Amino acid replacement: W22term.
G16053370A
W22term | Mbs-PG; W22term | Mbs-PH; W22term | Mbs-PI; W22term | Mbs-PJ; W22term | Mbs-PK; W22term | Mbs-PL; W22term | Mbs-PM; W22term | Mbs-PN; W22term | Mbs-PO; W22term | Mbs-PP; W22term | Mbs-PQ; W22term | Mbs-PV
W22term
G to A nucleotide change at the second or third position of the wild type Trp codon leads to a nonsense mutation (exact site of mutation unspecified). The mutation was annotated at the second base of the codon.
Egg chambers containing follicle cells mutant for MbsT541 display oocyte polarity defects.
MbsT541 mutant clones in the eye disc show a mislocalization of photoreceptors from the apical epithelium into the basal region, sometimes progressing into the optic stalk. The mislocalized photoreceptors retain their polarity and some epithelial characteristics. There is only a slight reduction in apical constriction in the morphogenetic furrow in MbsT541 clones and no ectopic apical constriction in more posterior regions of the disc.
MbsT541/Mbs[+] is a non-suppressor of abnormal planar polarity phenotype of dsh1
MbsT541 has eye disc | somatic clone phenotype, enhanceable by sqhA21.Tag:FLAG
MbsT541 has eye disc | somatic clone phenotype, non-enhanceable by Scer\GAL4Tub.PU/RokCAT.UAS
MbsT541 has eye disc | somatic clone phenotype, suppressible by sqhA21.Tag:FLAG
MbsT541 has eye disc | somatic clone phenotype, suppressible by zip[+]/zip1
MbsT541/Mbs[+] is a suppressor | partially of embryonic/first instar larval cuticle phenotype of PatjΔ1
MbsT541/Mbs[+] is a suppressor of wing hair | increased number phenotype of dsh1
MbsT541, disco1 has eye disc | somatic clone phenotype
MbsT541/+ reduces the frequency of embryonic lethality in PatjΔ1 homozygotes from 28 to 12%. In addition, the cuticle defects seen in PatjΔ1 embryos are strongly decreased in frequency in the MbsT541/+ background. PatjΔ1/MbsT541 PatjΔ1 pupae start metamorphosis (reflected by elongation and remodelling of the wing disc).
Removing one copy of Mbs antagonizes the multiple wing hair formation in dsh1/Y mutants but has no effect on the planar polarity defects. MbsT541 photoreceptor clones are restored to their wild-type apical location in the eye disc when discs carry one copy of the constitutively inactive sqhA21.T:Zzzz\FLAG transgene. However, the amount of photoreceptor basal mislocalization is increased when eye discs carry one copy of sqhE20.E21 (a transgene that contains two phosphomimetic mutations). The mislocalization of photoreceptors in MbsT541 clones is suppressed when eye discs have a zip1/+ background. The photoreceptor localization defect is not significantly enhanced when MbsT541 mutant clones express rokCAT.Scer\UAS under the control of Scer\GAL4tub. Photoreceptors still move basally in MbsT541 eye disc clones with a disco1 background. However, instead of moving toward the optic stalk, the mutant photoreceptors are found more centrally at the basal surface of the eye disc, and are concentrated at sites where many axons are present.
MbsT541/MbsT791 is partially rescued by Scer\GAL4da.G32/MbsUAS.cLa
MbsT541/MbsT666 is partially rescued by Scer\GAL4da.G32/MbsUAS.cLa
Expression of MbsScer\UAS.cLa, driven by Scer\GAL4da.G32, partially rescues the embryonic lethality of MbsT541/MbsT791 transheterozygotes, allowing over 90% of these mutants to survive to the pupal stage and 45% to survive to adulthood. Likewise, expression of the transgene allows 80% of MbsT541/MbsT666 mutants to survive to the pupal stage, but only 6% to survive to adulthood.
Selected as: a mutation affecting early eye development.