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1.
New Phytol ; 235(1): 220-233, 2022 07.
Article in English | MEDLINE | ID: mdl-35306666

ABSTRACT

Sensing carbohydrate availability is essential for plants to coordinate their growth and development. In Arabidopsis thaliana, TREHALOSE 6-PHOSPHATE SYNTHASE 1 (TPS1) and its product, trehalose 6-phosphate (T6P), are important for the metabolic control of development. tps1 mutants are embryo-lethal and unable to flower when embryogenesis is rescued. T6P regulates development in part through inhibition of SUCROSE NON-FERMENTING1 RELATED KINASE1 (SnRK1). Here, we explored the role of SnRK1 in T6P-mediated plant growth and development using a combination of a mutant suppressor screen and genetic, cellular and transcriptomic approaches. We report nonsynonymous amino acid substitutions in the catalytic KIN10 and regulatory SNF4 subunits of SnRK1 that can restore both embryogenesis and flowering of tps1 mutant plants. The identified SNF4 point mutations disrupt the interaction with the catalytic subunit KIN10. Contrary to the common view that the two A. thaliana SnRK1 catalytic subunits act redundantly, we found that loss-of-function mutations in KIN11 are unable to restore embryogenesis and flowering, highlighting the important role of KIN10 in T6P signalling.


Subject(s)
Arabidopsis Proteins , Arabidopsis , Sugar Phosphates , Arabidopsis/metabolism , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Gene Expression Regulation, Plant , Phosphates/metabolism , Plants/metabolism , Protein Serine-Threonine Kinases/genetics , Sugar Phosphates/metabolism , Transcription Factors/metabolism , Trehalose/metabolism
2.
Plant Physiol ; 182(4): 2081-2095, 2020 04.
Article in English | MEDLINE | ID: mdl-31996406

ABSTRACT

The floral transition is a critical step in the life cycle of flowering plants, and several mechanisms control this finely orchestrated process. TERMINAL FLOWER1 (TFL1) is a floral repressor and close relative of the florigen, FLOWERING LOCUS T (FT). During the floral transition, TFL1 expression is up-regulated in the inflorescence apex to maintain the indeterminate growth of the shoot apical meristem (SAM). Both TFL1 and FT are mobile proteins, but they move in different ways. FT moves from the leaves to the SAM, while TFL1 appears to move within the SAM. The importance of TFL1 movement for its function in the regulation of flowering time and shoot indeterminacy and its molecular function are still largely unclear. Our results using Arabidopsis (Arabidopsis thaliana) indicate that TFL1 moves from its place of expression in the center of the SAM to the meristem layer L1 and that the movement in the SAM is required for the regulation of the floral transition. Chromatin immunoprecipitation sequencing and RNA sequencing demonstrated that TFL1 functions as a cotranscription factor that associates with and regulates the expression of hundreds of genes. These newly identified direct TFL1 targets provide the possibility to discover new roles for TFL1 in the regulation of floral transition and inflorescence development.


Subject(s)
Arabidopsis Proteins/metabolism , Arabidopsis/metabolism , Meristem/metabolism , Plant Shoots/metabolism , Plants, Genetically Modified/metabolism , Arabidopsis/genetics , Arabidopsis Proteins/genetics , Gene Expression Regulation, Plant/genetics , Gene Expression Regulation, Plant/physiology , Meristem/genetics , Plant Shoots/genetics , Plants, Genetically Modified/genetics
3.
Nat Plants ; 3(11): 854-858, 2017 Nov.
Article in English | MEDLINE | ID: mdl-29085068

ABSTRACT

The outermost cell layer of plant roots (epidermis) constantly encounters environmental challenges. The epidermal outer plasma membrane domain harbours the PENETRATION3 (PEN3)/ABCG36/PDR8 ATP-binding cassette transporter that confers non-host resistance to several pathogens. Here, we show that the Arabidopsis ENDOPLASMIC RETICULUM-ARRESTED PEN3 (EAP3) BTB/POZ-domain protein specifically mediates PEN3 exit from the endoplasmic reticulum and confers resistance to a root-penetrating fungus, providing prime evidence for BTB/POZ-domain protein-dependent membrane trafficking underlying disease resistance.


Subject(s)
ATP-Binding Cassette Transporters/metabolism , Arabidopsis Proteins/metabolism , Arabidopsis/metabolism , Arabidopsis/microbiology , Arabidopsis/genetics , Arabidopsis Proteins/genetics , Chromosome Mapping , Chromosomes, Plant , Endoplasmic Reticulum/metabolism , Green Fluorescent Proteins/genetics , Membrane Proteins/metabolism , Mutation , Plant Roots/metabolism , Plant Roots/microbiology , Protein Domains
4.
Nat Commun ; 8: 15120, 2017 05 17.
Article in English | MEDLINE | ID: mdl-28513600

ABSTRACT

Plants can produce organs throughout their entire life from pluripotent stem cells located at their growing tip, the shoot apical meristem (SAM). At the time of flowering, the SAM of Arabidopsis thaliana switches fate and starts producing flowers instead of leaves. Correct timing of flowering in part determines reproductive success, and is therefore under environmental and endogenous control. How epigenetic regulation contributes to the floral transition has eluded analysis so far, mostly because of the poor accessibility of the SAM. Here we report the temporal dynamics of the chromatin modifications H3K4me3 and H3K27me3 and their correlation with transcriptional changes at the SAM in response to photoperiod-induced flowering. Emphasizing the importance of tissue-specific epigenomic analyses we detect enrichments of chromatin states in the SAM that were not apparent in whole seedlings. Furthermore, our results suggest that regulation of translation might be involved in adjusting meristem function during the induction of flowering.


Subject(s)
Arabidopsis/genetics , Arabidopsis/physiology , Flowers/genetics , Flowers/physiology , Gene Expression Regulation, Plant , Histone Code/genetics , Meristem/genetics , Chromatin/genetics , Gene Expression Profiling , Genes, Plant , Histones/metabolism , Lysine/metabolism , Methylation , Time Factors
5.
Elife ; 52016 07 11.
Article in English | MEDLINE | ID: mdl-27400267

ABSTRACT

A major feature of embryogenesis is the specification of stem cell systems, but in contrast to the situation in most animals, plant stem cells remain quiescent until the postembryonic phase of development. Here, we dissect how light and metabolic signals are integrated to overcome stem cell dormancy at the shoot apical meristem. We show on the one hand that light is able to activate expression of the stem cell inducer WUSCHEL independently of photosynthesis and that this likely involves inter-regional cytokinin signaling. Metabolic signals, on the other hand, are transduced to the meristem through activation of the TARGET OF RAPAMYCIN (TOR) kinase. Surprisingly, TOR is also required for light signal dependent stem cell activation. Thus, the TOR kinase acts as a central integrator of light and metabolic signals and a key regulator of stem cell activation at the shoot apex.


Subject(s)
Gene Expression Regulation, Plant/radiation effects , Light , Meristem/growth & development , Plant Shoots/growth & development , Stem Cells/metabolism , Stem Cells/radiation effects , Meristem/genetics , Meristem/metabolism , Meristem/radiation effects , Plant Shoots/genetics , Plant Shoots/metabolism , Plant Shoots/radiation effects
6.
Plant Signal Behav ; 11(5): e1176818, 2016 05 03.
Article in English | MEDLINE | ID: mdl-27088968

ABSTRACT

Plants compete with their neighbors via the release of chemical compounds into the rhizosphere. These phytotoxins originate from a series of secondary metabolites and can be processed further by soil-living microorganisms before exerting their activity on the target plant. To determine the molecular mode of action and the physiological relevance of potential phytotoxins, it is important to simulate true-to-life conditions in laboratory experiments, for example by applying physiologically relevant concentrations. Here, we report on an improved experimental setting to study the function of allelochemicals of the benzoxazolinone class. By adjusting the solvent and the application of the chemicals, we reduced by more than 2fold the concentration that is necessary to induce growth defects in the model plant Arabidopsis thaliana.


Subject(s)
Arabidopsis/physiology , Oxazines/pharmacology , Pheromones/pharmacology , Acetylation/drug effects , Arabidopsis/drug effects , Arabidopsis/growth & development , Culture Media/pharmacology , Histones/metabolism , Models, Biological , Plant Roots/drug effects , Plant Roots/growth & development
7.
Plant Cell ; 27(11): 3175-89, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26530086

ABSTRACT

To secure their access to water, light, and nutrients, many plant species have developed allelopathic strategies to suppress competitors. To this end, they release into the rhizosphere phytotoxic substances that inhibit the germination and growth of neighbors. Despite the importance of allelopathy in shaping natural plant communities and for agricultural production, the underlying molecular mechanisms are largely unknown. Here, we report that allelochemicals derived from the common class of cyclic hydroxamic acid root exudates directly affect the chromatin-modifying machinery in Arabidopsis thaliana. These allelochemicals inhibit histone deacetylases both in vitro and in vivo and exert their activity through locus-specific alterations of histone acetylation and associated gene expression. Our multilevel analysis collectively shows how plant-plant interactions interfere with a fundamental cellular process, histone acetylation, by targeting an evolutionarily highly conserved class of enzymes.


Subject(s)
Arabidopsis/growth & development , Histone Deacetylase Inhibitors/pharmacology , Histone Deacetylases/metabolism , Acetylation/drug effects , Arabidopsis/drug effects , Arabidopsis/enzymology , Arabidopsis/genetics , Gene Expression Regulation, Plant/drug effects , Genetic Loci , Herbicides/pharmacology , Histone Deacetylase Inhibitors/chemistry , Histones/metabolism , Models, Biological , Oxazines/chemistry , Oxazines/pharmacology , Pheromones/pharmacology , Stress, Physiological/drug effects , Stress, Physiological/genetics
9.
Pigment Cell Melanoma Res ; 28(5): 545-58, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26079969

ABSTRACT

Guppies (Poecilia reticulata) are colorful fish that have attracted the attention of pigmentation researchers for almost a century. Here, we report that the blond phenotype of the guppy is caused by a spontaneous mutation in the guppy ortholog of adenylate cyclase 5 (adcy5). Using double digest restriction site-associated DNA sequencing (ddRADseq) and quantitative trait locus (QTL) mapping, we linked the blond phenotype to a candidate region of 118 kb, in which we subsequently identified a 2-bp deletion in adcy5 that alters splicing and leads to a premature stop codon. We show that adcy5, which affects life span and melanoma growth in mouse, is required for melanophore development and formation of male orange pigmentation traits in the guppy. We find that some components of the male orange pattern are particularly sensitive to loss of Adcy5 function. Our work thus reveals a function for Adcy5 in patterning of fish color ornaments.


Subject(s)
Adenylyl Cyclases/physiology , Melanophores/metabolism , Poecilia/embryology , Animals , Body Patterning , Cell Differentiation , Codon, Terminator , Crosses, Genetic , Female , Gene Library , Genotype , Male , Melanosomes/metabolism , Microscopy, Electron, Transmission , Molecular Sequence Data , Mutation , Phenotype , Phylogeny , Pigmentation , Polymerase Chain Reaction , Quantitative Trait Loci , Sequence Analysis, DNA , Sex Differentiation , Species Specificity
10.
PLoS One ; 10(3): e0121056, 2015.
Article in English | MEDLINE | ID: mdl-25822541

ABSTRACT

Transcription activator-like effector nucleases (TALENs) are custom-made bi-partite endonucleases that have recently been developed and applied for genome engineering in a wide variety of organisms. However, they have been only scarcely used in plants, especially for germline-modification. Here we report the efficient creation of small, germline-transmitted deletions in Arabidopsis thaliana via TALENs that were delivered by stably integrated transgenes. Using meristem specific promoters to drive expression of two TALEN arms directed at the CLV3 coding sequence, we observed very high phenotype frequencies in the T2 generation. In some instances, full CLV3 loss-of-function was already observed in the T1 generation, suggesting that transgenic delivery of TALENs can cause highly efficient genome modification. In contrast, constitutive TALEN expression in the shoot apical meristem (SAM) did not cause additional phenotypes and genome re-sequencing confirmed little off-target effects, demonstrating exquisite target specificity.


Subject(s)
Arabidopsis Proteins/genetics , Arabidopsis/genetics , DNA Restriction Enzymes/genetics , Gene Targeting/methods , Genetic Engineering/methods , Germ-Line Mutation/genetics , Base Sequence , Molecular Sequence Data , Plasmids/genetics , Sequence Analysis, DNA , Transgenes/genetics
11.
Science ; 339(6120): 704-7, 2013 Feb 08.
Article in English | MEDLINE | ID: mdl-23393265

ABSTRACT

The timing of the induction of flowering determines to a large extent the reproductive success of plants. Plants integrate diverse environmental and endogenous signals to ensure the timely transition from vegetative growth to flowering. Carbohydrates are thought to play a crucial role in the regulation of flowering, and trehalose-6-phosphate (T6P) has been suggested to function as a proxy for carbohydrate status in plants. The loss of TREHALOSE-6-PHOSPHATE SYNTHASE 1 (TPS1) causes Arabidopsis thaliana to flower extremely late, even under otherwise inductive environmental conditions. This suggests that TPS1 is required for the timely initiation of flowering. We show that the T6P pathway affects flowering both in the leaves and at the shoot meristem, and integrate TPS1 into the existing genetic framework of flowering-time control.


Subject(s)
Arabidopsis/growth & development , Arabidopsis/metabolism , Flowers/growth & development , Glucosyltransferases/metabolism , Signal Transduction , Sugar Phosphates/metabolism , Trehalose/analogs & derivatives , Arabidopsis/genetics , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Circadian Rhythm , Flowers/metabolism , Gene Expression Regulation, Plant , Glucosyltransferases/genetics , Meristem/metabolism , MicroRNAs/genetics , MicroRNAs/metabolism , Phosphatidylethanolamine Binding Protein/genetics , Phosphatidylethanolamine Binding Protein/metabolism , Photoperiod , Plant Leaves/metabolism , Plant Shoots/metabolism , Trehalose/metabolism
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