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矮牵牛花朵衰老过程中PhEOL1和PhEOL2的表达及功能分析

Expression and functional analysis of PhEOL1 and PhEOL2 during flower senescence in petunia.

作者信息

Liu Juanxu, Zhao Ji, Xiao Zhina, Chang Xinlei, Chen Guoju, Yu Yixun

机构信息

Guangdong Key Laboratory for Innovative Development and Utilisation of Forest Plant Germplasm, College of Forestry and Landscape Architecture, South China Agricultural University, Guangzhou 510642, China.

College of Horticulture, South China Agricultural University, Guangzhou 510642, China.

出版信息

Funct Plant Biol. 2016 May;43(5):413-422. doi: 10.1071/FP15311.

Abstract

The ethylene biosynthesis pathway controls flower senescence. Previous studies have shown that Arabidopsis ETHYLENE-OVERPRODUCER1 (ETO1) interacts specifically with and negatively regulates type 2 1-aminocyclopropane-1-carboxylate synthases (ACSs), the rate-limiting enzymes of ethylene biosynthesis. The ethylene biosynthesis pathway controls flower senescence in petunias (Petunia hybrida Juss.). However, the role of ETO1-like genes (EOLs) during flower senescence has not been investigated. Here, two full-length petunia EOL cDNAs, PhEOL1 and PhEOL2, were isolated. RT-PCR assays indicated that the expression of PhEOL1 and PhEOL2 increased after exogenous ethylene treatment. The VIGS-mediated silencing of PhEOL1 accelerated flower senescence and produced more ethylene than the control condition, whereas the silencing of PhEOL2 did not. Notably, the effects caused by PhEOL1 suppression were not enhanced by PhEOL2 suppression in corollas. In addition, the expression of two petunia type 2 PhACS genes increased during flower senescence and after ethylene treatment. A yeast two-hybrid assay showed that PhEOL1 interacts with both PhACS2 and PhACS3. It is possible that PhEOL1 is involved in flower senescence by interacting with type 2 PhACSs in petunias.

摘要

乙烯生物合成途径控制花朵衰老。先前的研究表明,拟南芥乙烯过量产生1(ETO1)与乙烯生物合成的限速酶——2型1-氨基环丙烷-1-羧酸合成酶(ACSs)特异性相互作用并对其起负调控作用。乙烯生物合成途径控制矮牵牛(Petunia hybrida Juss.)的花朵衰老。然而,类ETO1基因(EOLs)在花朵衰老过程中的作用尚未得到研究。在此,分离出了两个矮牵牛EOL全长cDNA,即PhEOL1和PhEOL2。RT-PCR分析表明,外源乙烯处理后PhEOL1和PhEOL2的表达增加。VIGS介导的PhEOL1沉默加速了花朵衰老,并且比对照条件下产生了更多的乙烯,而PhEOL2的沉默则没有这种现象。值得注意的是,在花冠中,PhEOL2的抑制并没有增强PhEOL1抑制所产生的效果。此外,两个矮牵牛2型PhACS基因的表达在花朵衰老期间以及乙烯处理后增加。酵母双杂交试验表明,PhEOL1与PhACS2和PhACS3都相互作用。PhEOL1有可能通过与矮牵牛中的2型PhACSs相互作用而参与花朵衰老过程。

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