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两个基因变体与波多黎各帕索马的“虎眼”虹膜色素沉着有关。

Two Variants in Are Associated with "Tiger-Eye" Iris Pigmentation in Puerto Rican Paso Fino Horses.

作者信息

Mack Maura, Kowalski Elizabeth, Grahn Robert, Bras Dineli, Penedo Maria Cecilia T, Bellone Rebecca

机构信息

Veterinary Genetics Laboratory, School of Veterinary Medicine, University of California, Davis, California 95616.

Department of Biology, University of Tampa, Florida 33606.

出版信息

G3 (Bethesda). 2017 Aug 7;7(8):2799-2806. doi: 10.1534/g3.117.043786.

Abstract

A unique eye color, called tiger-eye, segregates in the Puerto Rican Paso Fino (PRPF) horse breed and is characterized by a bright yellow, amber, or orange iris. Pedigree analysis identified a simple autosomal recessive mode of inheritance for this trait. A genome-wide association study (GWAS) with 24 individuals identified a locus on ECA 1 reaching genome-wide significance ( = 1.32 × 10). This ECA1 locus harbors the candidate gene, (), (), with known roles in pigmentation in humans, mice, and zebrafish. Humans with compound heterozygous mutations in have oculocutaneous albinism (OCA) type 6 (OCA6), which is characterized by dilute skin, hair, and eye pigmentation, as well as ocular anomalies. Twenty tiger-eye horses were homozygous for a nonsynonymous mutation in exon 2 (p.Phe91Tyr) of (called here Tiger-eye 1), which is predicted to be deleterious to protein function. Additionally, eight of the remaining 12 tiger-eye horses heterozygous for the p.Phe91Tyr variant were also heterozygous for a 628 bp deletion encompassing all of exon 7 of (c.875-340_1081+82del), which we will call here the Tiger-eye 2 allele. None of the 122 brown-eyed horses were homozygous for either tiger-eye-associated allele or were compound heterozygotes. Further, neither variant was detected in 196 horses from four related breeds not known to have the tiger-eye phenotype. Here, we propose that two mutations in affect iris pigmentation in tiger-eye PRPF horses. Further, unlike OCA6 in humans, the Tiger-eye 1 mutation in its homozygous state or as a compound heterozygote (Tiger-eye 1/Tiger-eye 2) does not appear to cause ocular anomalies or a change in coat color in the PRPF horse.

摘要

一种名为虎眼的独特眼睛颜色在波多黎各帕索马(PRPF)品种中分离,其特征是虹膜呈亮黄色、琥珀色或橙色。系谱分析确定了该性状的简单常染色体隐性遗传模式。一项对24匹马的全基因组关联研究(GWAS)在ECA 1上确定了一个达到全基因组显著性水平的位点( = 1.32 × 10)。这个ECA1位点包含候选基因, (), (),在人类、小鼠和斑马鱼的色素沉着中具有已知作用。在 中具有复合杂合突变的人类患有6型眼皮肤白化病(OCA)(OCA6),其特征是皮肤、毛发和眼睛色素沉着变淡,以及眼部异常。20匹虎眼马在 外显子2(p.Phe91Tyr)(此处称为虎眼1)中存在一个非同义突变,预计该突变对蛋白质功能有害。此外,其余12匹虎眼马中,有8匹对于p.Phe91Tyr变异是杂合的,同时对于一个包含 外显子7全部的628 bp缺失(c.875 - 340_1081 + 82del)也是杂合的,我们在此将其称为虎眼2等位基因。122匹棕眼马中没有一匹对于任何与虎眼相关的等位基因是纯合的,也没有一匹是复合杂合子。此外,在来自四个已知没有虎眼表型的相关品种的196匹马中均未检测到这两种变异。在这里,我们提出 中的两个突变影响了虎眼PRPF马的虹膜色素沉着。此外,与人类的OCA6不同,虎眼1突变在其纯合状态或作为复合杂合子(虎眼1/虎眼2)时,似乎不会导致PRPF马出现眼部异常或毛色变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/444f/5555483/71973ee9a36b/2799f1.jpg

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