Specificity of ARGONAUTE7-miR390 interaction and dual functionality in TAS3 trans-acting siRNA formation

被引:604
作者
Montgomery, Taiowa A. [1 ,2 ]
Howell, Miya D. [1 ,3 ]
Cuperus, Josh T. [1 ,2 ]
Li, Dawei [4 ]
Hansen, Jesse E. [1 ]
Alexander, Amanda L. [1 ]
Chapman, Elisabeth J. [1 ,2 ]
Fahlgren, Noah [1 ,2 ]
Allen, Edwards [1 ,3 ]
Carrington, James C. [1 ,3 ]
机构
[1] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
[2] Oregon State Univ, Mol & Cellular Biol Program, Corvallis, OR 97331 USA
[3] Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USA
[4] China Agr Univ, State Key Lab Agro Biotechnol, Beijing 100094, Peoples R China
关键词
D O I
10.1016/j.cell.2008.02.033
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
Trans-acting siRNA form through a refined RNAi mechanism in plants. miRNA-guided cleavage triggers entry of precursor transcripts into an RNA-DEPENDENT RNA POLYMERASE6 pathway, and sets the register for phased tasiRNA formation by DICER-LIKE4. Here, we show that miR390-ARGONAUTE7 complexes function in distinct cleavage or noncleavage modes at two target sites in TAS3a transcripts. The AGO7 cleavage, but not the noncleavage, function could be provided by AGO1, the dominant miRNA-associated AGO, but only when AGO1 was guided to a modified target site through an alternate miRNA. AGO7 was highly selective for interaction with miR390, and miR390 in turn was excluded from association with AGO1 due entirely to an incompatible 50 adenosine. Analysis of AGO1, AGO2, and AGO7 revealed a potent 50 nucleotide discrimination function for some, although not all, ARGONAUTEs. miR390 and AGO7, therefore, evolved as a highly specific miRNA guide/effector protein pair to function at two distinct tasiRNA biogenesis steps.
引用
收藏
页码:128 / 141
页数:14
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