Mvl97f mutants exhibit an iron-deficient phenotype, but display comparable levels of copper, manganese and zinc to wild-type controls. A dietary supplement of 1 mmol/l CuSO[[4]] leads to a decrease in total body iron, yet these flies accumulate iron to similar levels as controls.
Mvl97f mutants accumulate less iron in ferritin than controls, except when fed on an iron-enriched food. There is a decrease in iron-loaded ferritin content following dietary copper supplementation in Mvl97f flies.
Dietary iron accumulates primarily in the anterior midgut and copper in the diet reduces iron content of the middle midgut. Intestines from Mvl97f homozygotes show severely reduced iron content in the middle midgut. Dietary iron fails to rescue iron storage in this region, whereas in the anterior midgut ferritin induction and iron accumulation are normal. The addition of copper to the diet reduces iron content in Mvl97f intestines to below levels of histochemical detection.
There is a 4-log reduction in viral titers of flies that are infected with Sindbis virus in Mvl97f mutants compared with heterozygous or wild-type controls, while vesicular stomatitis virus (VSV) infection is unaffected.
Mvl97f flies show no significant changes in pigmentation or cuticle morphology under basal, copper-limited, or copper-excessive conditions.
Mvl97f flies show a strong sensitivity to excess copper, with significant reduced viability at 1 mmol 1[-1] Cu and essentially no survival at 2 mmol 1[-1] Cu.
Under limiting Cu conditions Mvl97f females demonstrate reduced viability, but males are unaffected.
The pupae of Mvl97f larvae raised on basal food show 40% lower iron levels than controls. Copper, Zinc and Manganese levels are not significantly lower. Larvae raised under copper-limited conditions show significantly reduced copper levels in both Mvl97f and control pupae.
Mvl97f larvae raised under basal conditions and exposed to 6 mmol 1[-] copper for a 24 hour period as adults show dramatically higher levels of copper. These flies also contain significantly more manganese and zinc than controls, and iron levels are restored.
Mutants do not discriminate between tastes, showing no preference for sugar supplemented medium, unlike wild type flies. Addition of Mn2+ and Fe2+ reverses the mutant phenotype in a dose-dependent manner. Addition of Ca2+, Mg2+, or Zn2+ fails to revert the phenotype. Metal ions are not required for correct development to the nervous system components involved in taste perception: transfer of newly eclosed adults onto Mn2+ Fe2+ supplemented medium does not rescue the mutant taste phenotype. Mn2+ and Fe2+ are implicated in a signal transduction pathway underlying taste perception.
Heterozygotes and homozygotes show a reduced preference for several sugars and an increased acceptance of low concentrations of sodium chloride, though homozygotes show a significantly stronger phenotype. Homozygotes show a shift in the threshold of acceptance of sucrose, fructose and trehalose, as measured in the feeding preference test and the proboscis extension test. Higher concentrations of stimulus are required to elicit a maximal behavioral response.
Mvl97f has abnormal taste perception phenotype, suppressible by Hsap\SLC11A1hs.PD
Mvl97f/Mvl[+] is a non-enhancer of abnormal body color phenotype of ATP7UAS.Tag:FLAG, Scer\GAL4pnr-MD237
Mvl97f/Mvl[+] is a non-suppressor of abnormal body color phenotype of ATP7UAS.Tag:FLAG, Scer\GAL4pnr-MD237
Df(3R)Fer2LCHΔ17, Mvl97f has melanotic necrosis | embryonic stage phenotype
Mvl97f/Mvl[+] is a non-enhancer of adult thorax phenotype of ATP7UAS.Tag:FLAG, Scer\GAL4pnr-MD237
Mvl97f/Mvl[+] is a non-suppressor of adult thorax phenotype of ATP7UAS.Tag:FLAG, Scer\GAL4pnr-MD237
Df(3R)Fer2LCHΔ17;Mvl97f/+ embryos have necrotic patches in the cuticle (rarely seen in either single mutant), and the percentage of embryos with these patches further significantly increases in Df(3R)Fer2LCHΔ17;Mvl97f/Mvl97f embryos.
ATP7Scer\UAS.T:Zzzz\FLAG under the control of Scer\GAL4pnr-MD237 in a Mvl97f/+ background does not significantly affect pigmentation or thoracic development compared to overexpression in a wildtype background.
The defects shown by Mvl97f flies in a feeding preference assay are partially rescued, in a dose-dependent manner, by expression of Hsap\NRAMP1hs.PD when flies are reared at 25oC or 27oC.
Not a null mutation. Dysgenesis-induced excisions of the P{lacW} can revert the Mvl97f phenotype to wild type.