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人类天然反义转录本的计算机发现

In silico discovery of human natural antisense transcripts.

作者信息

Li Yuan-Yuan, Qin Lei, Guo Zong-Ming, Liu Lei, Xu Hao, Hao Pei, Su Jiong, Shi Yixiang, He Wei-Zhong, Li Yi-Xue

机构信息

Shanghai Center for Bioinformation Technology, Shanghai 200235, China.

出版信息

BMC Bioinformatics. 2006 Jan 13;7:18. doi: 10.1186/1471-2105-7-18.

Abstract

BACKGROUND

Several high-throughput searches for potential natural antisense transcripts (NATs) have been performed recently, but most of the reports were focused on cis type. A thorough in silico analysis of human transcripts will help expand our knowledge of NATs.

RESULTS

We have identified 568 NATs from human RefSeq RNA sequences. Among them, 403 NATs are reported for the first time, and at least 157 novel NATs are trans type. According to the pairing region of a sense and antisense RNA pair, hNATs are divided into 6 classes, of which about 87% involve 5' or 3' UTR sequences, supporting the regulatory role of UTRs. Among a total of 535 NAT pairs related with splice variants, 77.4% (414/535) have their pairing regions affected or completely eliminated by alternative splicing, suggesting significant relationship of alternative splicing and antisense-directed regulation. The extensive occurrence of splice variants in hNATs and other multiple pairing patterns results in a one-to-many relationship, allowing the formation of complex regulation networks. Based on microarray data from Stanford Microarray Database, two hNAT pairs were found to display significant inverse expression patterns before and after insulin injection.

CONCLUSION

NATs might carry out more extensive and complex functions than previously thought. Combined with endogenous micro RNAs, hNATs could be regarded as a special group of transcripts contributing to the complex regulation networks.

摘要

背景

最近已经进行了几次针对潜在天然反义转录本(NATs)的高通量搜索,但大多数报告都集中在顺式类型上。对人类转录本进行全面的计算机分析将有助于扩展我们对NATs的认识。

结果

我们从人类RefSeq RNA序列中鉴定出568个NATs。其中,403个NATs是首次报道,并且至少157个新的NATs是反式类型。根据正义和反义RNA对的配对区域,人类NATs(hNATs)分为6类,其中约87%涉及5'或3'非翻译区(UTR)序列,这支持了UTR的调控作用。在总共535个与剪接变体相关的NAT对中,77.4%(414/535)的配对区域受到可变剪接的影响或完全消除,这表明可变剪接与反义导向调控之间存在显著关系。hNATs中广泛存在的剪接变体和其他多种配对模式导致了一对多的关系,从而允许形成复杂的调控网络。基于斯坦福微阵列数据库的微阵列数据,发现两个hNAT对在胰岛素注射前后表现出显著的反向表达模式。

结论

NATs可能具有比以前认为的更广泛和复杂的功能。与内源性微小RNA结合,hNATs可被视为有助于复杂调控网络的一类特殊转录本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb46/1369008/2347d68d8118/1471-2105-7-18-1.jpg

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