首页> 外文期刊>Journal of Plant Biology >Comparative expression and characterization of dehydroascorbate reductase cDNA from transformed sesame hairy roots using real-time RT-PCR
【24h】

Comparative expression and characterization of dehydroascorbate reductase cDNA from transformed sesame hairy roots using real-time RT-PCR

机译:实时RT-PCR技术比较转化芝麻毛状根中脱氢抗坏血酸还原酶cDNA的表达和鉴定

获取原文
获取原文并翻译 | 示例
           

摘要

The differential transcription activity of dehydroascorbate reductase (DHAR) was scrutinized in the transformed hairy roots, leaves, stems, roots, and developing seeds of sesame (Sesamum indicum L.). Its relative levels of expression were compared via the threshold cycle (CT) method, using real-time RT-PCR. Ubiquitous expression of DHAR in all organs was confirmed with both reai-time and conventional RT-PCR. With the former, DHAR transcript levels were, unexpectedly, 4.7-fold higher in the stem tissue than in the hairy roots; the lowest levels were detected in the seeds. It was possible to determine the transcription activity of hairy root DHAR, with a low amount of total RNA (0.5 ng), using real-time RT-PCR but not with conventional RT-PCR gel analysis. This indicated that the former is more sensitive and efficient than the latter for the detection of gene expression. We also characterized DHAR cDNA cloned from transformed hairy roots, and found that sequence identity for the deduced amino acids of the DHAR enzyme was shared at 60 to 83% among plant species. The algorithm prediction and phylogenetic analysis suggested that the cloned cDNA polypeptide is cytosolic DHAR. Another feature of the cloned cDNA polypeptide was the presence of a CXXS instead of CXXC motif in the active center of the DHAR enzyme.
机译:仔细研究了转化后的毛状根,叶,茎,根和发育中的芝麻种子(Sesamum indicum L.)的脱氢抗坏血酸还原酶(DHAR)的差异转录活性。使用实时逆转录-聚合酶链反应(RT-PCR),通过阈值循环(CT )方法比较了其相对表达水平。用reai-time和常规RT-PCR都证实了DHAR在所有器官中的普遍表达。对于前者,出乎意料的是,茎组织中的DHAR转录水平比毛状根中高4.7倍。在种子中检测到最低水平。使用实时RT-PCR而非常规RT-PCR凝胶分析,可以测定毛根DHAR的转录活性,而总RNA量很低(0.5 ng)。这表明前者在检测基因表达方面比后者更灵敏和有效。我们还表征了从转化的毛根中克隆的DHAR cDNA,并发现DHAR酶的推导氨基酸的序列同一性在植物物种之间的共享率为60%至83%。算法预测和系统进化分析表明,克隆的cDNA多肽是胞质DHAR。克隆的cDNA多肽的另一个特征是在DHAR酶的活性中心存在CXXS而不是CXXC基序。

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