College of Horticulture, Northwest A&F University, Yangling, Shaanxi 712100, China.
State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China; China National Botanical Garden, Beijing 100093, China; Department of Computational and Systems Biology, John Innes Centre, Norwich Research Park, Colney Lane, Norwich NR4 7UH, UK.
Curr Biol. 2024 Feb 26;34(4):755-768.e4. doi: 10.1016/j.cub.2024.01.004. Epub 2024 Jan 24.
During the process of flower opening, most petals move downward in the direction of the pedicel (i.e., epinastic movement). In most Delphinium flowers, however, their two lateral petals display a very peculiar movement, the mirrored helical rotation, which requires the twist of the petal stalk. However, in some lineages, their lateral petals also exhibit asymmetric bending that increases the degree of mirrored helical rotation, facilitating the formation of a 3D final shape. Notably, petal asymmetric bending is a novel trait that has not been noticed yet, so its morphological nature, developmental process, and molecular mechanisms remain largely unknown. Here, by using D. anthriscifolium as a model, we determined that petal asymmetric bending was caused by the localized expansion of cell width, accompanied by the specialized array of cell wall nano-structure, on the adaxial epidermis. Digital gene analyses, gene expression, and functional studies revealed that a class I homeodomain-leucine zipper family transcription factor gene, DeanLATE MERISTEM IDENTITY1 (DeanLMI1), contributes to petal asymmetric bending; knockdown of it led to the formation of explanate 2D petals. Specifically, DeanLMI1 promotes cell expansion in width and influences the arrangement of cell wall nano-structure on the localized adaxial epidermis. These results not only provide a comprehensive portrait of petal asymmetric bending for the first time but also shed some new insights into the mechanisms of flower opening and helical movement in plants.
在花朵开放的过程中,大多数花瓣沿花梗(即内卷运动)方向向下移动。然而,在大多数飞燕草花朵中,它们的两个侧花瓣呈现出一种非常特殊的运动,即镜像螺旋旋转,这需要花瓣茎的扭曲。然而,在一些谱系中,它们的侧花瓣也表现出不对称弯曲,增加了镜像螺旋旋转的程度,从而促进了 3D 最终形状的形成。值得注意的是,花瓣不对称弯曲是一种尚未被注意到的新特征,因此其形态性质、发育过程和分子机制在很大程度上仍然未知。在这里,我们以 D. anthriscifolium 为模型,确定了花瓣不对称弯曲是由细胞宽度的局部扩张引起的,同时伴随着细胞细胞壁纳米结构的特殊排列,在近轴表皮上。数字基因分析、基因表达和功能研究表明,一类 homeodomain-leucine zipper 家族转录因子基因 DeanLATE MERISTEM IDENTITY1(DeanLMI1)有助于花瓣不对称弯曲;其敲低导致展开的 2D 花瓣形成。具体来说,DeanLMI1 促进细胞宽度的扩张,并影响局部近轴表皮上细胞壁纳米结构的排列。这些结果不仅首次提供了花瓣不对称弯曲的全面描述,而且为植物花朵开放和螺旋运动的机制提供了一些新的见解。