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根、循环与叶片。大豆中磷酸烯醇式丙酮酸羧化酶激酶基因家族的表达

Roots, cycles and leaves. Expression of the phosphoenolpyruvate carboxylase kinase gene family in soybean.

作者信息

Sullivan Stuart, Jenkins Gareth I, Nimmo Hugh G

机构信息

Plant Molecular Science Group, Division of Biochemistry and Molecular Biology, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.

出版信息

Plant Physiol. 2004 Aug;135(4):2078-87. doi: 10.1104/pp.104.042762. Epub 2004 Aug 6.

Abstract

Phosphorylation of phosphoenolpyruvate carboxylase (PEPc; EC 4.1.1.31) plays an important role in the control of central metabolism of higher plants. This phosphorylation is controlled largely at the level of expression of PEPc kinase (PPCK) genes. We have analyzed the expression of both PPCK genes and the PEPC genes that encode PEPc in soybean (Glycine max). Soybean contains at least four PPCK genes. We report the genomic and cDNA sequences of these genes and demonstrate the function of the gene products by in vitro expression and enzyme assays. For two of these genes, GmPPCK2 and GmPPCK3, transcript abundance is highest in nodules and is markedly influenced by supply of photosynthate from the shoots. One gene, GmPPCK4, is under robust circadian control in leaves but not in roots. Its transcript abundance peaks in the latter stages of subjective day, and its promoter contains a sequence very similar to the evening element found in Arabidopsis genes expressed at this time. We report the expression patterns of five PEPC genes, including one encoding a bacterial-type PEPc lacking the phosphorylation site of the plant-type PEPcs. The PEPc expression patterns do not match those of any of the PPCK genes, arguing against the existence of specific PEPc-PPCK expression partners. The PEPC and PPCK gene families in soybean are significantly more complex than previously understood.

摘要

磷酸烯醇式丙酮酸羧化酶(PEPc;EC 4.1.1.31)的磷酸化在高等植物中心代谢的调控中发挥着重要作用。这种磷酸化主要在PEPc激酶(PPCK)基因的表达水平上受到调控。我们分析了大豆(Glycine max)中编码PEPc的PPCK基因和PEPC基因的表达情况。大豆至少含有四个PPCK基因。我们报道了这些基因的基因组和cDNA序列,并通过体外表达和酶活性测定证明了基因产物的功能。对于其中两个基因GmPPCK2和GmPPCK3,转录本丰度在根瘤中最高,并且受到来自地上部光合产物供应的显著影响。一个基因GmPPCK4在叶片中受到强烈的昼夜节律控制,但在根中不受此控制。其转录本丰度在主观日的后期达到峰值,并且其启动子包含一个与此时在拟南芥中表达的基因中发现的晚间元件非常相似的序列。我们报道了五个PEPC基因的表达模式,其中一个编码的细菌型PEPc缺乏植物型PEPc的磷酸化位点。PEPC的表达模式与任何PPCK基因的表达模式均不匹配,这表明不存在特定的PEPc - PPCK表达伙伴。大豆中的PEPC和PPCK基因家族比之前所了解的要复杂得多。

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