Yamaguchi S, Sun T p, Kawaide H, Kamiya Y
Frontier Research Program, The Institute of Physical and Chemical Reasearch (RIKEN), hirosawa, Japan.
Plant Physiol. 1998 Apr;116(4):1271-8. doi: 10.1104/pp.116.4.1271.
The ga2 mutant of Arabidopsis thaliana is a gibberellin-deficient dwarf. Previous biochemical studies have suggested that the ga2 mutant is impaired in the conversion of copalyl diphosphate to ent-kaurene, which is catalyzed by ent-kaurene synthase (KS). Overexpression of the previously isolated KS cDNA from pumpkin (Cucurbita maxima) (CmKS) in the ga2 mutant was able to complement the mutant phenotype. A genomic clone coding for KS, AtKS, was isolated from A. thaliana using CmKS cDNA as a heterologous probe. The corresponding A. thaliana cDNA was isolated and expressed in Escherichia coli as a fusion protein. The fusion protein showed enzymatic activity that converted [3H]copalyl diphosphate to [3H]ent-kaurene. The recombinant AtKS protein derived from the ga2-1 mutant is truncated by 14 kD at the C-terminal end and does not contain significant KS activity in vitro. Sequence analysis revealed that a C-2099 to T base substitution, which converts Gln-678 codon to a stop codon, is present in the AtKS cDNA from the ga2-1 mutant. Taken together, our results show that the GA2 locus encodes KS.
拟南芥的ga2突变体是一种赤霉素缺陷型矮化植株。先前的生化研究表明,ga2突变体在由内根-贝壳杉烯合酶(KS)催化的内根-贝壳杉烯二磷酸转化为内根-贝壳杉烯的过程中存在缺陷。在ga2突变体中过表达先前从南瓜(南瓜属)分离的KS cDNA(CmKS)能够互补突变体表型。以CmKS cDNA作为异源探针,从拟南芥中分离出编码KS的基因组克隆AtKS。分离出相应的拟南芥cDNA并在大肠杆菌中作为融合蛋白表达。该融合蛋白表现出将[3H]内根-贝壳杉烯二磷酸转化为[3H]内根-贝壳杉烯的酶活性。来自ga2-1突变体的重组AtKS蛋白在C末端被截短了14 kD,并且在体外不具有显著的KS活性。序列分析表明,ga2-1突变体的AtKS cDNA中存在一个C-2099到T的碱基替换,该替换将Gln-678密码子转换为终止密码子。综上所述,我们的结果表明GA2基因座编码KS。