花生中6个ERF家族蛋白基因的克隆及非生物胁迫下的表达模式分析

来源 :中国作物学会油料作物专业委员会第七次会员代表大会暨学术年会 | 被引量 : 0次 | 上传用户:cooltcp
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  ERF家族蛋白在植物对低温、干旱及高盐胁迫的响应中具有重要的转录调控作用.然而花生中至今还没有有关该家族蛋白的报道.本研究从花生的cDNA文库中找到了40个编码AP2/ERF家族蛋白的EST序列,并对其中6个进行了基因全长的克隆.序列分析表明这6个基因编码的蛋白均只包含一个AP2/ERF保守结构域,属于ERF亚家族.6个基因分别命名为Arachis hypogaea ERF l-6(AhERF1-6).同时我们分析了这6个基因在低温、高盐和干旱胁迫下的表达模式.实验结果表明,AhERF4和AhERF6的表达对非生物胁迫具有快速明显的响应;AhERF1和AhERF5的转录在某些胁迫下略有提高.还有一些基因如盐处理叶片中AhERF3和干旱处理的叶片中AhERF2在胁迫下表达量有所降低.AhERF3和AhERF5则在花生干旱处理的叶片和根中表现出了相反的表达模式.以上结果表明不同的ERF蛋白在花生对非生物胁迫适应性中可能具有不同的功能.
其他文献
It is critical to develop a cost-effective quantitative/semiquantitative assay for rapid diagnosis and on-site detection of toxic or harmful substances.Here, a naked-eye based semiquantitative immunoc
We screened and established seven hybridoma cell lines that secrete anti-aflatoxin monoclonal antibodies with different sensitivities.Among these antibodies, 1 C11 exhibited the highest sensitivity ag
会议
Mycotoxin contamination in the food chain has caused serious health issues in humans and animals.Thus, a rapid on-site and lab-independent detection method for mycotoxins, such as aflatoxins (AFTs), i
The method of headspace coupled with comprehensive two-dimensional GC-time-of-flight MS (HS-GC × GC-TOF/MS) was applied to differentiate the volatile flavor compounds of three types of pure vegetable
The failure of peg penetration into the soil leads to seed abortion in peanut.Knowledge of genes involved in these processes is comparatively deficient.Here, we used RNA-seq to gain insights into tran
The peanut (Arachis hypogaea) is an important oil crop.Breeding for high oil content is becoming increasingly important.Wild Arachis species have been reported to harbor genes for many valuable traits
Although an important oil crop, peanut has only 162,030 expressed sequence tags (ESTs) publicly available, 86,943 of which are from cultivated plants.More ESTs from cultivated peanuts are needed for i
溶血磷脂酸酰基转移酶(LPAT)是植物油脂合成途径的关键酶,负责催化溶血磷脂酸(LPA)生成磷脂酸(PA)的反应.植物LPAT的编码基因是提高油料作物含油量和改良油脂组成的重要候选基因.本研究通过构建花生种子cDNA文库,采用RACE技术,克隆了花生AhLPA T4基因.该基因全长1631bp,编码一条383个氨基酸组成的多肽,预测分子量为43.8kD.AhLPAT4蛋白含有一个典型的酰基转移酶保
运用近红外技术,从油酸含量为44.2%的传统出口型大花生品种鲁丰2号EMS浸种诱变群体中筛选出油酸含量高达64.2%的突变体E2-4-83-12.FAD2基因克隆和序列分析表明,该突变体AD2B基因编码区第313位C碱基突变成T碱基,导致所编码的氨基酸第105为组氨酸突变成酪氨酸.该突变为新突变,其导致的氨基酸变化发生于第一个组氨酸盒内,进一步通过酵母表达系统检测了FAD2B基因活性.突变型FAD