Shenton Matt, Fontaine Véronique, Hartwell James, Marsh Justin T, Jenkins Gareth I, Nimmo Hugh G
Plant Science Group, Division of Biochemistry and Molecular Biology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G12 8QQ, UK.
Plant J. 2006 Oct;48(1):45-53. doi: 10.1111/j.1365-313X.2006.02850.x. Epub 2006 Aug 22.
We have examined the complexity of the phosphoenolpyruvate carboxylase kinase (PPCK) gene family in the C(4) monocots maize and sorghum. Maize contains at least four PPCK genes. The encoded proteins are similar to other phosphoenolpyruvate carboxylase (PEPC) kinases, in that they comprise a protein kinase domain with minimal extensions, except that two of the proteins contain unusual acidic insertions. The spatial and temporal expression patterns of the genes provide information about their presumed functions. Expression of ZmPPCK1 in leaves is mesophyll cell-specific and light-induced, indicating that it encodes the PEPC kinase that is responsible for the phosphorylation of leaf PEPC during C(4) photosynthesis. Surprisingly, ZmPPCK2 is expressed in leaf bundle sheath cells, preferentially in the dark. This suggests that a main function of the ZmPPCK2 gene product is to allow PEPC to function anaplerotically in bundle sheath cells in the dark without interfering with the C(4) cycle. ZmPPCK2, ZmPPCK3 and ZmPPCK4 are all induced by exposure of tissue to cycloheximide, whereas ZmPPCK1 is not. This suggests that the ZmPPCK2, ZmPPCK3 and ZmPPCK4 genes share the property that their expression is controlled by a rapidly turning over repressor. Sequence and expression data show that sorghum contains orthologues of ZmPPCK1 and ZmPPCK2.
我们研究了C4单子叶植物玉米和高粱中磷酸烯醇式丙酮酸羧化酶激酶(PPCK)基因家族的复杂性。玉米至少含有四个PPCK基因。编码的蛋白质与其他磷酸烯醇式丙酮酸羧化酶(PEPC)激酶相似,因为它们都包含一个蛋白激酶结构域,且延伸部分最少,只是其中两个蛋白质含有不寻常的酸性插入序列。这些基因的时空表达模式为其假定功能提供了信息。ZmPPCK1在叶片中的表达具有叶肉细胞特异性且受光诱导,这表明它编码的PEPC激酶负责C4光合作用过程中叶片PEPC的磷酸化。令人惊讶的是,ZmPPCK2在叶片维管束鞘细胞中表达,且在黑暗中表达更为优先。这表明ZmPPCK2基因产物的主要功能是使PEPC在黑暗中在维管束鞘细胞中发挥回补作用,而不干扰C4循环。ZmPPCK2、ZmPPCK3和ZmPPCK4都可通过将组织暴露于环己酰亚胺而被诱导,而ZmPPCK1则不然。这表明ZmPPCK2、ZmPPCK3和ZmPPCK4基因具有共同特性,即它们的表达受一个快速周转的阻遏物控制。序列和表达数据表明高粱含有ZmPPCK1和ZmPPCK2的直系同源基因。