Amino acid replacement: A263V.
C21778626T
A263V | tsl-PA; A263V | tsl-PB; A263V | tsl-PC
A263V
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
embryonic head (with tsl3)
embryonic telson (with tsl3)
filzkorper | embryonic stage | maternal effect (with tslΔ)
telson | embryonic stage | maternal effect (with tslΔ)
Late embryos from tsl4/tslΔ transheterozygous mothers exhibit a fully penetrant "terminal class mutant" phenotype, in which some terminal structures are missing (including head structures, abdominal segment 8, telson, and filzkorper), and exhibit a highly penetrant posterior-ventral cuticle hole phenotype, as compared to controls.
Pupariation is delayed in tsl4/Df(3R)cakiX-313 mutant larvae.
Pupariation is delayed in homozygous tsl4 mutant larvae.
tsl4/tsl3 has embryonic/larval segmentation phenotype phenotype, non-suppressible by gclrev390/gcl[+]
tsl4/tsl3 has embryonic/larval segmentation phenotype phenotype, non-suppressible by gclrev390/gclrev390
tsl4/tsl3 is a suppressor of decreased cell number | recessive | embryonic stage phenotype of gclrev390
tsl4/tsl[+] is a non-suppressor of decreased cell number | recessive | embryonic stage phenotype of gclrev390
gclrev390, tsl4/tsl3 has increased cell number | embryonic stage phenotype
tsl4/tsl3 has embryonic head phenotype, non-suppressible by gclrev390/gcl[+]
tsl4/tsl3 has embryonic telson phenotype, non-suppressible by gclrev390/gcl[+]
tsl4/tsl3 has primordial germ cell | embryonic stage phenotype, non-suppressible by gclrev390/gcl[+]
tsl4/tsl3 has embryonic head phenotype, non-suppressible by gclrev390/gclrev390
tsl4/tsl3 has embryonic telson phenotype, non-suppressible by gclrev390/gclrev390
tsl4/tsl3 has primordial germ cell | embryonic stage phenotype, non-suppressible by gclrev390/gclrev390
tsl4/tsl3 is a suppressor of germline cell | embryonic stage phenotype of gclrev390
tsl4/tsl[+] is a non-suppressor of germline cell | embryonic stage phenotype of gclrev390
gclrev390, tsl4/tsl3 has primordial germ cell | embryonic stage phenotype
The pole-hole phenotype in early embryonic stage and the patterning defects in late embryonic stage (i.e. head and telson defects in cuticle preparations) displayed by tsl4/tsl3 transheterozygotes are not suppressed by gclrev390 heterozygosity or homozygosity.
The decreased primordial germ cells in gclrev390 homozygous early embryos (i.e. mitotic cycles 12/13) is fully suppressed by tsl4/tsl3 transheterozygosity, but not by tsl4 heterozygosity. tsl4/tsl3, gclrev390/+ and tsl4/tsl3, gclrev390/gclrev390 double mutants do not present any obvious defects in either centrosome positioning or cell division of primordial germ cells in the early embryo, as compared to controls.
Clonal analysis indicates that tsl expression is required only in subpopulations of follicle cells located at the poles of the oocyte.
Allelic series: tsl5 = tsl4 > tsl3 > tsl1 > tsl2