FD and FDP bZIP transcription factors and FT florigen regulate floral development and control homeotic gene expression in Arabidopsis floral meristems.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2025-05-15 Epub Date: 2025-05-22 DOI:10.1242/dev.204241
Maida Romera-Branchat, Chloé Pocard, Coral Vincent, Martina Cerise, Vítor da Silveira Falavigna, Alice Pajoro, Na Ding, He Gao, Rainer Franzen, George Coupland
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引用次数: 0

Abstract

Arabidopsis florigen activation complex (FAC), formed by the interaction of the transcription factor FD and the florigen protein FT, activates gene expression in the shoot apical meristem to induce flowering. We show that FD and its paralog FDP are also expressed in partially overlapping patterns in the floral meristem and floral organs, and that FT is present in floral meristems. The flowers of mutants for FT and its paralog TSF (ft tsf), and of fd fdp mutants show variable numbers of sepals and petals, and larger floral meristems than wild type. In the floral meristem, fd fdp and ft tsf mutants show a significant reduction in the expression of SEP and AG genes, which encode MADS-domain transcription factors, as well as increased expression of the homeobox gene WUS. Binding of FD to SEP genes suggests that diminished SEP gene expression is a primary defect in the mutants. We conclude that, beyond their role in floral transition, FAC components regulate floral homeotic gene expression to control floral meristem size, and influence floral organ development and identity.

FD/FDP bZIP转录因子和FT花原调控拟南芥花分生组织的发育和同源基因表达。
拟南芥花原激活复合物(FAC)是由转录因子FD与花原蛋白FT相互作用形成的,激活茎尖分生组织基因表达,诱导开花。我们发现,FD及其同源基因FDP在花分生组织和花器官中也以部分重叠的模式表达,并且FT存在于花分生组织中。FT及其旁系TSF (FT - TSF)突变体和fd - fdp突变体的花具有不同数量的萼片和花瓣,花的分生组织比野生型大。在花分生组织中,fd fdp和ft tsf突变体编码mads结构域转录因子的SEP和AG基因的表达显著降低,同源异构体基因WUS的表达显著增加。FD与SEP基因结合表明SEP表达减少是突变体的主要缺陷。我们认为FAC成分除了在花的转变过程中发挥作用外,还通过调控花同源基因的表达来控制花分生组织的大小,影响花器官的发育和特性。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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