4.8 Article

SMAX1-LIKE/D53 Family Members Enable Distinct MAX2-Dependent Responses to Strigolactones and Karrikins in Arabidopsis

Journal

PLANT CELL
Volume 27, Issue 11, Pages 3143-3159

Publisher

AMER SOC PLANT BIOLOGISTS
DOI: 10.1105/tpc.15.00562

Keywords

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Funding

  1. University of Georgia Research Foundation
  2. National Science Foundation [IOS-1350561]
  3. NIGMS National Institutes of Health [T32GM007103]
  4. Chinese Government Scholarship PhD Program (Sichuan Agriculture University)
  5. European Research Council [294514 EnCoDe]
  6. Gatsby Foundation [GAT3272C]
  7. Direct For Biological Sciences
  8. Division Of Integrative Organismal Systems [1350561] Funding Source: National Science Foundation

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The plant hormones strigolactones and smoke-derived karrikins are butenolide signals that control distinct aspects of plant development. Perception of both molecules in Arabidopsis thaliana requires the F-box protein MORE AXILLARY GROWTH2 (MAX2). Recent studies suggest that the homologous SUPPRESSOR OF MAX2 1 (SMAX1) in Arabidopsis and DWARF53 (D53) in rice (Oryza sativa) are downstream targets of MAX2. Through an extensive analysis of loss-of-function mutants, we demonstrate that the Arabidopsis SMAX1-LIKE genes SMXL6, SMXL7, and SMXL8 are co-orthologs of rice D53 that promote shoot branching. SMXL7 is degraded rapidly after treatment with the synthetic strigolactone mixture rac-GR24. Like D53, SMXL7 degradation is MAX2- and D14-dependent and can be prevented by deletion of a putative P-loop. Loss of SMXL6,7,8 suppresses several other strigolactone-related phenotypes in max2, including increased auxin transport and PIN1 accumulation, and increased lateral root density. Although only SMAX1 regulates germination and hypocotyl elongation, SMAX1 and SMXL6,7,8 have complementary roles in the control of leaf morphology. Our data indicate that SMAX1 and SMXL6,7,8 repress karrikin and strigolactone signaling, respectively, and suggest that all MAX2-dependent growth effects are mediated by degradation of SMAX1/SMXL proteins. We propose that functional diversification within the SMXL family enabled responses to different butenolide signals through a shared regulatory mechanism.

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