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2025年5月11日 星期日
农业生物技术学报  2023, Vol. 31 Issue (12): 2674-2684    DOI: 10.3969/j.issn.1674-7968.2023.12.021
  研究资源与技术改进 本期目录 | 过刊浏览 | 高级检索 |
梅花花色合成基因的qPCR内参基因筛选及验证
叶勇1, Henry Lusekelo INGWE1, 郑子飞1, 陈樱之1, 赵宏波1,2, 董彬1,2,*
1 浙江农林大学 风景园林与建筑学院,杭州 311300;
2 浙江农林大学 浙江省园林植物种质创新与利用重点实验室,杭州 311300
Screening and Validation of Reference Genes for qPCR Analysis of Flower Color Synthesis Genes in Prunus mume
YE Yong1, Henry Lusekelo INGWE1, ZHENG Zi-Fei1, CHEN Ying-Zhi1, ZHAO Hong-Bo1,2, DONG Bin1,2,*
1 School of Landscape Architecture, Zhejiang A&F University, Hangzhou 311300, China;
2 Zhejiang Provincial Key Laboratory of Germplasm Innovation and Utilization for Garden Plants, Zhejiang A&F University, Hangzhou 311300, China
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摘要 梅花(Prunus mume)是中国十大传统名花之一,园林应用广泛。随着梅花分子生物学研究的不断深入,筛选出适用于梅花花色合成基因qPCR分析的内参基因至关重要。本研究选择3个不同色系的共计6个梅花栽培品种,进行花色表型分析和花青素含量测定,发现花青素含量与梅花花瓣的颜色呈正相关。同时,利用qPCR技术,在梅花不同色系品种间对14个候选内参基因的表达进行检测,使用3种软件geNorm、NormFinder、BestKeeper和ΔCt方法进行表达稳定性分析,最后用RefFinder程序综合分析,得出最佳内参基因,并利用花青素合成相关基因进行验证。实验结果表明,3-磷酸甘油醛脱氢酶(glyceraldehyde-3-phosphate dehydrogenase, GAPDH)和肌动蛋白1 (actin 1, ACT1)表达最为稳定,ACT3表达最不稳定。验证结果表明,以GAPDHACT1为内参基因时,花青素合成相关基因的表达模式相近,较多基因呈现显著的差异表达;当以ACT3作为内参基因时,花青素合成相关基因的表达模式与GAPDHACT1为内参基因的结果不同,而且只有少数基因呈现显著的差异表达。本研究为深入开展梅花花色合成相关基因的表达模式分析提供基础资料。
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叶勇
Henry Lusekelo INGWE
郑子飞
陈樱之
赵宏波
董彬
关键词 梅花qPCR内参基因花青素    
AbstractPrunus mume, one of the top 10 traditional famous flowers in China, is widely used in gardens. With the development of molecular biology research of P. mume, it is very important to screen reference genes suitable for qPCR analysis of flower color synthesis genes in P. mume. In this study, a total of 6 P. mume cultivars of 3 different color lines were selected for flower color phenotypic analysis and anthocyanin content determination, and it was found that anthocyanin content was positively correlated with the color of P. mume petals. Meanwhile, the expression of 14 candidate reference genes was detected among different color varieties of P. mume using qPCR, and their expression stability was analyzed using 3 software (including geNorm, NormFinder, BestKeeper) and ΔCt method. Finally, the best reference gene was synthesized using the RefFinder program and validated using genes related to anthocyanin synthesis. The experimental results showed that the expression of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and actin 1 (ACT1) were the most stable and ACT3 was the least stable. The validation results showed that when GAPDH and ACT1 were used as reference genes, the expression patterns of anthocyanin synthesis-related genes were similar, and more genes showed significant differential expression; when ACT3 was used as reference gene, the expression patterns of anthocyanin synthesis-related genes were different from the results of GAPDH and ACT1 as reference genes, and only a few genes showed significant differential expression. This study provides basic data for in-depth analysis of the expression patterns of genes related to flower color synthesis.
Key wordsPrunus mume    qPCR    Reference gene    Anthocyanin
收稿日期: 2023-02-24     
ZTFLH:  S685.17  
基金资助:国家重点研发计划(2019YFD1001500; 2018YFD100400); 浙江省农业(花卉新品种选育)新品种选育重大科技专项(2021C02071)
通讯作者: *dongbin@zafu.edu.cn   
引用本文:   
叶勇, Henry Lusekelo INGWE, 郑子飞, 陈樱之, 赵宏波, 董彬. 梅花花色合成基因的qPCR内参基因筛选及验证[J]. 农业生物技术学报, 2023, 31(12): 2674-2684.
YE Yong, Henry Lusekelo INGWE, ZHENG Zi-Fei, CHEN Ying-Zhi, ZHAO Hong-Bo, DONG Bin. Screening and Validation of Reference Genes for qPCR Analysis of Flower Color Synthesis Genes in Prunus mume. 农业生物技术学报, 2023, 31(12): 2674-2684.
链接本文:  
https://journal05.magtech.org.cn/Jwk_ny/CN/10.3969/j.issn.1674-7968.2023.12.021     或     https://journal05.magtech.org.cn/Jwk_ny/CN/Y2023/V31/I12/2674
 
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