Yanagisawa S, Izui K
Department of Chemistry, Faculty of Science, Kyoto University, Japan.
Plant Mol Biol. 1992 Jul;19(4):545-53. doi: 10.1007/BF00026781.
When gel shift assays were performed with maize nuclear extract and a DNA fragment containing the cauliflower mosaic virus (CaMV) 35S promoter, three DNA-protein complexes were observed. Analyses with nuclear extracts prepared from green leaves, etiolated leaves, stems and roots showed that the complexes resulted from the existence of at least two nuclear factors. One of them is presumably a constitutive nuclear factor found in all tissues tested, and another is a leaf-specific factor present both in green and etiolated leaves. This leaf-specific nuclear factor seemed to be identical to MNF1, previously identified as a factor interacting with the promoter of the maize gene for phosphoenolpyruvate carboxylase involved in the C4 photosynthesis. Deletion analysis revealed that MNF1 binds to the sequence from -281 to -235 relative to the transcription start site of the CaMV 35S promoter. MNF1-like nuclear protein was also found in tobacco nuclear extracts. The possibility that MNF1 participates as a positive trans-acting factor in the expression of genes in maize leaves is discussed.
当用玉米核提取物和一个含有花椰菜花叶病毒(CaMV)35S启动子的DNA片段进行凝胶迁移试验时,观察到三种DNA-蛋白质复合物。对从绿叶、黄化叶、茎和根制备的核提取物进行分析表明,这些复合物是由至少两种核因子的存在导致的。其中一种可能是在所测试的所有组织中都存在的组成型核因子,另一种是在绿叶和黄化叶中都存在的叶特异性因子。这种叶特异性核因子似乎与MNF1相同,MNF1先前被鉴定为一种与参与C4光合作用的玉米磷酸烯醇式丙酮酸羧化酶基因启动子相互作用的因子。缺失分析表明,MNF1与相对于CaMV 35S启动子转录起始位点从-281到-235的序列结合。在烟草核提取物中也发现了类似MNF1的核蛋白。本文讨论了MNF1作为正性反式作用因子参与玉米叶片基因表达的可能性。