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Binding of cell type-specific nuclear proteins to the 5 '-flanking region of maize C-4 phosphoenolpyruvate carboxylase gene confers its differential transcription in mesophyll cells

机译:Binding of cell type-specific nuclear proteins to the 5 '-flanking region of maize C-4 phosphoenolpyruvate carboxylase gene confers its differential transcription in mesophyll cells

摘要

C-4-type phosphenolpyruvate carboxylase (C4PEPC) acts as a primary carbon assimilatory enzyme in the C-4 photosynthetic pathway. The maize C4PEPC gene (C4Ppc1) is specifically expressed in mesophyll cells (MC) of light-grown leaves, but the molecular mechanism responsible for its cell type-specific expression has not been characterized. In this study, we introduced a chimeric maize C4Ppc1 5'-flanking region/beta -glucuronidase (GUS) gene into maize plants by Agrobacterium-mediated transformation. Activity assay and histochemical staining showed that GUS is almost exclusively localized in leaf MC of transgenic maize plants. This observation suggests that the introduced 5' region of maize C4Ppc1 contains the necessary cis element(s) for its specific expression in MC. Next, we investigated whether the 5' region of the maize gene interacts with nuclear proteins in a cell type-specific manner. By gel shift assays with nuclear extracts prepared from MC or bundle sheath cells (BSC), cell type-specific DNA-protein interactions were detected: nuclear factors PEPIb and PEPIc are specific to MC whereas PEPIa and PEPIIa are specific to BSC. Light alters the binding activity of these factors. These interactions were not detected in the assay with nuclear extract prepared from root, or competed out by oligonucleotides corresponding to the binding sites for the maize nuclear protein, PEP-I, which is known to bind specifically to the promoter region of C4Ppc1. The results suggest that novel cell type-specific positive and negative nuclear factors bind to the maize C4Ppc1 5'-flanking region and regulate its differential transcription in MC in a light-dependent manner.
机译:C-4型磷酸丙酮酸羧化酶(C4PEPC)在C-4光合作用途径中充当主要的碳同化酶。玉米C4PEPC基因(C4Ppc1)在光生叶的叶肉细胞(MC)中特异性表达,但尚未表征导致其细胞类型特异性表达的分子机制。在这项研究中,我们通过农杆菌介导的转化将嵌合的玉米C4Ppc1 5'侧翼区/β-葡萄糖醛酸苷酶(GUS)基因引入玉米植物。活性测定和组织化学染色显示,GUS几乎完全位于转基因玉米植物的叶MC中。该观察结果表明,导入的玉米C4Ppc1的5'区域含有在MC中特异性表达所必需的顺式元件。接下来,我们研究了玉米基因的5'区是否以细胞类型特异性方式与核蛋白相互作用。通过用从MC或束鞘细胞(BSC)制备的核提取物进行的凝胶位移分析,检测到细胞类型特异性的DNA-蛋白质相互作用:核因子PEPIb和PEPIc对MC具特异性,而PEPIa和PEPIIa对BSC具特异性。光会改变这些因子的结合活性。在用根部制备的核提取物的测定中未检测到这些相互作用,或未与对应于玉米核蛋白PEP-1结合位点的寡核苷酸竞争,该寡核苷酸已知与C4Ppc1的启动子区域特异性结合。结果表明,新型细胞类型特异性正负核因子与玉米C4Ppc1 5'侧翼区结合,并以光依赖方式调节其在MC中的差异转录。

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