4.6 Article

A conformational switch in the SCF-D3/MAX2 ubiquitin ligase facilitates strigolactone signalling

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NATURE PLANTS
卷 8, 期 5, 页码 561-+

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NATURE PORTFOLIO
DOI: 10.1038/s41477-022-01145-7

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资金

  1. National Science Foundation
  2. NSF-CAREER [2047396]
  3. NSF-EAGER [2028283]
  4. U.S. Department of Energy Office of Science User Facility [DE-AC02-05CH11231]
  5. ALS-ENABLE program - National Institutes of Health, National Institute of General Medical Sciences [P30 GM124169-01]
  6. National Science Foundation, NSF BTT EAGER [1844705]
  7. BARD, the United States-Israel Binational Agricultural Research and Development Fund, Vaadia-BARD Postdoctoral Fellowship [FI-559-2017]
  8. Direct For Biological Sciences [2047396, 2028283, 1844705] Funding Source: National Science Foundation
  9. Division Of Integrative Organismal Systems [1844705] Funding Source: National Science Foundation
  10. Div Of Molecular and Cellular Bioscience [2028283, 2047396] Funding Source: National Science Foundation

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This study reveals the mechanism of perception and signal activation of the plant hormone strigolactones, as well as the key factors regulating strigolactone signaling. Through the study of mutants, the importance of protein conformational switch in the signaling process is demonstrated. Additionally, an organic acid metabolite that can directly trigger the conformational switch is discovered.
Strigolactones (SLs) are a class of plant hormones that regulate numerous processes of growth and development. SL perception and signal activation involves interaction between F-box E3 ubiquitin ligase D3/MAX2 and DWARF14 (D14) alpha/beta-hydrolase in a SL-dependent manner and targeting of D53/SMXL6/7/8 transcriptional repressors (SMXLs) for proteasome-mediated degradation. D3/MAX2 has been shown to exist in multiple conformational states in which the C-terminal helix (CTH) undergoes a closed-to-open dynamics and regulates D14 binding and SL perception. Despite the multiple modes of D3-D14 interactions found in vitro, the residues that regulate the conformational switch of D3/MAX2 CTH in targeting D53/SMXLs and the subsequent effect on SL signalling remain unclear. Here we elucidate the functional dynamics of ASK1-D3/MAX2 in SL signalling by leveraging conformational switch mutants in vitro and in plants. We report the crystal structure of a dislodged CTH of the ASK1-D3 mutant and demonstrate that disruptions in CTH plasticity via either CRISPR-Cas9 genome editing or expression of point mutation mutants result in impairment of SL signalling. We show that the conformational switch in ASK1-D3/MAX2 CTH directly regulates ubiquitin-mediated protein degradation. A dislodged conformation involved in D53/SMXLs SL-dependent recruitment and ubiquitination and an engaged conformation are required for the release of polyubiquitinated D53/SMXLs and subsequently D14 for proteasomal degradation. Finally, we uncovered an organic acid metabolite that can directly trigger the D3/MAX2 CTH conformational switch. Our findings unravel a new regulatory function of a SKP1-CUL1-F-box ubiquitin ligase in plant signalling. This study elucidates the functional dynamics of the ubiquitin ligase SCF D3/MAX2 as a key element in strigolactone signalling. The switch between D3/MAX2 conformational states regulates substrate targeting and can be elicited by a primary metabolite.

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