Yohn C B, Cohen A, Danon A, Mayfield S P
Division of Plant Biology, Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Mol Cell Biol. 1996 Jul;16(7):3560-6. doi: 10.1128/MCB.16.7.3560.
Translational regulation has been identified as one of the key steps in chloroplast-encoded gene expression. Genetic and biochemical analysis with Chlamydomonas reinhardtii has implicated nucleus-encoded factors that interact specifically with the 5' untranslated region of chloroplast mRNAs to mediate light-activated translation. F35 is a nuclear mutation in C. reinhardtii that specifically affects translation of the psbA mRNA (encoding D1, a core polypeptide of photosystem II), causing a photosynthetic deficiency in the mutant strain. The F35 mutant has reduced ribosome association of the psbA mRNA as a result of decreased translation initiation. This reduction in ribosome association correlates with a decrease in the stability of the mRNA. Binding activity of the psbA specific protein complex to the 5' untranslated region of the mRNA is diminished in F35 cells, and two members of this binding complex (RB47 and RB55) are reduced compared with the wild type. These data suggest that alteration of members of the psbA mRNA binding complex in F35 cells results in a reduction in psbA mRNA-protein complex formation, thereby causing a decrease in translation initiation of this mRNA.
翻译调控已被确定为叶绿体编码基因表达的关键步骤之一。对莱茵衣藻进行的遗传和生化分析表明,细胞核编码的因子与叶绿体mRNA的5'非翻译区特异性相互作用,以介导光激活的翻译。F35是莱茵衣藻中的一种核突变,它特异性地影响psbA mRNA(编码D1,光系统II的核心多肽)的翻译,导致突变菌株出现光合缺陷。由于翻译起始减少,F35突变体中psbA mRNA的核糖体结合减少。核糖体结合的这种减少与mRNA稳定性的降低相关。在F35细胞中,psbA特异性蛋白复合物与mRNA的5'非翻译区的结合活性降低,并且与野生型相比,该结合复合物的两个成员(RB47和RB55)减少。这些数据表明,F35细胞中psbA mRNA结合复合物成员的改变导致psbA mRNA-蛋白质复合物形成减少,从而导致该mRNA的翻译起始减少。