首页> 外文期刊>Journal of Plant Biochemistry and Biotechnology >Differential expression of two members of the nuclear gene family encoding arginine decarboxylase in tobacco (Nicotiana tabacum L)
【24h】

Differential expression of two members of the nuclear gene family encoding arginine decarboxylase in tobacco (Nicotiana tabacum L)

机译:烟草(Nicotiana tabacum L)中编码精氨酸脱羧酶的两个核基因家族成员的差异表达

获取原文
获取原文并翻译 | 示例
           

摘要

Two nuclear genes (NtADC-1 and Nt ADC-2) encoding arginine decarboxylase (ADC, EC 4.1.1.19) have been characterized from Nicotiana tabacum cv Xanthi and their differential expression during development analyzed. The two nuclear genes are 95% identical in nucleotide sequence within their coding and 5'-and 3'-noncoding regions. Both genes contain a single open reading frame, uninterrupted by introns, encoding proteins of 720 (ADC1) and 721 (ADC2) amino acids. The predicted amino acid sequence of ADC1 is identical to that encoded by the cDNA PR24 previously isolated from N. tabacum cv Burley 21, and differs at 22 amino acids residues from ADC2 (96.4% identical). Transcripts encoding ADC1 and ADC2 are expressed predominantly in the root and floral tissues of wild-type tobacco plants. A small, transient increase in ADC transcript abundance is observed in the roots of wild-type Burley 21 tobacco within 24 h after topping (i.e., removal of the floral meristem and upper leaves and stem). Low alkaloid (nic1 nic2) mutants subjected to the same treatment showed no induction in ADC expression. Using semi-quantitative RT-PCR analysis and synthetic oligonucleotide primers capable of distinguishing between the two different ADC transcripts, it has been shown that NtADC2 is preferentially expressed in roots and accounts for the major portion of ADC transcripts present.
机译:从烟草(Nicotiana tabacum)cv Xanthi鉴定了编码精氨酸脱羧酶(ADC,EC 4.1.1.19)的两个核基因(NtADC-1和Nt ADC-2),并分析了它们在发育过程中的差异表达。这两个核基因在其编码区和5'-和3'-非编码区的核苷酸序列中95%相同。这两个基因都包含一个单一的开放阅读框,不受内含子干扰,编码720(ADC1)和721(ADC2)个氨基酸的蛋白质。 ADC1的预测氨基酸序列与先前从烟草(N.tabacum cv Burley)21中分离的cDNA PR24编码的序列相同,并且与ADC2的22个氨基酸残基不同(96.4%相同)。编码ADC1和ADC2的转录物主要在野生型烟草植物的根和花组织中表达。摘心后24小时内(即去除花分生组织,上部叶和茎)在野生型白肋烟21烟草的根中观察到ADC转录丰度有短暂的瞬时增加。接受相同处理的低生物碱(nic1 nic2)突变体在ADC表达中未显示出诱导作用。使用半定量RT-PCR分析和能够区分两个不同ADC转录物的合成寡核苷酸引物,已显示NtADC2在根中优先表达,并占存在的ADC转录物的主要部分。

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