...
首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Molecular cloning and expression analysis of an arginine decarboxylase gene from peach (Prunus persica).
【24h】

Molecular cloning and expression analysis of an arginine decarboxylase gene from peach (Prunus persica).

机译:桃(Prunus persica)精氨酸脱羧酶基因的分子克隆和表达分析。

获取原文
获取原文并翻译 | 示例
           

摘要

Arginine decarboxylase (ADC), one of the enzymes responsible for putrescine (Put) biosynthesis, has been shown to be implicated in stress response. In the current paper attempts were made to clone and characterize a gene encoding ADC from peach (Prunus persica (L.) Batsch, 'Akatsuki'). Rapid amplification of cDNA ends (RACE) gave rise to a full-length ADC cDNA (PpADC) with a complete open reading frame of 2178 bp, encoding a 725 amino acid polypeptide. Homology search and sequence multi-alignment demonstrated that the deduced PpADC protein sequence shared a high identity with ADCs from other plants, including several highly conservative motifs and amino acids. Southern blotting indicated that PpADC existed in peach genome as a single gene. Expression levels of PpADC in different tissues of peach (P. persica 'Akatsuki') were spatially and developmentally regulated. Treatment of peach shoots from 'Mochizuki' with exogenous 5 mM Put, an indirect product of ADC, remarkably induced accumulation of PpADC mRNA. Transcripts of PpADC in peach leaves from 'Mochizuki' were quickly induced, either transiently or continuously, in response to dehydration, high salinity (200 mM NaCl), low temperature (4 degrees C) and heavy metal (150 microM CdCl(2)), but repressed by high temperature 37 degrees C) during a 2-day treatment, which changed in an opposite direction when the stresses were otherwise removed with the exception of CdCl(2) treatment. In addition, steady-state of PpADC mRNA could be also transiently up-regulated by abscisic acid (ABA) in 'Mochizuki' leaves. All of these, taken together, suggest that PpADC is a stress-responsive gene and can be considered as a potential target that is genetically manipulated so as to create novel germplasms with enhanced stress tolerance in the future.
机译:精氨酸脱羧酶(ADC)是负责腐胺(Put)生物合成的酶之一,已被证明与应激反应有关。在当前的论文中,试图从桃(Prunus persica(L.)Batsch,“ Akatsuki”)克隆并表征编码ADC的基因。 cDNA末端的快速扩增(RACE)产生了全长ADC cDNA(PpADC),具有2178 bp的完整开放阅读框,编码725个氨基酸的多肽。同源搜索和序列多比对表明,推导的PpADC蛋白序列与其他植物的ADC具有高度同一性,包括几个高度保守的基序和氨基酸。 Southern印迹表明,PpADC作为单个基因存在于桃基因组中。 PpADC在桃(P. persica'Akatsuki')不同组织中的表达水平受到空间和发育的调节。 ADC的间接产物外源5 mM Put处理来自'Mochizuki'的桃芽,明显诱导了PpADC mRNA的积累。响应脱水,高盐度(200 mM NaCl),低温(4摄氏度)和重金属(150 microM CdCl(2))的响应,瞬间或连续快速诱导'Mochizuki'桃叶中的PpADC转录本。 ,但在2天的处理过程中受到高温(37摄氏度)的抑制,当以其他方式除去CdCl(2)处理的应力时,其方向相反。此外,脱落酸(ABA)在“ Mochizuki”叶片中也可以瞬时上调PpADC mRNA的稳态。所有这些加在一起,表明PpADC是一种应激反应基因,可以被认为是经过基因操作的潜在靶标,从而可以在将来创建具有增强的胁迫耐受性的新种质。

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