Gehrig Hans H, Wood Joshua A, Cushman Mary Ann, Virgo Aurelio, Cushman John C, Winter Klaus
Smithsonian Tropical Research Institute, P.O. Box 2072, Balboa, Ancón, Republic of Panama.
Department of Biochemistry and Molecular Biology, University of Nevada, Reno, NV 89557-0014, USA.
Funct Plant Biol. 2005 Jul;32(5):467-472. doi: 10.1071/FP05079.
Clones coding for a 1100-bp cDNA sequence of phosphoenolpyruvate carboxylase (PEPC) of the constitutive crassulacean acid metabolism (CAM) plant Kalanchoe pinnata (Lam.) Pers., were isolated by reverse transcription-polymerase chain reaction (RT-PCR) and characterised by restriction fragment length polymorphism analysis and DNA sequencing. Seven distinct PEPC isogenes were recovered, four in leaves and three in roots (EMBL accession numbers: AJ344052-AJ344058). Sequence similarity comparisons and distance neighbour-joining calculations separate the seven PEPC isoforms into two clades, one of which contains the three PEPCs found in roots. The second clade contains the four isoforms found in leaves and is divided into two branches, one of which contains two PEPCs most similar with described previously CAM isoforms. Of these two isoforms, however, only one exhibited abundant expression in CAM-performing leaves, but not in very young leaves, which do not exhibit CAM, suggesting this isoform encodes a CAM-specific PEPC. Protein sequence calculations suggest that all isogenes are likely derived from a common ancestor gene, presumably by serial gene duplication events. To our knowledge, this is the most comprehensive identification of a PEPC gene family from a CAM plant, and the greatest number of PEPC isogenes reported for any vascular plant to date.
通过逆转录聚合酶链反应(RT-PCR)分离出组成型景天酸代谢(CAM)植物落地生根(Kalanchoe pinnata (Lam.) Pers.)磷酸烯醇丙酮酸羧化酶(PEPC)1100 bp cDNA序列的编码克隆,并通过限制性片段长度多态性分析和DNA测序进行表征。回收了七个不同的PEPC同基因,四个在叶片中,三个在根中(EMBL登录号:AJ344052-AJ344058)。序列相似性比较和距离邻接法计算将七个PEPC同工型分为两个进化枝,其中一个包含在根中发现的三个PEPC。第二个进化枝包含在叶片中发现的四个同工型,并分为两个分支,其中一个分支包含与先前描述的CAM同工型最相似的两个PEPC。然而,在这两个同工型中,只有一个在进行CAM的叶片中大量表达,而在不表现出CAM的非常幼嫩的叶片中不表达,这表明该同工型编码一种CAM特异性PEPC。蛋白质序列计算表明,所有同基因可能都来自一个共同的祖先基因,大概是通过连续的基因复制事件。据我们所知,这是对CAM植物中PEPC基因家族最全面的鉴定,也是迄今为止报道的任何维管植物中PEPC同基因数量最多的。