Chihara Carol J, Song Chunyan, LaMonte Greg, Fetalvero Kristina, Hinchman Kristy, Phan Helen, Pineda Mario, Robinson Kelly, Schneider Gregory P
University of San Francisco, Department of Biology, 2130 Fulton St., San Francisco, CA 94117-1080, USA.
J Insect Sci. 2005 Nov 2;5:26. doi: 10.1093/jis/5.1.26.
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.
ω(ome)基因产物是黑腹果蝇三龄幼虫表皮蛋白5及其等位基因(和重复基因)的修饰因子。通过缺失定位,该基因座定位于3号染色体左臂的70F-71A区域。纯合子无效突变体(ome 1)表现出多效性表型,影响果蝇的大小、发育时间以及纯合突变雄性的生育力(或可能是行为)。通过遗传分析、底物特异性和最适pH值,证实ω基因产生二肽基肽酶IV(DPPIV)。该基因的身份在Celera数据库(伯克利果蝇基因组计划)中被确认为CG32145(细胞学位置70F4),这与其缺失图谱位置一致。描述了该基因的基因组结构,并表明突变体ome1中DPPIV活性的降低是由于基因CG32145(ω)所致。对黑腹果蝇ω DPPIV酶进行了部分纯化和特性分析。对ome1突变体的外显子进行了测序,在第4外显子中鉴定出一个碱基替代突变,该突变会导致由终止密码子引起的截短蛋白。还报道了对ω DPPIV酶在几个器官中的区室化的初步研究。