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对 3' 动物 miRNA 修饰事件的全面调查和 3' 腺苷酸化在调节 miRNA 靶向有效性中的可能作用。

A comprehensive survey of 3' animal miRNA modification events and a possible role for 3' adenylation in modulating miRNA targeting effectiveness.

机构信息

Omics Science Center (OSC), RIKEN Yokohama Institute, Tsurumi-ku, Yokohama-shi, Kanagawa 230-0045, Japan.

出版信息

Genome Res. 2010 Oct;20(10):1398-410. doi: 10.1101/gr.106054.110. Epub 2010 Aug 18.

Abstract

Animal microRNA sequences are subject to 3' nucleotide addition. Through detailed analysis of deep-sequenced short RNA data sets, we show adenylation and uridylation of miRNA is globally present and conserved across Drosophila and vertebrates. To better understand 3' adenylation function, we deep-sequenced RNA after knockdown of nucleotidyltransferase enzymes. The PAPD4 nucleotidyltransferase adenylates a wide range of miRNA loci, but adenylation does not appear to affect miRNA stability on a genome-wide scale. Adenine addition appears to reduce effectiveness of miRNA targeting of mRNA transcripts while deep-sequencing of RNA bound to immunoprecipitated Argonaute (AGO) subfamily proteins EIF2C1-EIF2C3 revealed substantial reduction of adenine addition in miRNA associated with EIF2C2 and EIF2C3. Our findings show 3' addition events are widespread and conserved across animals, PAPD4 is a primary miRNA adenylating enzyme, and suggest a role for 3' adenine addition in modulating miRNA effectiveness, possibly through interfering with incorporation into the RNA-induced silencing complex (RISC), a regulatory role that would complement the role of miRNA uridylation in blocking DICER1 uptake.

摘要

动物 microRNA 序列可进行 3' 核苷酸添加。通过对深度测序的短 RNA 数据集的详细分析,我们表明 miRNA 的腺苷酸化和尿苷酸化在果蝇和脊椎动物中普遍存在且保守。为了更好地理解 3' 腺苷酸化功能,我们在核苷酸转移酶酶敲低后对 RNA 进行了深度测序。PAPD4 核苷酸转移酶使广泛的 miRNA 基因座发生腺苷酸化,但腺苷酸化似乎不会影响 miRNA 在全基因组范围内的稳定性。腺嘌呤的添加似乎会降低 miRNA 靶向 mRNA 转录本的有效性,而对与 EIF2C2 和 EIF2C3 相关的 miRNA 进行 RNA 结合的 Argonaute(AGO)亚家族蛋白免疫沉淀的深度测序显示,与 EIF2C2 和 EIF2C3 相关的 miRNA 中腺嘌呤的添加大量减少。我们的研究结果表明,3' 添加事件在动物中广泛存在且保守,PAPD4 是 miRNA 的主要腺苷酸化酶,并表明 3' 腺嘌呤添加在调节 miRNA 有效性方面发挥作用,可能通过干扰其掺入 RNA 诱导的沉默复合物 (RISC) 发挥作用,这种调节作用将补充 miRNA 尿苷酸化在阻止 DICER1 摄取方面的作用。

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