 337(6101): 1536-41, 2012 Sep 21.
Article in English | MEDLINE | ID: mdl-22997338

ABSTRACT

Color markings among felid species display both a remarkable diversity and a common underlying periodicity. A similar range of patterns in domestic cats suggests a conserved mechanism whose appearance can be altered by selection. We identified the gene responsible for tabby pattern variation in domestic cats as Transmembrane aminopeptidase Q (Taqpep), which encodes a membrane-bound metalloprotease. Analyzing 31 other felid species, we identified Taqpep as the cause of the rare king cheetah phenotype, in which spots coalesce into blotches and stripes. Histologic, genomic expression, and transgenic mouse studies indicate that paracrine expression of Endothelin3 (Edn3) coordinates localized color differences. We propose a two-stage model in which Taqpep helps to establish a periodic pre-pattern during skin development that is later implemented by differential expression of Edn3.


Subject(s)
Aminopeptidases/genetics , Cats/genetics , Endothelin-3/genetics , Felidae/genetics , Hair Color/genetics , Metalloproteases/genetics , Skin/metabolism , Acinonyx/genetics , Acinonyx/metabolism , Alleles , Aminopeptidases/chemistry , Aminopeptidases/metabolism , Animals , Cats/embryology , Cats/growth & development , Cats/metabolism , Endothelin-3/metabolism , Epistasis, Genetic , Felidae/growth & development , Felidae/metabolism , Gene Expression Regulation , Gene Frequency , Genetic Variation , Hair/embryology , Hair/growth & development , Hair Follicle/embryology , Haplotypes , Metalloproteases/chemistry , Metalloproteases/metabolism , Mice , Mice, Transgenic , Panthera/genetics , Panthera/metabolism , Phenotype , Polymorphism, Single Nucleotide , Skin/anatomy & histology , Skin/embryology , Species Specificity
2.
Genetics ; 181(4): 1427-36, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19189957

ABSTRACT

Alternating patches of black and yellow pigment are a ubiquitous feature of mammalian color variation that contributes to camouflage, species recognition, and morphologic diversity. X-linked determinants of this pattern--recognized by variegation in females but not in males--have been described in the domestic cat as Orange, and in the Syrian hamster as Sex-linked yellow (Sly), but are curiously absent from other vertebrate species. Using a comparative genomic approach, we develop molecular markers and a linkage map for the euchromatic region of the Syrian hamster X chromosome that places Sly in a region homologous to the centromere-proximal region of human Xp. Comparison to analogous work carried out for Orange in domestic cats indicates, surprisingly, that the cat and hamster mutations lie in nonhomologous regions of the X chromosome. We also identify the molecular cause of recessively inherited black coat color in hamsters (historically referred to as nonagouti) as a Cys115Tyr mutation in the Agouti gene. Animals doubly mutant for Sly and nonagouti exhibit a Sly phenotype. Our results indicate that Sly represents a melanocortin pathway component that acts similarly to, but is genetically distinct from, Mc1r and that has implications for understanding both the evolutionary history and the mutational mechanisms of pigment-type switching.


Subject(s)
Genetic Linkage , Hair Color/genetics , Mesocricetus/genetics , X Chromosome/genetics , Agouti Signaling Protein/genetics , Animals , Cricetinae , Epistasis, Genetic/physiology , Female , Genetic Variation , Genetics, Population , Male , Mesocricetus/physiology , Models, Biological , Pedigree , Phenotype , Receptor, Melanocortin, Type 1/genetics
3.
PLoS Genet ; 1(1): 81-95, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16103921

ABSTRACT

Niemann-Pick type C is a neurodegenerative lysosomal storage disorder caused by mutations in either of two genes, npc1 and npc2. Cells lacking Npc1, which is a transmembrane protein related to the Hedgehog receptor Patched, or Npc2, which is a secreted cholesterol-binding protein, have aberrant organelle trafficking and accumulate large quantities of cholesterol and other lipids. Though the Npc proteins are produced by all cells, cerebellar Purkinje neurons are especially sensitive to loss of Npc function. Since Niemann-Pick type C disease involves circulating molecules such as sterols and steroids and a robust inflammatory response within the brain parenchyma, it is crucial to determine whether external factors affect the survival of Purkinje cells (PCs). We investigated the basis of neurodegeneration in chimeric mice that have functional npc1 in only some cells. Death of mutant npc1 cells was not prevented by neighboring wild-type cells, and wild-type PCs were not poisoned by surrounding mutant npc1 cells. PCs undergoing cell-autonomous degeneration have features consistent with autophagic cell death. Chimeric mice exhibited a remarkable delay and reduction of wasting and ataxia despite their substantial amount of mutant tissue and dying cells, revealing a robust mechanism that partially compensates for massive PC death.

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