Amino acid replacement: A147T. Residue is located 2 positions downstream of the DFG triplet.
Amino acid replacement: A?T. Mutation is in the kinase domain.
restriction map normal
G18658350A
G1414A
A147T | fu-PA
A147T
Polar follicle cell specification occurs in clones induced in somatic stem cells and their descendents. Relatively large somatic clones that include the anterior region of the follicular epithelium of an egg chamber are associated with the production of egg chambers with abnormal numbers of germline cells.
Germ cells in embryos lacking maternal fu function (derived from females carrying fumH63 germline clones and fertilised with a wild-type sperm) migrate towards the somatic gonadal precursor cells but fail to properly associate with them and instead scatter through the posterior half of the embryo. These embryos do not hatch.
Mutant embryos derived from homozygous germline clones lack Bolwig's organs.
Homozygotes display a strong fu wing phenotype.
Pharates die with a strong fused wing phenotype.
Homozygous and hemizygous females and hemizygous males die in pupal stage; lethality suppressible by Su(fu). fumH63/fu41 and fumH63/Y have all segments entirely duplicated; lack mouth hooks and some have no head. fumH63/+ embryos from such clones exhibit very low paternal rescue; small correction of segmental phenotype, low hatch and preadult mortality (Busson et al. 1988). pupal lethal
fumH63, ptcS2 has increased occurrence of cell division | somatic clone | oogenesis phenotype
The lack of Bolwig's organs seen in embryos derived from homozygous germline is partially rescued by expression of hhScer\UAS.cKa under the control of Scer\GAL4da.G32.
Hanratty.
Class I fu allele.
Class I mutation based on interaction with Su(fu)LP, suppression of embryonic and adult phenotype.