A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Chihara, C.J., Song, C., LaMonte, G., Fetalvero, K., Hinchman, K., Phan, H., Pineda, M., Robinson, K., Schneider, G.P. (2005). Identification and partial characterization of the enzyme of omega: one of five putative DPP IV genes in Drosophila melanogaster.  J. Insect Sci. 5(): 26. (Export to RIS)
FlyBase ID FBrf0194259
Publication Type Research paper
PubMed ID 17119608
PubMed 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 (ome 1) 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 ome1 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.
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Secondary IDs FBrf0191767
Language of Publication English
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Publication Type Journal
Abbreviation J. Insect Sci.
Title Journal of insect science (Online)
Publication Year 2001-
ISBN/ISSN 1536-2442
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