韩新蕊1, 2,
袁欣2, 高杰2, 王亮生3, 王晓晖4, 贾文庆1*, 符真珠2*, 张和臣2*
收稿日期:
2025-01-15
修回日期:
2025-03-13
出版日期:
2025-03-18
发布日期:
2025-03-18
通讯作者:
贾文庆, 符真珠, 张和臣
基金资助:
国家自然科学基金(No.32030095)、河南省联合基金(No.242301420128)、河南省农业科学院创新团队项目(No.2024TD36)、河南省科技攻关项目“切花牡丹核心种质资源构建及应用”(No.242102110269)和中央引导计划项目(No.Z20241471128)
Xinrui Han1, 2, Xin Yuan2, Jie Gao2, Liangsheng Wang3, Xiaohui Wang4, Wenqing Jia1*, Zhenzhu Fu2*, Hechen Zhang2*
1Henan Institute of Science and Technology, Xinxiang 453003, China; 2Horticultural Research Institute, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China; 3Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China; 4Luoyang Academy of Agricultural and Forestry Sciences, Luoyang 471026, China
Received:
2025-01-15
Revised:
2025-03-13
Online:
2025-03-18
Published:
2025-03-18
Contact:
Wenqing Jia, Zhenzhu Fu, Hecheng Zhang
摘要: 为了研究TCP转录因子家族在牡丹(Paeonia sect. Moutan)花瓣呈色过程中的作用, 为牡丹花色改良和分子育种提供候选基因。本研究对牡丹TCP家族进行鉴定、生物信息学分析, 并对可能参与花色调控的基因TCP13、TCP15a进行功能分析。研究结果表明: 在3个牡丹基因组中共鉴定出26个TCP家族成员, 分为2个亚族3个亚类, 不规则的分布在5条染色体上; 不同成员的理化性质、基因结构存在差异, 但均含有TCP保守结构域。矮牵牛(Petunia hybrida)花瓣瞬时表达TCP13、TCP15a, 发现TCP13对MYB57诱导的紫色表型无明显作用, 而TCP15a可显著抑制; 荧光定量PCR分析表明, TCP15a可以显著抑制MYB57诱导浸染的花瓣组织内花青苷合成酶基因CHSa、DFR、ANS的表达。进一步通过蛋白互作鉴定发现, TCP15a与MBW蛋白复合体成员WD40-1、WD40-2互作。TCP15a通过与MYB57竞争与WD40的相互作用, 影响了MBW复合体的形成, 进而抑制了MYB57对花青苷合成酶基因的调控作用。本研究为深入研究牡丹TCP家族基因功能奠定理论基础, 为牡丹花色定向育种提供了有价值的线索。
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