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利用连锁不平衡对德国荷斯坦奶牛18号染色体上影响体细胞评分的数量性状位点进行精细定位。

Refined positioning of a quantitative trait locus affecting somatic cell score on chromosome 18 in the German Holstein using linkage disequilibrium.

作者信息

Baes C, Brand B, Mayer M, Kühn C, Liu Z, Reinhardt F, Reinsch N

机构信息

Forschungsinstitut für die Biologie Landwirtschaftlicher Nutztiere, 18196 Dummerstorf, Germany.

出版信息

J Dairy Sci. 2009 Aug;92(8):4046-54. doi: 10.3168/jds.2008-1742.

Abstract

Combined linkage and linkage disequilibrium analysis (LALD) was conducted to more accurately map a previously reported quantitative trait locus (QTL) affecting somatic cell score on bovine chromosome 18. A grand-daughter design consisting of 6 German Holstein grandsire families with 1,054 progeny-tested genotyped sons was used in this study. Twenty microsatellite markers, 5 single nucleotide polymorphisms, and an erythrocyte antigen marker with an average marker spacing of 1.95 cM were analyzed along a chromosomal segment of 50.80 cM. Variance components were estimated and restricted maximum likelihood test statistics were calculated at the midpoint of each marker interval. The test statistics calculated in single-QTL linkage analysis exceeded the genome-wide significance threshold at several putative QTL positions. Using LALD, we were successful in assigning a genome-wide significant QTL to a confidence interval of 10.8 cM between the markers ILSTS002 and BMS833. The QTL in this marker interval was estimated to be responsible for between 5.89 and 13.86% of the genetic variation in somatic cell score. In contrast to the single-QTL linkage analysis model, LALD analyses with a 2-QTL model confirmed the position of one QTL, but gave no conclusive evidence for the existence or position of a second QTL. Ultimately, the QTL position was narrowed down considerably compared with previous results with a refined confidence interval of less than 11 cM.

摘要

进行了联合连锁与连锁不平衡分析(LALD),以更精确地定位先前报道的影响牛18号染色体体细胞评分的数量性状基因座(QTL)。本研究采用了由6个德国荷斯坦祖父系家族组成的孙女设计,这些家族中有1054头经过后裔测定并进行基因分型的儿子。沿着50.80 cM的染色体片段分析了20个微卫星标记、5个单核苷酸多态性以及一个红细胞抗原标记,平均标记间距为1.95 cM。估计了方差成分,并在每个标记区间的中点计算了限制最大似然检验统计量。在单QTL连锁分析中计算出的检验统计量在几个假定的QTL位置超过了全基因组显著性阈值。使用LALD,我们成功地将一个全基因组显著的QTL定位到标记ILSTS002和BMS833之间10.8 cM的置信区间内。该标记区间内的QTL估计占体细胞评分遗传变异的5.89%至13.86%。与单QTL连锁分析模型不同,使用双QTL模型的LALD分析证实了一个QTL的位置,但没有给出第二个QTL存在或位置的确凿证据。最终,与先前结果相比,QTL位置被大幅缩小,精细置信区间小于11 cM。

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