lethal | pupal stage (with Df(3R)Exel6147)
lethal | pupal stage (with Sgt1c01428)
Sgt1s2383 mutants exhibit a modest decrease in neuroblast number, and larval/pupal lethality.
Sgt1s2383/Df(3R)Exel6147 mutants exhibit a modest decrease in neuroblast number, and larval/pupal lethality.
Sgt1s2383/Sgt1c01428 mutants exhibit a modest decrease in neuroblast number, and larval/pupal lethality.
Sgt1s2383 mutants exhibit slower cell cycle progression, cytokinesis failure, polyploidy, multiple centrosomes, and malformed mitotic spindles. Sgt1s2383 mutants also exhibit defects in neuroblast cell polarity, with Sgt1 being required for establishing apical cortical polarity during prophase. Sgt1s2383 mutants show a strong loss of cortical scrib localization during metaphase and interphase; they also show a loss of the uniform cortical pool of dlg1 protein at interphase and mitosis, with retention of the pol of dlg1 asymmetrically colocalised with raps at the apical cortex at metaphase.
Sgt1s2383 mutant neuroblasts treated with colcemid lack all detectable apical cortical polarity.
Time-lapse imaging of Sgt1s2383 mutant larval neuroblasts show highly abnormal cortical protrusions, misshapen cells, and failure of cytokinesis.
Sgt1s2383 has abnormal cell polarity phenotype, enhanceable by pinsP62
Sgt1s2383 has abnormal cell polarity phenotype, non-suppressible by sqhE21.Tag:FLAG
Sgt1s2383 has abnormal cell polarity phenotype, non-suppressible by sqhA20.A21.Tag:FLAG
Sgt1s2383 is an enhancer of abnormal cell polarity phenotype of pinsP62
Sgt1s2383 has neuroblast phenotype, suppressible by pinsP62
Sgt1s2383 has neuroblast phenotype, non-suppressible by sqhE21.Tag:FLAG
Sgt1s2383 has neuroblast phenotype, non-suppressible by sqhA20.A21.Tag:FLAG
Sgt1s2383 is a suppressor of neuroblast phenotype of pinsP62
Sgt1s2383, pinsP62 has neuroblast | increased number phenotype
Sgt1s2383 rapsP62 double mutant neuroblasts establish little or no apical or basal cortical polarity. The developmental consequences of this loss of polarity are the formation of ectopic neuroblasts throughout the brain. This is in striking contrast to either single mutant, where the brains are smaller with reduced neuroblast numbers.
The presence of sqhE21.T:Zzzz\FLAG fails to suppress the Sgt1s2383 neuroblast cortical polarity phenotype.
The presence of sqhA20.A21.T:Zzzz\FLAG fails to suppress the Sgt1s2383 neuroblast cortical polarity phenotype.
M. Scott.
The lethality and defects in neuroblast number which are seen in the l(3)s2383 insertion line do not map to the P{lacW}s2383 insertion (which is at 66E), but instead map to a separate lesion (represented by Sgt1s2383) that maps to 84F6-84F13.
This allele was listed in the BDGP database as a lethal or sterile line during the period 1994-1999, but was discarded from the gene disruption project prior to the summary publication (FBrf0111489). Reasons for excluding lines from the collection described in FBrf0111489 include presence of more than one P insertion on the mutant chromosome, separation of lethality (or sterility) from the location of the insertion, and loss of lethality (or sterility) from the stock. Further information is available from http://www.fruitfly.org/bfd/ and from Dr. Spradling (spradling@mail1.ciwemb.edu).
Complements: l(3)0162901629. Complements: msn03349. Complements: l(3)0626406264. Complements: dally06464. Complements: mRpL1210534. Complements: mRpL12j4B2.