Genetic dissection of plant cell-wall biosynthesis

被引:27
|
作者
Bonetta, DT [1 ]
Facette, M [1 ]
Raab, TK [1 ]
Somerville, CR [1 ]
机构
[1] Carnegie Inst Washington, Dept Plant Biol, Stanford, CA 94305 USA
关键词
Arabidopsis; cellulose synthase; Fourer-transform IR; polysaccharide biosynthesis;
D O I
10.1042/BST0300298
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The plant cell wall is a complex structure consisting of a variety of polymers including cellulose, xyloglucan, xylan and polygalacturonan. Biochemical and genetic analysis has made it possible to clone genes encoding cellulose synthases (CesA). A comparison of the predicted protein sequences in the Arabidopsis genome indicates that 30 divergent genes with similarity to CesAs exist. It is possible that these cellulose synthase-like (Csl) proteins do not contribute to cellulose synthesis, but rather to the synthesis of other wall polymers. A major challenge is, therefore, to assign biological function to these genes. In an effort to address this issue we have systematically identified T-DNA or transposon insertions in 17 Arabidopsis Csls. Phenotypic characterization of 'knock-out' mutants includes the determination of spectroscopic profile differences in mutant cell walls from wild-type plants by Fourier-transform IR microscopy. A more precise characterization includes cell wall fractionation followed by neutral sugar composition analysis by anionic exchange chromatography.
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页码:298 / 301
页数:4
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