Schopen G C B, Koks P D, van Arendonk J A M, Bovenhuis H, Visker M H P W
Animal Breeding and Genomics Centre, Wageningen University, PO Box 338, 6700 AH Wageningen, the Netherlands.
Anim Genet. 2009 Aug;40(4):524-37. doi: 10.1111/j.1365-2052.2009.01880.x. Epub 2009 Apr 7.
The objective of this study was to perform a whole genome scan to detect quantitative trait loci (QTL) for milk protein composition in 849 Holstein-Friesian cows originating from seven sires. One morning milk sample was analysed for the major milk proteins using capillary zone electrophoresis. A genetic map was constructed with 1341 single nucleotide polymorphisms, covering 2829 centimorgans (cM) and 95% of the cattle genome. The chromosomal regions most significantly related to milk protein composition (P(genome) < 0.05) were found on Bos taurus autosomes (BTA) 6, 11 and 14. The QTL on BTA6 was found at about 80 cM, and affected alpha(S1)-casein, alpha(S2)-casein, beta-casein and kappa-casein. The QTL on BTA11 was found at 124 cM, and affected beta-lactoglobulin, and the QTL on BTA14 was found at 0 cM, and affected protein percentage. The proportion of phenotypic variance explained by the QTL was 3.6% for beta-casein and 7.9% for kappa-casein on BTA6, 28.3% for beta-lactoglobulin on BTA11, and 8.6% for protein percentage on BTA14. The QTL affecting alpha(S2)-casein on BTA6 and 17 showed a significant interaction. We investigated the extent to which the detected QTL affecting milk protein composition could be explained by known polymorphisms in beta-casein, kappa-casein, beta-lactoglobulin and DGAT1 genes. Correction for these polymorphisms decreased the proportion of phenotypic variance explained by the QTL previously found on BTA6, 11 and 14. Thus, several significant QTL affecting milk protein composition were found, of which some QTL could partially be explained by polymorphisms in milk protein genes.
本研究的目的是对来自7头公牛的849头荷斯坦-弗里生奶牛进行全基因组扫描,以检测乳蛋白组成的数量性状基因座(QTL)。采集一份早晨的乳样,采用毛细管区带电泳分析主要乳蛋白。构建了一个包含1341个单核苷酸多态性的遗传图谱,覆盖2829厘摩(cM)和95%的牛基因组。在牛1号常染色体(BTA)6、11和14上发现了与乳蛋白组成最显著相关的染色体区域(P(基因组)<0.05)。BTA6上的QTL位于约80 cM处,影响α(S1)-酪蛋白、α(S2)-酪蛋白、β-酪蛋白和κ-酪蛋白。BTA11上的QTL位于124 cM处,影响β-乳球蛋白,BTA14上的QTL位于0 cM处,影响蛋白质百分比。BTA6上β-酪蛋白的QTL解释的表型变异比例为3.6%,κ-酪蛋白为7.9%;BTA11上β-乳球蛋白的QTL解释的表型变异比例为28.3%;BTA14上蛋白质百分比的QTL解释的表型变异比例为8.6%。BTA6和17上影响α(S2)-酪蛋白的QTL表现出显著的相互作用。我们研究了检测到的影响乳蛋白组成的QTL在多大程度上可以由β-酪蛋白、κ-酪蛋白、β-乳球蛋白和DGAT1基因中的已知多态性来解释。对这些多态性进行校正后,BTA6、11和14上先前发现的QTL解释的表型变异比例降低。因此,发现了几个影响乳蛋白组成的显著QTL,其中一些QTL可以部分由乳蛋白基因中的多态性来解释。