Christians Matthew J, Larsen Paul B
Department of Biochemistry, University of California, Riverside, CA 92521, USA.
J Exp Bot. 2007;58(8):2237-48. doi: 10.1093/jxb/erm086. Epub 2007 May 24.
The eer3-1 loss-of-function mutant, which was identified by screening for Arabidopsis mutant seedlings with an enhanced ethylene response, has both increased sensitivity and profound exaggeration of response to ethylene when visually assessed, yet exhibits partial ethylene insensitivity at the molecular level. The eer3-1 mutation represents a conditional allele with an ethylene-dependent phenotype that results from an amino acid substitution in the previously uncharacterized prohibitin, AtPHB3, with complete loss of EER3 function resulting in an extreme constitutive ethylene response in air. Prohibitins in other organisms have diverse roles including transcriptional regulation, with loss of prohibitin function in this capacity associated with tumour formation in mammals. Subcellular localization of AtPHB3 indicates that it is found in several cellular locations, including the nucleus and throughout the cytoplasm. Genetic analysis demonstrates that EER3 functions downstream of EIN2, since an ein2-5;eer3-2 double mutant has the same profound hypocotyl inhibition phenotype seen with the eer3-2 mutant. Based on the presented work, AtPHB3 probably functions as a positive regulator of expression of a subset of ethylene-regulated genes along with a group of genes required to maintain growth in the presence of ethylene.
eer3-1功能缺失突变体是通过筛选具有增强乙烯反应的拟南芥突变幼苗而鉴定出来的。在视觉评估时,它对乙烯的敏感性增加且反应极度夸张,但在分子水平上表现出部分乙烯不敏感性。eer3-1突变代表一个具有乙烯依赖性表型的条件等位基因,该表型是由先前未表征的禁止素AtPHB3中的氨基酸取代导致的,EER3功能完全丧失会导致在空气中出现极端组成型乙烯反应。其他生物体中的禁止素具有多种作用,包括转录调控,这种功能丧失在哺乳动物中与肿瘤形成有关。AtPHB3的亚细胞定位表明它存在于几个细胞位置,包括细胞核和整个细胞质中。遗传分析表明EER3在EIN2下游起作用,因为ein2-5;eer3-2双突变体具有与eer3-2突变体相同的严重下胚轴抑制表型。基于所展示的工作,AtPHB3可能与一组在乙烯存在下维持生长所需的基因一起,作为乙烯调节基因子集表达的正调节因子发挥作用。