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PROCUSTE1 Encodes a Cellulose Synthase Required for Normal Cell Elongation Specifically in Roots and Dark-Grown Hypocotyls of Arabidopsis

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TLDR
Mutants at the PROCUSTE1 (PRC1) locus show decreased cell elongation, specifically in roots and dark-grown hypocotyls, suggesting that cellulose synthesis in these organs requires the coordinated expression of at least two distinct cellulose synthase isoforms.
Abstract
Mutants at the PROCUSTE1 (PRC1) locus show decreased cell elongation, specifically in roots and dark-grown hypocotyls. Cell elongation defects are correlated with a cellulose deficiency and the presence of gapped walls. Map-based cloning of PRC1 reveals that it encodes a member (CesA6) of the cellulose synthase catalytic subunit family, of which at least nine other members exist in Arabidopsis. Mutations in another family member, RSW1 (CesA1), cause similar cell wall defects in all cell types, including those in hypocotyls and roots, suggesting that cellulose synthesis in these organs requires the coordinated expression of at least two distinct cellulose synthase isoforms.

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Journal ArticleDOI

Growth of the plant cell wall

TL;DR: Recent discoveries have uncovered how plant cells synthesize wall polysaccharides, assemble them into a strong fibrous network and regulate wall expansion during cell growth.
Journal ArticleDOI

Visualization of Cellulose Synthase Demonstrates Functional Association with Microtubules

TL;DR: Inhibition of microtubule polymerization changed the fine-scale distribution and pattern of moving CESA complexes in the membrane, indicating a relatively direct mechanism for guidance of cellulose deposition by the cytoskeleton.
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Cellulose Synthesis in Higher Plants

TL;DR: Genetic studies in Arabidopsis have identified a number of genes that contribute to the overall process of cellulose synthesis, but the role of these proteins is not yet known.
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Interactions among three distinct CesA proteins essential for cellulose synthesis

TL;DR: Data suggest that IRX5, IRX3, and IRX1 are all essential components of the cellulose synthesizing complex and the presence of all three subunits is required for the correct assembly of this complex.
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Identification of genes required for cellulose synthesis by regression analysis of public microarray data sets

TL;DR: To identify factors involved in cellulose biosynthesis, a regression method was used to analyze 408 publicly available Affymetrix Arabidopsis microarrays and found the general approach developed here is useful for identification of elements of multicomponent processes.
References
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Journal ArticleDOI

A revised medium for rapid growth and bio assays with tobacco tissue cultures

TL;DR: In vivo redox biosensing resolves the spatiotemporal dynamics of compartmental responses to local ROS generation and provide a basis for understanding how compartment-specific redox dynamics may operate in retrograde signaling and stress 67 acclimation in plants.
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Genomic sequencing

TL;DR: The genomic sequencing procedures are applicable to the analysis of genetic polymorphisms, DNA methylation at deoxycytidines, and nucleic acid-protein interactions at single nucleotide resolution.
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Structural models of primary cell walls in flowering plants: consistency of molecular structure with the physical properties of the walls during growth

TL;DR: This review integrates information on the chemical structure of individual polymers with data obtained from new techniques used to probe the arrangement of the polymers within the walls of individual cells consistent with the physical properties of the wall and its components.
Journal ArticleDOI

A simple and rapid method for the preparation of plant genomic DNA for PCR analysis.

TL;DR: This work has developed a method for the rapid extraction of small amounts of plant genomic DNA suitable for PCR analysis that is applicable to a variety of plant species and has the added advantage of not requiring any phenol or chloroform extraction.
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Semimicro determination of cellulose in biological materials.

TL;DR: The semimicro method gives quantitative recovery of purified cellulose from microbiological culture media, and also appears to be satisfactory for cellulOSE from paper pulp.
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