Cytokinin signalling regulates two-stage inflorescence arrest in Arabidopsis

To maximise their reproductive success, flowering plants must correctly time their entry into and exit from the reproductive phase (flowering). While much is known about the mechanisms that regulate the initiation of flowering, the regulation of end-of-flowering remains largely uncharacterised. End-of-flowering in Arabidopsis thaliana consists of the quasi-synchronous arrest of individual inflorescences, but it is unclear how this arrest is correctly timed with respect to environmental stimuli and ongoing reproductive success. Here we show that Arabidopsis inflorescence arrest is a complex developmental phenomenon which includes a decline in size and cessation of activity in the inflorescence meristem (IM), coupled with a separable developmental arrest in all unopened floral primordia (floral arrest); these events occur well before the visible arrest of the inflorescence. We show that global removal of inflorescences can delay both IM arrest and floral arrest, but that local fruit removal only delays floral arrest, emphasising the separability of these processes. We test a role for cytokinin in regulating inflorescence arrest, and find that cytokinin treatment can delay arrest. We further show that gain-of-function cytokinin receptor hypersensitive mutants can delay floral arrest, and also IM arrest, depending on the expression pattern of the receptor; conversely, loss-of-function mutants prevent extension of flowering in response to inflorescence removal. Collectively, our data suggest that the dilution of cytokinin among an increasing number of sink organs leads to end-of-flowering in Arabidopsis by triggering IM and floral arrest, conversely meaning that a lack of reproductive success can homeostatically extend flowering in compensation.

RcAP1, a Homolog of APETALA1, is Associated with Flower Bud Differentiation and Floral Organ Morphogenesis in Rosa chinensis

Rosa chinensis is one of the most popular flower plants worldwide. The recurrent flowering trait greatly enhances the ornamental value of roses, and is the result of the constant formation of new flower buds. Flower bud differentiation has always been a major topic of interest among researchers. The APETALA1 (AP1) MADS-box (Mcm1, Agamous, Deficiens and SRF) transcription factor-encoding gene is important for the formation of the floral meristem and floral organs. However, research on the rose AP1 gene has been limited. Thus, we isolated AP1 from Rosa chinensis ‘Old Blush’. An expression analysis revealed that RcAP1 was not expressed before the floral primordia formation stage in flower buds. The overexpression of RcAP1 in Arabidopsis thaliana resulted in an early-flowering phenotype. Additionally, the virus-induced down-regulation of RcAP1 expression delayed flowering in ‘Old Blush’. Moreover, RcAP1 was specifically expressed in the sepals of floral organs, while its expression was down-regulated in abnormal sepals and leaf-like organs. These observations suggest that RcAP1 may contribute to rose bud differentiation as well as floral organ morphogenesis, especially the sepals. These results may help for further characterization of the regulatory mechanisms of the recurrent flowering trait in rose.

Gibberellin Control of Reproductive Transitions in Brassica oleracea Curd Development

Cauliflower (Brassica oleracea var. botrytis) and broccoli (B. oleracea var. italica) differ in the developmental stage of the reproductive meristem at harvest. A cauliflower head is formed by arrest at the inflorescence meristem stage and broccoli at the flower bud stage, and the horticultural value of the crop depends on synchronous development across the head. In other plant species, gibberellin (GA) can promote floral development and is therefore a candidate for providing the early developmental cues that shape the curd morphology. This research investigated the effect of GAs on the two horticulturally important transitions of the reproductive meristem: initiation of the inflorescence meristem and initiation of floral primordia on the proliferated inflorescence meristems. GA is known to affect the former in many species, but effects on the latter have not been determined. It is also not known whether one or both active forms produced by the two GA biosynthetic pathways is involved in the reproductive transitions in this crop. GAs from the early-13 hydroxylation pathway (GA3) and the non-13 hydroxylation pathway (GA4+7) were applied to the shoot apical meristems of cauliflower and broccoli at three developmental stages: adult-vegetative, curd initiation, and curd enlargement. GAs applied during the adult vegetative stage caused the curd to form faster and after fewer additional nodes in both cauliflower and broccoli. GAs applied to the inflorescence meristem did not cause floral primordia to form nor did the expression of transition-associated genes change. Integrator genes BoLFY and SOC1 had constant expression over 24 hours, and meristem-identity genes BoAP1-a and BoAP1-c remained undetectable. However, GAs applied early during the reproductive phase increased bract development in cauliflower curds. This study shows that GAs from both pathways can trigger the vegetative-to-reproductive transition in both cauliflower and broccoli, resulting in earlier curd formation. However, GAs did not advance the inflorescence-meristem-to-floral-primordium transition; on the contrary, they increased bract incidence in cauliflower, a sign of reversion toward the vegetative stage, suggesting that another pathway is responsible for this second transition in cauliflower and broccoli.

Ontogenesis of the Potamogeton flower and fruitlet in SEM research

The morphological development of fruitlets representing the four sections of the genus <em>Potamogeton</em> was investigated. Evident morphological differences in the course of the development of fruitlets between the species studied were found. They concern: a) size, shape and outline of carpels and fruitlets, b) individual rate of fruitlet development, c) angle arrangement of the fruitlets, and d) structure of the basal and the apical parts of the fruitlets. Acropetal initiating of the floral primordia was found, as well as the fact that the fruitlet surfaces are very variable and thus useless for taxonomical purposes.

A nucleostemin-like GTPase required for normal apical and floral meristem development in Arabidopsis

Mammalian nucleostemin (NS) is preferentially expressed in stem cells and acts to promote cell cycle progression. In plants, stem cell activities have to be terminated during flower development, and this process requires the activation of AGAMOUS (AG) gene expression. Here, a nucleostemin-like 1 gene, NSN1, is shown to be required for flower development in Arabidopsis. The NSN1 mRNA was found in the inflorescence meristem and floral primordia, and its protein was localized to the nucleoli. Both heterozygous and homozygous plants developed defective flowers on inflorescences that were eventually terminated by the formation of carpelloid flowers. Overexpression of NSN1 resulted in loss of apical dominance and formation of defective flowers. Expression of the AG gene was found to be up-regulated in nsn1. The carpelloid flower defect of nsn1 was suppressed by the ag mutation in the nsn1 ag double mutant, whereas double mutants of nsn1 apetala2 (ap2) displayed enhanced defective floral phenotypes. These results suggest that in the delicately balanced regulatory network, NSN1 acts to repress AG and plays an additive role with AP2 in floral organ specification. As a midsize nucleolar GTPase, NSN1 represents a new class of regulatory proteins required for flower development in Arabidopsis.