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鉴定和分子分析绒山羊长非编码 RNA,揭示其在次级毛囊中的综合调控网络和潜在作用。

Identification and molecular analysis of cashmere goat lncRNAs reveal their integrated regulatory network and potential roles in secondary hair follicle.

机构信息

College of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang, P.R. China.

Academy of Animal Husbandry Science of Liaoning Province, Liaoyang, P.R. China.

出版信息

Anim Biotechnol. 2021 Dec;32(6):719-732. doi: 10.1080/10495398.2020.1747477. Epub 2020 Apr 1.

Abstract

Long non-coding RNAs (lncRNAs) is a class of eukaryotic transcripts with length of more than 200 bp. They contribute to the regulation of gene expressions involved in multiple processes including the skin cell proliferation, differentiation, and reconstruction of the secondary hair follicles (SHFs). In this study, firstly, we identified 16 putative lncRNAs from SHFs of cashmere goat based on the EST sequences from NCBI database. Secondly, we investigated their transcriptional pattern in SHFs of cashmere goat, and constructed their ceRNA regulatory networks. The RT-qPCR results showed four lncRNAs (lncRNA-475074, -052149, -052140, and -051789) were significantly up-regulated, and nine lncRNAs (lncRNA-711032, -475083, -475070, -052139, -052127, -052037, -051903, -051847, and -051804) were significantly down-regulatd in anagen SHFs of cashmere goat. CeRNA networks analysis revealed complex interactional relationship among lncRNAs, miRNAs and mRNAs. Further, the KEGG pathway enrichment was performed for the potential target genes of the identified lncRNAs based on bioinformatics technique, and the results indicated that differentially expressed lncRNAs directly or indirectly might regulate potential target genes. Our results from this study will provide a significant information for further exploring the functions and possible mechanisms of the identified lncRNAs in SHFs of cashmere goat.

摘要

长链非编码 RNA(lncRNA)是一类长度超过 200bp 的真核转录本。它们参与了多个过程的基因表达调控,包括皮肤细胞的增殖、分化和次级毛囊(SHFs)的重建。在这项研究中,首先,我们基于 NCBI 数据库中的 EST 序列,从羊绒山羊的 SHFs 中鉴定了 16 个推定的 lncRNA。其次,我们研究了它们在羊绒山羊 SHFs 中的转录模式,并构建了它们的 ceRNA 调控网络。RT-qPCR 结果显示,有 4 个 lncRNA(lncRNA-475074、-052149、-052140 和-051789)显著上调,有 9 个 lncRNA(lncRNA-711032、-475083、-475070、-052139、-052127、-052037、-051903、-051847 和-051804)在羊绒山羊的生长期 SHFs 中显著下调。ceRNA 网络分析揭示了 lncRNA、miRNA 和 mRNA 之间复杂的相互作用关系。此外,我们还基于生物信息学技术对鉴定出的 lncRNA 的潜在靶基因进行了 KEGG 通路富集分析,结果表明差异表达的 lncRNA 可能直接或间接调节潜在的靶基因。本研究的结果将为进一步探索鉴定出的 lncRNA 在羊绒山羊 SHFs 中的功能和可能机制提供重要信息。

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