Robles Linda M, Wampole Jessica S, Christians Matthew J, Larsen Paul B
Department of Biochemistry, University of California, Riverside, CA 92521, USA.
J Exp Bot. 2007;58(10):2627-39. doi: 10.1093/jxb/erm080. Epub 2007 May 26.
eer4 was isolated as an Arabidopsis mutant with an extreme response to ethylene in dark-grown seedlings that was also found to have partial ethylene insensitivity at the level of ethylene-dependent gene expression, including ERF1. Subsequent cloning of eer4 revealed an inappropriate stop codon in a previously uncharacterized TFIID-interacting transcription factor homologous to human TAF12 and yeast TAF61. Genetic and pharmacological analysis demonstrated that the eer4 phenotype is strictly ethylene dependent in seedlings, yet a double mutant with the partially ethylene-insensitive Arabidopsis mutant, ein3-1, had restored ethylene responsiveness, indicating that eer4 also regulates a previously unknown resetting or dampening mechanism for the ethylene signalling pathway. Consistent with the absolute requirement of EER4 for ERF1 expression, biochemical analysis showed that EER4 is localized to the nucleus where it probably recruits EIN3 and probably other transcription factors along with components of the TFIID complex for expression of a subset of genes required for either manifestation or subsequent dampening of the response to ethylene.
eer4作为拟南芥突变体被分离出来,该突变体在黑暗生长的幼苗中对乙烯有极端反应,并且在乙烯依赖基因表达水平上也表现出部分乙烯不敏感性,包括ERF1。随后对eer4的克隆揭示了一个与人类TAF12和酵母TAF61同源的、以前未被表征的与TFIID相互作用的转录因子中存在不适当的终止密码子。遗传和药理学分析表明,eer4表型在幼苗中严格依赖乙烯,然而,与部分乙烯不敏感的拟南芥突变体ein3-1的双突变体恢复了乙烯反应性,这表明eer4还调节了乙烯信号通路中一个以前未知的重置或抑制机制。与EER4对ERF1表达的绝对需求一致,生化分析表明EER4定位于细胞核,在那里它可能招募EIN3以及可能的其他转录因子,连同TFIID复合体的成分,用于表达对乙烯反应的表现或随后抑制所必需的一组基因。