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1.
Plant Mol Biol ; 94(3): 267-280, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28364389

ABSTRACT

The structure of a pectin network requires both calcium (Ca2+) and boron (B). Ca2+ is involved in crosslinking pectic polysaccharides and arbitrarily induces the formation of an "egg-box" structure among pectin molecules, while B crosslinks rhamnogalacturonan II (RG-II) side chain A apiosyl residues in primary cell walls to generate a borate-dimeric-rhamnogalacturonan II (dRG-II-B) complex through a boron-bridge bond, leading to the formation of a pectin network. Based on recent studies of dRG-II-B structures, a hypothesis has been proposed suggesting that Ca2+is a common component of the dRG-II-B complex. However, no in vivo evidence has addressed whether B affects the stability of Ca2+ crosslinks. Here, we investigated the L-fucose-deficient dwarf mutant mur1, which was previously shown to require exogenous B treatment for phenotypic reversion. Imbibed Arabidopsis thaliana seeds release hydrated polysaccharides to form a halo of seed mucilage covering the seed surface, which consists of a water-soluble outer layer and an adherent inner layer. Our study of mur1 seed mucilage has revealed that the pectin in the outer layer of mucilage was relocated to the inner layer. Nevertheless, the mur1 inner mucilage was more vulnerable to rough shaking or ethylene diamine tetraacetic acid (EDTA) extraction than that of the wild type. Immunolabeling analysis suggested that dRG-II-B was severely decreased in mur1 inner mucilage. Moreover, non-methylesterified homogalacturonan (HG) exhibited obvious reassembly in the mur1 inner layer compared with the wild type, which may imply a possible connection between dRG-II-B deficiency and pectin network transformation in the seed mucilage. As expected, the concentration of B in the mur1 inner mucilage was reduced, whereas the distribution and concentration of Ca2+in the inner mucilage increased significantly, which could be the reason why pectin relocates from the outer mucilage to the inner mucilage. Consequently, the disruption of B bridges appears to result in the extreme sensitivity of the mur1 mucilage pectin complex to EDTA extraction, despite the reinforcement of the pectin network by excessive Ca2+. Therefore, we propose a hypothesis that B, in the form of dRG-II-B, works together with Ca2+to maintain pectin network crosslinks and ultimately the mucilage ultrastructure in seed mucilage. This work may serve to complement our current understanding of mucilage configuration.


Subject(s)
Arabidopsis/physiology , Boron/chemistry , Calcium/physiology , Plant Mucilage/chemistry , Polysaccharides/metabolism , Seeds/physiology , Arabidopsis/chemistry , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Calcium/chemistry , Gene Expression Regulation, Plant/physiology , Polysaccharides/chemistry
2.
Yi Chuan ; 37(1): 91-97, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25608819

ABSTRACT

Genetic linkage map is helpful for analysis on heredity of some gene families and map-based gene cloning because of its simple and elegant manifestation. One software is in need to draw a gene physical map, which shows a manner similar to the genetic linkage map, based on the relative physical distance between genes. Although some tools like GBrowse and MapViewer etc. are available to draw gene physical map, there are obvious limitations for them: (1) the data need to be decorated in advance; (2) users can't modify results. Therefore, we developed a bio-assisted mapping software--MapGene2Chrom with PC and web versions, which is based on Perl and SVG languages. The software can be used to draw the corresponding physical map quickly in SVG format based on the input data. It will become a useful tool for drawing gene physical map with the advantages of simple input data format, easily modified output and very good portability.


Subject(s)
Physical Chromosome Mapping/instrumentation , Software , Internet , Physical Chromosome Mapping/methods , Plants/genetics
3.
Yi Chuan Xue Bao ; 32(10): 1082-8, 2005 Oct.
Article in Chinese | MEDLINE | ID: mdl-16252704

ABSTRACT

Using an estrogen-inducible expression XVE (LexA-VP16-Estragon Receptor) system, we have generated approximately 40 000 independent T-DNA insertion lines of Arabidopsis thaliana. Segregation analyses of about 18000 lines indicated that 51.6% of them contain single T-DNA insertions and that the average insertion number is 1.38 copies per line. Mutants displaying a variety of morphological alterations were identified, including those that affect development of roots,hypocotyls, leaves, floral organs and seeds as well as the flowering time.


Subject(s)
Arabidopsis/genetics , DNA, Bacterial/genetics , Mutagenesis, Insertional/methods , Plants, Genetically Modified/genetics , Arabidopsis/anatomy & histology , Arabidopsis/growth & development , Bacterial Proteins/genetics , Cloning, Molecular , Estrogens/pharmacology , Genetic Vectors/genetics , Herpes Simplex Virus Protein Vmw65/genetics , Mutagenesis, Insertional/drug effects , Phenotype , Plants, Genetically Modified/anatomy & histology , Plants, Genetically Modified/growth & development , Plasmids/genetics , Receptors, Estrogen/genetics , Serine Endopeptidases/genetics , Transcriptional Activation/drug effects
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