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1.
PLoS Genet ; 10(3): e1004221, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24625826

ABSTRACT

Arabidopsis seeds rapidly release hydrophilic polysaccharides from the seed coat on imbibition. These form a heavy mucilage layer around the seed that makes it sink in water. Fourteen natural Arabidopsis variants from central Asia and Scandinavia were identified with seeds that have modified mucilage release and float. Four of these have a novel mucilage phenotype with almost none of the released mucilage adhering to the seed and the absence of cellulose microfibrils. Mucilage release was modified in the variants by ten independent causal mutations in four different loci. Seven distinct mutations affected one locus, coding the MUM2 ß-D-galactosidase, and represent a striking example of allelic heterogeneity. The modification of mucilage release has thus evolved a number of times independently in two restricted geographical zones. All the natural mutants identified still accumulated mucilage polysaccharides in seed coat epidermal cells. Using nuclear magnetic resonance (NMR) relaxometry their production and retention was shown to reduce water mobility into internal seed tissues during imbibition, which would help to maintain seed buoyancy. Surprisingly, despite released mucilage being an excellent hydrogel it did not increase the rate of water uptake by internal seed tissues and is more likely to play a role in retaining water around the seed.


Subject(s)
Arabidopsis Proteins/genetics , Arabidopsis/genetics , Seeds/growth & development , beta-Galactosidase/genetics , Arabidopsis/growth & development , Arabidopsis Proteins/metabolism , Evolution, Molecular , Magnetic Resonance Spectroscopy , Mutation , Plant Mucilage/genetics , Seeds/genetics , Water/chemistry , Water/metabolism
2.
Mol Plant Microbe Interact ; 25(3): 341-54, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22088194

ABSTRACT

Five tomato mutants affected in the Rx-mediated resistance against Potato virus X (PVX) were identified by screening a mutagenized population derived from a transgenic, Rx1-expressing 'Micro-Tom' line. Contrary to their parental line, they failed to develop lethal systemic necrosis upon infection with the virulent PVX-KH2 isolate. Sequence analysis and quantitative reverse-transcription polymerase chain reaction experiments indicated that the mutants are not affected in the Rx1 transgene or in the Hsp90, RanGap1 and RanGap2, Rar1 and Sgt1 genes. Inoculation with the PVX-CP4 avirulent isolate demonstrated that the Rx1 resistance was still effective in the mutants. In contrast, the virulent PVX-KH2 isolate accumulation was readily detectable in all mutants, which could further be separated in two groups depending on their ability to restrict the accumulation of PVX-RR, a mutant affected at two key positions for Rx1 elicitor activity. Finally, transient expression of the viral capsid protein elicitor indicated that the various mutants have retained the ability to mount an Rx1-mediated hypersensitive response. Taken together, the results obtained are consistent with a modification of the specificity or intensity of the Rx1-mediated response. The five Micro-Tom mutants should provide very valuable resources for the identification of novel tomato genes affecting the functioning of the Rx gene.


Subject(s)
Disease Resistance/genetics , Plant Diseases/immunology , Potexvirus/pathogenicity , Solanum lycopersicum/genetics , Solanum lycopersicum/immunology , Capsid Proteins/genetics , Capsid Proteins/metabolism , Chromosome Mapping , DNA, Plant/genetics , Disease Resistance/immunology , Genes, Plant/genetics , Host-Pathogen Interactions , Solanum lycopersicum/virology , Mutagenesis , Mutation , Phenotype , Plant Diseases/virology , Plant Leaves/virology , Plants, Genetically Modified , Potexvirus/physiology , RNA, Plant/genetics , RNA, Viral/genetics , Species Specificity , Nicotiana/virology , Transcription, Genetic , Transgenes/genetics , Virulence
3.
Mol Plant ; 1(1): 145-54, 2008 Jan.
Article in English | MEDLINE | ID: mdl-20031921

ABSTRACT

Light and temperature are key external factors in the control of Arabidopsis thaliana seed germination and dormancy mechanisms. Perception and response to these stimuli have to ensure that seedling emergence and growth occur at the most advantageous time for correct establishment. Analysis of over 300 Arabidopsis accessions identified 14, from 12 different geographical locations, that were able to germinate to greater than 20% at 6 degrees C in the dark. This natural variation was exploited to identify genetic loci responsible for cold-tolerant, dark germination. A quantitative trait loci approach was used on recombinant inbred line progeny of a cross between Bay-0 and Shahdara. Six distinct quantitative trait loci were identified, three of which were major loci, each responsible for 17-25% of the phenotypic variability in this trait. Parental phenotypes indicated that the majority of the cold-tolerant, dark-germination characteristics are related to light responses. Validation of the three major loci using heterogeneous inbred families confirmed the feasibility of fine mapping and cloning the genes at the quantitative trait loci responsible for cold-tolerant, dark germination.


Subject(s)
Arabidopsis/physiology , Genetic Variation , Germination/radiation effects , Light , Quantitative Trait Loci/radiation effects , Arabidopsis/genetics , Arabidopsis/radiation effects , Cold Temperature , Darkness , France , Geography , Homozygote , Phenotype , Quantitative Trait Loci/genetics , Signal Transduction/radiation effects , Temperature
4.
Plant Cell Physiol ; 48(7): 984-99, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17540691

ABSTRACT

A comprehensive analysis was carried out of the composition of seed coat mucilage from Arabidopsis thaliana using the Columbia-0 accession. Pectinaceous mucilage is released from myxospermous seeds upon imbibition, and in Arabidopsis consists of a water-soluble, outer layer and an adherent, inner layer. Analysis of monosaccharide composition in conjunction with digestion with pectolytic enzymes conclusively demonstrated that the principal pectic domain of both layers was rhamnogalacturonan I, and that in the outer layer this was unbranched. The macromolecular characteristics of the water-soluble mucilage indicated that the rhamnogalacturonan molecules in the outer layer were in a slightly expanded random-coil conformation. The inner, adherent layer remained attached to the seed, even after extraction with acid and alkali, suggesting that its integrity was maintained by covalent bonds. Confocal microscopy and monosaccharide composition analyses showed that the inner layer can be separated into two domains. The internal domain contained cellulose microfibrils, which could form a matrix with RGI and bind it to the seed. In effect, in the mum5-1 mutant where most of the inner and outer mucilage layers were water soluble, cellulose remained attached to the seed coat. Immunolabeling with anti-pectin antibodies indicated the presence of galactan and arabinan in the inner layer, with the latter only present in the non-cellulose-containing external domain. In addition, JIM5 and JIM7 antibodies labeled different domains of the inner layer, suggesting the presence of stretches of homogalacturonan with different levels of methyl esterification.


Subject(s)
Adhesives/chemistry , Adhesives/metabolism , Arabidopsis/metabolism , Seeds/metabolism , Antibodies , Carbohydrates/chemistry , Staining and Labeling
5.
Plant Cell ; 19(12): 3990-4006, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18165330

ABSTRACT

The Arabidopsis thaliana accession Shahdara was identified as a rare naturally occurring mutant that does not liberate seed mucilage on imbibition. The defective locus was found to be allelic to the mum2-1 and mum2-2 mutants. Map-based cloning showed that MUCILAGE-MODIFIED2 (MUM2) encodes the putative beta-D-galactosidase BGAL6. Activity assays demonstrated that one of four major beta-D-galactosidase activities present in developing siliques is absent in mum2 mutants. No difference was observed in seed coat epidermal cell structure between wild-type and mutant seed; however, weakening of the outer tangential cell wall by chemical treatment resulted in the release of mucilage from mum2 seed coat epidermal cells, and the mum2 mucilage only increased slightly in volume, relative to the wild type. Consistent with the absence of beta-D-galactosidase activity in the mutant, the inner layer of mucilage contained more Gal. The allocation of polysaccharides between the inner and outer mucilage layers was also modified in mum2. Mass spectrometry showed that rhamnogalacturonan I in mutant mucilage had more branching between rhamnose and hexose residues relative to the wild type. We conclude that the MUM2/BGAL6 beta-D-galactosidase is required for maturation of rhamnogalacturonan I in seed mucilage by the removal of galactose/galactan branches, resulting in increased swelling and extrusion of the mucilage on seed hydration.


Subject(s)
Adhesives/metabolism , Arabidopsis/metabolism , Pectins/metabolism , Seeds/metabolism , beta-Galactosidase/metabolism , Amino Acid Sequence , Arabidopsis/genetics , Arabidopsis/ultrastructure , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Gene Expression Regulation, Plant , Hexoses/chemistry , Hexoses/metabolism , In Situ Hybridization , Microscopy, Electron, Scanning , Models, Genetic , Molecular Sequence Data , Mutation , Pectins/chemistry , Phenotype , Plants, Genetically Modified , Rhamnose/chemistry , Rhamnose/metabolism , Seeds/genetics , Seeds/ultrastructure , Sequence Homology, Amino Acid , beta-Galactosidase/genetics
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