Amino acid replacement: Q98term.
C13677407T
Q100term | Lkb1-PA; Q100term | Lkb1-PB; Q100term | Lkb1-PC; Q100term | Lkb1-PD; Q100term | Lkb1-PE; Q100term | Lkb1-PF; Q100term | Lkb1-PH; Q100term | Lkb1-PI; Q100term | Lkb1-PJ
Q98term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. Position of mutation on reference sequence inferred by FlyBase curator.
oocyte & microtubule | germ-line clone
Lkb14B1-11 mutant class IV dendritic arborizing neuron MARCM clones display mild pruning defects at 18 h after pupariation.
Mutant third instar larvae show normal clearance of dyed food from the gut.
Heterozygous females have a mild border follicle cell migration defect.
lkb14B1-11 germ line clones cause loss of anterior-posterior polarisation of the oocyte. bcd and osk mRNA localisation fails. Mutant oocytes show loss of anterior-posterior microtubule gradient, with a high density of microtubules round the cortex and the lowest concentration in the centre. The progeny of these females are developmentally arrested before cellularization. A proportion of the mutant oocytes exit meiosis and adopt a nurse cell fate. The penetrance of this phenotype increases with age. This may be due to perdurance of the lkb1 gene product in germ-line clones.
Lkb14B1-11/lkb1[+] is a suppressor of lethal | pupal stage phenotype of Hsap\HTTQ138.UAS.mRFP1, Scer\GAL4elav-C155
Lkb14B1-11/lkb1[+] is an enhancer of border follicle cell phenotype of Scer\GAL4slbo.2.6, par-1UAS.C*.GFP
Lkb14B1-11 is an enhancer of embryonic abdominal segment | maternal effect phenotype of par-1k06821b/par-1W3
lkb14B1-11 heterozygous animals expressing Hsap\HTTQ138.Scer\UAS.T:Disc\RFP-mRFP pan-neuronally (under the control of Scer\GAL4elav-C155) exhibit an adult escaper frequency of 1.8% and 3.7% respectively. These animals are viable and have a relatively normal walking ability, although they do not inflate their wings.
lkb14B1-11/+ significantly enhances the border follicle cell migration defects caused by expression of par-1Scer\UAS.C*.T:Avic\GFP under the control of Scer\GAL4slbo.2.6.
The maternal effect embryonic phenotype of par-1k06821b/par-1W3 is enhanced by heterozygosity for lkb14B1-11.
Lkb14B1-11/Lkb14A4-2 is partially rescued by Lkb1S535A.UASp.GFP/Scer\GAL4VP16.mat.αTub67C
Lkb14B1-11/Lkb14A4-2 is partially rescued by Scer\GAL4arm.PS/Lkb1S535A.UASp.GFP
Lkb14B1-11/Lkb14A4-2 is partially rescued by Lkb1C537A.UASp.GFP/Scer\GAL4arm.PS
Lkb14B1-11/Lkb14A4-2 is partially rescued by Lkb1C537A.UASp.GFP/Scer\GAL4VP16.mat.αTub67C
Lkb14B1-11/Lkb14A4-2 is partially rescued by Scer\GAL4arm.PS/Lkb1UASp.GFP
lkb14B1-11 was identified in a genetic screen for germ-line clone mutants that disrupt the localization of the product of the transgene stauαTub67C.T:Avic\GFP-m6 in the oocyte.