Feldbrügge M, Hahlbrock K, Weisshaar B
Max-Planck-Institut für Züchtungsforschung. Abteilung Biochemie, Köln, Germany.
Mol Gen Genet. 1996 Jul 26;251(6):619-27. doi: 10.1007/BF02174110.
Many eukaryotic DNA-binding proteins share a conserved amino acid sequence known as the basic region leucine zipper (bZIP) domain. bZIP proteins recognise DNA, upon dimerization, in a sequence-specific manner. The Common Plant Regulatory Factor 1 (CPRF1) is a bZIP transcription factor from parsley (Petroselinum crispum), which recognises defined elements containing ACGT cores. CPRF1 genomic DNA was cloned and the gene was sequenced. Analysis of the sequence data revealed the existence of 12 exons and 11 introns within a stretch of about 9 kb. A second RNA species hybridising to CPRF1 probes was identified as an alternatively spliced, additional CPRF1 transcript containing intron 8. This polyadenylated RNA species showed accumulation characteristics very similar to those of the CPRF1 mRNA. CPRF1 specifically binds an ACGT-containing element which is located within the composite regulatory unit that is necessary and sufficient for light activation of the parsley chalcone synthase (CHS) minimal promoter. Expression studies at the mRNA level demonstrated that CPRF1 mRNA is present in all organs of light-grown plants in which CHS mRNA expression is detectable, and light-dependent CHS mRNA accumulation was shown to be blocked by cycloheximide. Therefore, translation of a protein factor, possibly CPRF1, may be a prerequisite for CHS promoter activation.
许多真核生物的DNA结合蛋白都共享一种保守的氨基酸序列,即碱性区域亮氨酸拉链(bZIP)结构域。bZIP蛋白在二聚化后以序列特异性方式识别DNA。普通植物调控因子1(CPRF1)是来自欧芹(Petroselinum crispum)的一种bZIP转录因子,它能识别含有ACGT核心的特定元件。克隆了CPRF1基因组DNA并对该基因进行了测序。序列数据分析显示,在约9 kb的片段中存在12个外显子和11个内含子。另一种与CPRF1探针杂交的RNA物种被鉴定为一种选择性剪接的额外CPRF1转录本,它含有内含子8。这种多聚腺苷酸化的RNA物种显示出与CPRF1 mRNA非常相似的积累特征。CPRF1特异性结合一个含有ACGT的元件,该元件位于复合调控单元内,对于欧芹查尔酮合酶(CHS)最小启动子的光激活是必需且充分的。在mRNA水平上的表达研究表明,CPRF1 mRNA存在于光照生长植物中所有可检测到CHS mRNA表达的器官中,并且光照依赖性的CHS mRNA积累被环己酰亚胺阻断。因此,一种蛋白质因子(可能是CPRF1)的翻译可能是CHS启动子激活的先决条件。