Transcriptomic analysis of Arabidopsis developing stems: a close-up on cell wall genes

被引:58
作者
Minic, Zoran [1 ,2 ]
Jamet, Elisabeth [3 ]
San-Clemente, Helene [3 ]
Pelletier, Sandra [4 ]
Renou, Jean-Pierre [4 ]
Rihouey, Christophe [5 ]
Okinyo, Denis P. O. [1 ]
Proux, Caroline [4 ]
Lerouge, Patrice [5 ]
Jouanin, Lise [2 ]
机构
[1] Univ Saskatchewan, Dept Chem, Saskatoon, SK S7N 5C9, Canada
[2] INRA, Biol Cellulaire Lab, F-78026 Versailles, France
[3] Univ Toulouse, CNRS, UPS, UMR 5546, F-31326 Castanet Tolosan, France
[4] UEVE, INRA, CNRS 8114, Unite Rech Genom Vegetale,UMR 1165, F-91057 Evry, France
[5] Univ Rouen, IFRMP23, CNRS, Fac Sci,FRE 3090, F-76821 Mont St Aignan, France
关键词
CARBOHYDRATE-ACTIVE ENZYMES; ARABINOGALACTAN-PROTEINS; SECONDARY GROWTH; FUNCTIONAL GENOMICS; LIGNIN BIOSYNTHESIS; CROSS-LINKING; THALIANA; IDENTIFICATION; EXPRESSION; POLYMERS;
D O I
10.1186/1471-2229-9-6
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Different strategies (genetics, biochemistry, and proteomics) can be used to study proteins involved in cell biogenesis. The availability of the complete sequences of several plant genomes allowed the development of transcriptomic studies. Although the expression patterns of some Arabidopsis thaliana genes involved in cell wall biogenesis were identified at different physiological stages, detailed microarray analysis of plant cell wall genes has not been performed on any plant tissues. Using transcriptomic and bioinformatic tools, we studied the regulation of cell wall genes in Arabidopsis stems, i.e. genes encoding proteins involved in cell wall biogenesis and genes encoding secreted proteins. Results: Transcriptomic analyses of stems were performed at three different developmental stages, i.e., young stems, intermediate stage, and mature stems. Many genes involved in the synthesis of cell wall components such as polysaccharides and monolignols were identified. A total of 345 genes encoding predicted secreted proteins with moderate or high level of transcripts were analyzed in details. The encoded proteins were distributed into 8 classes, based on the presence of predicted functional domains. Proteins acting on carbohydrates and proteins of unknown function constituted the two most abundant classes. Other proteins were proteases, oxido-reductases, proteins with interacting domains, proteins involved in signalling, and structural proteins. Particularly high levels of expression were established for genes encoding pectin methylesterases, germin-like proteins, arabinogalactan proteins, fasciclin-like arabinogalactan proteins, and structural proteins. Finally, the results of this transcriptomic analyses were compared with those obtained through a cell wall proteomic analysis from the same material. Only a small proportion of genes identified by previous proteomic analyses were identified by transcriptomics. Conversely, only a few proteins encoded by genes having moderate or high level of transcripts were identified by proteomics. Conclusion: Analysis of the genes predicted to encode cell wall proteins revealed that about 345 genes had moderate or high levels of transcripts. Among them, we identified many new genes possibly involved in cell wall biogenesis. The discrepancies observed between results of this transcriptomic study and a previous proteomic study on the same material revealed post-transcriptional mechanisms of regulation of expression of genes encoding cell wall proteins.
引用
收藏
页数:17
相关论文
共 99 条
[1]   Analysis of xylem formation in pine by cDNA sequencing [J].
Allona, I ;
Quinn, M ;
Shoop, E ;
Swope, K ;
St Cyr, S ;
Carlis, J ;
Riedl, J ;
Retzel, E ;
Campbell, MM ;
Sederoff, R ;
Whetten, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9693-9698
[2]   Carbohydrate-active enzymes involved in the secondary cell wall biogenesis in hybrid aspen [J].
Aspeborg, H ;
Schrader, J ;
Coutinho, PM ;
Stam, M ;
Kallas, Å ;
Djerbi, S ;
Nilsson, P ;
Denman, S ;
Amini, B ;
Sterky, F ;
Master, E ;
Sandberg, G ;
Mellerowicz, E ;
Sundberg, B ;
Henrissat, B ;
Teeri, TT .
PLANT PHYSIOLOGY, 2005, 137 (03) :983-997
[3]  
BALDWIN NTC, 1993, PLANT PHYSIOL, V13, P115
[4]   Extracellular proteomes of Arabidopsis thaliana and Brassica napus roots:: analysis and comparison by MudPIT and LC-MS/MS [J].
Basu, Urmila ;
Francis, Jennafer L. ;
Whittal, Randy M. ;
Stephens, Julie L. ;
Wang, Yang ;
Zaiane, Osmar R. ;
Goebel, Randy ;
Muench, Douglas G. ;
Good, Allen G. ;
Taylor, Gregory J. .
PLANT AND SOIL, 2006, 286 (1-2) :357-376
[5]  
Bhatia Prakash K., 1999, V64, P155
[6]   Brassinosteroids and plant steroid hormone signaling [J].
Bishop, GJ ;
Koncz, C .
PLANT CELL, 2002, 14 :S97-S110
[7]   A SIMPLE AND RAPID PREPARATION OF ALDITOL ACETATES FOR MONOSACCHARIDE ANALYSIS [J].
BLAKENEY, AB ;
HARRIS, PJ ;
HENRY, RJ ;
STONE, BA .
CARBOHYDRATE RESEARCH, 1983, 113 (02) :291-299
[8]   Lignin biosynthesis [J].
Boerjan, W ;
Ralph, J ;
Baucher, M .
ANNUAL REVIEW OF PLANT BIOLOGY, 2003, 54 :519-546
[9]   Proteomics of loosely bound cell wall proteins of Arabidopsis thaliana cell suspension cultures:: A critical analysis [J].
Borderies, G ;
Jamet, E ;
Lafitte, C ;
Rossignol, M ;
Jauneau, A ;
Boudart, G ;
Monsarrat, B ;
Esquerrè-Tugayé, MT ;
Boudet, A ;
Pont-Lezica, R .
ELECTROPHORESIS, 2003, 24 (19-20) :3421-3432
[10]   Identification of glycosylphosphatidylinositol-anchored proteins in Arabidopsis. A proteomic and genomic analysis [J].
Borner, GHH ;
Lilley, KS ;
Stevens, TJ ;
Dupree, P .
PLANT PHYSIOLOGY, 2003, 132 (02) :568-577