Lincoln J E, Campbell A D, Oetiker J, Rottmann W H, Oeller P W, Shen N F, Theologis A
Plant Gene Expression Center, Albany, California 94710.
J Biol Chem. 1993 Sep 15;268(26):19422-30.
ACC (1-aminocyclopropane-1-carboxylic acid) synthase is the key regulatory enzyme in the biosynthetic pathway of the plant hormone ethylene and is encoded by a highly divergent multigene family in tomato (Rottmann, W. H., Peter, G. F., Oeller, P. W., Keller, J. A., Shen, N. F., Nagy, B. P., Taylor, L. P., Campbell, A. D., and Theologis, A. (1991) J. Mol. Biol. 222, 937-961). Two members of the family, LE-ACS2 and LE-ACS4, are induced during fruit ripening and upon treatment of mature green fruits with exogenous ethylene (C2H4) in a dose-dependent manner. Both genes are superinduced by wounding of pericarp tissue during various stages of ripening. The wound-induced accumulation of LE-ACS2 mRNA is more rapid and greater than that of LE-ACS4. Both mRNAs accumulate in the absence of protein synthesis, suggesting that their induction is a primary response to the inducer. The LE-ACS4 gene was isolated and structurally characterized. The function of the LE-ACS4 protein (53,509 Da, pI 5.4) was verified by expression experiments in Escherichia coli. The promoters of LE-ACS2 and LE-ACS4 contain potential cis-acting regulatory elements responsible for induction by ethylene, wounding, and anaerobiosis. In addition, elements for binding the transcriptional factors EmBP1, GBF-1, and OCSBF-1 are also present. Phylogenetic analysis of 20 ACC synthases from dicots and monocots indicate that the LE-ACS2 and LE-ACS4 proteins belong to an unique sublineage that includes an additional member of the tobacco family, NT-ACS1. The divergence of this sublineage is a relatively recent event in the evolution of ACC synthase protein.
1-氨基环丙烷-1-羧酸(ACC)合酶是植物激素乙烯生物合成途径中的关键调节酶,由番茄中一个高度分化的多基因家族编码(罗特曼,W.H.,彼得,G.F.,奥勒,P.W.,凯勒,J.A.,沈,N.F.,纳吉,B.P.,泰勒,L.P.,坎贝尔,A.D.,和西奥洛吉斯,A.(1991年)《分子生物学杂志》222卷,937 - 961页)。该家族的两个成员,LE - ACS2和LE - ACS4,在果实成熟期间以及用外源乙烯(C2H4)处理成熟绿色果实后以剂量依赖方式被诱导。在成熟的各个阶段,果皮组织受伤都会使这两个基因超诱导表达。伤口诱导的LE - ACS2 mRNA积累比LE - ACS4更快且更多。两种mRNA在没有蛋白质合成的情况下积累,这表明它们的诱导是对诱导剂的初级反应。LE - ACS4基因被分离并进行了结构表征。LE - ACS4蛋白(53,509道尔顿,pI 5.4)的功能通过在大肠杆菌中的表达实验得到验证。LE - ACS2和LE - ACS4的启动子含有负责乙烯、伤口和厌氧诱导的潜在顺式作用调节元件。此外,还存在与转录因子EmBP1、GBF - 1和OCSBF - 1结合的元件。对双子叶植物和单子叶植物的20种ACC合酶的系统发育分析表明,LE - ACS2和LE - ACS4蛋白属于一个独特的亚谱系,该亚谱系还包括烟草家族的另一个成员NT - ACS1。在ACC合酶蛋白的进化过程中,这个亚谱系的分化是一个相对较新的事件。