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绵羊睾丸成熟过程中长链非编码 RNA 和信使 RNA 表达谱的综合分析

Comprehensive analysis of long noncoding RNA and mRNA expression patterns in sheep testicular maturation.

机构信息

Jiangsu Livestock Embryo Engineering Laboratory, College of Animal Science and Technology, Nanjing Agricultural University, NO. 1 Weigang, Nanjing, 210095, P.R. China.

出版信息

Biol Reprod. 2018 Sep 1;99(3):650-661. doi: 10.1093/biolre/ioy088.

Abstract

Long noncoding RNAs (LncRNAs) have been identified as important regulators of testis development; however, their expression patterns and roles in sheep are not yet clear. Thus, we used stranded specific RNA-seq to profile the testis transcriptome (lncRNAs and mRNAs) in premature and mature sheep. Hormone levels and the testis index were examined, and histological analyses were performed at five stages of testis development, 5-day-old (D5), 3-month-old (3M), 6-month-old (6M), 9-month-old (9M), and 2-year-old (2Y), the results of which indicate a significant difference in hormone levels and testis morphometries between the 3M and 9M stages (P < 0.05). Based on the comparison between 3M and 9M samples, we found 1,118 differentially expressed (DE) lncRNAs and 7,253 DE mRNAs in the testes, and qRT-PCR analysis showed that the results correlated well with the transcriptome data. Furthermore, we constructed lncRNA-protein-coding gene interaction networks. Forty-seven DE lncRNA-targeted genes enriched for male reproduction were obtained by cis- and trans-acting; 51 DE lncRNAs and 45 cis-targets, 2 DE lncRNAs and 2 trans-targets were involved in this network. Of these, 5 lncRNAs and their targets, PRKCD, NANOS3, SERPINA5, and CYP19A1, were enriched for spermatogenesis and male gonad development signaling pathways. We further examined the expression levels of 5 candidate lncRNAs and their target genes during testis development. Lastly, the interaction of lncRNA TCONS__00863147 and its target gene PRKCD was validated in vitro in sheep Leydig cells. This study provides a valuable resource for further study of lncRNA function in sheep testis development and spermatogenesis.

摘要

长链非编码 RNA(lncRNAs)已被鉴定为睾丸发育的重要调节因子;然而,它们在绵羊中的表达模式和作用尚不清楚。因此,我们使用有向特异性 RNA-seq 来描绘早产儿和成熟绵羊睾丸的转录组(lncRNAs 和 mRNAs)。在睾丸发育的五个阶段(5 天龄(D5)、3 月龄(3M)、6 月龄(6M)、9 月龄(9M)和 2 岁龄(2Y))检查了激素水平和睾丸指数,并进行了组织学分析,结果表明 3M 和 9M 阶段之间的激素水平和睾丸形态学有显著差异(P < 0.05)。基于 3M 和 9M 样本之间的比较,我们在睾丸中发现了 1118 个差异表达(DE)lncRNAs 和 7253 个 DE mRNAs,qRT-PCR 分析表明结果与转录组数据吻合良好。此外,我们构建了 lncRNA-蛋白编码基因相互作用网络。通过顺式和反式作用获得了 47 个 DE lncRNA 靶向基因,这些基因富集于雄性生殖;51 个 DE lncRNAs 和 45 个顺式靶基因,2 个 DE lncRNAs 和 2 个反式靶基因参与了该网络。其中,5 个 lncRNA 及其靶基因 PRKCD、NANOS3、SERPINA5 和 CYP19A1 与精子发生和雄性性腺发育信号通路有关。我们进一步检测了 5 个候选 lncRNA 及其靶基因在睾丸发育过程中的表达水平。最后,在绵羊 Leydig 细胞中体外验证了 lncRNA TCONS__00863147 与其靶基因 PRKCD 的相互作用。本研究为进一步研究 lncRNA 在绵羊睾丸发育和精子发生中的功能提供了有价值的资源。

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