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Relationship of polymorphisms in the fsh beta subunit gene with reproduction in Bos taurus and Bos indicus cattle.

机译:fshβ亚基基因多态性与金牛座和印度in牛繁殖的关系。

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摘要

Two experiments were conducted to characterize polymorphisms (SNP) in the bovine FSHbeta gene promoter region to examine breed differences in SNP, and to determine effects of SNP on reproduction in beef cattle. Experiment 1 - DNA samples were collected from 5 Angus (ANG), 13 Balancer (BAL), & 16 Brahman influenced (BI) bulls. Polymorphisms were identified by sequencing of 3 sequential PCR products from the promoter region revealed 17 SNP & 4 insertion/deletions (INDEL). Semen samples were collected and sperm quality variables determined via computer assisted sperm analysis (CASA) or stained smears. The MIXED procedure for ANG & BAL indicated interactions of week and SNP 485for LIN, AREA, & MINAB (P ≤ 0.05), effects of SNP 169 & 170 on MINAB & TOTAB (P ≤ 0.07), SNP 485 on MOT, PROG, RAP, VAP, VSL, VCL, ALH, BCF, AREA, & LIVE (P ≤ 0.05),and SNP 1130 on VCL, ALH, LIN (P ≤ 0.05), & STR (P = 0.06). For BI bulls effects of SNP 171, 225, 353, 410, 411, 412, & INDEL 413-414 on MINAB & TOTAB (P ≤ 0.09), SNP 783 on MINAB & TOTAB (P ≤ 0.03), BCF & MAJAB (P ≤ 0.09), SNP 1130 on VCL (P = 0.05), VAP, & VSL (P ≤ 0.09), and SNP 1702 on MINAB & TOTAB (P ≤ 0.04). Experiment 2 - DNA samples were collected from early & late pubertal Brahman heifers and SNP were identified by sequencing 2 upstream segments of FSHâ promoter region. Chi square revealed effects upon puberty for SNP 783 (P = 0.02) and 171 (P = 0.08), breed differences in frequency of occurrence for 10 SNP (171, 225, 321, 353, 410, 411, 412, 783, 887, 1702), and 2 INDEL (411-412 INDEL & 413-414 INDEL). Results indicate breed differences in frequency of occurrence of SNP in FSHâ promoter region, and that SNP may be useful as markers related to semen quality in bulls and puberty in Brahman heifers.
机译:进行了两个实验来表征牛FSHbeta基因启动子区域的多态性(SNP),以检查SNP的品种差异,并确定SNP对肉牛繁殖的影响。实验1-从5个安格斯(ANG),13个平衡器(BAL)和16个受到婆罗门影响(BI)的公牛中收集了DNA样品。通过对来自启动子区域的3种顺序PCR产物进行测序,鉴定出多态性,揭示了17个SNP和4个插入/缺失(INDEL)。收集精液样本,并通过计算机辅助精子分析(CASA)或染色涂片确定精子质量变量。 ANG和BAL的混合过程表明LIN,AREA和MINAB的周与SNP 485相互作用(P≤0.05),SNP 169和170对MINAB和TOTAB的影响(P≤0.07),SNP 485对MOT,PROG,RAP的影响,VAP,VSL,VCL,ALH,BCF,AREA和LIVE(P≤0.05),以及VCL,ALH,LIN(P≤0.05)和STR上的SNP 1130(P = 0.06)。对于BI Bulls,SNP 171、225、353、410、411、412和INDEL 413-414对MINAB和TOTAB(P≤0.09),SNP 783对MINAB和TOTAB(P≤0.03),BCF和MAJAB(P ≤0.09),VCL上的SNP 1130(P = 0.05),VAP和VSL(P≤0.09),MINAB和TOTAB上的SNP 1702(P≤0.04)。实验2-从早期和晚期青春期婆罗门小母牛收集DNA样本,并通过对FSHα启动子区域的2个上游片段进行测序来鉴定SNP。卡方显示了SNP 783(P = 0.02)和171(P = 0.08)对青春期的影响,10 SNP的出现频率差异(171、225、321、353、410、411、412、412、783、887, 1702)和2 INDEL(411-412 INDEL和413-414 INDEL)。结果表明,FSHα启动子区域中SNP发生频率的品种差异,SNP可用作与公牛和婆罗门小母牛的青春期精液质量有关的标志物。

著录项

  • 作者

    Davis, Amanda Jo.;

  • 作者单位

    University of Arkansas.;

  • 授予单位 University of Arkansas.;
  • 学科 Animal sciences.
  • 学位 M.S.
  • 年度 2012
  • 页码 94 p.
  • 总页数 94
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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