Curi Graciela C, Chan Raquel L, Gonzalez Daniel H
Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, CC 242 Paraje El Pozo, 3000 Santa Fe, Argentina.
J Exp Bot. 2005 Sep;56(419):2563-71. doi: 10.1093/jxb/eri250. Epub 2005 Aug 1.
The involvement of regions located upstream of the translation start site in the expression of two Arabidopsis thaliana nuclear COX5c genes encoding subunit 5c of mitochondrial cytochrome c oxidase has been analysed. It was observed that these regions, which include a leader intron, direct the tissue-specific expression of the gus reporter gene, mainly in root and shoot meristems, actively growing tissues and vascular strands. Expression was also observed in flowers, specifically localized in anthers, stigma, and the receptacle, and in developing seeds. GUS activity measurements in protein extracts from transformed plants indicated that expression levels are higher than those observed with the constitutive CaMV 35S promoter. Removal of the leader intron produced a significant decrease in expression to values only slightly higher than those observed with a promoterless gus gene. Histochemical staining of plants transformed with the intronless construct revealed expression only in pollen, suggesting that regulatory elements capable of directing pollen-specific expression are present upstream of the intron. The COX5c-2 intron also increased GUS expression levels when fused in the correct orientation with the promoter of the unrelated COX5b-1 gene. Comparison of GUS activity values with the transcript levels suggests that the intron also increases translation efficiency of the corresponding mRNA. The results obtained point to an essential role of the intron present in the 5'-non-coding region of all known COX5c genes in directing the expression of these genes in plants.
对拟南芥中两个编码线粒体细胞色素c氧化酶亚基5c的核COX5c基因表达过程中翻译起始位点上游区域的参与情况进行了分析。结果发现,这些区域包括一个前导内含子,可指导gus报告基因的组织特异性表达,主要在根和茎的分生组织、活跃生长的组织以及维管束中表达。在花中也观察到了表达,具体定位于花药、柱头和花托以及发育中的种子中。对转化植物蛋白质提取物中的GUS活性测量表明,其表达水平高于组成型CaMV 35S启动子所观察到的水平。去除前导内含子导致表达显著下降,降至仅略高于无启动子gus基因所观察到的值。用无内含子构建体转化的植物的组织化学染色显示仅在花粉中表达,这表明能够指导花粉特异性表达的调控元件存在于内含子上游。当以正确方向与不相关的COX5b - 1基因的启动子融合时,COX5c - 2内含子也提高了GUS表达水平。将GUS活性值与转录水平进行比较表明,该内含子还提高了相应mRNA的翻译效率。所得结果表明,所有已知COX5c基因5'-非编码区中存在的内含子在指导这些基因在植物中的表达方面起着至关重要的作用。