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水曲柳FmPIF基因家族克隆及表达模式分析
引用本文:吕义品,梁楠松,宋婷婷,崔靖弘,于磊,詹亚光.水曲柳FmPIF基因家族克隆及表达模式分析[J].北京林业大学学报,2022,44(1):58-68.
作者姓名:吕义品  梁楠松  宋婷婷  崔靖弘  于磊  詹亚光
作者单位:东北林业大学“东北盐碱植被恢复与重建”教育部重点实验室,东北林业大学生命科学学院,黑龙江 哈尔滨 150040
基金项目:黑龙江省应用技术研究与开发计划项目(GA19B201)。
摘    要:目的]探究水曲柳光敏色素互作因子(FmPIFs)在激素调控与非生物胁迫应答过程中的重要作用,为揭示水曲柳抗逆分子机制和制定林木遗传育种策略提供理论依据.方法]在水曲柳中克隆FmPIFs基因,并对其基因结构、蛋白质理化性质、保守基序、系统进化关系等进行生物信息学分析.采用qRT-PCR方法分析水曲柳中FmPIFs基因...

关 键 词:水曲柳  光敏色素互作因子  基因克隆  生物信息分析  表达模式
收稿时间:2020-12-01

Cloning and expression pattern analysis of FmPIF gene family in Fraxinus mandshurica
Lü Yipin,Liang Nansong,Song Tingting,Cui Jinghong,Yu Lei,Zhan Yaguang.Cloning and expression pattern analysis of FmPIF gene family in Fraxinus mandshurica[J].Journal of Beijing Forestry University,2022,44(1):58-68.
Authors:Lü Yipin  Liang Nansong  Song Tingting  Cui Jinghong  Yu Lei  Zhan Yaguang
Institution:Key Laboratory of Saline-Alkali Vegetation Ecology Restoration of Ministry of Education, College of Life Science,Northeast Forestry University, Harbin 150040, Heilongjiang, China
Abstract:  Objective  This paper aims to explore the important role of Fraxinus mandshurica phytochrome interaction factors (PIFs) in the process of hormone regulation and abiotic stress response, and provide theoretical basis for revealing the molecular mechanism of Fraxinus mandshurica resistance and formulating forest genetic breeding strategies.   Method  The FmPIFs gene was cloned from Fraxinus mandshurica, and its gene structure, protein physicochemical properties, conserved motifs, and phylogenetic relationships were analyzed by bioinformatics. The qRT-PCR method was used to analyze the expression patterns of FmPIFs genes in Fraxinus mandshurica in different tissues and under different hormones and stress conditions.   Result  Five members of FmPIFs gene family of Fraxinus mandshurica were obtained and named as FmPIF1, FmPIF3, FmPIF4, FmPIF7 and FmPIF8. The corresponding proteins were all hydrophilic and unstable proteins, all of which were located in the nucleus. The results of multiple sequence alignment showed that FmPIFs all had APB conserved domains, and members FmPIF1 and FmPIF3 had unique APA domains. Tissue-specific analysis showed that FmPIFs were all expressed in leaves at the highest level, and member FmPIF8 expressed at the highest level, which was 3.96 times of control. However, it was expressed in a small amount in the stem, and the highest expression in stem was FmPIF3, which was only 0.21 time of control. The expression in root was extremely low. Stress response analysis showed that FmPIFs positively regulated the resistance of Fraxinus mandshurica plants to salt, alkali and drought stress, while negatively regulated plant cold resistance. The member FmPIF3 responded significantly to cold and salt stress, and the expression of FmPIF8 was significantly up-regulated under alkali stress, the expression of FmPIF1 was significantly up-regulated under drought stress. In the hormone response results, FmPIFs hadrelatively consistent responses to abscisic acid (ABA), salicylic acid (SA) and gibberellin (GA3), while responses to auxin (IAA) and methyl jasmonate (MeJA) existed difference. FmPIF1 responded violently after MeJA application and its expression was significantly up-regulated, FmPIF7 was significantly up-regulated after SA treatment, and FmPIF3 and FmPIF4 were significantly up-regulated after GA3 treatment.   Conclusion  FmPIFs show high consistency in gene and protein structure. RT-qPCR results show that FmPIFs express the highest amount in the leaves of Fraxinus mandshurica. FmPIFs are induced to express by salt, alkali, drought and cold stress, and most of the expression patterns are similar. FmPIFs also play an important role in the regulation of Fraxinus mandshurica in response to IAA, ABA, MeJA, SA and GA3 hormones. 
Keywords:Fraxinus mandschurica  phytochrome interacting factor  gene clone  bioinformatics analysis  expression pattern
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