Insertion in the second intron.
Transheterozygous combination of Sec61αk04917/Sec61αEP2567 suppresses neurodegenerative disease induced by Hsap\ATXN3tr.Q78.Scer\UAS.T:Ivir\HA1.
lethal (with Df(2L)BSC296)
lethal | embryonic stage (with Sec61α1)
autophagic vacuole & larval fat body | somatic clone | cell autonomous
lysosome & larval fat body | somatic clone | cell autonomous
Sec61α1/Sec61αk04917 animals show 46 +/- 6% embryonic lethality, with the majority of the animals dying during the early first larval instar.
Homozygous animals show 58 +/- 8% embryonic lethality, with the remainder of the animals dying during the early first larval instar.
Sec61αk04917 clones in fat bodies from well-fed early third instar larvae accumulate lysosomes, as indicated by elevated LysoTracker staining, and show redistribution of the Atg8a product into autophagosomes.
Sec61αk04917/Sec61alpha[+] is a suppressor of visible | heat sensitive phenotype of peb1
Sec61αk04917/Sec61alpha[+] is a suppressor of eye | heat sensitive phenotype of peb1
Sec61αk04917 is a suppressor of eye phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
Sec61αk04917 is a suppressor of ommatidium phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PF
Sec61αk04917 is partially rescued by Sec61αt4.4
Sec61αt4.4 rescues the lethality of Sec61αk04917 so that more than 70% of the rescued animals are viable as adults.
Lethality is revertable on excision of the P{lacW}.
Fails to complement: l(2)00455b00455b.