Zhao Lingxia, Lu Liya, Zhang Lida, Wang Aoxue, Wang Ning, Liang Zhuobin, Lu Xiaowen, Tang Kexuan
Plant Biotechnology Research Center, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
J Biosci. 2009 Mar;34(1):71-83. doi: 10.1007/s12038-009-0010-x.
The E8 gene is related to ethylene biosynthesis in plants. To explore the effect of the expression pattern of the E8 gene on different E8 promoters, the molecular evolution of E8 promoters was investigated. A total of 16 E8 promoters were cloned from 16 accessions of seven tomato species,and were further analysed. The results from 19 E8 promoters including three previously cloned E8 promoters (X13437,DQ317599 and AF515784) showed that the size of the E8 promoters varied from 2101 bp (LA2150) to 2256 bp (LA2192); their sequences shared 69.9% homology and the average A/T content was 74.9%. Slide-window analysis divided E8 promoters into three regions -A,B and C - and the sequence identity in these regions was 72.5%, 41.2% and 70.8%, respectively. By searching the cis -elements of E8 promoters in the PLACE database, mutant nucleotides were found in some functional elements,and deletions or insertions were also found in regions responsible for ethylene biosysnthesis (-1702 to -1274) and the negative effect region (-1253 to -936). Our results indicate that the size of the functional region for ethylene biosynthesis in the E8 promoter could be shortened from 429 bp to 113 bp (-1612 to -1500). The results of molecular evolution analysis showed that the 19 E8 promoters could be classified into four clade groups, which is basically consistent with evolution of the tomato genome. Southern blot analysis results showed that the copy number of E8 promoters in tomato and some other wild species changed from 1 to 4. Taken together, our study provides important information for further elucidating the E8 gene expression pattern in tomato, analysing functional elements in the E8 promoter and reconstructing the potent E8 promoter.
E8基因与植物中的乙烯生物合成有关。为了探究E8基因表达模式对不同E8启动子的影响,对E8启动子的分子进化进行了研究。从7个番茄物种的16个种质中克隆了总共16个E8启动子,并进行了进一步分析。包括3个先前克隆的E8启动子(X13437、DQ317599和AF515784)在内的19个E8启动子的结果表明,E8启动子的大小从2101 bp(LA2150)到2256 bp(LA2192)不等;它们的序列具有69.9%的同源性,平均A/T含量为74.9%。滑动窗口分析将E8启动子分为A、B和C三个区域,这些区域的序列同一性分别为72.5%、41.2%和70.8%。通过在PLACE数据库中搜索E8启动子的顺式元件,在一些功能元件中发现了突变核苷酸,并且在负责乙烯生物合成的区域(-1702至-1274)和负效应区域(-1253至-936)也发现了缺失或插入。我们的结果表明,E8启动子中乙烯生物合成功能区域的大小可以从429 bp缩短到113 bp(-1612至-1500)。分子进化分析结果表明,19个E8启动子可分为四个进化枝组,这与番茄基因组的进化基本一致。Southern杂交分析结果表明,番茄和其他一些野生物种中E8启动子的拷贝数从1变为4。综上所述,我们的研究为进一步阐明番茄中E8基因的表达模式、分析E8启动子中的功能元件以及重建有效的E8启动子提供了重要信息。