二穗短柄草RING Finger基因家族的鉴定及表达分析OA北大核心CSTPCD
Identification and Expression Analysis of the RING Finger Gene Family in Brachypodium distachyon
RING finger蛋白通常具有E3泛素连接酶活性,在调节植物生长发育和响应生物和非生物胁迫过程中具有重要作用.然而,目前对于二穗短柄草(Brachypodium distachyon)RING finger基因家族的研究非常有限.本研究利用生物信息学方法系统对二穗短柄草RING finger基因家族进行了系统分析,通过qPCR对其在干旱、盐和脱落酸(abscisic acid,ABA)胁迫处理下的表达进行了初步分析.结果表明,在二穗短柄草基因组中共鉴定到了666个RING finger基因,在5条染色体上不均匀分布,并发生了39次基因间的复制.系统进化分析将RING finger基因家族划分为9个亚族,每个亚族的成员同源性较高,并含有相似的保守结构域和基序.物种间的共线性分析显示,RING finger基因家族源自基因组复制,基因片段重复和串联重复在其扩张和进化中起关键作用.水稻(Oryza sativa)和二穗短柄草有303对RING finger共线性基因,而拟南芥(Arabidopsis thaliana)和二穗短柄草只有48对,在二穗短柄草基因组内则共有39对RING finger共线性基因.组织表达谱显示,共547个RING finger基因在二穗短柄草不同组织中表达,39.8%的基因在二穗短柄草雄花中高度表达.基因差异表达分析显示,29个RING finger基因可能参与到干旱、盐和ABA胁迫的应答反应.qPCR结果显示,共有26个RING finger基因在干旱胁迫中显著上调表达(P<0.05),3个RING finger基因下调表达;27个RING finger基因参与盐胁迫的上调表达,2个下调表达;在ABA胁迫下,15个RING finger基因上调表达,9个RING finger基因下调表达,5个RING finger基因表达水平和对照持平.本研究为揭示RING finger基因家族的功能、进化及其在调节干旱胁迫中的作用机制提供了理论依据.
RING finger proteins,which usually have E3 ubiquitin ligase activity,are important in regulating plant growth and development and in response to biotic and abiotic stresses.However,studies on the RING finger gene family of Brachypodium distachyon are limited.In this study,the RING finger gene family of B.distachyon was systematically analyzed using bioinformatics methods,and its expression under drought,salt,and abscisic acid(ABA)stress treatments was preliminarily analyzed by qPCR.The results showed that a total of 666 RING finger genes were identified in the B.distachyon genome,which were unevenly distributed on 5 chromosomes,and 39 intergenic duplications occurred.The phylogenetic analysis divided the RING finger gene family into 9 subclusters,and the members of each subcluster were highly homologous and contained similar conserved structural domains and motifs.The covariance analysis among species showed that the RING finger gene family originated from genome duplication,and that gene fragment duplications and tandem duplications played a key role in its expansion and evolution.There were 303 RING finger collinearity gene pairs in rice(Oryza sativa)and B.distachyon,whereas there were only 48 pairs in Arabidopsis thaliana and B.distachyon,and a total of 39 RING finger gene pairs in B.distachyon genomes.Tissue expression profiles showed that 547 RING finger genes were expressed in different tissues of B.distachyon,and 39.8%of the genes were highly expressed in male flowers of B.distachyon.Differential expression analysis showed that 29 RING finger genes might be involved in the response to drought,salt and abscisic acid(ABA)stress.qPCR results showed that 26 RING finger genes were significantly up-regulated in drought stress(P<0.05),3 RING finger genes were down-regulated,27 RING finger genes were up-regulated and 2 were down-regulated in salt stress;15 RING finger genes were up-regulated,9 RING finger genes were down-regulated,and 5 RING finger genes were at the same level as the control in ABA stress.The present study provides a theoretical basis for revealing the function and evolution of the RING finger gene family and its role in the regulation of drought stress.
曾德二;张丽萍;倪馨悦;徐丽;胡婧;赵杨子俊;魏和平
安庆师范大学生命科学学院,安庆 246133安庆市林业创新研究院,安庆 246000
农业科学
二穗短柄草RING Finger基因家族遗传进化干旱胁迫
Brachypodium distachyonRING FingerGene familyGenetic evolutionStress response
《农业生物技术学报》 2024 (006)
1316-1328 / 13
安徽省自然科学基金面上项目(1908085MC81)
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