Robles Pedro, Pelaz Soraya
División de Genética and Instituto de Bioingeniería, Universidad Miguel Hernández, Campus de Elche, Elche, Alicante, Spain.
Int J Dev Biol. 2005;49(5-6):633-43. doi: 10.1387/ijdb.052020pr.
The study of flower development has experienced great advances over the last 15 years. The most important landmark was the proposal of the ABC model in which three different functions of overlapping activities account for the development of the four rings of organs of the eudicot flower. Most interestingly, during recent years this simple and elegant model has been broadly accepted and is applicable to a wide range of plant species. However, recent advances in the characterization of protein interactions and the discovery of the SEPALLATA genes that are required for proper floral organ development have led to a revision of the ABC model. The largely accepted floral quartet model, which includes the new SEPALLATA function, postulates that the development of a specific floral organ is achieved by the formation of a single complex of different MADS-box proteins. The ultimate fate of the flower is to become a fruit, ensuring dispersal of the seeds and therefore survival of the species. The Arabidopsis fruit is a silique or pod. Only in the last five years important advances have been made in establishing the differentiation of the tissues required for the opening of the fruit: the valve margins and dehiscence zone. Classical genetic analyses and molecular biology approaches have pointed to the involvement of the transcription factors SHP, ALC and IND in the formation of these tissues and of FUL and RPL in repressing this identity in the bordering tissues, valves and replum, respectively.
在过去15年里,花发育的研究取得了巨大进展。最重要的里程碑是ABC模型的提出,其中三种重叠活动的不同功能解释了双子叶植物花的四轮器官的发育。最有意思的是,近年来这个简单而优雅的模型已被广泛接受,并适用于多种植物物种。然而,蛋白质相互作用表征方面的最新进展以及花器官正常发育所需的SEPALLATA基因的发现,导致了ABC模型的修订。目前广泛接受的花四重奏模型,包括新的SEPALLATA功能,假定特定花器官的发育是通过形成不同MADS-box蛋白的单一复合体来实现的。花的最终命运是变成果实,确保种子传播,从而保证物种的生存。拟南芥的果实是长角果或荚果。仅在过去五年里,在确定果实开裂所需组织(瓣膜边缘和开裂区)的分化方面取得了重要进展。经典遗传学分析和分子生物学方法表明,转录因子SHP、ALC和IND参与这些组织的形成,而FUL和RPL分别在相邻组织(瓣膜和胎座框)中抑制这种特性。