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未成熟和成熟牛睾丸中长链非编码RNA和mRNA表达谱分析

Analysis of Long Non-Coding RNA and mRNA Expression Profiling in Immature and Mature Bovine () Testes.

作者信息

Gao Yuan, Li Shipeng, Lai Zhenyu, Zhou Zihui, Wu Fei, Huang Yongzhen, Lan Xianyong, Lei Chuzhao, Chen Hong, Dang Ruihua

机构信息

Key Laboratory of Animal Genetics, Breeding and Reproduction of Shaanxi Province, College of Animal Science and Technology, Northwest A&F University, Yangling, China.

出版信息

Front Genet. 2019 Jul 5;10:646. doi: 10.3389/fgene.2019.00646. eCollection 2019.

Abstract

Testis development and spermatogenesis are strictly regulated by numbers of genes and non-coding genes. However, long non-coding RNAs (lncRNAs) as key regulators in multitudinous biological processes have not been systematically identified in bovine testes during sexual maturation. In this study, we comprehensively analyzed lncRNA and mRNA expression profiling of six bovine testes at 3 days after birth and 13 months by RNA sequencing. 23,735 lncRNAs and 22,118 mRNAs were identified, in which 540 lncRNAs (-value < 0.05) and 3,525 mRNAs (-adjust < 0.05) were significantly differentially expressed (DE) between two stages. Correspondingly, the results of RT-qPCR analysis showed well correlation with the transcriptome data. Moreover, GO and KEGG enrichment analyses showed that DE genes and target genes of DE lncRNAs were enriched in spermatogenesis. Furthermore, we constructed lncRNA-gene interaction networks; consequently, 15 DE lncRNAs and 12 -target genes were involved. The target genes (, , , , , , , and ) were found associated with bovine sexual maturation. In addition, the expression of lncRNAs and -target genes was detected in bovine Leydig cells, Sertoli cells, and spermatogonia. Our study identified and analyzed lncRNAs and mRNAs in testis tissues, suggesting that lncRNAs may regulate testis development and spermatogenesis. Our findings provided new insights for further investigation of biological function in bovine lncRNA.

摘要

睾丸发育和精子发生受到众多基因和非编码基因的严格调控。然而,作为众多生物学过程关键调节因子的长链非编码RNA(lncRNA)在牛性成熟过程中的睾丸中尚未得到系统鉴定。在本研究中,我们通过RNA测序全面分析了出生后3天和13个月的6个牛睾丸的lncRNA和mRNA表达谱。共鉴定出23,735个lncRNA和22,118个mRNA,其中在两个阶段之间有540个lncRNA(P值<0.05)和3,525个mRNA(P调整后<0.05)显著差异表达(DE)。相应地,RT-qPCR分析结果与转录组数据显示出良好的相关性。此外,GO和KEGG富集分析表明,DE基因和DE lncRNA的靶基因在精子发生过程中富集。此外,我们构建了lncRNA-基因相互作用网络;结果,涉及15个DE lncRNA和12个靶基因。发现靶基因(、、、、、、和)与牛的性成熟有关。此外,在牛睾丸间质细胞、支持细胞和精原细胞中检测到lncRNA和靶基因的表达。我们的研究鉴定并分析了睾丸组织中的lncRNA和mRNA,表明lncRNA可能调节睾丸发育和精子发生。我们的发现为进一步研究牛lncRNA的生物学功能提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf4/6624472/18efc6837027/fgene-10-00646-g001.jpg

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