首页|基于基因组重测序技术筛选小尾寒羊高繁基因的研究

基于基因组重测序技术筛选小尾寒羊高繁基因的研究

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本研究旨在筛选影响小尾寒羊高繁殖力的相关基因,为小尾寒羊的品种选育及杂交改良提供理论依据.试验选取21只具有稳定系谱的经产纯种小尾寒羊,其中,11只来自吉林地区(高产羔率组6只,低产羔率组5只)、10只来自山东地区(高产羔率组、低产羔率组各5只),采集血液样本进行全基因组重测序,进行差异等位基因频率检测及全基因组选择信号分析.分析结果显示,基于差异等位基因频率共筛选到两个地区共有的候选基因3 074个;基于群体分化指数筛选到两个地区共有的候选基因16个;基于核苷酸多样性比值筛选到两个地区共有的候选基因511个.以上三种方法取交集,获得共享基因6个,分别是CPNE4、CTNNA2、LOC114114249、LOC132659407、MBD5和SLC6A15,预期可作为影响小尾寒羊高繁殖力的候选基因.
Research on Screening High Fecundity Genes of Small-Tailed Han Sheep Based on the Genome Resequencing Technology
The purpose of the research is to screen the genes that affect the high fecundity of small-tailed Han sheep,and to provide theoretical basis for breeding improvement and crossbreeding improvement of small-tailed Han sheep.In this study,a total of 21 purebred and pluriparous small-tailed Han sheep with stable pedigree were selected in which 11 sheep(6 in the high-yield lambing group and 5 in the low-yield lambing group)from Jilin and 10 sheep(5 in each of the high-yield lambing group and low-yield lambing group)from Shandong,and blood samples were collected for the whole genome resequencing.The results showed that a total of 3,074 candidate genes shared by the two regions were screened based on the difference in allele frequency,16 candidate genes shared by the two regions were screened based on the population differentiation index,and 511 candidate genes shared by the two regions were screened based on the nucleotide diversity ratio.Six shared genes were obtained by the intersection of the above three methods,namely CPNE4,CTNNA2,LOC1 14114249,LOC132659407,MBD5 and SLC6A15,which are expected to be candidate genes affecting high fecundity of small-tailed Han sheep.

Small-tailed Han sheepGenome resequencingHigh fecundityGenesGenetic improvement

方文文、缪立生、刘宇、王维婷、刘昭华、杨少滢、王可、曹阳

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吉林省农业科学院,长春 130033

山东省农业科学院畜牧兽医研究所,济南 250100

中国农业科学院特产研究所,长春 130117

小尾寒羊 基因组重测序 高繁殖力 基因 遗传改良

2024

东北农业科学
吉林省农业科学院

东北农业科学

CSTPCD
影响因子:0.449
ISSN:1003-8701
年,卷(期):2024.49(5)