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影响瑞典奶牛健康性状的数量性状基因座

Quantitative trait loci affecting health traits in Swedish dairy cattle.

作者信息

Holmberg M, Andersson-Eklund L

机构信息

Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, S-750 07 Uppsala, Sweden.

出版信息

J Dairy Sci. 2004 Aug;87(8):2653-9. doi: 10.3168/jds.s0022-0302(04)73391-3.

Abstract

The purpose of this study was to map quantitative trait loci (QTL) affecting health traits in Swedish dairy cattle. A genome scan covering 17 chromosomes was performed. Ten grandsire families were used in a granddaughter design. Nine of the families belonged to the Swedish Red and White breed, which is related to other Nordic Ayrshire breeds, and one family was of the Swedish Holstein breed. A total of 417 bulls were genotyped for 116 microsatellite markers distributed over 17 chromosomes. Daughter yield deviations for clinical mastitis, somatic cell count (SCC), and other diseases (OD) were included in the analysis. Least squares interval mapping using putative QTL as cofactors was applied both within and across grandsire families. Significance thresholds were set by permutation tests. In the across-family analysis, we detected 8 suggestive QTL and 3 QTL significant at the genome level. The QTL affecting clinical mastitis were found on 3 chromosomes (9, 11, and 25), 4 QTL for SCC were found (on chromosomes 5, 9, 11, and 23), and we detected 4 QTL for OD (on chromosomes 9, 11, 15, and 25). In addition, we found several QTL that segregated within single families but where the QTL effect was not significant in the across-family analysis. In conclusion, we were able to locate QTL for all 3 analyzed traits, and overlapping QTL for several traits were observed.

摘要

本研究的目的是绘制影响瑞典奶牛健康性状的数量性状基因座(QTL)图谱。进行了覆盖17条染色体的全基因组扫描。采用孙女设计,使用了10个祖父系家系。其中9个家系属于瑞典红白奶牛品种,该品种与其他北欧艾尔夏奶牛品种相关,1个家系为瑞典荷斯坦奶牛品种。对分布于17条染色体上的116个微卫星标记进行基因分型,共检测了417头公牛。分析中纳入了临床乳腺炎、体细胞计数(SCC)和其他疾病(OD)的女儿产奶偏差。以假定的QTL作为辅助因子,在祖父系家系内和家系间进行最小二乘区间定位分析。通过排列检验设定显著性阈值。在家系间分析中,我们检测到8个暗示性QTL和3个在基因组水平上显著的QTL。影响临床乳腺炎的QTL位于3条染色体上(9号、11号和25号),检测到4个影响SCC的QTL(位于5号、9号、11号和23号染色体上),以及4个影响OD的QTL(位于9号、11号、15号和25号染色体上)。此外,我们还发现了几个在单个家系中分离但在家系间分析中QTL效应不显著的QTL。总之,我们能够定位所有3个分析性状的QTL,并观察到几个性状的重叠QTL。

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