An Ning, Huang Xiaowei, Yang Zhao, Zhang Minhua, Ma Miaolian, Yu Fang, Jing Lianyan, Du Boya, Wang Yong-Fei, Zhang Xue, Zhang Peng
National Key Laboratory of Plant Molecular Genetics, Centre for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, China.
Key Laboratory of Plant Carbon Capture, Chinese Academy of Sciences, Shanghai, China.
Nat Plants. 2024 Dec;10(12):2052-2061. doi: 10.1038/s41477-024-01839-0. Epub 2024 Nov 4.
Jasmonates (JAs) are a class of oxylipin phytohormones including jasmonic acid (JA) and derivatives that regulate plant growth, development and biotic and abiotic stress. A number of transporters have been identified to be responsible for the cellular and subcellular translocation of JAs. However, the mechanistic understanding of how these transporters specifically recognize and transport JAs is scarce. Here we determined the cryogenic electron microscopy structure of JA exporter AtABCG16 in inward-facing apo, JA-bound and occluded conformations, and outward-facing post translocation conformation. AtABCG16 structure forms a homodimer, and each monomer contains a nucleotide-binding domain, a transmembrane domain and an extracellular domain. Structural analyses together with biochemical and plant physiological experiments revealed the molecular mechanism by which AtABCG16 specifically recognizes and transports JA. Structural analyses also revealed that AtABCG16 features a unique bifurcated substrate translocation pathway, which is composed of two independent substrate entrances, two substrate-binding pockets and a shared apoplastic cavity. In addition, residue Phe608 from each monomer is disclosed to function as a gate along the translocation pathway controlling the accessing of substrate JA from the cytoplasm or apoplast. Based on the structural and biochemical analyses, a working model of AtABCG16-mediated JA transport is proposed, which diversifies the molecular mechanisms of ABC transporters.
茉莉酸类物质(JAs)是一类氧化脂质植物激素,包括茉莉酸(JA)及其衍生物,它们调控植物的生长、发育以及生物和非生物胁迫。已鉴定出多种转运蛋白负责JAs的细胞和亚细胞转运。然而,对于这些转运蛋白如何特异性识别和转运JAs的机制了解甚少。在这里,我们确定了JA输出蛋白AtABCG16在向内的空载、JA结合和封闭构象以及向外的转运后构象下的低温电子显微镜结构。AtABCG16结构形成一个同二聚体,每个单体包含一个核苷酸结合结构域、一个跨膜结构域和一个细胞外结构域。结构分析以及生化和植物生理学实验揭示了AtABCG16特异性识别和转运JA的分子机制。结构分析还表明,AtABCG16具有独特的分叉底物转运途径,该途径由两个独立的底物入口、两个底物结合口袋和一个共享的质外体腔组成。此外,每个单体的苯丙氨酸残基Phe608被揭示在转运途径中起门控作用,控制底物JA从细胞质或质外体进入。基于结构和生化分析,提出了AtABCG16介导的JA转运的工作模型,这使ABC转运蛋白的分子机制更加多样化。