梅花PmERF4基因的克隆及其表达分析
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贵州省科技支撑计划([2018]2302);贵州省教育厅青年科技人才成长项目([2017]112)


Cloning and expression of PmERF4 gene in Prunus mume
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    摘要:

    为阐明梅花(Prunus mume)ERF基因的功能,采用RTPCR技术从梅花品种‘雪梅’中克隆获得1个PmERF4基因。生物信息学分析表明该基因cDNA全长序列为842 bp,完整开放阅读框(ORF)为690 bp,编码229个氨基酸。氨基酸序列比对发现,PmERF4蛋白包含1个AP2/ERF保守结构域。系统进化分析结果显示,梅花PmERF4蛋白与李亚科李属植物的ERF蛋白高度同源。利用荧光定量PCR(qRTPCR)检测PmERF4基因在非生物胁迫和激素处理下的表达,结果表明:PmERF4基因受低温、氧化胁迫的诱导,但响应程度不同,它能够持续且强烈地响应低温胁迫,对甘露醇、MeJA、SA处理不敏感,而高盐和ABA则抑制其表达;PmERF4基因可能在梅花低温胁迫应答中发挥重要作用。

    Abstract:

    ERF (ethylene response factor) transcription factor plays a critical role in response to environmental stress and hormonal signal transduction in plants.To elucidate the function of ERF gene in Prunus mume,the PmERF4 gene was cloned from a Prunus mume ‘Xuemei’ by RTPCR.The fulllength cDNA sequence of PmERF4 was 842 bp with an open reading frame (ORF) of 690 bp,encoding 229 amino acids.The deduced amino acid sequence alignment of PmERF4 contained a conserved AP2/ERF domain.The result of phylogenetic analysis showed the PmERF4 was highly homologous to other proteins in Prunus genus.qRTPCR was conducted to examine the expression patterns of PmERF4 under abiotic stress and hormone treatment.The results showed that PmERF4 was induced by cold and H2O2 stress.The induction levels of the gene were different between cold and H2O2 stress.A continuous and strong response of PmERF4 was triggered by cold.PmERF4 was insensitive to mannitol,MeJA and SA treatment and its expression was inhibited by NaCl and ABA.It is indicated that PmERF4 from Prunus mume may be involved in response to cold and H2O2 stress.

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彭婷,冯蓝萍,王艺琴,任静,包满珠,张俊卫.梅花PmERF4基因的克隆及其表达分析[J].华中农业大学学报,2019,38(4):

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  • 收稿日期:2019-02-26
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  • 在线发布日期: 2019-06-25
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