G to A mutation in a splicing donor site The P{GSV1}lolaGS88A8 insertion is still present on the chromosome.
G10561955A
G?A
Position of mutation on reference sequence inferred by FlyBase curator based on author statement. See Supplementary Data Figure S3. Mutation is in splice donor site leading to the retention of the 72 bp intron. This causes in frame addition of 24 aa within the BTB/POZ domain.
Flies expressing DlScer\UAS.cDa under the control of Scer\GAL4ey.PH and also carrying lolaGS88A8 and psqrev9 do not produce eye tumours or metastases.
Induced on: the P{GSV1}lolaGS88A8 chromosome. Selected as: a mutation that reverts the tumour phenotype caused by overexpression of both psq and lola from the P{GSV1}lolaGS88A8 insertion under the control of Scer\GAL4ey.PH in the presence of DlScer\UAS.cDa.