Suppr超能文献

通过应用锁定核酸和深度测序获得的 pre-miRNA 谱揭示了复杂的 5'/3'臂变异,包括伴随的切割和聚尿嘧啶化模式。

pre-miRNA profiles obtained through application of locked nucleic acids and deep sequencing reveals complex 5'/3' arm variation including concomitant cleavage and polyuridylation patterns.

机构信息

Omics Science Center, RIKEN Yokohama Institute, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama-shi, Kanagawa 230-0045, Japan.

出版信息

Nucleic Acids Res. 2012 Feb;40(4):1424-37. doi: 10.1093/nar/gkr903. Epub 2011 Nov 3.

Abstract

Recent research hints at an underappreciated complexity in pre-miRNA processing and regulation. Global profiling of pre-miRNA and its potential to increase understanding of the pre-miRNA landscape is impeded by overlap with highly expressed classes of other non coding (nc) RNA. Here, we present a data set excluding these RNA before sequencing through locked nucleic acids (LNA), greatly increasing pre-miRNA sequence counts with no discernable effect on pre-miRNA or mature miRNA sequencing. Analysis of profiles generated in total, nuclear and cytoplasmic cell fractions reveals that pre-miRNAs are subject to a wide range of regulatory processes involving loci-specific 3'- and 5'-end variation entailing complex cleavage patterns with co-occurring polyuridylation. Additionally, examination of nuclear-enriched flanking sequences of pre-miRNA, particularly those derived from polycistronic miRNA transcripts, provides insight into miRNA and miRNA-offset (moRNA) production, specifically identifying novel classes of RNA potentially functioning as moRNA precursors. Our findings point to particularly intricate regulation of the let-7 family in many ways reminiscent of DICER1-independent, pre-mir-451-like processing, introduce novel and unify known forms of pre-miRNA regulation and processing, and shed new light on overlooked products of miRNA processing pathways.

摘要

最近的研究表明 miRNA 前体的加工和调控存在被低估的复杂性。miRNA 前体的全局分析及其增加对 miRNA 前体景观理解的潜力受到与高度表达的其他非编码(nc)RNA 重叠的阻碍。在这里,我们通过锁定核酸(LNA)在测序前排除这些 RNA,极大地增加了 miRNA 前体序列的数量,而对 miRNA 前体或成熟 miRNA 测序没有明显影响。对总细胞、核细胞和胞质细胞分数生成的图谱进行分析表明,miRNA 前体受到涉及基因座特异性 3' 和 5' 端变化的广泛调控过程的影响,涉及具有共同多聚尿苷酸化的复杂切割模式。此外,对 miRNA 前体富含核的侧翼序列(特别是那些源自多顺反子 miRNA 转录物的序列)的检查提供了对 miRNA 和 miRNA 偏移(moRNA)产生的深入了解,特别是确定了可能作为 moRNA 前体的新型 RNA 类别。我们的研究结果表明,let-7 家族受到特别复杂的调控,在许多方面类似于 DICER1 独立的 pre-mir-451 样加工,引入了新的和统一的已知 miRNA 前体调控和加工形式,并为 miRNA 加工途径中被忽视的产物提供了新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3323/3287202/2e984c6ade4a/gkr903f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验