首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >The characterization of GmTIP, a root-specific gene from soybean, and the expression analysis of its promoter
【24h】

The characterization of GmTIP, a root-specific gene from soybean, and the expression analysis of its promoter

机译:大豆根特异性基因GmTIP的鉴定及其启动子的表达分析

获取原文
获取原文并翻译 | 示例
           

摘要

The soybean encounters severe root-related biotic and abiotic stresses causing extensive yield losses annually. The use of a root-specific promoter to confer expression of genes in a targeted manner has the potential to benefit the genetic improvement of the soybean. Several tonoplast intrinsic protein genes (TIPs) in plants like tobacco, strawberry, tomato, maize, pine, have been identified exhibiting root-specific expression. To explore the possibility of root-specific gene and promoter utilizations in soybean, we cloned soybean GmTIP and the upstream promoter sequence from soybean, and examined the expression patterns and promoter activity. Fluorometric GUS assays revealed that the GUS activity was obviously higher in roots than in leaves in transgenic Arabidopsis, regardless of the length of the promoter fragment. Weak GUS expression was found in other organs except root in transgenic Arabidopsis with the GmTIPp-2054 construct. Deletion analysis of the GmTIP promoter displayed that it still keep root-specific expression and can also be induced by various factors, such as methyl jasmonate, salicylic acid, abscisic acid, gibberellins acid, indole-3-acetic acid, NaCl, and PEG6000. This study provides a useful tool for soybean root improvement by genetic engineering.
机译:大豆遇到严重的根系相关生物和非生物胁迫,每年导致大量的产量损失。使用根特异性启动子以靶向方式赋予基因表达具有潜在有益于大豆遗传改良的潜力。已经确定了烟草,草莓,番茄,玉米,松树等植物中的几个液泡内在蛋白基因(TIP)表现出根特异性表达。为了探索在大豆中利用根特异性基因和启动子的可能性,我们从大豆中克隆了大豆GmTIP和上游启动子序列,并检查了表达模式和启动子活性。荧光GUS分析表明,无论启动子片段的长度如何,转基因拟南芥中根部的GUS活性明显高于叶中的GUS活性。在带有GmTIPp-2054构建体的转基因拟南芥中,除了根部以外,其他器官中均发现了弱的GUS表达。 GmTIP启动子的缺失分析表明,它仍然保持根特异性表达,并且也可以由多种因素诱导,例如茉莉酸甲酯,水杨酸,脱落酸,赤霉素,吲哚-3-乙酸,NaCl和PEG6000。该研究为通过基因工程改良大豆根系提供了有用的工具。

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