首页> 外文期刊>Molecular Plant-Microbe Interactions >Promoters of Orthologous Glycine max and Lotus japonicus Nodulation Autoregulation Genes Interchangeably Drive Phloem-Specific Expression in Transgenic Plants
【24h】

Promoters of Orthologous Glycine max and Lotus japonicus Nodulation Autoregulation Genes Interchangeably Drive Phloem-Specific Expression in Transgenic Plants

机译:直系最大大豆和日本莲结瘤调控基因的启动子可互换地驱动转基因植物韧皮部特异性表达。

获取原文
           

摘要

The nodule autoregulation receptor kinase (GmNARK) of soybean (Glycine max) is essential for the systemic auto-regulation of nodulation. Based on quantitative reverse-transcriptase polymerase chain reaction, GmNARK is expressed to varying levels throughout the plant; the transcript was detected at high levels in mature leaves and roots but to a lesser extent in young leaves, shoot tips, and nodules. The transcript level was not significantly affected by Bradyrhizobium japonicum during the first week following inoculation. In addition, the activities of the promoters of GmNARK and Lotus japonicus HAR1, driving a β-glucuronidase (GUSPlus) reporter gene, were examined in stably transformed L. japonicus and transgenic hairy roots of soybean. Histochemical GUS activity in L. japonicus plants carrying either a 1.7-kb GmNARKprGUS or 2.0-kb LjHAR1prGUS construct was clearly localized to living cells within vascular bundles, especially phloem cells in leaves, stems, roots, and nodules. Phloem-specific expression also was detected in soybean hairy roots carrying these constructs. Our study suggests that regulatory elements required for the transcription of these orthologous genes are conserved. Moreover, rapid amplification of 5' cDNA ends (5' rapid amplification of cDNA ends) revealed two major transcripts of GmNARK potentially originating from two TATA boxes. Further analysis of the GmNARK promoter has confirmed that these two TATA boxes are functional. Deletion analysis also located a region controlling phloem-specific expression to a DNA sequence between 908 bp and 1.7 kb upstream of the translation start site of GmNARK.
机译:大豆(Glycine max)的结节自动调节受体激酶(GmNARK)对于结瘤的全身自动调节至关重要。基于定量逆转录酶聚合酶链反应,GmNARK在整个植物中表达的水平各不相同;在成熟叶片和根中检测到高水平的转录本,而在幼叶,枝梢和根瘤中检出的水平较低。接种后第一周,日本根瘤菌对Bra本水平没有明显影响。另外,在稳定转化的大豆和大豆毛状根中检测了驱动β-葡萄糖醛酸苷酶(GUSPlus)报告基因的GmNARK和日本莲HAR1启动子的活性。携带1.7 kb GmNARKprGUS或2.0 kb LjHAR1prGUS构建体的日本血吸虫植物的组织化学GUS活性显然位于血管束内的活细胞中,尤其是叶,茎,根和根瘤中的韧皮部细胞。在携带这些构建体的大豆毛状根中也检测了韧皮部特异性表达。我们的研究表明,这些直系同源基因转录所需的调控元件是保守的。此外,5'cDNA末端的快速扩增(cDNA末端的5'迅速扩增)显示了GmNARK的两个主要转录本,它们可能源自两个TATA盒。对GmNARK启动子的进一步分析已确认这两个TATA盒具有功能。缺失分析还将控制韧皮部特异性表达的区域定位在GmNARK翻译起始位点上游908 bp和1.7 kb之间的DNA序列上。

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