A single miR390 targeting event is sufficient for triggering TAS3-tasiRNA biogenesis in Arabidopsis

被引:46
作者
de Felippes, Felipe Fenselau [1 ]
Marchais, Antonin [1 ]
Sarazin, Alexis [1 ]
Oberlin, Stefan [1 ]
Voinnet, Olivier [1 ]
机构
[1] ETH Z, Swiss Fed Inst Technol Zurich, Chair RNA Biol, Dept Biol, CH-8092 Zurich, Switzerland
基金
欧洲研究理事会;
关键词
TRANS-ACTING SIRNAS; SMALL RNAS; REGULATORY NETWORKS; INTERFERING RNAS; PLANTS; THALIANA; MIRNAS; SECONDARY; COMPLEX; SGS3;
D O I
10.1093/nar/gkx119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In plants, tasiRNAs form a class of endogenous secondary siRNAs produced through the action of RNA-DEPENDENT-RNA-POLYMERASE-6 (RDR6) upon microRNA-mediated cleavage of non-coding TAS RNAs. In Arabidopsis thaliana, TAS1, TAS2 and TAS4 tasiRNA production proceeds via a single cleavage event mediated by 22nt-long or/and asymmetric miRNAs in an ARGONAUTE-1 (AGO1)-dependent manner. By contrast, tasiRNA production from TAS3 seems to follow the so-called 'two-hit' process, where dual targeting of TAS3, specifically mediated by the 21nt-long, symmetric miR390, initiates AGO7-dependent tasiRNA production. Interestingly, features for TAS3 tasiRNA production differ in other plant species and we show here that such features also enable TAS3 tasiRNA biogenesis in Arabidopsis, and that a single miR390 targeting event is, in fact, sufficient for this process, suggesting that the 'one-hit' model underpins all the necessary rudiments of secondary siRNA biogenesis from plant TAS transcripts. Further results suggest that the two-hit configuration likely enhances the fidelity of tasiRNA production and, hence, the accuracy of downstream gene regulation. Finally, we show that a 'non-cleavable one-hit' process allows tasiRNA production from both TAS1 and TAS3 transcripts, indicating that RDR6 recruitment does not require miRNA cleavage, nor does the recruitment, as we further show, of SUPRRESSOR-OF-GENE-SILENCING-3, indispensable for tasiRNA generation.
引用
收藏
页码:5539 / 5554
页数:16
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