Bruick R K, Mayfield S P
Department of Cell Biology and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
J Cell Biol. 1998 Nov 30;143(5):1145-53. doi: 10.1083/jcb.143.5.1145.
The 5' untranslated region of the chloroplast psbA mRNA, encoding the D1 protein, is processed in Chlamydomonas reinhardtii. Processing occurs just upstream of a consensus Shine-Dalgarno sequence and results in the removal of 54 nucleotides from the 5' terminus, including a stem-loop element identified previously as an important structure for D1 expression. Examination of this processing event in C. reinhardtii strains containing mutations within the chloroplast or nuclear genomes that block psbA translation reveals a correlation between processing and ribosome association. Mutations within the 5' untranslated region of the psbA mRNA that disrupt the Shine-Dalgarno sequence, acting as a ribosome binding site, preclude translation and prevent mRNA processing. Similarly, nuclear mutations that specifically affect synthesis of the D1 protein specifically affect processing of the psbA mRNA. In vitro, loss of the stem-loop element does not prohibit the binding of a message-specific protein complex required for translational activation of psbA upon illumination. These results are consistent with a hierarchical maturation pathway for chloroplast messages, mediated by nuclear-encoded factors, that integrates mRNA processing, message stability, ribosome association, and translation.
编码D1蛋白的叶绿体psbA mRNA的5'非翻译区在莱茵衣藻中会进行加工。加工发生在一个共有Shine-Dalgarno序列的上游,导致从5'末端去除54个核苷酸,包括一个先前被确定为对D1表达很重要的茎环结构。在叶绿体或核基因组中含有阻断psbA翻译的突变的莱茵衣藻菌株中对这一加工事件进行研究,发现加工与核糖体结合之间存在相关性。psbA mRNA的5'非翻译区内破坏作为核糖体结合位点的Shine-Dalgarno序列的突变会阻止翻译并防止mRNA加工。同样,特异性影响D1蛋白合成的核突变也会特异性影响psbA mRNA的加工。在体外,茎环结构的缺失并不妨碍光照后psbA翻译激活所需的信使特异性蛋白复合物的结合。这些结果与由核编码因子介导的叶绿体信使的分级成熟途径一致,该途径整合了mRNA加工、信使稳定性、核糖体结合和翻译。