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MAC3A 和 MAC3B,MOS4 相关复合物的两个核心亚基,正向影响 miRNA 的生物发生。

MAC3A and MAC3B, Two Core Subunits of the MOS4-Associated Complex, Positively Influence miRNA Biogenesis.

机构信息

Qingdao Engineering Research Center of Biomass Resources and Environment, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China.

Center for Plant Science Innovation University of Nebraska-Lincoln, Lincoln, Nebraska 68588-0666.

出版信息

Plant Cell. 2018 Feb;30(2):481-494. doi: 10.1105/tpc.17.00953. Epub 2018 Feb 5.

Abstract

MAC3A and MAC3B are conserved U-box-containing proteins in eukaryotes. They are subunits of the MOS4-associated complex (MAC) that plays essential roles in plant immunity and development in However, their functional mechanisms remain elusive. Here, we show that Arabidopsis MAC3A and MAC3B act redundantly in microRNA (miRNA) biogenesis. Lack of both MAC3A and MAC3B in the double mutant reduces the accumulation of miRNAs, causing elevated transcript levels of miRNA targets. also decreases the levels of primary miRNA transcripts (pri-miRNAs). However, MAC3A and MAC3B do not affect the promoter activity of genes encoding miRNAs ( genes), suggesting that they may not affect transcription. This result, together with the fact that MAC3A associates with pri-miRNAs in vivo, indicates that MAC3A and MAC3B may stabilize pri-miRNAs. Furthermore, we find that MAC3A and MAC3B interact with the DCL1 complex that catalyzes miRNA maturation, promote DCL1 activity, and are required for the localization of HYL1, a component of the DCL1 complex. Besides MAC3A and MAC3B, two other MAC subunits, CDC5 and PRL1, also function in miRNA biogenesis. Based on these results, we propose that MAC functions as a complex to control miRNA levels through modulating pri-miRNA transcription, processing, and stability.

摘要

MAC3A 和 MAC3B 是真核生物中保守的 U -box 蛋白。它们是 MOS4 相关复合物(MAC)的亚基,在植物免疫和发育中发挥重要作用。然而,它们的功能机制尚不清楚。在这里,我们表明拟南芥 MAC3A 和 MAC3B 在 microRNA (miRNA) 生物发生中起冗余作用。在 双突变体中缺乏两者都会减少 miRNA 的积累,导致 miRNA 靶标转录本水平升高。也降低了初级 miRNA 转录物 (pri-miRNAs) 的水平。然而,MAC3A 和 MAC3B 不影响编码 miRNA 的基因( 基因)的启动子活性,表明它们可能不影响 转录。这一结果,加上 MAC3A 与体内 pri-miRNAs 相关的事实,表明 MAC3A 和 MAC3B 可能稳定 pri-miRNAs。此外,我们发现 MAC3A 和 MAC3B 与催化 miRNA 成熟的 DCL1 复合物相互作用,促进 DCL1 活性,并需要 HYL1 的定位,HYL1 是 DCL1 复合物的一个组成部分。除了 MAC3A 和 MAC3B 之外,另外两个 MAC 亚基 CDC5 和 PRL1 也参与了 miRNA 的生物发生。基于这些结果,我们提出 MAC 作为一个复合物通过调节 pri-miRNA 转录、加工和稳定性来控制 miRNA 水平。

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