4.7 Review

Characterizing visible and invisible cell wall mutant phenotypes

Journal

JOURNAL OF EXPERIMENTAL BOTANY
Volume 66, Issue 14, Pages 4145-4163

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erv090

Keywords

Capillary electrophoresis; cell wall synthesis; cell wall mutant; electrospray ionization (ESI); Fourier transform infrared (FTIR); matrix-assisted laser desorption ionization (MALDI); mass spectrometry (MS); methylation analysis; principal components analysis (PCA)

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Funding

  1. Center for Direct Catalytic Conversion of Biomass to Biofuels (C3Bio), an Energy Frontiers Research Center - US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0000997]

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About 10% of a plant's genome is devoted to generating the protein machinery to synthesize, remodel, and deconstruct the cell wall. High-throughput genome sequencing technologies have enabled a reasonably complete inventory of wall-related genes that can be assembled into families of common evolutionary origin. Assigning function to each gene family member has been aided immensely by identification of mutants with visible phenotypes or by chemical and spectroscopic analysis of mutants with 'invisible' phenotypes of modified cell wall composition and architecture that do not otherwise affect plant growth or development. This review connects the inference of gene function on the basis of deviation from the wild type in genetic functional analyses to insights provided by modern analytical techniques that have brought us ever closer to elucidating the sequence structures of the major polysaccharide components of the plant cell wall.

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