4.7 Article

Structural Flexibility Enables Alternative Maturation, ARGONAUTE Sorting and Activities of miR168, a Global Gene Silencing Regulator in Plants

期刊

MOLECULAR PLANT
卷 11, 期 8, 页码 1008-1023

出版社

CELL PRESS
DOI: 10.1016/j.molp.2018.05.006

关键词

microRNA; miR168; Dicer; ARGONAUTE; tombusvirus; P19

资金

  1. Swiss National Science Foundation (SNF) [51NF40_141735]
  2. IIF Marie Curie fellowship [329029]
  3. European Research Council (ERC) advanced grant Frontiers of RNAi-II'' [323071]
  4. Swiss National Science Foundation (SNF) [51NF40_141735] Funding Source: Swiss National Science Foundation (SNF)
  5. European Research Council (ERC) [323071] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

In eukaryotes, the RNase-III Dicer often produces length/sequence microRNA (miRNA) variants, called isomiRs, owing to intrinsic structural/sequence determinants of the miRNA precursors (pre-miRNAs). In this study, we combined biophysics, genetics and biochemistry approaches to study Arabidopsis miR168, the key feedback regulator of central plant silencing effector protein ARGONAUTE1 (AGO1). We identified a motif conserved among plant pre-miR168 orthologs, which enables flexible internal base-pairing underlying at least three metastable structural configurations. These configurations promote alternative, accurate Dicer cleavage events generating length and structural isomiR168 variants with distinctive AGO sorting properties and modes of action. Among these isomiR168s, a duplex with a 22-nt guide strand exhibits strikingly preferential affinity for AGO10, the closest AGO1 paralog. The 22-nt miR168-AGO10 complex antagonizes AGO1 accumulation in part via transitive RNAi, a silencing-amplification process, to maintain appropriate AGO1 cellular homeostasis. Furthermore, we found that the tombusviral P19 silencing-suppressor protein displays markedly weaker affinity for the 22-nt form among its isomiR168 cargoes, thereby promoting AGO10-directed suppression of AGO1-mediated antiviral silencing. Taken together, these findings indicate that structural flexibility, a previously overlooked property of pre-miRNAs, considerably increases the versatility and regulatory potential of individual MIRNA genes, and that some pathogens might have evolved the capacity or mechanisms to usurp this property.

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