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绵羊和山羊表型致因变异的基因检测。

Genetic testing for phenotype-causing variants in sheep and goats.

机构信息

Department of Animal Breeding and Genetics, Justus-Liebig University of Giessen, Ludwigstrasse 21B, 35390 Giessen, Germany.

出版信息

Mol Cell Probes. 2012 Dec;26(6):231-7. doi: 10.1016/j.mcp.2012.04.005. Epub 2012 Apr 23.

DOI:10.1016/j.mcp.2012.04.005
PMID:22554501
Abstract

This review gives an overview on ovine and caprine defects/disorders, disease predispositions, production traits and coat colours for which causal gene variants are known. Most phenotypes are inherited autosomal-recessive or dominant and in the majority are caused by single nucleotide substitutions or deletions. Causative sequence variants mainly were identified by sequencing candidate genes in the past, and recently also by whole genome analysis using the ovine 50k SNP chip. While PCR-fragment length polymorphism analyses were developed for the majority of causative sequence variants, other low- to medium-throughput PCR-based methods as PCR-single strand conformation analysis and allele-specific PCR were also established frequently. For processing large sample numbers, high-throughput methods as MALDI-ToF MS or real-time PCR are available for some gene variants. Further progress in development of ovine and caprine genome sequences and SNP chips will be beneficial for the discovery of additional causative variants in these two species.

摘要

这篇综述概述了已知引起绵羊和山羊缺陷/疾病、疾病易感性、生产性状和毛色的候选基因变异。大多数表型是常染色体隐性或显性遗传的,大多数是由单个核苷酸替换或缺失引起的。过去,候选基因的测序主要用于鉴定致病序列变异,最近也可以使用绵羊 50kSNP 芯片进行全基因组分析。虽然大多数致病序列变异都开发了 PCR-片段长度多态性分析,但也经常建立其他低到中通量的基于 PCR 的方法,如 PCR-单链构象分析和等位基因特异性 PCR。对于处理大量样本数量,对于一些基因变异,MALDI-TOF MS 或实时 PCR 等高通量方法是可用的。绵羊和山羊基因组序列和 SNP 芯片的进一步发展将有助于发现这两个物种中的其他致病变异。

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