Seo Dong Hye, Ahn Min Yong, Park Ki Youl, Kim Eun Yu, Kim Woo Taek
Department of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul 120-749, Korea.
Department of Systems Biology, College of Life Science and Biotechnology, Yonsei University, Seoul 120-749, Korea
Plant Cell. 2016 Dec;28(12):2952-2973. doi: 10.1105/tpc.16.00347. Epub 2016 Dec 12.
The Arabidopsis thaliana U-box E3 ligases PUB18/PUB19 and PUB22/PUB23 are negative regulators of drought stress responses. PUB18/PUB19 regulate the drought stress response in an abscisic acid (ABA)-dependent manner, whereas PUB22/PUB23 regulate this response in an ABA-independent manner. A major structural difference between PUB18/PUB19 and PUB22/PUB23 is the presence of the UND (U-box N-terminal domain). Here, we focused on elucidating the molecular mechanism that mediates the functional difference between PUB18 and PUB22 and found that the UND was critically involved in the negative regulation of ABA-mediated stomatal movements. Exo70B1, a subunit of the exocyst complex, was identified as a target of PUB18, whereas Exo70B2 was a substrate of PUB22. However, the ∆UND-PUB18 derivative failed to ubiquitinate Exo70B1, but ubiquitinated Exo70B2. By contrast, the UND-PUB22 chimeric protein ubiquitinated Exo70B1 instead of Exo70B2, suggesting that the ubiquitination specificities of PUB18 and PUB22 to Exo70B1 and Exo70B2, respectively, are dependent on the presence or absence of the UND motif. The ABA-insensitive phenotypes of the pub18 pub19 exo70b1 triple mutant were reminiscent of those of exo70b1 rather than pub18 pub19, indicating that Exo70B1 functions downstream of PUB18. Overall, our results suggest that the UND motif is crucial for the negative regulation of ABA-dependent stomatal movement and for determination of its ubiquitination specificity to Exo70B1.
拟南芥U-box E3连接酶PUB18/PUB19和PUB22/PUB23是干旱胁迫响应的负调控因子。PUB18/PUB19以脱落酸(ABA)依赖的方式调控干旱胁迫响应,而PUB22/PUB23以ABA非依赖的方式调控此响应。PUB18/PUB19和PUB22/PUB23之间的一个主要结构差异是存在UND(U-box N端结构域)。在此,我们专注于阐明介导PUB18和PUB22功能差异的分子机制,发现UND关键参与ABA介导的气孔运动的负调控。Exo70B1是外泌体复合体的一个亚基,被鉴定为PUB18的靶标,而Exo70B2是PUB22的底物。然而,∆UND-PUB18衍生物无法泛素化Exo70B1,但能泛素化Exo70B2。相反,UND-PUB22嵌合蛋白泛素化的是Exo70B1而非Exo70B2,这表明PUB18和PUB22分别对Exo70B1和Exo70B2的泛素化特异性取决于UND基序的有无。pub18 pub19 exo70b1三重突变体的ABA不敏感表型使人联想到exo70b1而非pub18 pub19的表型,表明Exo70B1在PUB18下游发挥作用。总体而言,我们的结果表明UND基序对于ABA依赖的气孔运动的负调控及其对Exo70B1的泛素化特异性的确定至关重要。