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苦荞转录因子基因FtNAC16的克隆、亚细胞定位及表达分析OACSTPCD

Cloning,Subcellular Localization and Expression Analysis of the Transcription Factor Gene FtNAC16 in Fagopyrum tataricum

中文摘要英文摘要

NAC(petunia NAM and Arabidopsis thaliana ATAF1,ATAF2,and CUC2)转录因子在植物次生壁加厚过程中具有重要调控作用.为探究苦荞(Fagopyrum tataricum)中NAC转录因子在果壳次生壁形成中的功能和分子机制,本研究采用逆转录PCR(reverse transcription,RT-PCR)技术从苦荞中克隆到1个参与调控苦荞果壳细胞次生壁合成的NAC转录因子基因,命名为FtNAC16.对FtNAC16进行生物信息学、亚细胞定位及基因表达等分析,结果表明,FtNAC16(GenBank No.OR723785)全长CDS序列为1 086 bp,编码361个氨基酸.对FtNAC16进行蛋白多序列比对和系统进化树分析,结果表明,FtNAC16是NAC转录因子家族成员,且与拟南芥(A.thaliana)中调控次生壁加厚的AtNST2(NAC secondary wall thickening)亲缘关系最近.亚细胞定位显示,FtNAC16定位于细胞核.基因表达分析表明,FtNAC16主要在根、茎、花和早期发育的籽粒中高表达.此外,在厚壳苦荞和薄壳苦荞不同发育时期籽粒中的表达分析表明,FtNAC16在厚壳苦荞和薄壳苦荞中具有相似的表达模式,即其表达呈先增后减趋势,且在授粉后7d籽粒中表达量最高,在籽粒发育早期,FtNAC16在厚壳苦荞中的表达量显著高于薄壳苦荞.进一步表达分析显示,次生壁形成的下游调控基因FtMYB103与纤维素合成酶4(cellulose synthase 4,FtCESA4)和FtCESA8在厚壳苦荞和薄壳苦荞不同发育时期籽粒中的表达与FtNAC16高度正相关.推测FtNAC16可能通过正向调控苦荞次生壁生物合成相关的基因表达,进一步调控苦荞发育过程中不同组织部位尤其是苦荞果壳细胞次生壁的生物合成.本研究为培育高产、优质、适应性强的薄壳苦荞新品种提供优异的基因资源和理论依据.

NAC(petunia NAM and Arabidopsis thaliana ATAF1,ATAF2,and CUC2)transcription factors play important regulatory roles in plant secondary wall thickening.In order to explore the function and molecular mechanism of NAC transcription factor in the formation of secondary wall of tartary buckwheat(Fagopyrum tataricum),reverse transcription PCR(RT-PCR)was used to clone a candidate NAC transcription factor previously identified by comparative transcriptome,named FtNAC16,which might be involved in regulating the synthesis of secondary wall of tartary buckwheat shell cells.Then the bioinformatics,subcellular localization and gene expression analysis of FtNAC16 were conducted.As results,the CDS length of FtNAC16(GenBank No.OR723785)was 1 086 bp and it encoded 361 amino acids.Multiple sequence alignment and phylogenetic tree analysis indicated that FtNAC16 belonged to the NAC transcription factor family and was closely related to AtNST2(NAC secondary wall thickening),which regulated secondary wall thickening in Arabidopsis thaliana.Subcellular localization showed that FtNAC16 was located in the nucleus.Gene expression analysis suggested that FtNAC16 was highly expressed in roots,stems,flowers and early developing grains with high cellulose content.In addition,the expression analysis of FtNAC16 in thick shell tartary buckwheat and thin shell tartary buckwheat at different developmental stages showed a similar expression pattern,with a trend of increasing and then decreasing,and the highest expression was observed at 7 d after pollination.However,the expression of FtNAC16 in thick shell tartary buckwheat was significantly higher than that in thin shell tartary buckwheat at early stage of development.Further expression analysis revealed that the expression of the downstream regulatory gene FtMYB103,cellulose synthase 4(FtCESA4)and FtCESA8 involved in cellulose synthesis were highly positively correlated with FtNAC16 in the grains of thick shell tartary buckwheat and thin shell tartary buckwheat at different developmental stages.All these results suggested that FtNAC16 was a nucleo-specific NAC transcription factor,which may positively regulate the biosynthesis of secondary walls by positively regulating the expression of genes further related to the biosynthesis of cell secondary walls of tartary buckwheat in different tissue parts,especially in the fruit shell cells.It provides excellent genetic resources and theoretical basis for breeding new varieties of buckwheat with high yield,high quality and strong adaptability.

柯瑾;陈庆富;李洪有

贵州师范大学生命科学学院/荞麦产业技术研究中心,贵阳 550001

农业科学

苦荞NAC转录因子FtNAC16基因克隆亚细胞定位表达分析

Fagopyrum tataricumNAC transcription factorFtNAC16Gene cloningSubcellular localizationExpression analysis

《农业生物技术学报》 2024 (001)

新类型易脱壳苦荞薄壳特性的细胞学、转录组学及遗传定位研究

39-49 / 11

国家自然科学基金(32260461;31860408);国家燕麦荞麦现代农业产业技术体系专项资金(CARS-07-A5);国家基金委-贵州喀斯特中心重大研发计划项目(U1812401);贵州省科技计划(黔科合基础-ZK[2021]重点035);云南省重大科技专项计划(202202AE090020)

10.3969/j.issn.1674-7968.2024.01.004

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