Cho Young-Hee, Yoo Sang-Dong
Division of Life Sciences, College of Life Sciences and Biotechnology, Korea University , Seoul, South Korea.
Front Plant Sci. 2015 Jan 5;5:733. doi: 10.3389/fpls.2014.00733. eCollection 2014.
The signaling of the plant hormone ethylene has been studied genetically, resulting in the identification of signaling components from membrane receptors to nuclear effectors. Among constituents of the hormone signaling pathway, functional links involving a putative mitogen-activated protein kinase kinase CONSTITUTIVE TRIPLE RESPONSE1 (CTR1) and a membrane transporter-like protein ETHYLENE INSENSITIVE2 (EIN2) have been missing for a long time. We now learn that EIN2 is cleaved and its C-terminal end moves to the nucleus upon ethylene perception at the membrane receptors, and then the C-terminal end of EIN2 in the nucleus supports EIN3-dependent ethylene-response gene expression. CTR1 kinase activity negatively controls the EIN2 cleavage process through direct phosphorylation. Despite the novel connection of CTR1 with EIN2 that explains a large portion of the missing links in ethylene signaling, our understanding still remains far from its completion. This focused review will summarize recent advances in the EIN3-dependent ethylene signaling mechanisms including CTR1-EIN2 functions with respect to EIN3 regulation and ethylene responses. This will also present several emerging issues that need to be addressed for the comprehensive understanding of signaling pathways of the invaluable plant hormone ethylene.
植物激素乙烯的信号传导已通过遗传学方法进行了研究,从而鉴定出了从膜受体到核效应子的信号传导成分。在激素信号传导途径的组成成分中,涉及一种假定的丝裂原活化蛋白激酶激酶组成型三重反应1(CTR1)和一种膜转运蛋白样蛋白乙烯不敏感2(EIN2)的功能联系长期以来一直缺失。我们现在了解到,EIN2在膜受体感知乙烯后会被切割,其C末端会转移到细胞核中,然后细胞核中的EIN2的C末端支持依赖EIN3的乙烯反应基因表达。CTR1激酶活性通过直接磷酸化负向控制EIN2的切割过程。尽管CTR1与EIN2之间的新联系解释了乙烯信号传导中很大一部分缺失环节,但我们的理解仍远未完成。这篇重点综述将总结依赖EIN3的乙烯信号传导机制的最新进展,包括CTR1-EIN2在EIN3调节和乙烯反应方面的功能。这还将提出几个新出现的问题,为全面理解这种重要植物激素乙烯的信号传导途径,这些问题需要得到解决。