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1.
J Exp Bot ; 58(14): 3829-40, 2007.
Article in English | MEDLINE | ID: mdl-18162628

ABSTRACT

Plant epidermal cells are morphologically diverse, differing in size, shape, and function. Their unique morphologies reflect the integral function each cell performs in the organ to which it belongs. Cell morphogenesis involves multiple cellular processes acting in concert to create specialized shapes. The Arabidopsis epidermis contains numerous cell types greatly differing in shape, size, and function. Work on three types of epidermal cells, namely trichomes, root hairs, and pavement cells, has made significant progress towards understanding how plant cells reach their final morphology. These three cell types have highly distinct morphologies and each has become a model cell for the study of morphological processes. A growing body of knowledge is creating a picture of how endoreduplication, cytoskeletal dynamics, vesicle transport, and small GTPase signalling, work in concert to create specialized shapes. Similar mechanisms that determine cell shape and polarity are shared between these cell types, while certain mechanisms remain specific to each.


Subject(s)
Arabidopsis/cytology , Cell Differentiation , Plant Epidermis/cytology , Arabidopsis/genetics , Arabidopsis/metabolism , Gene Expression Regulation, Plant
2.
J Plant Physiol ; 164(8): 980-92, 2007 Aug.
Article in English | MEDLINE | ID: mdl-16904792

ABSTRACT

Arabidopsis is currently the most studied organism in plant biology. Its short life cycle and small genome size have rendered it one of the principal model systems. Additionally, numerous large T-DNA insertion mutant collections are available. The advent of molecular biology and the completion of the Arabidopsis genome sequence have contributed to helping researchers discover a large variety of mutants identified for their phenotypes. Yet, it is important to consider that natural phenotypic variations exist and appear in natural ecotypes, differing greatly in several traits. Although there are a vast number of ecotypes available, only a few have been extensively studied, and some have been created in laboratories. In order to identify new phenotypic differences, we chose to study the differences observed between three ecotypes: Columbia (Col-0), Landsberg erecta (Laer-0) and Wassilewskija (Ws-0). Our research focuses on observable morphological traits throughout plant growth and development along the entire plant life cycle. We then attempted to shed some light on phenotypic discrepancies through the study of the class III peroxidase protein family, which is involved in many aspects of plant growth and tissue differentiation. Both morphological and molecular aspects reveal that there are major variations between ecotypes, hence indicating a possibly interesting heterotic effect in the F1 from crosses between different Arabidopsis ecotypes.


Subject(s)
Arabidopsis/classification , Arabidopsis/physiology , Arabidopsis/genetics , DNA, Plant/genetics , Ecosystem , Flowers/physiology , Gene Library , Oligonucleotide Array Sequence Analysis , Plant Roots/physiology , Plant Stems/physiology , Regeneration , Seedlings/physiology , Seeds/physiology , Switzerland
3.
Trends Plant Sci ; 11(12): 601-9, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17088095

ABSTRACT

Cell fate determination in the Arabidopsis epidermis has been extensively studied for over a decade. Epidermal cells become either trichoblasts (hair-forming cells) or atrichoblasts (non-hair-forming cells). In Arabidopsis, two types of trichoblasts are formed in defined patterns: trichomes and root hairs. Both cell types are specified through the action of a common set of transcriptional regulators that define cell pattern. Recent studies also characterize epigenetic factors in the determination of cell fate in the root, suggesting a default pattern for epidermal cell fate that can be overridden by environmental stimuli. These results reveal how plant cell developmental plasticity is controlled at the molecular level.


Subject(s)
Arabidopsis/cytology , Body Patterning , Cell Differentiation , Epigenesis, Genetic , Body Patterning/genetics , Chromatin Assembly and Disassembly , Gene Expression Regulation, Plant , Models, Genetic , Transcription Factors/physiology
4.
Proc Natl Acad Sci U S A ; 102(22): 8066-70, 2005 May 31.
Article in English | MEDLINE | ID: mdl-15905328

ABSTRACT

Glomalean fungi induce and colonize symbiotic tissue called arbuscular mycorrhiza on the roots of most land plants. Other fungi also colonize plants but cause disease not symbiosis. Whole-transcriptome analysis using a custom-designed Affymetrix Gene-Chip and confirmation with real-time RT-PCR revealed 224 genes affected during arbuscular mycorrhizal symbiosis. We compared these transcription profiles with those from rice roots that were colonized by pathogens (Magnaporthe grisea and Fusarium moniliforme). Over 40% of genes showed differential regulation caused by both the symbiotic and at least one of the pathogenic interactions. A set of genes was similarly expressed in all three associations, revealing a conserved response to fungal colonization. The responses that were shared between pathogen and symbiont infection may play a role in compatibility. Likewise, the responses that are different may cause disease. Some of the genes that respond to mycorrhizal colonization may be involved in the uptake of phosphate. Indeed, phosphate addition mimicked the effect of mycorrhiza on 8% of the tested genes. We found that 34% of the mycorrhiza-associated rice genes were also associated with mycorrhiza in dicots, revealing a conserved pattern of response between the two angiosperm classes.


Subject(s)
Fungi , Gene Expression Profiling , Gene Expression Regulation, Plant , Genes, Plant/genetics , Mycorrhizae , Oryza/genetics , Oryza/microbiology , DNA, Complementary/genetics , Fusarium , Magnaporthe , Oligonucleotide Array Sequence Analysis , Oryza/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Symbiosis
5.
Cell ; 116(6): 843-53, 2004 Mar 19.
Article in English | MEDLINE | ID: mdl-15035986

ABSTRACT

The Arabidopsis seedpod opens through a spring-loaded mechanism known as pod shatter, which is essential for dispersal of the seeds. Here, we identify INDEHISCENT (IND), an atypical bHLH protein, that is necessary for fruit opening and is involved in patterning each of the three fruit cell types required for seed dispersal. Previous studies suggested that FRUITFULL (FUL), a member of the MADS-domain transcription factor family, is required for fruit growth since ful mutant fruit fail to undergo the dramatic enlargement that normally occurs after fertilization. Here we show, however, that FUL is not directly required for fruit elongation and instead is required to prevent ectopic activity of IND. Our molecular and genetic studies suggest a model for the regulatory interactions among the genes that control fruit development and the mechanism that results in the expression of IND in a narrow stripe of cells.


Subject(s)
Arabidopsis Proteins/genetics , Arabidopsis/genetics , Fruit/genetics , Gene Expression Regulation, Plant/genetics , Seeds/genetics , Arabidopsis/growth & development , Arabidopsis/metabolism , Arabidopsis Proteins/isolation & purification , Arabidopsis Proteins/metabolism , Base Sequence/genetics , Basic Helix-Loop-Helix Transcription Factors , Cell Differentiation/genetics , DNA, Complementary/analysis , DNA, Complementary/genetics , Fruit/growth & development , Fruit/metabolism , Helix-Loop-Helix Motifs/genetics , Molecular Sequence Data , Morphogenesis/genetics , Mutation/genetics , Phenotype , Reproduction/genetics , Seeds/growth & development , Seeds/metabolism , Transcription Factors/genetics
6.
Proc Natl Acad Sci U S A ; 100(8): 4945-50, 2003 Apr 15.
Article in English | MEDLINE | ID: mdl-12684538

ABSTRACT

We used a systematic approach to build a network of genes associated with developmental and stress responses in rice by identifying interaction domains for 200 proteins from stressed and developing tissues, by measuring the associated gene expression changes in different tissues exposed to a variety of environmental, biological, and chemical stress treatments, and by localizing the cognate genes to regions of stress-tolerance trait genetic loci. The integrated data set suggests that similar genes respond to environmental cues and stresses, and some may also regulate development. We demonstrate that the data can be used to correctly predict gene function in monocots and dicots. As a result, we have identified five genes that contribute to disease resistance in Arabidopsis.


Subject(s)
Genes, Plant , Oryza/genetics , 14-3-3 Proteins , Arabidopsis/genetics , DNA, Plant/genetics , Gene Expression , Molecular Sequence Data , Oryza/growth & development , Oryza/metabolism , Phenotype , Phosphoprotein Phosphatases/chemistry , Phosphoprotein Phosphatases/genetics , Phosphoprotein Phosphatases/metabolism , Plant Diseases/genetics , Plant Proteins/genetics , Plant Proteins/metabolism , Plants, Genetically Modified , Protein Subunits , Quantitative Trait Loci , Seeds/growth & development , Transcription Factors/genetics , Transcription Factors/metabolism , Two-Hybrid System Techniques , Tyrosine 3-Monooxygenase/genetics , Tyrosine 3-Monooxygenase/metabolism
7.
Plant Biotechnol J ; 1(1): 59-70, 2003 Jan.
Article in English | MEDLINE | ID: mdl-17147681

ABSTRACT

Cereal grains accumulate carbohydrates, storage proteins and fatty acids via different pathways during their development. Many genes that participate in nutrient partitioning during grain filling and that affect starch quality have been identified. To understand how the expression of these genes is coordinated during grain development, a genomic approach to surveying the participation and interactions of all the pathways is necessary. Using recently published rice genome information, we designed a rice GeneChip microarray that covers half the rice genome. By monitoring the expression of 21,000 genes in parallel, we identified genes involved in the grain filling process and found that the expression of genes involved in different pathways is coordinately controlled in a synchronized fashion during grain filling. Interestingly, a known promoter element in genes encoding seed storage proteins, AACA, is statistically over-represented among the 269 genes in different pathways with diverse functions that are significantly up-regulated during grain filling. By expression pattern matching, a group of transcription factors that have the potential to interact with this element was identified. We also found that most genes in the starch biosynthetic pathway show multiple distinct spatial and temporal expression patterns, suggesting that different isoforms of a given enzyme are expressed in different tissues and at different developmental stages. Our results reveal key regulatory machinery and provide an opportunity for modifying multiple pathways by manipulating key regulatory elements for improving grain quality and quantity.

8.
Plant Mol Biol ; 53(3): 273-9, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14750518

ABSTRACT

Yeast two-hybrid assays were used to identify rice proteins interacting with two rice cyclins and other proteins potentially involved in cell cycling. The DNA sequences encoding 119 protein fragments identified were then compared by BLAST against proteins in GenBank. The proteins found include myosin-like proteins, transcription factors, kinesins, centromere proteins and undefined proteins. Based on interactions with cyclins and other elements required for cycling, we believe the undefined proteins may be involved in associated cycling processes. The identification of proteins involved in cell cycle regulation in rice may allow for the control of agronomic traits involving plant growth or development.


Subject(s)
Cell Cycle/physiology , Cyclins/metabolism , Oryza/genetics , Plant Proteins/genetics , Plant Proteins/metabolism , Cell Cycle/genetics , Cyclins/genetics , DNA, Complementary/chemistry , DNA, Complementary/genetics , Molecular Sequence Data , Protein Binding , Saccharomyces cerevisiae/genetics , Sequence Analysis, DNA , Two-Hybrid System Techniques
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