The Amsterdam petunia germplasm collection: A tool in plant science

Petunia hybrida is a plant model system used by many researchers to investigate a broad range of biological questions. One of the reasons for the success of this organism as a lab model is the existence of numerous mutants, involved in a wide range of processes, and the ever-increasing size of this collection owing to a highly active and efficient transposon system. We report here on the origin of petunia-based research and describe the collection of petunia lines housed in the University of Amsterdam, where many of the existing genotypes are maintained

Insight into the evolution of the Solanaceae from the parental genomes of Petunia hybrida

Petunia hybrida is a popular bedding plant that has a long history as a genetic model system. We report the whole-genome sequencing and assembly of inbred derivatives of its two wild parents, P. axillaris N and P. inflata S6. The current assemblies include 91.3% and 90.2% coverage of their diploid genomes (1.4 Gb; 2n=14) containing 32,928 and 36,697 protein-coding genes, respectively. The Petunia lineage has experienced at least two rounds of paleohexaploidization, the older gamma hexaploidy event, which is shared with other Eudicots, and the more recent Solanaceae paleohexaploidy event that is shared with tomato and other Solanaceae species. Transcription factors that were targets of selection during the shift from bee- to moth pollination reside in particularly dynamic regions of the genome, which may have been key to the remarkable diversity of floral color patterns and pollination systems. The high quality genome sequences will enhance the value of Petunia as a model system for basic and applied research on a variety of unique biological phenomena

Insight into the evolution of the Solanaceae from the parental genomes of Petunia hybrida

Petunia hybrida is a popular bedding plant that has a long history as a genetic model system. We report the whole-genome sequencing and assembly of inbred derivatives of its two wild parents, P. axillaris N and P. inflata S6. The assemblies include 91.3% and 90.2% coverage of their diploid genomes (1.4 Gb; 2n = 14) containing 32,928 and 36,697 protein-coding genes, respectively. The genomes reveal that the Petunia lineage has experienced at least two rounds of hexaploidization: the older gamma event, which is shared with most Eudicots, and a more recent Solanaceae event that is shared with tomato and other solanaceous species. Transcription factors involved in the shift from bee to moth pollination reside in particularly dynamic regions of the genome, which may have been key to the remarkable diversity of floral colour patterns and pollination systems. The high-quality genome sequences will enhance the value of Petunia as a model system for research on unique biological phenomena such as small RNAs, symbiosis, self-incompatibility and circadian rhythms

Salt and heavy metal tolerance and expression levels of candidate tolerance genes among four extremophile Cochlearia species with contrasting habitat preferences

To test the concept of a general “mineral stress tolerance”, we compared four extremophile Cochlearia species for salt (NaCl), zinc (Zn) and cadmium (Cd) tolerance and accumulation, and for expression of candidate tolerance genes for salt and Zn tolerance. Salt tolerance decreased in the order C. anglica > C. x hollandica > C. danica > C. pyrenaica, corresponding with the average salinity levels in the species' natural environments. The glycophytic metallophyte, C. pyrenaica, showed a relatively high level of salt tolerance, compared to other glycophytic Brassicaceae. Salt tolerance was positively correlated with HKT1 expression and the K+ concentration in roots under salt exposure, but uncorrelated with the Na+ concentrations in roots and shoots. All the species accumulated Na+ primarily in their leaves, and exhibited a high NHX1 expression in leaves, in comparison with other glycophytic Brassicaceae, suggesting that salt tolerance in Cochlearia is based on an efficient vacuolar sequestration of Na+ in leaves. The metallicolous C. pyrenaica population was hypertolerant to Zn, but not to Cd, in comparison with the other Cochlearia species. All the Cochlearia species accumulated Zn and Cd primarily in roots, and showed high levels of Cd and Zn tolerance, with unusually low rates of metal accumulation, in comparison with non-metallophytes, or non-metallicolous metallophyte populations, of species belonging to other genera or families. Although Cochlearia, as a genus, shows relatively high levels of tolerance to both salt and heavy metals, this is most probably not due to a common ‘mineral stress tolerance’ mechanism

Salt and heavy metal tolerance and expression levels of candidate tolerance genes among four extremophile Cochlearia species with contrasting habitat preferences

To test the concept of a general “mineral stress tolerance”, we compared four extremophile Cochlearia species for salt (NaCl), zinc (Zn) and cadmium (Cd) tolerance and accumulation, and for expression of candidate tolerance genes for salt and Zn tolerance. Salt tolerance decreased in the order C. anglica > C. x hollandica > C. danica > C. pyrenaica, corresponding with the average salinity levels in the species' natural environments. The glycophytic metallophyte, C. pyrenaica, showed a relatively high level of salt tolerance, compared to other glycophytic Brassicaceae. Salt tolerance was positively correlated with HKT1 expression and the K+ concentration in roots under salt exposure, but uncorrelated with the Na+ concentrations in roots and shoots. All the species accumulated Na+ primarily in their leaves, and exhibited a high NHX1 expression in leaves, in comparison with other glycophytic Brassicaceae, suggesting that salt tolerance in Cochlearia is based on an efficient vacuolar sequestration of Na+ in leaves. The metallicolous C. pyrenaica population was hypertolerant to Zn, but not to Cd, in comparison with the other Cochlearia species. All the Cochlearia species accumulated Zn and Cd primarily in roots, and showed high levels of Cd and Zn tolerance, with unusually low rates of metal accumulation, in comparison with non-metallophytes, or non-metallicolous metallophyte populations, of species belonging to other genera or families. Although Cochlearia, as a genus, shows relatively high levels of tolerance to both salt and heavy metals, this is most probably not due to a common ‘mineral stress tolerance’ mechanism

Patterning of Inflorescences and Flowers by the F-Box Protein DOUBLE TOP and the LEAFY Homolog ABERRANT LEAF AND FLOWER of Petunia[W]

Angiosperms display a wide variety of inflorescence architectures differing in the positions where flowers or branches arise. The expression of floral meristem identity (FMI) genes determines when and where flowers are formed. In Arabidopsis thaliana, this is regulated via transcription of LEAFY (LFY), which encodes a transcription factor that promotes FMI. We found that this is regulated in petunia (Petunia hybrida) via transcription of a distinct gene, DOUBLE TOP (DOT), a homolog of UNUSUAL FLORAL ORGANS (UFO) from Arabidopsis. Mutation of DOT or its tomato (Solanum lycopersicum) homolog ANANTHA abolishes FMI. Ubiquitous expression of DOT or UFO in petunia causes very early flowering and transforms the inflorescence into a solitary flower and leaves into petals. Ectopic expression of DOT or UFO together with LFY or its homolog ABERRANT LEAF AND FLOWER (ALF) in petunia seedlings activates genes required for identity or outgrowth of organ primordia. DOT interacts physically with ALF, suggesting that it activates ALF by a posttranslational mechanism. Our findings suggest a wider role than previously thought for DOT and UFO in the patterning of flowers and indicate that the different roles of LFY and UFO homologs in the spatiotemporal control of floral identity in distinct species result from their divergent expression patterns

FLOOZY of petunia is a flavin mono-oxygenase-like protein required for the specification of leaf and flower architecture

The mechanisms that determine the relative positions of floral organs, and thereby their numbers, is a poorly understood aspect of flower development. We isolated a petunia mutant, floozy (fzy), in which the formation of floral organ primordia in the outermost three floral whorls and one of the two bracts at the base of the flower is blocked at an early stage. In addition, fzy mutants fail to generate secondary veins in leaves and bracts and display a decreased apical dominance in the inflorescence. FZY encodes an enzyme with homology to flavin mono-oxygenases and appears to be the ortholog of YUCCA genes of Arabidopsis. FZY is expressed in young leafs and bracts and in developing flowers. In young floral meristems FZY is expressed in the center of the meristem dome and, later, expression becomes localized on the flanks of the initiating petal and stamen primordia and at several sites in maturing anthers and carpels. These findings indicate that FZY is involved in synthesizing a signaling compound that is required for floral organ initiation and specification of the vascularization pattern in leaves. Although fzy mutants contain normal auxin levels, ectopic expression of FZY results in excessive auxin accumulation, suggesting that the signaling compound is auxin

An ancient RAB5 governs the formation of additional vacuoles and cell shape in petunia petals

International audienceHomologous ("canonical'') RAB5 proteins regulate endosomal trafficking to lysosomes in animals and to the central vacuole in plants. Epidermal petal cells contain small vacuoles (vacuolinos) that serve as intermediate stations for proteins on their way to the central vacuole. Here, we show that transcription factors required for vacuolino formation in petunia induce expression of RAB5a. RAB5a defines a previously unrecognized clade of canonical RAB5s that is evolutionarily and functionally distinct from ARA7-type RAB5s, which act in trafficking to the vacuole. Loss of RAB5a reduces cell height and abolishes vacuolino formation, which cannot be rescued by the ARA7 homologs, whereas constitutive RAB5a (over)expression alters the conical cell shape and promotes homotypic vacuolino fusion, resulting in oversized vacuolinos. These findings provide a rare example of how gene duplication and neofunctionalization increased the complexity ofmembrane trafficking during evolution and suggest a mechanism by which cells may form multiple vacuoles with distinct content and function

Evolution of tonoplast P-ATPase transporters involved in vacuolar acidification

Li Y, Provenzano S, Bliek M, et al. Evolution of tonoplast P-ATPase transporters involved in vacuolar acidification. New Phytologist. 2016;211(3):1092-1107

Hyperacidification of Vacuoles by the Combined Action of Two Different P-ATPases in the Tonoplast Determines Flower Color

The acidification of endomembrane compartments is essential for enzyme activities, sorting, trafficking, and trans-membrane transport of various compounds. Vacuoles are mildly acidic inmost plant cells because of the action of V-ATPase and/or pyrophosphatase proton pumps but are hyperacidified in specific cells by mechanisms that remained unclear. Here, we show that the blue petal color of petunia ph mutants is due to a failure to hyperacidify vacuoles. We report that PH1 encodes a P-3B-ATPase, hitherto known as Mg2+ transporters in bacteria only, that resides in the vacuolar membrane (tonoplast). In vivo nuclear magnetic resonance and genetic data show that PH1 is required and, together with the tonoplast H+ P-3A-ATPase PH5, sufficient to hyperacidify vacuoles. PH1 has no H+ transport activity on its own but can physically interact with PH5 and boost PH5 H+ transport activity. Hence, the hyperacidification of vacuoles in petals, and possibly other tissues, relies on a heteromeric P-ATPase pump