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cDNA sequence, mRNA expression and genomic DNA of trypsinogen from the Indianmeal moth, Plodia interpunctella
Author(s) -
Zhu Y. C.,
Oppert B.,
Kramer K. J.,
McGaughey W. H.,
Dowdy A. K.
Publication year - 2000
Publication title -
insect molecular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.955
H-Index - 93
eISSN - 1365-2583
pISSN - 0962-1075
DOI - 10.1046/j.1365-2583.2000.00138.x
Subject(s) - biology , complementary dna , microbiology and biotechnology , open reading frame , nucleic acid sequence , cdna library , peptide sequence , biochemistry , trypsinogen , trypsin , enzyme , gene
Trypsin‐like enzymes are major insect gut enzymes that digest dietary proteins and proteolytically activate insecticidal proteins produced by the bacterium Bacillus thuringiensis (Bt). Resistance to Bt in a strain of the Indianmeal moth, Plodia interpunctella , was linked to the absence of a major trypsin‐like proteinase (Oppert et al. , 1997). In this study, trypsin‐like proteinases, cDNA sequences, mRNA expression levels and genomic DNAs from Bt‐susceptible and ‐resistant strains of the Indianmeal moth were compared. Proteinase activity blots of gut extracts indicated that the susceptible strain had two major trypsin‐like proteinases, whereas the resistant strain had only one. Several trypsinogen‐like cDNA clones were isolated and sequenced from cDNA libraries of both strains using a probe deduced from a conserved sequence for a serine proteinase active site. cDNAs of 852 nucleotides from the susceptible strain and 848 nucleotides from the resistant strain contained an open reading frame of 783 nucleotides which encoded a 261‐amino acid trypsinogen‐like protein. There was a single silent nucleotide difference between the two cDNAs in the open reading frame and the predicted amino acid sequence from the cDNA clones was most similar to sequences of trypsin‐like proteinases from the spruce budworm, Choristoneura fumiferana , and the tobacco hornworm, Manduca sexta . The encoded protein included amino acid sequence motifs of serine proteinase active sites, conserved cysteine residues, and both zymogen activation and signal peptides. Northern blotting analysis showed no major difference between the two strains in mRNA expression in fourth‐instar larvae, indicating that transcription was similar in the strains. Southern blotting analysis revealed that the restriction sites for the trypsinogen genes from the susceptible and resistant strains were different. Based on an enzyme size comparison, the cDNA isolated in this study corresponded to the gene for the smaller of two trypsin‐like proteinases, which is found in both the Bt‐susceptible and ‐resistant strains of the Indianmeal moth. The sequences reported in this paper have been deposited in the GenBank database (accession numbers AF064525 for the RC688 strain and AF064526 for HD198).