Abstract:Cellulose, an abundant, crystalline polysaccharide, is central to plant morphogenesis and to many industries. Chemical and ultrastructural analyses together with map-based cloning indicate that the RSW1 locus of Arabidopsis encodes the catalytic subunit of cellulose synthase. The cloned gene complements the rsw1 mutant whose temperature-sensitive allele is changed in one amino acid. The mutant allele causes a specific reduction in cellulose synthesis, accumulation of noncrystalline beta-1,4-glucan, disassembly… Show more
“…(ixr1) and CESA6 (prc, ixr2) genes in most tissues is also compatible with the observations from genetic studies that these genes are involved in primary wall synthesis throughout the plants (also see below) (Arioli et al 1998;Fagard et al 2001;Scheible et al 2001). A CESA10::GUS promoter fusion indicates that CESA10 is expressed at the base of rosette leaves in Arabidopsis, which correlates with the very weak expression of the gene on the gene chips (Doblin et al 2002).…”
We have used Affymetrix gene chips to measure the expression of 10 CESA and 29 CSL genes of Arabidopsis in different developmental stages or organs. These measurements reveal that many of the genes exhibit different levels of expression in the various organs. While several CESA genes are highly expressed in all the tissues examined, very few CSL genes approach such high levels of expression. This suggests that the CSL genes either encode enzymes for the synthesis of minor components of cell walls or are expressed only in specific cell types. The expression data also highlights the potential importance of the CESA genes for primary and secondary cell wall formation during different developmental stages and in the different organs examined.Abbreviations: FTIR -Fourier transform infrared spectroscopy; CESA -cellulose synthase; cev 1 -constitutive expression of VSP1;
“…(ixr1) and CESA6 (prc, ixr2) genes in most tissues is also compatible with the observations from genetic studies that these genes are involved in primary wall synthesis throughout the plants (also see below) (Arioli et al 1998;Fagard et al 2001;Scheible et al 2001). A CESA10::GUS promoter fusion indicates that CESA10 is expressed at the base of rosette leaves in Arabidopsis, which correlates with the very weak expression of the gene on the gene chips (Doblin et al 2002).…”
We have used Affymetrix gene chips to measure the expression of 10 CESA and 29 CSL genes of Arabidopsis in different developmental stages or organs. These measurements reveal that many of the genes exhibit different levels of expression in the various organs. While several CESA genes are highly expressed in all the tissues examined, very few CSL genes approach such high levels of expression. This suggests that the CSL genes either encode enzymes for the synthesis of minor components of cell walls or are expressed only in specific cell types. The expression data also highlights the potential importance of the CESA genes for primary and secondary cell wall formation during different developmental stages and in the different organs examined.Abbreviations: FTIR -Fourier transform infrared spectroscopy; CESA -cellulose synthase; cev 1 -constitutive expression of VSP1;
“…[6][7][8][9] We recently showed that in Arabidopsis thaliana cellulose-deficient thanatos and pom2-4 mutants, of AtCesA3 and AtCSI1 respectively, suppression of cell expansion results in cortical microtubule reorientation in the fast elongation zone. 10 As both genes are involved in cellulose synthesis in primary cell walls, we examined the orientation of microtubules in 2 additional primary wall-related mutants, radially swollen1 (rsw1) 11,12 and procuste1 (prc1) 13 of AtCesA1 and AtCesA6, respectively.…”
Section: Cortical Microtubule Patterning Is Aberrant In the Fast Elonmentioning
confidence: 99%
“…On the contrary, in the meristematic and transition zones cortical microtubules exhibit transverse orientation (black lines) reminiscent of the pattern in wild-type roots. The mutants are: pom2-4 of Cellulose Synthase Interacting1 protein (CSI1), 3 prc1 (procuste1 of CesA6), 13 rsw1 (radially swollen1 of CesA1), 11,12 and than (thanatos of CesA3). 19 …”
Section: Disclosure Of Potential Conflicts Of Interestmentioning
“…(ii) Proper assembly of CelS depends on protein encoded by AtCesA1: To demonstrate that rosettes are made up of intact CESAs, the temperature-sensitive mutant rsw1 was analyzed (Arioli et al, 1998). It displayed disassembly of CelS (or rosettes) in the plasma membrane, altered cellulose crystallinity (or production of non-crystalline cellulose), and interrupted morphogenesis.…”
Section: Cels Is Composed Of Cesa Isoforms That Are Encoded By Cesa Gmentioning
confidence: 99%
“…It was proposed that the rsw1 mutant allele interrupts assembly of glucan chains into microfibrils. In the mutant, at the restrictive temperature, CelS is not properly assembled suggesting that the proper assembly of CelS depends on the presence of wild-type AtCesA1 (Arioli et al, 1998).…”
Section: Cels Is Composed Of Cesa Isoforms That Are Encoded By Cesa Gmentioning
Annually, plants produce about 180 billion tons of cellulose making it the largest reservoir of organic carbon on Earth. Cellulose is a linear homopolymer of beta(1-4)-linked glucose residues. The coordinated synthesis of glucose chains is orchestrated by specific plasma membrane-bound cellulose synthase complexes (CelS). The CelS is postulated to be composed of approximately 36 cellulose synthase (CESA) subunits. The CelS synthesizes 36 glucose chains in close proximity before they are further organized into microfibrils that are further associated with other cell wall polymers. The 36 glucose chains in a microfibril are stabilized by intra- and inter-hydrogen bonding which confer great stability on microfibrils. Several elementary microfibrils come together to form macrofibrils. Many CESA isoforms appear to be involved in the cellulose biosynthetic process and at least three types of CESA isoforms appear to be necessary for the functional organization of CelS in higher plants.
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