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转录因子 GhTCP7 通过与拟南芥 WIP 型锌指蛋白 GhWIP2 互作抑制非洲菊花瓣的伸展。

The transcription factor GhTCP7 suppresses petal expansion by interacting with the WIP-type zinc finger protein GhWIP2 in Gerbera hybrida.

机构信息

State Key Laboratory of Conservation and Utilization of Bio-Resources in Yunnan, Center for Life Sciences, School of Life Sciences, Yunnan University, Kunming, Yunnan 650091, China.

Key Laboratory of Southern Subtropical Plant Diversity, Fairy Lake Botanical Garden, Shenzhen & Chinese Academy of Sciences, Shenzhen, Guangdong 518004, China.

出版信息

J Exp Bot. 2023 Aug 3;74(14):4093-4109. doi: 10.1093/jxb/erad152.

Abstract

Petal size is a critical factor in plant reproduction and horticulture, and is largely determined by cell expansion. Gerbera hybrida is an important horticultural plant and serves as a model for studying petal organogenesis. We have previously characterized GhWIP2, a Trp-Ile-Pro (WIP)-type zinc protein, that constrains petal size by suppressing cell expansion. However, the underlying molecular mechanism remains largely unclear. Using yeast two-hybrid screening, bimolecular fluorescence complementation, and co-immunoprecipitation, we identified a TEOSINTE BRANCHED1/CYCLOIDEA/PROLIFERATING CELL FACTOR (TCP) family transcription factor, GhTCP7, that interacts with GhWIP2 both in vitro and in vivo. Using reverse genetic approaches, we elucidated the function of the GhTCP7-GhWIP2 complex in controlling petal expansion. GhTCP7 overexpression severely reduced cell expansion and petal size, whereas GhTCP7 silencing resulted in increased cell expansion and petal size. GhTCP7 showed similar expression patterns to GhWIP2 in various types of G. hybrida petals. We further identified GhIAA26, which encodes an auxin signalling regulator, that is activated by the GhTCP7-GhWIP2 complex, leading to the suppression of petal expansion. Our findings reveal a previously unknown transcriptional regulatory mechanism that involves protein-protein interactions between two different transcription factor families to activate a negative regulator of petal organogenesis.

摘要

花瓣大小是植物繁殖和园艺学的关键因素,主要由细胞扩张决定。大丁草是一种重要的园艺植物,可作为研究花瓣器官发生的模型。我们之前已经对 GhWIP2 进行了特征描述,它是一种 Trp-Ile-Pro (WIP)- 型锌蛋白,通过抑制细胞扩张来限制花瓣大小。然而,其潜在的分子机制在很大程度上仍不清楚。通过酵母双杂交筛选、双分子荧光互补和共免疫沉淀,我们鉴定了一个 TEOSINTE BRANCHED1/CYCLOIDEA/PROLIFERATING CELL FACTOR (TCP) 家族转录因子 GhTCP7,它在体外和体内都与 GhWIP2 相互作用。通过反向遗传学方法,我们阐明了 GhTCP7-GhWIP2 复合物在控制花瓣扩张中的功能。GhTCP7 的过表达严重减少了细胞扩张和花瓣大小,而 GhTCP7 的沉默导致细胞扩张和花瓣大小增加。GhTCP7 在各种类型的大丁草花瓣中的表达模式与 GhWIP2 相似。我们进一步鉴定了 GhIAA26,它编码一个生长素信号调节剂,被 GhTCP7-GhWIP2 复合物激活,导致花瓣扩张受到抑制。我们的研究结果揭示了一个以前未知的转录调控机制,涉及两个不同转录因子家族之间的蛋白-蛋白相互作用,以激活花瓣器官发生的负调节剂。

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