Zerges William, Auchincloss Andrea H, Rochaix Jean-David
Biology Department, Concordia University, Montreal, Quebec H3G 1M8, Canada.
Genetics. 2003 Mar;163(3):895-904. doi: 10.1093/genetics/163.3.895.
Translation of the chloroplast psbC mRNA in the unicellular eukaryotic alga Chlamydomonas reinhardtii is controlled by interactions between its 547-base 5' untranslated region and the products of the nuclear loci TBC1, TBC2, and possibly TBC3. In this study, a series of site-directed mutations in this region was generated and the ability of these constructs to drive expression of a reporter gene was assayed in chloroplast transformants that are wild type or mutant at these nuclear loci. Two regions located in the middle of the 5' leader and near the initiation codon are important for translation. Other deletions still allow for partial expression of the reporter gene in the wild-type background. Regions with target sites for TBC1 and TBC2 were identified by estimating the residual translation activity in the respective mutant backgrounds. TBC1 targets include mostly the central part of the leader and the translation initiation region whereas the only detected TBC2 targets are in the 3' part. The 5'-most 93 nt of the leader are required for wild-type levels of transcription and/or mRNA stabilization. The results indicate that TBC1 and TBC2 function independently and further support the possibility that TBC1 acts together with TBC3.
单细胞真核藻类莱茵衣藻中叶绿体psbC mRNA的翻译受其547个碱基的5'非翻译区与核基因座TBC1、TBC2以及可能的TBC3产物之间相互作用的控制。在本研究中,在该区域产生了一系列定点突变,并在这些核基因座为野生型或突变型的叶绿体转化体中检测了这些构建体驱动报告基因表达的能力。位于5'前导序列中间和起始密码子附近的两个区域对翻译很重要。其他缺失在野生型背景下仍允许报告基因部分表达。通过估计各自突变背景下的残余翻译活性,确定了TBC1和TBC2的靶位点区域。TBC1的靶位点主要包括前导序列的中央部分和翻译起始区域,而唯一检测到的TBC2靶位点在3'部分。前导序列最5'端的93个核苷酸是野生型转录水平和/或mRNA稳定性所必需的。结果表明,TBC1和TBC2独立发挥作用,并进一步支持TBC1与TBC3共同作用的可能性。