Amino acid replacement: T415S.
A5978347T
T415S | mle-PA; T58S | mle-PC
T415S
Amino acid replacement reported as reported as Thr to Ser, which could result from a nucleotide substitution in the first or second base of the codon. The mutation was annotated at the first base of the codon.
Males arise at a low frequency when raised at a permissive temperature. These rare escapers are sterile and produce non-motile sperm.
Homozygous adult males escape lethality at a rate of 1/150 at 18oC. In prunspecified males, gl60j males and pp males that are also mutant for mle4, the eyes are darker than for their mle4/+ sibs. rsP1 and Nspl-1 males that are also homozygous for mle4 show a less severe phenotype than their mle4/+ sibs. vg79d5 males that are also mutant for mle4 show less severe phenotype than females also mutant for mle4. mle4 has very little effect on the dosage compensation of wa : homozygous males have slightly darker eyes than their heterozygous brothers. wAdh.PB males that are also mutant for mle4 show paler eye pigmentation with respect their mle4/+ sibs. KrIf-1 and B1 males that are also mutant for mle4 show a more severe phenotype than their mle4/+ sibs.
Homozygous males show abnormal dosage compensation as determined by tritiated uridine labeling of polytene chromosomes.
male-lethal temperature-sensitive male-lethal 18oC survivors sterile, small and slow to develop
Sxlf1, mle4 has abnormal sex-determination | dominant | female phenotype
Sxlf2, mle4 has abnormal sex-determination | female phenotype
Sxlf2, mle4 has abnormal sex-determination | dominant | female phenotype
Sxlf1, mle4 has abnormal sex-determination | female phenotype
Sxlfhv1/Sxlf1, mle4 has abnormal sex-determination | female phenotype
Sxlf1, mle4 has prothoracic metatarsus | female phenotype
Sxlf2, mle4 has prothoracic metatarsus | female phenotype
Occasionally females heterozygous for Sxlf2 and homozygous for mle4 (at 18oC) have sex combs on the basitarsi of their forelegs. Some females homozygous for mle4 and heterozygous for Sxlf1 have sex combs on the basitarsi of their forelegs at 25oC (restrictive temperature). This phenotype occurs with a higher frequency in females with homozygous mle4 mothers. Intersexes are seen in females which are homozygous for mle4 and either carrying one functional copy of Sxl or transheterozygous for Sxlf1 and Sxlfhv1.
Belote, 1977.
mle4 has no effect on the dosage compensation of we, wapl, wF4-2, wa2, Dp(1;1)w+61e19 or wi.
Single amino acid change is not responsible for the mutant phenotype: transgenic copy (P{HA-ts}) binds to the X chromosome and fails to complement mle mutants.