Polytene chromosomes normal. not a duplication at either the cytological level or at the DNA level.
Canton-S-like on the basis of restriction enzyme site polymorphisms.
Dual phenotype of elevated DDC activity and increased resistance to dietary α methyl dopa relative to Oregon-R derived controls (DdcC). Specific DDC activity of newly eclosed adults 158% and DDC crossreacting material (CRM) 156% of the DdcC control. LD50 for α methyl dopa is about 0.4 mM vs. about 0.2 mM for the DdcC control. Gene dosage studies with Ddc+ and amd+ demonstrate that increased resistance to α methyl dopa is not the result of increased DDC activity. Thus, the dual phenotype is inferred to arise from a coordinated increase in Ddc+ activity and amd+ activity produced either by accumulated changes in a genetic element (or elements) in the close proximity to the Ddc and amd genes. Specific DDC activity of newly eclosed adult CyO/Ddc heterozygotes, as percentage of CyO/+ control: 158
Sherald.
Originally reported as being EMS-induced in Oregon-R but probably a Canton-S contaminant. Made coisogenic with DdcC strain.
Coordinately increases the function of Ddc and amd. Mutation is not a duplication.