Franzetti B, Zhou D X, Mache R
Laboratoire de Biologie Moléculaire Végétale, CNRS (URA 1178), Grenoble, France.
Nucleic Acids Res. 1992 Aug 25;20(16):4153-7. doi: 10.1093/nar/20.16.4153.
The chloroplast ribosomal protein CS1 is an essential component of the plastids translational machinery involved in translation initiation. Southern analysis suggests that the corresponding nuclear gene is present in one copy in the spinach genome. We have isolated and sequenced the gene (rps1) to study its expression at the transcriptional level. The gene consists of 7 exons and 6 introns including an unusually large intron in the 5' coding region. No canonical TATA-box is found in the 5' upstream region of the gene. rps1 transcripts are detected early during germination and a significant accumulation is observed after the protrusion of the radicle. CS1 mRNAs are present in all organs of young seedlings although there are dramatic differences in the steady state level of the mRNAs between leaves and roots tissues. Transcripts accumulate independently of the presence or absence of light. Band shift analysis shows that the +1, -400 bp region of the gene can bind different sets of proteins isolated from roots and leaves nuclei. We suggest that the expression of the housekeeping plastid-related rps1 gene is regulated in a tissue-specific manner by transcriptional trans-acting factors.
叶绿体核糖体蛋白CS1是参与翻译起始的质体翻译机制的重要组成部分。Southern分析表明,相应的核基因在菠菜基因组中以单拷贝形式存在。我们已经分离并测序了该基因(rps1),以研究其在转录水平上的表达。该基因由7个外显子和6个内含子组成,其中包括5'编码区一个异常大的内含子。在该基因的5'上游区域未发现典型的TATA框。在萌发早期检测到rps1转录本,在胚根突出后观察到显著积累。CS1 mRNA存在于幼苗的所有器官中,尽管叶和根组织中mRNA的稳态水平存在显著差异。转录本的积累与光照的有无无关。凝胶迁移分析表明,该基因的+1,-400 bp区域可以结合从根和叶细胞核中分离出的不同蛋白质组。我们认为,管家质体相关rps1基因的表达受转录反式作用因子以组织特异性方式调控。