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Published on October 24, 2002; 10.1104/pp.008888


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Received May 29, 2002
Returned for revision July 9, 2002
Accepted July 22, 2002

Expression of {alpha}-Expansin and Expansin-Like Genes in Deepwater Rice

Yi Lee and Hans Kende *

Department of Energy Plant Research Laboratory (Y.L., H.K.) and Department of Plant Biology (H.K.), Michigan State University, East Lansing, Michigan 48824-1312

* Corresponding author; email: hkende{at}msu.edu.

Previously, we have studied the expression and regulation of four {alpha}- and 14 ß-expansin genes in deepwater rice (Oryza sativa). We now report on the structure, expression, and regulation of 22 additional {alpha}-expansin (Os-EXP) genes, four expansin-like (Os-EXPL) genes, and one expansin-related (Os-EXPR) gene, which have recently been identified in the expressed sequence tag and genomic databases of rice. {alpha}-Expansins are characterized by a series of conserved Cys residues in the N-terminal half of the protein, a histidine-phenylalanine-aspartate (HFD) motif in the central region, and a series of tryptophan residues near the carboxyl terminus. Of the 22 additional {alpha}-expansin genes, five are expressed in internodes and leaves, three in coleoptiles, and nine in roots, with high transcript levels in the growing regions of these organs. Transcripts of five {alpha}-expansin genes were found in roots only. Expression of five {alpha}-expansin genes was induced in the internode by treatment with gibberellin (GA) and by wounding. The wound response resulted from excising stem sections or from piercing pinholes into the stem of intact plants. EXPL proteins lack the HFD motif and have two additional Cys residues in their C- and N-terminal regions. The positions of conserved tryptophan residues at the C-terminal region are different from those of {alpha}- and ß-expansins. Expression of the Os-EXPL3 gene is correlated with elongation and slightly induced by applied GA. However, the expression of the Os-EXPL1 and Os-EXPL2 genes showed limited correlation with cell elongation and was not induced by GA. We found no expression of the Os-EXPR1 gene in the organs examined.




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