...
首页> 外文期刊>Acta Horticulturae >SNPs within the glutathione S-transferase genes as markers for the identification of more or less stress responsive sweet orange varieties
【24h】

SNPs within the glutathione S-transferase genes as markers for the identification of more or less stress responsive sweet orange varieties

机译:谷胱甘肽S-转移酶基因内的SNP可作为鉴定或多或少的胁迫响应性甜橙品种的标记

获取原文
获取原文并翻译 | 示例
           

摘要

The glutathione S-transferases (GSTs) are ubiquitous dimeric enzymes catalyzing the nucleophilic addition of glutathione (GSH) to the electrophilic groups of a large variety of toxic chemicals. The resulting GS-conjugates are sequestered into the vacuoles where further transformation processes can promote their partial salvage, substitution or degradation. Subunits of all known GSTs exhibit a two-domain fold, the N-terminal domain, including the highly conserved GSH-binding site (G-site), and the C-terminal domain which represents the more divergent cosubstrate-binding site (H-site). Previously, two GST genes sharing 98.6% homology (Ul and U2) have been isolated from sweet orange. The encoded enzymes differ in three amino acids, all of them localized in the H-site of the proteins. Despite the fact that the enzymes share very high sequence similarity, they have been found to show different substrate specificity as well as different catalytic efficiency towards l-chloro-2,4-dinitrobenzene (CDNB). Inthe present work, the analysis of single nucleotide polymorphisms (SNPs) among members of nine Citrus sinensis varieties was performed by genotype sequencing. The data showed that all SNPs, which lead to one or to the other GST isoform, are as differentalleles in a heterozygosis status at the GST locus thus suggesting that all the varieties under investigation could potentially express both isoforms in their organs. The analysis of gene expression highlighted that the GST isoforms show different distribution between leaf and flesh as well as that they are differently involved in abiotic stress response. Therefore, the regulation of GST gene expression certainly fulfils a crucial role in citrus plant defense mechanisms. Moreover, gene sequencing revealed the presence of other still unidentified SNPs, most of them leading to conservative amino acid substitutions. In a particular case ('Tarocco dal muso'), the newly individuated SNP inserts an in frame stop codon within the protein coding region which prematurely interrupts the mRNA translation process producing an incomplete, most likely inactive, form of enzyme. Therefore, SNP genotyping might represent a powerful tool to identify among varieties those potentially more responsive to environmental stresses.
机译:谷胱甘肽S-转移酶(GST)是普遍存在的二聚酶,催化谷胱甘肽(GSH)亲核加成到各种有毒化学物质的亲电子基团上。将得到的GS-缀合物螯合到液泡中,在液泡中进一步的转化过程可以促进它们的部分挽救,取代或降解。所有已知GST的亚基均具有两个结构域折叠,即N端结构域(包括高度保守的GSH结合位点(G位置))和C端结构域(代表更为分散的共底物结合位点(H-现场)。以前,已经从甜橙中分离出两个具有98.6%同源性的GST基因(U1和U2)。所编码的酶的三个氨基酸不同,它们全部位于蛋白质的H位点。尽管这些酶具有非常高的序列相似性,但是发现它们显示出不同的底物特异性以及对1-氯-2,4-二硝基苯(CDNB)的不同催化效率。在本工作中,通过基因型测序分析了九个柑橘品种成员之间的单核苷酸多态性(SNPs)。数据表明,导致一个或另一个GST同工型的所有SNP在GST位点处于杂合状态的等位基因不同,因此表明所研究的所有变体都可能在其器官中表达两种同工型。基因表达分析强调,GST亚型在叶片和果肉之间显示出不同的分布,并且它们在非生物胁迫响应中的参与程度也不同。因此,GST基因表达的调控当然在柑橘植物防御机制中起着至关重要的作用。此外,基因测序揭示了其他仍未鉴定的SNP的存在,其中大多数导致保守的氨基酸取代。在特定情况下('Tarocco dal muso'),新近个体化的SNP在蛋白质编码区域内插入了一个框内终止密码子,该密码子过早地中断了mRNA的翻译过程,从而产生了一种不完全的,最有可能失活的酶形式。因此,SNP基因分型可能是一个强大的工具,可以在品种中识别出可能对环境压力反应更强的品种。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号