Schepetilnikov Mikhail, Makarian Joelle, Srour Ola, Geldreich Angèle, Yang Zhenbiao, Chicher Johana, Hammann Philippe, Ryabova Lyubov A
Institut de Biologie Moléculaire des Plantes, Centre National de la Recherche Scientifique, UPR 2357, Université de Strasbourg, Strasbourg, France.
Department of Botany and Plant Sciences, Center for Plant Cell Biology, University of California, Riverside, CA, USA.
EMBO J. 2017 Apr 3;36(7):886-903. doi: 10.15252/embj.201694816. Epub 2017 Feb 28.
Target of rapamycin (TOR) promotes reinitiation at upstream ORFs (uORFs) in genes that play important roles in stem cell regulation and organogenesis in plants. Here, we report that the small GTPase ROP2, if activated by the phytohormone auxin, promotes activation of TOR, and thus translation reinitiation of uORF-containing mRNAs. Plants with high levels of active ROP2, including those expressing constitutively active ROP2 (CA-ROP2), contain high levels of active TOR ROP2 physically interacts with and, when GTP-bound, activates TOR TOR activation in response to auxin is abolished in ROP-deficient plants. GFP-TOR can associate with endosome-like structures in ROP2-overexpressing plants, indicating that endosomes mediate ROP2 effects on TOR activation. CA-ROP2 is efficient in loading uORF-containing mRNAs onto polysomes and stimulates translation in protoplasts, and both processes are sensitive to TOR inhibitor AZD-8055. TOR inactivation abolishes ROP2 regulation of translation reinitiation, but not its effects on cytoskeleton or intracellular trafficking. These findings imply a mode of translation control whereby, as an upstream effector of TOR, ROP2 coordinates TOR function in translation reinitiation pathways in response to auxin.
雷帕霉素靶蛋白(TOR)促进植物中在干细胞调控和器官发生中起重要作用的基因在上游开放阅读框(uORF)处重新起始翻译。在此,我们报道小GTP酶ROP2若被植物激素生长素激活,会促进TOR的激活,从而促进含uORF的mRNA的翻译重新起始。具有高水平活性ROP2的植物,包括那些组成型表达活性ROP2(CA-ROP2)的植物,含有高水平的活性TOR。ROP2与TOR发生物理相互作用,并且在结合GTP时激活TOR。在ROP缺陷型植物中,生长素诱导的TOR激活被消除。GFP-TOR可与过表达ROP2的植物中的类内体结构相关联,表明内体介导了ROP2对TOR激活的作用。CA-ROP2能有效地将含uORF的mRNA加载到多聚核糖体上,并刺激原生质体中的翻译,这两个过程都对TOR抑制剂AZD-8055敏感。TOR失活消除了ROP2对翻译重新起始的调控,但不影响其对细胞骨架或细胞内运输的作用。这些发现暗示了一种翻译控制模式,即作为TOR的上游效应物,ROP2在响应生长素时协调TOR在翻译重新起始途径中的功能。