人类长链非编码rna的全基因组分析:一个具有争议性的综述。

IF 7.7 2区 生物学 Q1 GENETICS & HEREDITY Annual review of genomics and human genetics Pub Date : 2022-08-31 DOI:10.1146/annurev-genom-112921-123710
Chris P Ponting, Wilfried Haerty
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引用次数: 35

摘要

长链非编码rna (lncRNAs)对人类生物学的贡献是小还是大?为了解决lncRNA位点及其转录本、结构、相互作用和功能如何影响人类特征和疾病,我们采用全基因组视角。我们打算激发对可疑证据的不同解释,并对未经证实的说法进行彻底调查。我们讨论lncRNA实验和计算方法的缺陷,以及对其结果的对立解释。我们认为,大多数证据表明,大多数lncRNA转录模型反映了转录噪声或提供次要的调节作用,留下相对较少的人类lncRNA对人类发育,生理或行为起主要作用。这些重要的少数倾向于拼接和更好地保守,但缺乏与结构和机制相关的简单语法序列,因此无法进行简单的分类。这种全基因组的观点应该有助于研究人员根据lncrna对人类生物学的可能贡献来优先考虑单个lncrna。
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Genome-Wide Analysis of Human Long Noncoding RNAs: A Provocative Review.

Do long noncoding RNAs (lncRNAs) contribute little or substantively to human biology? To address how lncRNA loci and their transcripts, structures, interactions, and functions contribute to human traits and disease, we adopt a genome-wide perspective. We intend to provoke alternative interpretation of questionable evidence and thorough inquiry into unsubstantiated claims. We discuss pitfalls of lncRNA experimental and computational methods as well as opposing interpretations of their results. The majority of evidence, we argue, indicates that most lncRNA transcript models reflect transcriptional noise or provide minor regulatory roles, leaving relatively few human lncRNAs that contribute centrally to human development, physiology, or behavior. These important few tend to be spliced and better conserved but lack a simple syntax relating sequence to structure and mechanism, and so resist simple categorization. This genome-wide view should help investigators prioritize individual lncRNAs based on their likely contribution to human biology.

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来源期刊
CiteScore
14.90
自引率
1.10%
发文量
29
期刊介绍: Since its inception in 2000, the Annual Review of Genomics and Human Genetics has been dedicated to showcasing significant developments in genomics as they pertain to human genetics and the human genome. The journal emphasizes genomic technology, genome structure and function, genetic modification, human variation and population genetics, human evolution, and various aspects of human genetic diseases, including individualized medicine.
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