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The mRNA expression profile of the goat prion protein testis-specific (PRNT) gene and its associations with litter size

机译:山羊朊病毒蛋白睾丸特异性(PRNT)基因的mRNA表达谱及其与凋落物尺寸的关联

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摘要

The goat PRNT gene was initially identified as a testis-specific gene with a role in spermatogenesis. In this study, we used quantitative real-time PCR (qPCR) to first determine the mRNA expression profile of this gene in different goat tissues. Surprisingly, we found that PRNT was expressed not only in the testis but also in nine other tissues in goats. Moreover, PRNT was weakly expressed in the testis, while its expression was strongest in the ovary. These results, combined with those of other studies, led us to hypothesize that the goat PRNT gene has a role in both male and female reproduction. We further used direct DNA sequencing to detect potential SNPs within this gene in Shaanbei whit cashmere (SBWC) rams and ewes, and identified three SNPs within the PRNT gene, namely, c.-58C > T, c.71A > G (p.Alanine24Valine), and c.102C > T (synonymous). In rams, c.-58C > T and c.102C > T were strongly linked with each other (D' = 1.000, r(2) = 0.504), whereas no significant association (P > 0.05) was found between the three SNPs and semen quality, which was consistent with the low expression of the PRNT gene in the testis. Interestingly, in ewes (n = 502), c.-58C > T and c.71A > G were also strongly linked with each other (D' = 0.973, r(2) = 0.537). Additionally, the c.71A > G locus, especially the AA genotype, had a significant influence on litter size (P = 0.006), consistent with the high PRNT expression in the ovary. Combined, the results of the expression profiling and analysis of the association between the SNPs and reproductive traits showed that two strongly linked nucleotide sequence variants within PRNT were significantly associated with goat litter size. These findings provide potential DNA markers for use in the marker-assisted selection (MAS) of goats with high-fertility traits. (C) 2021 Elsevier Inc. All rights reserved.
机译:山羊PRNT基因最初被鉴定为睾丸特异性基因,在精子发生中发挥作用。在本研究中,我们使用定量实时PCR(qPCR)首次确定该基因在不同山羊组织中的mRNA表达谱。令人惊讶的是,我们发现PRNT不仅在睾丸中表达,而且在山羊的其他九个组织中也表达。此外,PRNT在睾丸中表达较弱,而在卵巢中表达最强。这些结果,加上其他研究的结果,使我们假设山羊PRNT基因在雄性和雌性生殖中都有作用。我们进一步使用直接DNA测序来检测陕北白绒山羊(SBWC)公羊和母羊中该基因内的潜在SNP,并在PRNT基因内鉴定出三个SNP,即c.-58C>T、c.71A>G(p.Alanine24Valine)和c.102C>T(同义)。在公羊中,c.-58C>T和c.102C>T之间存在着紧密的联系(D'=1.000,r(2)=0.504),而这三个SNP与精液质量之间没有显著关联(P>0.05),这与睾丸中PRNT基因的低表达相一致。有趣的是,在母羊(n=502)中,c.-58C>T和c.71A>G也彼此紧密相连(D'=0.973,r(2)=0.537)。此外,c.71A>G基因座,尤其是AA基因型,对产仔数有显著影响(P=0.006),与卵巢中高PRNT表达一致。结合表达谱分析和SNPs与繁殖性状之间的关联分析的结果表明,PRNT中的两个强连锁核苷酸序列变异与山羊产仔数显著相关。这些发现为标记辅助选择(MAS)高育性山羊提供了潜在的DNA标记。(c)2021爱思唯尔公司保留所有权利。

著录项

  • 来源
    《Theriogenology》 |2021年第1期|共7页
  • 作者单位

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

    Northwest A&

    F Univ Coll Anim Sci &

    Technol Key Lab Anim Genet Breeding &

    Reprod Shaanxi Prov Yangling 712100 Shaanxi Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 动物学;
  • 关键词

    Goat; PRNT gene; mRNA expression; SNP; Litter size;

    机译:山羊;prnt基因;mRNA表达;SNP;垃圾尺寸;

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