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一个进化上保守的、可变剪接的 p68/DDX5 DEAD-box RNA 解旋酶基因内含子编码一个新的 miRNA。

An evolutionarily conserved, alternatively spliced, intron in the p68/DDX5 DEAD-box RNA helicase gene encodes a novel miRNA.

出版信息

RNA. 2011 Apr;17(4):555-62. doi: 10.1261/rna.2591611. Epub 2011 Feb 23.

Abstract

The DEAD-box RNA helicase p68 (DDX5) plays important roles in several cellular processes, including transcription, pre-mRNA processing, and microRNA (miRNA) processing. p68 expression is growth and developmentally regulated, and alterations in p68 expression and/or function have been implicated in tumor development. The p68 gene encodes an evolutionarily conserved, alternatively spliced, intron the function of which has to date remained unclear. Although the intron-containing p68 RNA does not appear to yield an alternative p68 protein, it is differentially expressed in cell lines and tissues, indicating regulation of expression. Here we show that the p68 conserved intron encodes a novel putative miRNA, suggesting a previously unknown possible regulatory function for the p68 intron. We show that this miRNA (referred to as p68 miRNA) is processed from the intron via the canonical miRNA-processing pathway and that it associates with the Argonaute protein Ago2. Finally we show that the p68 miRNA suppresses an mRNA bearing complementary target sequences, suggesting that it is functional. These findings suggest a novel mechanism by which alterations in p68 expression may impact on the cell.

摘要

DEAD -box RNA 解旋酶 p68(DDX5)在多个细胞过程中发挥重要作用,包括转录、前体 mRNA 加工和 microRNA(miRNA)加工。p68 的表达受到生长和发育的调控,p68 表达和/或功能的改变与肿瘤的发生有关。p68 基因编码一个进化上保守的、可变剪接的内含子,其功能迄今仍不清楚。尽管含有内含子的 p68 RNA 似乎不会产生替代的 p68 蛋白,但它在细胞系和组织中的表达存在差异,表明其受到调控。在这里,我们表明 p68 保守内含子编码一种新的潜在 miRNA,这表明 p68 内含子具有以前未知的可能的调节功能。我们表明,这种 miRNA(称为 p68 miRNA)通过经典的 miRNA 加工途径从内含子中加工而来,并与 Argonaute 蛋白 Ago2 结合。最后,我们表明 p68 miRNA 抑制具有互补靶序列的 mRNA,表明其具有功能。这些发现表明,p68 表达的改变可能通过一种新的机制影响细胞。

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本文引用的文献

1
Critical association of ncRNA with introns.
Nucleic Acids Res. 2011 Mar;39(6):2357-66. doi: 10.1093/nar/gkq1080. Epub 2010 Nov 10.
2
HSP90 protein stabilizes unloaded argonaute complexes and microscopic P-bodies in human cells.
Mol Biol Cell. 2010 May 1;21(9):1462-9. doi: 10.1091/mbc.e09-10-0885. Epub 2010 Mar 17.
3
Causes and consequences of microRNA dysregulation in cancer.
Nat Rev Genet. 2009 Oct;10(10):704-14. doi: 10.1038/nrg2634.
5
Limitations and possibilities of small RNA digital gene expression profiling.
Nat Methods. 2009 Jul;6(7):474-6. doi: 10.1038/nmeth0709-474.
6
Biogenesis of small RNAs in animals.
Nat Rev Mol Cell Biol. 2009 Feb;10(2):126-39. doi: 10.1038/nrm2632.
8
A multifunctional human Argonaute2-specific monoclonal antibody.
RNA. 2008 Jun;14(6):1244-53. doi: 10.1261/rna.973808. Epub 2008 Apr 22.
9
The Argonaute protein family.
Genome Biol. 2008;9(2):210. doi: 10.1186/gb-2008-9-2-210. Epub 2008 Feb 26.
10
Argonaute proteins: key players in RNA silencing.
Nat Rev Mol Cell Biol. 2008 Jan;9(1):22-32. doi: 10.1038/nrm2321.

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