Heterozygous RpL27A1 mutant females exhibit a dilated cardiomyopathy phenotype, including an increased end-systolic dimension (EDD) and a decreased fractional shortening (FS) compared to controls. Bristles appear short and thin compared to wild type (Minute phenotype).
Mutants show a significant developmental delay and somewhat smaller larval body sizes than normal, but no obvious morphological neuromuscular junction phenotypes.
Heterozygotes have a Minute bristle phenotype and appreciably larger and rougher eyes than normal. Larval development of heterozygotes is delayed by about 1.2 days at 25oC compared to control siblings.
RK2.
RpL27A1, Scer\GAL4en.PU, l(2)glGD4047 has neoplasia phenotype, suppressible by bskDN.UAS, Scer\GAL4en.PU
RpL27A[+]/RpL27A1 is a suppressor | partially of abnormal cell growth phenotype of PNUTS13B
RpL27A1, Scer\GAL4en.PU, l(2)glGD4047 has neoplasia phenotype
RpL27A1, Scer\GAL4en.PU, bskDN.UAS, l(2)glGD4047 has partially lethal - majority die phenotype
RpL27A1, Scer\GAL4en.PU, l(2)glGD4047 has tracheal section | ectopic phenotype, suppressible by bskDN.UAS, Scer\GAL4en.PU
RpL27A1, Scer\GAL4en.PU, l(2)glGD4047 has wing disc phenotype, suppressible by bskDN.UAS, Scer\GAL4en.PU
RpL27A1, Scer\GAL4en.PU, l(2)glGD4047 has wing disc phenotype
RpL27A1, Scer\GAL4en.PU, l(2)glGD4047 has tracheal section | ectopic phenotype
Delta1, RpL27A1 has tarsal segment phenotype
Dl[+]/Delta1, RpL27A1 has macrochaeta phenotype
Dl[+]/Delta1, RpL27A1 has tarsal segment phenotype
Larvae expressing l(2)glGD4047 under the control of Scer\GAL4en.PU in a minute background (RpL27A1) live for about 11 days after egg laying and die with no signs of differentiation. The cells of the P-compartment of the wing disc appear highly disorganised due to loss of apical-basal polarity and increased hypoxia is seen compared to controls. At the extreme end of the larval stage these tumor cells are highly migratory, migrating towards the tracheal tubes and contacting their filopodia. The tumor cells also form new tracheal branches and can migrate along tracheal vessels and fuse with them. Tumor cells are seen to migrate from one disc to another, for example from the haltere disc, along a tracheal scaffold, to the wing disc.
Expression of bskDN.Scer\UAS suppresses the tumor growth seen when l(2)glGD4047 is expressed under the control of Scer\GAL4en.PU in a minute background (RpL27A1). Individuals differentiate into adult pharates and a small proportion of the pupae eclose into adults with no evident phenotypic alterations.
Dl1 M(2)24F1 double heterozygotes do not eclose, although many flies form pharate adults. These flies have many abnormalities, including shortening of the legs. The tarsus, which is primarily affected, is sometimes reduced to half the size of the tibia. The femur is bent like a bow. One pair of legs (usually the last pair) may be more affected than the others. The wings are often scalloped and have an extreme Dl mutant phenotype; showing both thickening at the crossveins and deltas at the wing margin. The texture of the wing is very brittle. The eye are very rough or may be reduced in size. The ocelli are sometimes fused or one of them may be missing. The bristles are larger than seen in the M(2)24F1 single heterozygote and are often duplicated. Irregular additional hairs are seen on the thorax, as in Dl1 single heterozygotes.
Schultz.
Not suppressed by RpL32+t3.3.