Department of Bioscience, Tokyo University of Agriculture, Tokyo, 156-8502, Japan.
Graduate School of Science and Engineering, Saitama University, Saitama, 338-8570, Japan.
Biochem Biophys Res Commun. 2022 Dec 31;637:93-99. doi: 10.1016/j.bbrc.2022.11.009. Epub 2022 Nov 8.
Land plants exhibit various adaptation responses to unfavorable water environments, such as drought and flooding. The phytohormone abscisic acid (ABA) and ethylene play essential roles in plant adaptation to drought and flooding, respectively. It remains largely unknown how plants integrate environmental information for water availability. In the moss Physcomitrium patens, we recently reported that not only ethylene/flooding signaling but also ABA/osmostress signaling are mediated by ethylene receptor-related sensor histidine kinases (ETR-HKs). Subfamily I ETR-HKs of this moss were found to interact with a RAF kinase (ARK) and were required for ABA-dependent activation of SNF1-related protein kinase 2 (SnRK2) via ARK activation. To elucidate the mechanisms of ARK regulation by ETR-HKs, here we employed targeted in vivo mutagenesis of PpHK5, a member of subfamily I ETR-HKs. Analyses of ABA-insensitive Pphk5 mutants indicated that PpHK5 mutations affecting the interaction with ARK resulted in loss of PpHK5 function to activate ABA signaling. We also identified a PpHK5 mutation that does not affect ARK interaction but resulted in loss of PpHK5 function. These results suggest that physical interaction between ETR-HK and ARK is essential but not sufficient for the regulation of ARK activity, and the C-terminal response regulator domain is involved in regulating ARK activation.
陆生植物表现出各种适应不利水环境的反应,如干旱和洪水。植物激素脱落酸(ABA)和乙烯分别在植物适应干旱和洪水方面发挥着重要作用。植物如何整合环境信息以感知水分可用性在很大程度上仍不清楚。在藓类植物Physcomitrium patens 中,我们最近报道,不仅乙烯/洪水信号转导,而且 ABA/渗透胁迫信号转导,都由乙烯受体相关传感器组氨酸激酶(ETR-HK)介导。该藓类植物的 I 亚家族 ETR-HK 被发现与 RAF 激酶(ARK)相互作用,并通过 ARK 激活,参与 ABA 依赖的 SNF1 相关蛋白激酶 2(SnRK2)的激活。为了阐明 ETR-HK 对 ARK 的调节机制,我们在此使用了靶向 PpHK5(I 亚家族 ETR-HK 的成员)的体内诱变。对 ABA 不敏感的 Pphk5 突变体的分析表明,影响与 ARK 相互作用的 PpHK5 突变导致 PpHK5 功能丧失,从而无法激活 ABA 信号。我们还鉴定了一个不影响 ARK 相互作用但导致 PpHK5 功能丧失的 PpHK5 突变。这些结果表明,ETR-HK 和 ARK 之间的物理相互作用对于 ARK 活性的调节是必需的,但不是充分的,并且 C 端响应调节子结构域参与调节 ARK 的激活。