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通过分析人类 miRNA 靶标的特征来深入了解 miRNA 的调控作用。

Insight into microRNA regulation by analyzing the characteristics of their targets in humans.

机构信息

Center for Computational Research, New York State Center of Excellence in Bioinformatics & Life Sciences, Department of Biostatistics, Department of Medicine, State University of New York (SUNY), Buffalo, NY 14260, USA.

出版信息

BMC Genomics. 2009 Dec 10;10:594. doi: 10.1186/1471-2164-10-594.

Abstract

BACKGROUND

microRNAs (miRNAs) are believed to regulate their targets through posttranscriptional gene regulation and have the potential to silence gene expression via multiple mechanisms. Despite previous advances on miRNA regulation of gene expression, little has been investigated from a genome scale.

RESULTS

To gain new insight into miRNA regulation in humans, we used large scale data and carried out a series of studies to compare various features of miRNA target genes to that of non-miRNA target genes. We observed significant differences between miRNA and non-miRNA target genes for a number of characteristics, including higher and broader mRNA expression, faster mRNA decay rate, longer protein half-life, and longer gene structures. Based on these features and by analyzing their relationships we found that miRNA target genes, other than having miRNA repression, were most likely under more complex regulation than non-miRNA target genes, which was evidenced by their higher and broader gene expression but longer gene structures. Our results of higher and broader gene expression but fast mRNA decay rates also provide evidence that miRNA dampening of the output of preexisting transcripts facilitates a more rapid and robust transition to new expression programs. This could be achieved by enhancing mRNA degradation through an additive effect from multiple miRNA targeting.

CONCLUSION

Genome-scale analysis on the nature of miRNA target genes has revealed a general mechanism for miRNA regulation of human gene expression. The results of this study also indicate that miRNA target genes, other than having miRNA repression, are under more complex gene regulation than non-miRNA target genes. These findings provide novel insight into miRNA regulation of human gene expression.

摘要

背景

microRNAs(miRNAs)被认为通过转录后基因调控来调节其靶标,并具有通过多种机制沉默基因表达的潜力。尽管之前已经在 miRNA 对基因表达的调控方面取得了进展,但从基因组规模上进行的研究却很少。

结果

为了深入了解 miRNA 在人类中的调控作用,我们使用了大规模数据并进行了一系列研究,比较了 miRNA 靶基因和非 miRNA 靶基因的各种特征。我们观察到 miRNA 和非 miRNA 靶基因在许多特征上存在显著差异,包括更高和更广泛的 mRNA 表达、更快的 mRNA 降解率、更长的蛋白质半衰期和更长的基因结构。基于这些特征,并通过分析它们之间的关系,我们发现 miRNA 靶基因除了受到 miRNA 抑制外,可能受到比非 miRNA 靶基因更复杂的调控,这一点可以从它们更高和更广泛的基因表达但更长的基因结构中得到证明。我们的研究结果表明,更高和更广泛的基因表达以及快速的 mRNA 降解率也提供了证据,表明 miRNA 对预先存在的转录本输出的抑制有助于更快、更稳健地向新的表达程序过渡。这可以通过多个 miRNA 靶向的加性效应来增强 mRNA 降解来实现。

结论

对 miRNA 靶基因性质的全基因组分析揭示了 miRNA 调控人类基因表达的一般机制。本研究的结果还表明,除了受到 miRNA 抑制外,miRNA 靶基因受到的基因调控比非 miRNA 靶基因更为复杂。这些发现为 miRNA 对人类基因表达的调控提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d38/2799441/b8fad1539cb5/1471-2164-10-594-1.jpg

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