生物技术通报2024,Vol.40Issue(2) :146-159.DOI:10.13560/j.cnki.biotech.bull.1985.2023-0676

'红满堂'苹果MbbZIP43基因的克隆与功能研究

Cloning and Functional Analysis of MbbZIP43 Gene in'Hongmantang'Red-flesh Apple

杨艳 胡洋 刘霓如 殷璐 杨锐 王鹏飞 穆霄鹏 张帅 程春振 张建成
生物技术通报2024,Vol.40Issue(2) :146-159.DOI:10.13560/j.cnki.biotech.bull.1985.2023-0676

'红满堂'苹果MbbZIP43基因的克隆与功能研究

Cloning and Functional Analysis of MbbZIP43 Gene in'Hongmantang'Red-flesh Apple

杨艳 1胡洋 1刘霓如 1殷璐 1杨锐 1王鹏飞 1穆霄鹏 1张帅 1程春振 1张建成1
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作者信息

  • 1. 山西农业大学园艺学院,太谷 030801
  • 折叠

摘要

[目的]为探究碱性亮氨酸拉链(bZIP)转录因子在'红满堂'苹果花青素代谢中的调控作用.[方法]从'红满堂'苹果克隆得到一个bZIP基因,分析了其基因及编码蛋白序列特性,利用洋葱表皮细胞瞬时转化确定其编码蛋白亚细胞定位,利用实时荧光定量PCR(RT-qPCR)研究了该基因在不同成熟时期'红满堂'果实中的表达情况,基于烟草叶片、苹果叶片以及苹果果实瞬时转化研究了其对花青素积累和花青素合成相关结构基因表达的调控作用.[结果]该基因不含内含子,与MdbZIP43(XP_008393381.1)相似度最高,故命名为MbbZIP43.其编码序列长为 522 bp,可编码由 173 aa组成、含有bZIP_plant_GBF1 结构域、定位于细胞核的亲水蛋白.RT-qPCR分析结果显示,随着果实成熟,MbbZIP43在'红满堂'果实中的表达水平呈"先升后降"的变化趋势,在花后 11 周的果实中表达量最高.相关性分析显示MbbZIP43 基因表达量与总黄酮和花青素含量正相关.瞬时过表达该基因的烟草叶片、苹果叶片和果皮中花青素含量分别提高了 17.42%、25.66%和 48.99%,过表达MbbZIP43的苹果叶片中花青素合成结构基因CHI、F3'H、DFR和UFGT分别提高了 2.27 倍、1.84 倍、2.39 倍和 2.89 倍;过表达MbbZIP43 的苹果果皮中CHI、F3'H、DFR和UFGT分别提高了 1.79 倍、1.70 倍、1.35 倍和 1.51 倍,说明MbbZIP43 可以通过上调这些结构基因的表达正调控苹果花青素合成.[结论]MbbZIP43 可通过激活花青素合成相关结构基因CHI和UFGT等的表达进而促进花青素的积累.

Abstract

[Objective]To investigate the regulatory role of basic leucine zipper(bZIP)transcription factors in anthocyanin metabolism in'Hongmantang'apple.[Method]We cloned a bZIP gene from'Hongmantang'red-flesh apple,analyzed it and its sequence characteristics,studied the subcellular localization of its encoded protein using onion epidermis cell transient overexpression,and investigated its expression pattern in'Hongmantang'red-flesh apple fruits at different ripening stages using quantitative real time PCR(RT-qPCR).Furthermore,we explored its regulatory roles in the expressions of genes related to anthocyanin accumulation and biosynthesis based on the transient overexpression experiments in tobacco leaves,apple leaves and fruits.[Result]This bZIP gene was intron-less and shared the highest similarity with MdbZIP43(XP_008393381.1),thus was named as MbbZIP43.Its coding sequence was 522 bp,which encoded a 173 aa hydrophilic nucleus-localized protein with conserved bZIP_plant_GBF1 domain.RT-qPCR analysis revealed that MbbZIP43 showed a'rise-fall'expression change pattern in'Hongmantang'fruits during ripening,with the highest expression in the fruits at 11 weeks post flowering.Correlation analysis results showed that MbbZIP43 expression was positively correlated with the total flavonoids and anthocyanin contents in'Hongmantang'fruits,indicating that it might play regulatory roles in flavonoid biosynthesis.Consistently,transient overexpression of MbbZIP43 improved significantly the anthocyanin accumulations by 17.42%,25.66%and 48.99%in tobacco leaves,apple leaves and apple fruits,respectively.Moreover,RT-qPCR analysis results showed that,compared to the empty vector control,the expressions of anthocyanin biosynthesis related structural genes(CHI,F3'H,DFR and UFGT)in the apple leaves overexpressing MbbZIP43 were up-regulated by 2.27-,1.84-,2.39-and 2.89-fold,respectively.And their expressions in the peels of apple fruits overexpressing MbbZIP43 were up-regulated by 1.79-,1.70-,1.35-and 1.51-fold,respectively.These results indicated that the gene's transient overexpression may improve anthocyanin accumulation by activating the expressions of the anthocyanin biosynthesis related structural genes.[Conclusion]MbbZIP43 can promote anthocyanins accumulation by activating the expression of anthocyanin biosynthesis related structural genes,including CHI,UFGT and so on.

关键词

bZIP转录因子/苹果/花青素合成调控/基因克隆/瞬时转化/表达分析/亚细胞定位

Key words

bZIP transcription factor/apple/regulation to anthocyanin biosynthesis/gene cloning/transient overexpression/expression analysis/subcellular localization

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基金项目

山西省科技重大专项计划"揭榜挂帅"项目(202201140601027)

山西省果树产业技术体系项目(2023CYJSTX07)

出版年

2024
生物技术通报
中国农业科学院农业信息研究所

生物技术通报

CSTPCDCSCD北大核心
影响因子:0.505
ISSN:1002-5464
参考文献量56
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