Molecular cloning and functional characterization of an endogenous endoglucanase belonging to GHF45 from the western corn rootworm, Diabrotica virgifera virgifera

A novel insect β-1,4-endoglucanase (DvvENGaseI) gene belonging to the glycoside hydrolase family (GHF) 45 was identified from the western corn rootworm, Diabrotica virgifera virgifera. The cDNA of the DvvENGaseI consisted of a 720bp open reading frame encoding a 239 amino-acid protein. Analysis of t...

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Veröffentlicht in:Gene 2013-01, Vol.513 (2), p.260-267
Hauptverfasser: Valencia, Arnubio, Alves, Analiza P., Siegfried, Blair D.
Format: Artikel
Sprache:eng
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Zusammenfassung:A novel insect β-1,4-endoglucanase (DvvENGaseI) gene belonging to the glycoside hydrolase family (GHF) 45 was identified from the western corn rootworm, Diabrotica virgifera virgifera. The cDNA of the DvvENGaseI consisted of a 720bp open reading frame encoding a 239 amino-acid protein. Analysis of the amino acid sequence revealed that DvvENGaseI exhibits 60% protein sequence identity when compared with an endoglucanase belonging to GHF45 from another beetle, Leptinotarsa decemlineata. Western blot analyses using a polyclonal antiserum developed from a partial peptide sequence revealed that DvvENGaseI expression coincided with body regions corresponding to the fore-, mid- and hindgut, although regions corresponding to the midgut and hindgut were the primary sites for DvvENGaseI expression. Functional analysis of the DvvENGaseI by RNA interference (RNAi) indicated that nearly complete knock-down of gene expression could be obtained by injection of dsRNA based on qRT-PCR and western blot analysis. However, suppression only resulted in slight developmental delays suggesting that this gene may be part of a larger system of cellulose degrading enzymes. ► An endoglucanase gene was identified from western corn rootworm larvae. ► The midgut and hindgut are the primary sites of expression. ► Nearly complete knock-down of gene expression could be obtained by RNA interference. ► Only slight developmental delays were observed after RNAi suppression. ► The gene may be part of a larger system of cellulose degrading enzymes.
ISSN:0378-1119
1879-0038
DOI:10.1016/j.gene.2012.10.046