Walling G A, Wilson A D, Mcteir B L, Bishop S C
Department of Genetics and Biometry, Roslin Institute (Edinburgh), Roslin, Midlothian EH25 9PS, UK.
Heredity (Edinb). 2004 Feb;92(2):102-9. doi: 10.1038/sj.hdy.6800389.
In this study, the Suffolk and Texel sheep breeds were compared for microsatellite marker heterozygosity throughout seven chromosomal regions in the sheep genome. A total of 623 Texel animals and 489 Suffolk animals in five and three half-sib families, respectively, were genotyped for microsatellite markers across the seven different chromosomes. Using the observed allele frequencies, the expected levels of heterozygosity were calculated for each family. The expected levels of heterozygosity did not significantly differ between the breeds across all regions studied. However, levels of expected heterozygosity were 32% higher in Texel animals on chromosome 4 due to a region of increased heterozygosity between BMS648 and BM3212. The number of allelic variants significantly differed between the breeds, solely due to a region of increased number of alleles on chromosome 20. This region of higher numbers of allele variants in the Texel breed extended from the MHC to c. 15 cM distal to the MHC region incorporating markers OMHC1, CSRD226, TGLA387 and BM1818, which had 3.30, 7.02, 3.09 and 6.75 more alleles in Texel than in Suffolk animals, respectively. No difference was observed in the variance of allele frequency between the two breeds. It is proposed that previous selective sweeps may have reduced numbers of alleles and levels of heterozygosity in the Suffolk breed.
在本研究中,对萨福克羊和特克塞尔羊两个品种在绵羊基因组的七个染色体区域的微卫星标记杂合性进行了比较。分别在五个和三个半同胞家系中,对总共623只特克塞尔羊和489只萨福克羊进行了七个不同染色体上微卫星标记的基因分型。利用观察到的等位基因频率,计算每个家系的预期杂合性水平。在所研究的所有区域中,两个品种的预期杂合性水平没有显著差异。然而,由于BMS648和BM3212之间杂合性增加的区域,4号染色体上特克塞尔羊的预期杂合性水平高出32%。两个品种之间等位基因变体的数量存在显著差异,这完全是由于20号染色体上等位基因数量增加的区域所致。特克塞尔品种中这个等位基因变体数量较多的区域从主要组织相容性复合体(MHC)延伸至MHC区域远端约15厘摩处,包含标记OMHC1、CSRD226、TGLA387和BM1818,在这些标记上,特克塞尔羊的等位基因分别比萨福克羊多3.30、7.02、3.09和6.75个。两个品种之间等位基因频率的方差没有差异。有人提出,先前的选择性清除可能减少了萨福克品种的等位基因数量和杂合性水平。