Kano-Murakami Y, Suzuki I, Sugiyama T, Matsuoka M
Fruit Tree Research Center, Tsukuba, Ibaraki, Japan.
Mol Gen Genet. 1991 Feb;225(2):203-8. doi: 10.1007/BF00269849.
A plant nuclear protein PEP-I, which binds specifically to the promoter region of the phosphoenolpyruvate carboxylase (PEPC) gene, was identified. Methylation interference analysis and DNA binding assays using synthetic oligonucleotides revealed that PEP-I binds to GC-rich elements. These elements are directly repeated sequences in the promoter region of the PEPC gene and we have suggested that they may be cis-regulatory elements of this gene. The consensus sequence of the element is CCCTCTCCACATCC and the CTCC is essential for binding of PEP-I. PEP-I is present in the nuclear extracts of green leaves, where the PEPC gene is expressed. However, no binding was detected in tissues where the PEPC gene is not expressed in vivo, such as roots or etiolated leaves. Thus, PEP-I is the first factor identified in plants which has different binding activity in light-grown compared with dark-grown tissue. PEP-I binding is also tissue-specific, suggesting that PEP-I may function to coordinate PEPC gene expression with respect to light and tissue specificity. This report describes the identification and characterization of the sequences required for PEP-I binding.
一种植物核蛋白PEP-I被鉴定出来,它能特异性地结合磷酸烯醇式丙酮酸羧化酶(PEPC)基因的启动子区域。甲基化干扰分析和使用合成寡核苷酸的DNA结合试验表明,PEP-I与富含GC的元件结合。这些元件是PEPC基因启动子区域中的直接重复序列,我们认为它们可能是该基因的顺式调控元件。该元件的共有序列是CCCTCTCCACATCC,其中CTCC对于PEP-I的结合至关重要。PEP-I存在于绿叶的核提取物中,PEPC基因在绿叶中表达。然而,在体内不表达PEPC基因的组织,如根或黄化叶中,未检测到结合。因此,PEP-I是在植物中鉴定出的第一个在光生长组织与暗生长组织中具有不同结合活性的因子。PEP-I的结合也是组织特异性的,这表明PEP-I可能在协调PEPC基因表达的光和组织特异性方面发挥作用。本报告描述了PEP-I结合所需序列的鉴定和特征。