Kasai Seitaro, Yoshimura Satomi, Ishikura Kiyohide, Takaoka Yasuko, Kobayashi Kei, Kato Ko, Shinmyo Astuhiko
Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5 Takayama, Ikoma, Nara 630-0101, Japan.
J Biosci Bioeng. 2003;95(3):276-82. doi: 10.1016/s1389-1723(03)80029-4.
An exogenous gene, placed between the 5'-upstream regions of the Chlamydomonas reinhardtii chloroplast genes, rbcL or psbA, and the 3'-end of the rbcL gene, do not have the same expression pattern as endogenous genes in the C. reinhardtii chloroplast. Here, we chose four chloroplast genes, rbcL, psbA, psbD and atpA, and examine the effects of chloroplast gene coding regions on gene expression in C. reinhardtii. We constructed chimeric genes composed of the promoter, 5'- and 3'-untranslated regions, varying lengths of protein coding regions of the chloroplast genes, and the bacterial beta-glucuronidase (GUS) gene (uidA) as a reporter gene, and introduced into chloroplast genomes. The transformants, which contained the rbcL-uidA and psbA-uidA chimeric genes fused to the coding region of each gene, showed high expression of uidA mRNA as compared with the previously generated transformants, RG and PG, in which uidA was only fused to the promoter and 5'-UTR of each gene. The difference in the accumulation of uidA transcripts among the transformants was the result of different rates of transcription. This result indicates that the coding region is necessary for sufficient expression of rbcL and psbA. On the other hand, the psbD and atpA coding region portions did not affect chimeric gene expression.
置于莱茵衣藻叶绿体基因rbcL或psbA的5'-上游区域与rbcL基因3'-末端之间的外源基因,其表达模式与莱茵衣藻叶绿体中的内源基因不同。在此,我们选择了四个叶绿体基因rbcL、psbA、psbD和atpA,并研究叶绿体基因编码区对莱茵衣藻基因表达的影响。我们构建了嵌合基因,其由启动子、5'-和3'-非翻译区、不同长度的叶绿体基因蛋白质编码区以及作为报告基因的细菌β-葡萄糖醛酸酶(GUS)基因(uidA)组成,并导入叶绿体基因组。含有与每个基因编码区融合的rbcL-uidA和psbA-uidA嵌合基因的转化体,与之前产生的转化体RG和PG相比,uidA mRNA表达量较高,在RG和PG中uidA仅与每个基因的启动子和5'-UTR融合。转化体中uidA转录本积累的差异是转录速率不同的结果。这一结果表明编码区对于rbcL和psbA的充分表达是必要的。另一方面,psbD和atpA编码区部分不影响嵌合基因的表达。