Amino acid replacement: Q361term.
C3458610T
Q361term | Sec5-PA
Q361term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
clathrin-coated vesicle & oocyte | germ-line clone
coated pit & oocyte | germ-line clone
cytoplasmic vesicle & oocyte | germ-line clone
nurse cell & plasma membrane | germ-line clone
Adults in which eye tissue has been made homozygous for sec5E13 during development (using the EGUF method) show ablation of the eye.
sec5E13 mutant larvae display tracheal fusion defects in 20% of the examined tracheal dorsal branches.
Oocytes derived from sec5E13 germline clones show the normal large increase in nurse cell and oocyte size that occurs during oogenesis, but the final eggs are flaccid and often collapse after oviposition as a result of the lack of yolk granules that fill up the wild type egg.
The amount of yolk is reduced from approximately 35% of the cytoplasm in wild type eggs to approximately 4.1% of the cytoplasm in oocytes derived from sec5E13 germline clones.
Oocytes derived from sec5E13 germline clones have a reduced number of vesicles and tubules beneath the oocyte surface as well as an approximately 7-fold decrease in the number of clathrin-coated pits and vesicles compared to wild type.
Both the Golgi stack and the trans-Golgi network are approximately 2-fold larger in oocytes derived from sec5E13 germline clones compared to wild type.
Females carrying sec5E13 germ-line clones are fertile, but lay eggs in which the dorsal appendages are either too closely spaced or are fused. Some egg chambers in these animals lack membranes between some of the germ-cells, resulting in nurse cell nuclei falling into the oocyte and aggregation of ring canals. In some of these egg chambers the oocyte nucleus is mislocalized away from the dorsal membrane, although in all such cases the nucleus is localized in the anterior (as in wild-type).
The eye is completely ablated in mosaic animals in which the eye is homozygous for sec5E13. Females with homozygous germline clones do not produce eggs.
RopG27/Rop[+], Sec5E13 has abnormal neuroanatomy | third instar larval stage phenotype
Sec5E13 is an enhancer of embryonic/first instar larval cuticle phenotype of Exo84Z4840/Df(3R)Espl3
RopG27/Rop[+], Sec5E13 has larval multidendritic class IV neuron | third instar larval stage phenotype
Scer\GAL4nanos.PG, Sec5E13, Sec8UASp.Tag:HA has oocyte phenotype
Scer\GAL4nanos.PG, Sec5E13, Sec8UASp.Tag:HA has nurse cell phenotype
Scer\GAL4nanos.PG, Sec5E13, Sec8UASp.Tag:HA has egg chamber phenotype
Scer\GAL4nanos.PG, Sec5E13, Sec8UASp.Tag:HA has nurse cell ring canal phenotype
The cuticle defects seen at 25[o]C in embryos derived from exo84onr/Df(3R)Espl3 females mated to exo84onr heterozygous males are enhanced by sec5E13 (both parents are heterozygous for the second mutation).
Expression of sec8Scer\UAS.P\T.T:Ivir\HA1 under the control of Scer\GAL4nos.PG in homozygous female sec5E13 germline clones results in egg chamber development arresting between stages 7 and 9, such that these females lay no eggs. The oocyte nucleus migrates appropriately to the anterior end of the cell in the double mutant germlines at stage 7, but the oocyte fails to enlarge, remaining comparable in size to the nurse cells. Some disruption of the nurse cell membranes is seen, with some cells fused and the ring canals clustered together.
Sec5E13 is rescued by Sec5+t11.0