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1.
Plant Physiol ; 161(4): 1930-51, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23439917

ABSTRACT

Phytohormones regulate plant growth from cell division to organ development. Jasmonates (JAs) are signaling molecules that have been implicated in stress-induced responses. However, they have also been shown to inhibit plant growth, but the mechanisms are not well understood. The effects of methyl jasmonate (MeJA) on leaf growth regulation were investigated in Arabidopsis (Arabidopsis thaliana) mutants altered in JA synthesis and perception, allene oxide synthase and coi1-16B (for coronatine insensitive1), respectively. We show that MeJA inhibits leaf growth through the JA receptor COI1 by reducing both cell number and size. Further investigations using flow cytometry analyses allowed us to evaluate ploidy levels and to monitor cell cycle progression in leaves and cotyledons of Arabidopsis and/or Nicotiana benthamiana at different stages of development. Additionally, a novel global transcription profiling analysis involving continuous treatment with MeJA was carried out to identify the molecular players whose expression is regulated during leaf development by this hormone and COI1. The results of these studies revealed that MeJA delays the switch from the mitotic cell cycle to the endoreduplication cycle, which accompanies cell expansion, in a COI1-dependent manner and inhibits the mitotic cycle itself, arresting cells in G1 phase prior to the S-phase transition. Significantly, we show that MeJA activates critical regulators of endoreduplication and affects the expression of key determinants of DNA replication. Our discoveries also suggest that MeJA may contribute to the maintenance of a cellular "stand-by mode" by keeping the expression of ribosomal genes at an elevated level. Finally, we propose a novel model for MeJA-regulated COI1-dependent leaf growth inhibition.


Subject(s)
Acetates/pharmacology , Arabidopsis/cytology , Arabidopsis/genetics , Cyclopentanes/pharmacology , Endoreduplication/drug effects , Oxylipins/pharmacology , Plant Leaves/cytology , Plant Leaves/growth & development , Arabidopsis/drug effects , Arabidopsis/growth & development , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Cell Count , Cell Nucleus/drug effects , Cell Nucleus/metabolism , Cell Nucleus Size/drug effects , Cell Proliferation/drug effects , Cell Size/drug effects , Cluster Analysis , Cotyledon/drug effects , Cotyledon/growth & development , DNA Replication/drug effects , DNA, Plant/metabolism , Down-Regulation/drug effects , Endoreduplication/genetics , Gene Expression Profiling , Gene Expression Regulation, Plant/drug effects , Meristem/cytology , Meristem/drug effects , Mitosis/drug effects , Mitosis/genetics , Models, Biological , Phenotype , Plant Leaves/drug effects , Ribosomal Proteins/genetics , Ribosomal Proteins/metabolism
2.
Plant J ; 67(4): 635-47, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21554449

ABSTRACT

PtdIns-4,5-bisphosphate is a lipid messenger of eukaryotic cells that plays a critical role in processes such as cytoskeleton organization, intracellular vesicular trafficking, secretion, cell motility, regulation of ion channels and nuclear signalling pathways. The enzymes responsible for the synthesis of PtdIns(4,5)P2 are phosphatidylinositol phosphate kinases (PIPKs). The moss Physcomitrella patens contains two PIPKs, PpPIPK1 and PpPIPK2. To study their physiological role, both genes were disrupted by targeted homologous recombination and as a result mutant plants with lower PtdIns(4,5)P2 levels were obtained. A strong phenotype for pipk1, but not for pipk2 single knockout lines, was obtained. The pipk1 knockout lines were impaired in rhizoid and caulonemal cell elongation, whereas pipk1-2 double knockout lines showed dramatic defects in protonemal and gametophore morphology manifested by the absence of rapidly elongating caulonemal cells in the protonemal tissue, leafy gametophores with very short rhizoids, and loss of sporophyte production. pipk1 complemented by overexpression of PpPIPK1 fully restored the wild-type phenotype whereas overexpression of the inactive PpPIPK1E885A did not. Overexpression of PpPIPK2 in the pipk1-2 double knockout did not restore the wild-type phenotype demonstrating that PpPIPK1 and PpPIPK2 are not functionally redundant. In vivo imaging of the cytoskeleton network revealed that the shortened caulonemal cells in the pipk1 mutants was the result of the absence of the apicobasal gradient of cortical F-actin cables normally observed in wild-type caulonemal cells. Our data indicate that both PpPIPKs play a crucial role in the development of the moss P. patens, and particularly in the regulation of tip growth.


Subject(s)
Actin Cytoskeleton/ultrastructure , Bryopsida/physiology , Phosphatidylinositol 4,5-Diphosphate/metabolism , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Actin Cytoskeleton/drug effects , Actin Cytoskeleton/metabolism , Actins/metabolism , Amino Acid Substitution , Bridged Bicyclo Compounds, Heterocyclic/pharmacology , Bryopsida/enzymology , Bryopsida/genetics , Bryopsida/ultrastructure , Cytochalasin B/pharmacology , Gene Expression Regulation, Plant , Homologous Recombination , Phenotype , Phosphatidylinositol 4,5-Diphosphate/analysis , Phosphotransferases (Alcohol Group Acceptor)/genetics , Plant Proteins/genetics , Plant Proteins/metabolism , Sequence Deletion , Thiazolidines/pharmacology
3.
Plant Cell Physiol ; 50(3): 595-609, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19188261

ABSTRACT

Phosphoinositides (PIs) play a major role in eukaryotic cells, despite being a minor component of most membranes. This is the first report on PI metabolism in a bryophyte, the moss Physcomitrella patens. Moss PI composition is similar to that of other land plants growing under normal conditions. In contrast to the large number of PIPK genes present in flowering plants, the P. patens genome encodes only two type I/II PIPK genes, PpPIPK1 and PpPIPK2, which are very similar at both the nucleotide and protein product levels. However, the expression of the two genes is differentially regulated, and in vitro biochemical characterization shows that the resulting enzymes have different substrate specificities. PpPIPK1 uses PtdIns4P and PtdIns3P with similar preference and also metabolizes PtdIns(3,4)P(2) to produce PtdIns(3,4,5)P(3), a PI not yet detected in intact plant cells. PpPIPK2 prefers PtdIns as substrate and is much less active towards PtdIns4P and PtdIns3P. Thus, PpPIPK2 shows properties reminiscent of both PtdInsP-kinase and PtdIns-kinases. Moreover, a substitution of glutamic acid by alanine in the activation loop drastically reduced PpPIPK1 activity and altered the substrate specificity to PtdIns5P being the preferred substrate compared with PtdIns4P and PtdIns3P. These findings demonstrate that the substrate specificity of plant PIPKs is determined in a plant-specific manner, which provides new insights into the regulatory modes of PIPK activity in plants.


Subject(s)
Bryopsida/enzymology , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Amino Acid Sequence , Amino Acid Substitution , Bryopsida/genetics , Cell Membrane/enzymology , Cloning, Molecular , Gene Expression Regulation, Plant , Genes, Plant , Molecular Sequence Data , Phosphatidylinositol Phosphates/metabolism , Phosphotransferases (Alcohol Group Acceptor)/genetics , Phylogeny , RNA, Plant/genetics , Sequence Alignment , Substrate Specificity
4.
New Phytol ; 177(2): 301-318, 2008.
Article in English | MEDLINE | ID: mdl-18042205

ABSTRACT

Plant development and stress responses are regulated by complex signalling networks that mediate specific and dynamic plant responses upon activation by various types of exogenous and endogenous signal. In this review, we focus on the latest published work on jasmonate (JA) signalling components and new regulatory nodes in the transcriptional network that regulates a number of diverse plant responses to developmental and environmental cues. Not surprisingly, the majority of the key revelations in the field have been made in Arabidopsis thaliana. However, for comparative reasons, we integrate information on Arabidopsis with recent reports for other plant species (when available). Recent findings on the regulation of plant responses to pathogens by JAs, as well as new evidence implicating JAs in the regulation of senescence, suggest a common mechanism of JA action in these responses via distinct groups of transcription factors. Moreover, a significant increase in the amount of evidence has allowed placing of specific mitogen-activated protein kinases (MAPKs) as crucial regulatory nodes in the defence signalling network. In addition, we report on new physiological scenarios for JA signalling, such as organogenesis of nitrogen-fixing nodules and anticancer therapy.


Subject(s)
Arabidopsis/metabolism , Cyclopentanes/metabolism , Oxylipins/metabolism , Signal Transduction/physiology
5.
Plant Physiol ; 131(1): 186-97, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12529527

ABSTRACT

The vegetative phenotype of the auxin-resistant diageotropica (dgt) mutant of tomato (Lycopersicon esculentum Mill.) includes reduced gravitropic response, shortened internodes, lack of lateral roots, and retarded vascular development. Here, we report that early fruit development is also dramatically altered by the single-gene dgt lesion. Fruit weight, fruit set, and numbers of locules and seeds are reduced in dgt. In addition, time to flowering and time from anthesis to the onset of fruit ripening are increased by the dgt lesion, whereas ripening is normal. The dgt mutation appears to affect only the early stages of fruit development, irrespective of allele or genetic background. Expression of members of the LeACS (1-aminocyclopropane-1-carboxylic acid synthase, a key regulatory enzyme of ethylene biosynthesis) and LeIAA (Aux/IAA, auxin-responsive) gene families were quantified via real-time reverse transcriptase-polymerase chain reaction in both dgt and wild-type fruits, providing the first analysis of Aux/IAA gene expression in fruit. The dgt lesion affects the expression of only certain members of both the LeACS and LeIAA multigene families. Different subsets of LeIAA gene family members are affected by the dgt mutation in fruits and hypocotyls, indicating that the DGT gene product functions in a developmentally specific manner. The differential expression of subsets of LeIAA and LeACS gene family members as well as the alterations in dgt fruit morphology and growth suggest that the early stages of fruit development in tomato are regulated, at least in part, by auxin- and ethylene-mediated gene expression.


Subject(s)
Fruit/genetics , Indoleacetic Acids/genetics , Solanum lycopersicum/genetics , Ethylenes/metabolism , Flowers/genetics , Flowers/growth & development , Fruit/anatomy & histology , Fruit/growth & development , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , Gravitropism/genetics , Gravitropism/physiology , Indoleacetic Acids/metabolism , Lyases/genetics , Lyases/metabolism , Solanum lycopersicum/growth & development , Multigene Family/genetics , Mutation , Phenotype , Plant Proteins/genetics , Plant Proteins/metabolism , Plant Roots/genetics , Plant Roots/growth & development , Signal Transduction/genetics , Signal Transduction/physiology , Time Factors
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