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猪肛门闭锁的全基因组扫描确定了与猪1号染色体上一个染色体区域的连锁和关联。

Genomewide scan for anal atresia in swine identifies linkage and association with a chromosome region on Sus scrofa chromosome 1.

作者信息

Wiedemann Sabine, Fries Ruedi, Thaller Georg

机构信息

Lehrstuhl für Tierzucht, Technische Universität München, D-85350 Freising-Weihenstephan, Germany.

出版信息

Genetics. 2005 Nov;171(3):1207-17. doi: 10.1534/genetics.104.032805. Epub 2005 Jul 14.

Abstract

Anal atresia is a rare and severe disorder in swine occurring with an incidence of 0.1-1.0%. A whole-genome scan based on affected half-sibs was performed to identify susceptibility loci for anal atresia. The analysis included 27 families with a total of 95 animals and 65 affected piglets among them. Animals were genotyped for 126 microsatellite markers distributed across the 18 autosomal porcine chromosomes and the X chromosome, covering an estimated 2080 cM. Single-point and multipoint nonparametric linkage scores were calculated using the computer package ALLEGRO 1.0. Significant linkage results were obtained for chromosomes 1, 3, and 12. Markers on these chromosomes and additionally on chromosomes for which candidate genes have been postulated in previous studies were subjected to the transmission disequilibrium test (TDT). The test statistic exceeded the genomewide significance level for adjacent markers SW1621 (P = 7 x 10(-7)) and SW1902 (P = 3 x 10(-3)) on chromosome 1, supporting the results of the linkage analysis. A specific haplotype associated with anal atresia that could prove useful for selection against the disorder was revealed. Suggestive linkage and association were also found for markers S0081 on chromosome 9 and SW957 on chromosome 12.

摘要

肛门闭锁是猪中一种罕见且严重的疾病,发病率为0.1 - 1.0%。基于患病半同胞进行了全基因组扫描,以确定肛门闭锁的易感基因座。分析包括27个家系,共95只动物,其中65只为患病仔猪。对分布在18条常染色体猪染色体和X染色体上的126个微卫星标记进行基因分型,覆盖约2080厘摩。使用计算机软件包ALLEGRO 1.0计算单点和多点非参数连锁分数。在1号、3号和12号染色体上获得了显著的连锁结果。对这些染色体上以及先前研究中已假定有候选基因的染色体上的标记进行传递不平衡检验(TDT)。检验统计量超过了1号染色体上相邻标记SW1621(P = 7×10⁻⁷)和SW1902(P = 3×10⁻³)的全基因组显著水平,支持了连锁分析的结果。揭示了一种与肛门闭锁相关的特定单倍型,这可能对针对该疾病的选择有用。在9号染色体上的标记S0081和12号染色体上的SW957也发现了提示性的连锁和关联。

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