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Genomic and cDNA clones for maize phosphoenolpyruvate carboxylase and pyruvate,orthophosphate dikinase: Expression of different gene-family members in leaves and roots

机译:玉米磷酸烯醇丙酮酸羧化酶和丙酮酸,正磷酸二激酶的基因组和cDNA克隆:叶和根中不同基因家族成员的表达

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摘要

We have isolated cDNA clones for the maize leaf enzymes phosphoenolpyruvate (P-ePrv) carboxylase [orthophosphate:oxaloacetate carboxy-lyase (phosphorylating) EC 4.1.1.31] and pyruvate,orthophosphate (Prv,Pi) dikinase (ATP:pyruvate,orthophosphate phosphotransferase, EC 2.7.9.1) by exploiting the light-inducibility and large size of the mRNAs (3.5 kilobases) that encode the two enzymes. The clones were identified by hybrid-selection and immunoprecipitation assays. From a maize genomic library, two different types of genomic clones were screened with both the P-ePrv carboxylase and the Prv,Pi dikinase cDNA clones. Information from these genomic clones and genome blots indicates that the P-ePrv carboxylase gene family has at least three members and the Prv,Pi dikinase family at least two. Transcripts for both enzymes were detected in green leaves, etiolated leaves, and roots. The results show that the P-ePrv carboxylase mRNAs in green leaves and roots are encoded by different genes. Whereas the P-ePrv carboxylase mRNAs in all three tissues appear to be the same size, the Prv,Pi dikinase mRNA in green leaves is about 0.5 kilobases longer than the Prv,Pi dikinase mRNAs in etiolated leaves and roots. It is possible that all these Prv,Pi dikinase transcripts are encoded by one gene, and the size differences may correspond to the presence or absence of a sequence encoding a chloroplast transit peptide.
机译:我们已经为玉米叶酶磷酸烯醇丙酮酸(P-ePrv)羧化酶[正磷酸盐:草酰乙酸羧化酶(磷酸化)EC 4.1.1.31]和丙酮酸,正磷酸盐(Prv,Pi)二激酶(ATP:丙酮酸,正磷酸盐磷酸转移酶, EC 2.7.9.1),通过利用光诱导性和编码这两种酶的mRNA的大尺寸(3.5千碱基)来实现。通过杂交选择和免疫沉淀测定法鉴定克隆。从玉米基因组文库中,使用P-ePrv羧化酶和Prv,Pi二激酶cDNA克隆筛选了两种不同类型的基因组克隆。来自这些基因组克隆和基因组印迹的信息表明,P-ePrv羧化酶基因家族具有至少三个成员,Prv,Pi二激酶家族至少具有两个成员。在绿叶,黄化叶和根中均检测到两种酶的转录本。结果表明,绿叶和根中的P-ePrv羧化酶mRNA由不同的基因编码。尽管所有三个组织中的P-ePrv羧化酶mRNA大小都相同,但绿叶中的Prv,Pi二激酶的mRNA比黄化叶片和根中的Prv,Pi二激酶的mRNA长约0.5个碱基。所有这些Prv,Pi双激酶转录物都可能由一个基因编码,其大小差异可能对应于是否存在编码叶绿体转运肽的序列。

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