Identification and partial characterization of the enzyme of omega: One of five putative DPP IV genes in Drosophila melanogaster

Carol J. Chihara*, Chunyan Song, Greg LaMonte, Kristina Fetalvero, Kristy Hinchman, Helen Phan, Mario Pineda, Kelly Robinson, Gregory P. Schneider

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The omega (ome) gene product is a modifier of larval cuticle protein 5 and its alleles (and duplicates) in the third instar of Drosophila melanogaster. Using deletion mapping the locus mapped to 70F-71A on the left arm of chromosome 3. A homozygote null mutant (ome1) shows a pleiotropic phenotype that affected the size, developmental time of the flies, and the fertility (or perhaps the behavior) of homozygous mutant males. The omega gene was verified as producing a dipeptidyl peptidase IV (DPPIV) by genetic analysis, substrate specificity and pH optimum. The identity of the gene was confirmed as CG32145 (cytology 70F4) in the Celera Database (Berkeley Drosophila Genome Project), which is consistent with its deletion map position. The genomic structure of the gene is described and the decrease in DPPIV activity in the mutant ome 1 is shown to be due to the gene CG32145 (omega). The D. melanogaster omega DPPIV enzyme was partially purified and characterized. The exons of the ome1 mutant were sequenced and a base substitution mutation in exon 4 was identified that would yield a truncated protein caused by a stop codon. A preliminary study of the compartmentalization of the omega DPPIV enzyme in several organs is also reported.

Original languageEnglish (US)
JournalJournal of insect science (Online)
Volume5
DOIs
StatePublished - Nov 2 2005

Keywords

  • CD26
  • Dipeptidyl peptidase IV
  • DPPIV
  • Drosophila melanogaster
  • Enzyme compartmentalization
  • Gene identification
  • omega

ASJC Scopus subject areas

  • Insect Science

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