Arabidopsis Argonaute10 Specifically Sequesters miR166/165 to Regulate Shoot Apical Meristem Development
The shoot apical meristem (SAM) comprises a group of undifferentiated cells that divide to maintain the plant meristem and also give rise to all shoot organs. SAM fate is specified by class III HOMEODOMAIN-LEUCINE ZIPPER ( HD-ZIP III) transcription factors, which are targets of miR166/165. In Arabid...
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Published in: | Cell Vol. 145; no. 2; pp. 242 - 256 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Elsevier Inc
15-04-2011
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Subjects: | |
Online Access: | Get full text |
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Summary: | The shoot apical meristem (SAM) comprises a group of undifferentiated cells that divide to maintain the plant meristem and also give rise to all shoot organs. SAM fate is specified by class III
HOMEODOMAIN-LEUCINE ZIPPER (
HD-ZIP III) transcription factors, which are targets of miR166/165. In
Arabidopsis,
AGO10 is a critical regulator of SAM maintenance, and here we demonstrate that AGO10 specifically interacts with miR166/165. The association is determined by a distinct structure of the miR166/165 duplex. Deficient loading of miR166 into AGO10 results in a defective SAM. Notably, the miRNA-binding ability of AGO10, but not its catalytic activity, is required for SAM development, and AGO10 has a higher binding affinity for miR166 than does AGO1, a principal contributor to miRNA-mediated silencing. We propose that AGO10 functions as a decoy for miR166/165 to maintain the SAM, preventing their incorporation into AGO1 complexes and the subsequent repression of
HD-ZIP III gene expression.
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Arabidopsis AGO10 predominantly associates with miR166/165 ► The duplex structure of miR166/165 determines their specific association with AGO10 ► AGO10 competes with AGO1 for miR166/165 binding ► The decoy activity of AGO10 drives shoot apical meristem development |
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Bibliography: | http://dx.doi.org/10.1016/j.cell.2011.03.024 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0092-8674 1097-4172 |
DOI: | 10.1016/j.cell.2011.03.024 |