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作 者:刘娟[1,2] 孙艳[2] 姜强[2] 杨春红[2] 黄金明[2] 李建斌[2] 侯明海[2] 仲跻峰[2] 王长法[2] 刘保申[1]
机构地区:[1]山东农业大学农学院,泰安271000 [2]山东省农业科学院奶牛研究中心,济南250131
出 处:《遗传》2016年第1期62-71,共10页Hereditas(Beijing)
基 金:国家自然科学基金项目(编号:31401049;31401050);山东省农业良种工程种质创新应用项目(编号:2014LZ);现代农业产业技术体系奶牛岗位科学家项目(编号:CARS-37);山东省农业产业技术体系牛产业创新团队项目(编号:SDAIT-12-011-02)资助~~
摘 要:为研究内着丝粒蛋白(Inner centromere protein,INCENP)基因启动子区单核苷酸多态性(SNPs)与精液品质的相关性,本文利用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测了250头中国荷斯坦公牛INCENP基因的基因型。在INCENP基因启动子区鉴定出两个SNPs(g.-556 G>T,rs 136823901和g.-692 C>T,rs 211010999),发现了3种单倍型(CG、TT、TG)。分析两个SNP位点的基因型频率和等位基因频率,各SNP及单倍型组合与中国荷斯坦公牛精液品质的相关性,结果表明SNP位点g.-556 G>T GT基因型个体的鲜精活力显著高于GG基因型个体(P<0.05),单倍型组合H1H1(CCGG)、H1H3(CTGT)、H2H3(TTGT)和H3H3(TTTT)个体的鲜精活力和冻精解冻后活力均显著高于H1H2个体(P<0.05)。为进一步研究g.-556 G>T和g.-692 C>T影响精液品质的可能机理,本文将3种单倍型质粒分别转染小鼠睾丸间质细胞(MLTC-1),结果显示含TG单倍型的载体荧光素酶活性最高。由此推测,g.-556 G>T和g.-692 C>T为启动子区功能性突变位点,可通过调节启动子活性来调控INCENP基因表达,进而影响精液品质。To explore the association between single nucleotide polymorphisms(SNPs) in the promoter region ofthe inner centromere protein(INCENP) gene and bovine semen quality, the haplotypes in 250 Chinese Holstein bulls were detected using PCR-RFLP method in this study. Two SNPs(g.-556 G〉T, rs 136823901 and g.-692 C〉T,rs 211010999) and three haplotypes(CG, TT, TG) were identified in the promoter region of INCENP. The genotype frequency and allele frequency of these two SNPs as well as the correlation between different SNP haplotype combinations and bovine semen quality were then analyzed. Our results showed that fresh sperm motility of the GT genotype was significantly higher than that of the GG genotype(P〈0.05) at the SNP site g.-556 G〉T, while fresh and frozen-thawed sperm motilities of the haplotype combinations H1H1(CCGG), H1H3(CTGT), H2H3(TTGT) and H3H3(TTTT) were significantly higher than that of H1H2(P〈0.05). To further study the possible mechanisms by which g.-556 G〉T and g.-692 C〉T affect semen quality, three haplotype plasmids were respectively transfected into MLTC-1 cells. The TG haplotype demonstrated the highest luciferase activity, suggesting that g.-556 G〉T and g.-692 C〉T are functional mutations which could regulate INCENP gene expression by affecting promoter activity and thus affect semen quality.
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