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Merck
CN
  • The nonphototrophic hypocotyl 3 (NPH3) domain protein NRL5 is a trafficking-associated GTPase essential for drought resistance.

The nonphototrophic hypocotyl 3 (NPH3) domain protein NRL5 is a trafficking-associated GTPase essential for drought resistance.

Science advances (2024-08-09)
Neha Upadhyay-Tiwari, Xin-Jie Huang, Yi-Chen Lee, Shashi Kant Singh, Chuan-Chi Hsu, Shih-Shan Huang, Paul E Verslues
摘要

The mechanisms of plant drought resistance are unclear but may involve membrane trafficking and metabolic reprogramming, including proline accumulation. Forward genetic screening using a proline dehydrogenase 1 (ProDH1) promoter:reporter identified a drought hypersensitive mutant with a single-amino acid substitution (P335L) in the nonphototrophic hypocotyl 3 (NPH3) domain of NPH3/root phototropism 2-like 5 (NRL5)/naked pins in Yucca 8 (NPY8). Further experiments found that NRL5 and other NPH3 domain proteins are guanosine triphosphatases (GTPases). NRL5, but not NRL5P335L, interacted with the RABE1c and RABH1b GTPases and the soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs) Vesicle-Associated Membrane Protein (VAMP)721/722. These proteins controlled NRL5 localization and connection to trafficking while also being genetically downstream of, and potentially regulated by, NRL5. These data demonstrate that NRL5-mediated restraint of proline catabolism is required for drought resistance and also reveal unexpected functions of the NPH3 domain such that the role of NPH3 domain proteins in signaling, trafficking, and cellular polarity can be critically reevaluated.

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Roche
抗-GFP, from mouse IgG1κ (clones 7.1 and 13.1)
Sigma-Aldrich
聚组氨酸单克隆抗体 小鼠抗, clone HIS-1, ascites fluid
Sigma-Aldrich
Anti-Glutathione-S-Transferase (GST) antibody, Mouse monoclonal, clone GST-2, purified from hybridoma cell culture