首页> 美国卫生研究院文献>Nucleic Acids Research >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
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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

机译:通过应用锁定核酸和深度测序获得的pre-miRNA图谱显示复杂的5/ 3臂变异包括伴随的裂解和多尿化模式

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摘要

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.
机译:最近的研究表明,pre-miRNA加工和调控的复杂性未得到充分认识。与其他非编码(nc)RNA的高表达类别重叠,阻碍了pre-miRNA的全球概况分析及其增强对pre-miRNA状况的了解的潜力。在这里,我们介绍了通过锁定核酸(LNA)测序之前不包含这些RNA的数据集,大大增加了pre-miRNA序列计数,而对pre-miRNA或成熟的miRNA测序没有明显的影响。分析在总细胞,核细胞和细胞质细胞级分中产生的图谱表明,pre-miRNA受到多种调节过程的影响,涉及基因座特异性3'-和5'-端变异,需要复杂的裂解模式并同时发生多尿苷化。另外,检查pre-miRNA的富核侧翼序列,尤其是衍生自多顺反子miRNA转录的那些序列,可深入了解miRNA和miRNA偏移(moRNA)的产生,特别是鉴定可能充当moRNA前体的新型RNA。我们的发现指出,let-7家族在许多方面特别复杂的调控,让人想起DICER1独立的,mir-451样前加工,引入新颖和统一的已知形式的mimi调控和加工,并为被忽视的miRNA加工途径产物。

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