首页> 美国卫生研究院文献>Genes >Identification of a Missense Variant in MFSD12 Involved in Dilution of Phaeomelanin Leading to White or Cream Coat Color in Dogs
【2h】

Identification of a Missense Variant in MFSD12 Involved in Dilution of Phaeomelanin Leading to White or Cream Coat Color in Dogs

机译:MFSD12的一个错义变体的鉴定该变体参与了导致花粉蛋白稀释的犬的白色或奶油色外套颜色

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

White coat color in mammals has been selected several times during the domestication process. Numerous dog breeds are fixed for one form of white coat color that involves darkly pigmented skin. The genetic basis of this color, due to the absence of pigment in the hairs, was suggested to correspond to extreme dilution of the phaeomelanin, by both the expression of only phaeomelanin (locus E) and its extreme dilution (locus I). To go further, we performed genome-wide association studies (GWAS) using a multiple breed approach. The first GWAS, using 34 white dogs and 128 non-white dogs, including White Shepherds, Poodles, Cotons de Tulear and Bichons allowed us to identify two significantly associated loci on the locus E and a novel locus on chromosome 20. A second GWAS using 15 other breeds presenting extreme phaeomelanin dilution confirmed the position of locus I on the chromosome 20 (position 55 Mb pcorrected = 6 × 10−13). Using whole-genome sequencing, we identified a missense variant in the first exon of MFSD12, a gene recently identified to be involved in human, mouse and horse pigmentation. We confirmed the role of this variant in phaeomelanin dilution of numerous canine breeds, and the conserved role of MFSD12 in mammalian pigmentation.
机译:在驯化过程中,已经多次选择了哺乳动物的白大衣颜色。许多狗品种固定为一种白色外套颜色,涉及深色皮肤。这种颜色的遗传基础,由于在头发中不存在色素,通过仅表达酞菁黑素(基因座E)和其极端稀释度(基因座I),被认为对应于邻苯二甲酰亚胺的极度稀释。更进一步,我们使用多品种方法进行了全基因组关联研究(GWAS)。第一个GWAS使用34个白狗和128个非白狗,包括White Shepherds,Poodles,Cotons de Tulear和Bichons,使我们能够在E基因座上鉴定两个显着相关的基因座,并在20号染色体上鉴定出一个新基因座。其他15个表现出极大的苯丙氨酸甲酯稀释的品种确认了基因座I在20号染色体上的位置(校正后的55 Mb = 6×10 −13 )。使用全基因组测序,我们在MFSD12的第一个外显子中发现了一个错义变体,该基因最近被发现与人,小鼠和马的色素沉着有关。我们证实了该变体在众多犬科动物的苯丙氨酸甲酯稀释中的作用,以及MFSD12在哺乳动物色素沉着中的保守作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号