Brassinosteroids inhibit miRNA-mediated translational repression by decreasing AGO1 on the endoplasmic reticulum
- PMID: 34020507
- DOI: 10.1111/jipb.13139
Brassinosteroids inhibit miRNA-mediated translational repression by decreasing AGO1 on the endoplasmic reticulum
Abstract
Translational repression is a conserved mechanism in microRNA (miRNA)-guided gene silencing. In Arabidopsis, ARGONAUTE1 (AGO1), the major miRNA effector, localizes in the cytoplasm for mRNA cleavage and at the endoplasmic reticulum (ER) for translational repression of target genes. However, the mechanism underlying miRNA-mediated translational repression is poorly understood. In particular, how the subcellular partitioning of AGO1 is regulated is largely unexplored. Here, we show that the plant hormone brassinosteroids (BRs) inhibit miRNA-mediated translational repression by negatively regulating the distribution of AGO1 at the ER in Arabidopsis thaliana. We show that the protein levels rather than the transcript levels of miRNA target genes were reduced in BR-deficient mutants but increased under BR treatments. The localization of AGO1 at the ER was significantly decreased under BR treatments while it was increased in the BR-deficient mutants. Moreover, ROTUNDIFOLIA3 (ROT3), an enzyme involved in BR biosynthesis, co-localizes with AGO1 at the ER and interacts with AGO1 in a GW motif-dependent manner. Complementation analysis showed that the AGO1-ROT3 interaction is necessary for the function of ROT3. Our findings provide new clues to understand how miRNA-mediated gene silencing is regulated by plant endogenous hormones.
Keywords: AGO1; Arabidopsis thaliana; brassinosteroids; endoplasmic reticulum; miRNA; translational repression.
© 2021 The Authors. Journal of Integrative Plant Biology published by John Wiley & Sons Australia, Ltd on behalf of Institute of Botany, Chinese Academy of Sciences.
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References
REFERENCES
-
- Asami, T., and Yoshida, S. (1999). Brassinosteroid biosynthesis inhibitors. Trends Plant Sci. 4: 348-353.
-
- Aukerman, M.J., and Sakai, H. (2003). Regulation of flowering time and floral organ identity by a microRNA and its APETALA2-like target genes. Plant Cell 15: 2730-2741.
-
- Axtell, M.J. (2017). Lost in translation? microRNAs at the rough ER. Trends Plant Sci. 22: 273-274.
-
- Bajczyk, M., Bhat, S.S., Szewc, L., Szweykowska-Kulinska, Z., Jarmolowski, A., and Dolata, J. (2019). Novel nuclear functions of Arabidopsis ARGONAUTE1: Beyond RNA interference. Plant Physiol. 179: 1030-1039.
-
- Barman, B., and Bhattacharyya, S.N. (2015). mRNA targeting to endoplasmic reticulum precedes Ago protein interaction and microRNA (miRNA)-mediated translation repression in mammalian cells. J. Biol. Chem. 290: 24650-24656.
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