Wang Xiaoyan, Zhang Shuxin, Dou Yongchao, Zhang Chi, Chen Xuemei, Yu Bin, Ren Guodong
State Key Laboratory of Genetic Engineering, Institute of Plant Biology and Department of Biochemistry, School of Life Sciences, Fudan University, Shanghai, China.
Center for Plant Science Innovation & School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska, United States of America.
PLoS Genet. 2015 Apr 30;11(4):e1005091. doi: 10.1371/journal.pgen.1005091. eCollection 2015 Apr.
All types of small RNAs in plants, piwi-interacting RNAs (piRNAs) in animals and a subset of siRNAs in Drosophila and C. elegans are subject to HEN1 mediated 3' terminal 2'-O-methylation. This modification plays a pivotal role in protecting small RNAs from 3' uridylation, trimming and degradation. In Arabidopsis, HESO1 is a major enzyme that uridylates small RNAs to trigger their degradation. However, U-tail is still present in null hen1 heso1 mutants, suggesting the existence of (an) enzymatic activities redundant with HESO1. Here, we report that UTP: RNA uridylyltransferase (URT1) is a functional paralog of HESO1. URT1 interacts with AGO1 and plays a predominant role in miRNA uridylation when HESO1 is absent. Uridylation of miRNA is globally abolished in a hen1 heso1 urt1 triple mutant, accompanied by an extensive increase of 3'-to-5' trimming. In contrast, disruption of URT1 appears not to affect the heterochromatic siRNA uridylation. This indicates the involvement of additional nucleotidyl transferases in the siRNA pathway. Analysis of miRNA tailings in the hen1 heso1 urt1 triple mutant also reveals the existence of previously unknown enzymatic activities that can add non-uridine nucleotides. Importantly, we show HESO1 may also act redundantly with URT1 in miRNA uridylation when HEN1 is fully competent. Taken together, our data not only reveal a synergistic action of HESO1 and URT1 in the 3' uridylation of miRNAs, but also independent activities of multiple terminal nucleotidyl transferases in the 3' tailing of small RNAs and an antagonistic relationship between uridylation and trimming. Our results may provide further insight into the mechanisms of small RNA 3' end modification and stability control.
植物中的所有类型的小RNA、动物中的piwi相互作用RNA(piRNA)以及果蝇和秀丽隐杆线虫中的一部分小干扰RNA(siRNA)都要经历HEN1介导的3'末端2'-O-甲基化。这种修饰在保护小RNA免受3'尿苷酸化、修剪和降解方面起着关键作用。在拟南芥中,HESO1是一种主要的酶,它对小RNA进行尿苷酸化以触发其降解。然而,在HEN1基因敲除的HESO1基因敲除突变体中仍然存在U尾,这表明存在与HESO1功能冗余的酶活性。在这里,我们报告UTP:RNA尿苷酰转移酶(URT1)是HESO1的功能同源物。当不存在HESO1时,URT1与AGO1相互作用并在miRNA尿苷酸化中起主要作用。在HEN1基因敲除的HESO1基因敲除的URT1三重突变体中,miRNA的尿苷酸化被完全消除,同时伴随着3'到5'修剪的广泛增加。相反,URT1的破坏似乎不影响异染色质siRNA的尿苷酸化。这表明在siRNA途径中还有其他核苷酸转移酶参与。对HEN1基因敲除的HESO1基因敲除的URT1三重突变体中miRNA加尾的分析还揭示了存在以前未知的可以添加非尿苷核苷酸的酶活性。重要的是,我们表明当HEN1完全有功能时,HESO1在miRNA尿苷酸化中也可能与URT1起冗余作用。综上所述,我们的数据不仅揭示了HESO1和URT1在miRNA的3'尿苷酸化中的协同作用,还揭示了多种末端核苷酸转移酶在小RNA的3'加尾中的独立活性以及尿苷酸化和修剪之间的拮抗关系。我们的结果可能为小RNA 3'末端修饰和稳定性控制的机制提供进一步的见解。