Laboratoire Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRAE, Lyon, France.
Methods Mol Biol. 2023;2686:39-58. doi: 10.1007/978-1-0716-3299-4_2.
Flower development is the process leading from a reproductive meristem to a mature flower with fully developed floral organs. This multi-step process is complex and involves thousands of genes in intertwined regulatory pathways; navigating through the FLOR-ID website will give an impression of this complexity and of the astonishing amount of work that has been carried on the topic (Bouché et al., Nucleic Acids Res 44:D1167-D1171, 2016). Our understanding of flower development mostly comes from the model species Arabidopsis thaliana, but numerous other studies outside of Brassicaceae have helped apprehend the conservation of these mechanisms in a large evolutionary context (Moyroud and Glover, Curr Biol 27:R941-R951, 2017; Smyth, New Phytol 220:70-86, 2018; Soltis et al., Ann Bot 100:155-163, 2007). Integrating additional species and families to the research on this topic can only advance our understanding of flower development and its evolution.In this chapter, we review the contribution that the Solanaceae family has made to the comprehension of flower development. While many of the general features of flower development (i.e., the key molecular players involved in flower meristem identity, inflorescence architecture or floral organ development) are similar to Arabidopsis, our main objective in this chapter is to highlight the points of divergence and emphasize specificities of the Solanaceae. We will not discuss the large topics of flowering time regulation, inflorescence architecture and fruit development, and we will restrict ourselves to the mechanisms included in a time window after the floral transition and before the fertilization. Moreover, this review will not be exhaustive of the large amount of work carried on the topic, and the choices that we made to describe in large details some stories from the literature are based on the soundness of the functional work performed, and surely as well on our own preferences and expertise.First, we will give a brief overview of the Solanaceae family and some of its specificities. Then, our focus will be on the molecular mechanisms controlling floral organ identity, for which extended functional work in petunia led to substantial revisions to the famous ABC model. Finally, after reviewing some studies on floral organ initiation and growth, we will discuss floral organ maturation, using the examples of the inflated calyx of the Chinese lantern Physalis and petunia petal pigmentation.
花的发育是从生殖分生组织到具有完全发育的花器官的成熟花的多步骤过程。这个多步骤的过程非常复杂,涉及到数以千计的基因在相互交织的调控途径中;浏览 FLOR-ID 网站将使人们对这种复杂性以及在该主题上所进行的大量工作有一个印象(Bouché 等人,Nucleic Acids Res 44:D1167-D1171, 2016)。我们对花发育的理解主要来自模式物种拟南芥,但在芸薹科之外的许多其他研究帮助我们理解了这些机制在大进化背景下的保守性(Moyroud 和 Glover,Curr Biol 27:R941-R951, 2017; Smyth,New Phytol 220:70-86, 2018; Soltis 等人,Ann Bot 100:155-163, 2007)。将其他物种和科系纳入对该主题的研究只会促进我们对花发育及其进化的理解。在这一章中,我们回顾了茄科对花发育理解的贡献。虽然花发育的许多一般特征(即参与花分生组织身份、花序结构或花器官发育的关键分子参与者)与拟南芥相似,但我们在本章中的主要目标是强调分歧点,并强调茄科的特异性。我们不会讨论开花时间调控、花序结构和果实发育等大话题,我们将把自己限制在花转变后和受精前的时间窗口内的机制。此外,本综述不会详尽地涵盖该主题上的大量工作,我们选择详细描述文献中的一些故事的原因是基于功能工作的合理性,当然还有我们自己的偏好和专业知识。首先,我们将简要概述茄科及其一些特异性。然后,我们将重点介绍控制花器官身份的分子机制,在对矮牵牛的扩展功能研究中,这导致了著名的 ABC 模型的重大修订。最后,在回顾了一些关于花器官起始和生长的研究之后,我们将以中国灯笼椒 Physalis 的膨胀花萼和矮牵牛花瓣色素沉着为例,讨论花器官成熟。