abnormal cell number | oogenesis (with dally80)
lamina anlage & mitotic cell cycle
ovary | adult stage (with dally80)
ovary | larval stage (with dally80)
The ovarioles of dally06464/dally80 females show progressive loss of the germline stem cells (GSCs), with 59% of ovarioles containing no GSCs in the niche at day 10 after eclosion.
Wings of homozygous adults are smaller than normal, primarily due to a reduction in cell number rather than cell size.
dally06464 mutants display ISNb bypass at a similar rate to wild-type embryos.
Homozygotes have rough eyes, a reduced antenna, incomplete wing vein 5 and reduced genitalia, with incomplete penetrance. The ability of the lamina precursor neurons to enter a second division cycle is reduced in homozygous larvae.
The number of the multiply innervated (recurved) bristles in the dorsal row of dally06464/dallygem wings decreases to 55% of that of wild-type flies. Homozygotes exhibit defects the formation of macrochaetae. They lack anterior dorsocentral (aDC) and posterior supralar (pSA) bristles. the posterior dorsocentral (pDC) is displaced anteriorly or forms at an intermediate position between the aDC and pDC. Homozygotes also defects in microchaetae. Numbers are reduced and occur irregularly. In dallygem/dally06464 flies, 86% of animals lack the posterior supraalar bristle (pSA), 24% the anterior dorsocentral bristles (aDC) and 1% the posterior supraalar bristle (pSA).
3% of homozygous dally06464 flies exhibit a wing notching phenotype.
dallyΔP-527/dally06464 mutant embryos show a loss of naked cuticle and abnormalities with segment polarity (21% penetrance). About 70% of dally06464/dallygem flies show abnormalities in their genitalia.
Semilethal. Reduction or complete loss of genitalia, disordering and reduction in the number of ommatidia, reductions and duplications of the antenna and incomplete wing vein V and wing notching. Disruptions in the cell cycle progression of lamina precursors and of G2-M progression in the eye disc.
Homozygotes have wing vein defect.
some visible defects in eyes, wing veins, genitalia, male sterile
dally06464 has visible | recessive phenotype, enhanceable by wg[+]/wgl-8
dally06464 has visible | recessive phenotype, enhanceable by dppd-blk/dpp[+]
dally06464 has visible | recessive phenotype, enhanceable by dppd14/dpp[+]
dally06464 has partially lethal phenotype, non-enhanceable by Df(2R)59AB/+
dally80/dally06464 has abnormal cell number | oogenesis phenotype, suppressible by Scer\GAL4C587/dppUAS.cUa.GFP
dally80/dally06464 has abnormal cell number | oogenesis phenotype, suppressible by Scer\GAL4nanos.PG/KrUASz.Tag:HA
dally06464 has visible phenotype, suppressible by CycA3/CycA[+]
dally06464 has visible phenotype, suppressible by CycA[+]/CycA5
dally06464 has partially lethal phenotype, suppressible by CycA3/CycA[+]
dally06464 has partially lethal phenotype, suppressible by CycA[+]/CycA5
dally06464 has visible | recessive phenotype, suppressible by dppd14/dpp[+]
dally06464 has partially lethal phenotype, non-suppressible by Df(2R)59AB/+
dally06464 is an enhancer of visible phenotype of Scer\GAL4bbg-C96, fz2UAS.N
dally[+]/dally06464 is a non-enhancer of visible | dominant phenotype of sogEP7
dally[+]/dally06464 is a non-enhancer of visible | dominant phenotype of sogEP11
dally06464 is a suppressor of visible phenotype of Scer\GAL469B, fz2UAS.cCa
dally[+]/dally06464 is a non-suppressor of visible | dominant phenotype of sogEP7
dally[+]/dally06464 is a non-suppressor of visible | dominant phenotype of sogEP11
Scer\GAL4tj.PU, dally80/dally06464, tslUAS.cSa has abnormal cell number | oogenesis phenotype
Scer\GAL4nanos.PG, dally80/dally06464, tllUAS.ORF.GW.Tag:HA has abnormal cell number | oogenesis phenotype
KrKK105429, Scer\GAL4nanos.PG, dally80/dally06464 has abnormal cell number | oogenesis phenotype
dally06464, dppd-blk/dpp[+] has visible | dominant phenotype
dally[+]/dally06464, dppd-blk has visible | dominant phenotype
dally[+]/dally06464, dppd12 has visible | dominant phenotype
dally[+]/dally06464, dppd5 has visible | dominant phenotype
dallygem/dally06464 has anterior dorsocentral bristle phenotype, enhanceable by put10460
dallygem/dally06464 has posterior supraalar bristle phenotype, enhanceable by put10460
dallygem/dally06464 has posterior supraalar bristle phenotype, enhanceable by wgl-17
dally06464 has wing phenotype, enhanceable by wg[+]/wgl-8
dally06464 has wing margin bristle phenotype, enhanceable by wg[+]/wgl-8
dally06464 has phenotype, enhanceable by wg[+]/wgunspecified
dally06464 has embryo | segment polarity expression pattern | germline clone phenotype, enhanceable by wg[+]/wgunspecified
dally06464 has embryo | segment polarity expression pattern | germline clone phenotype, enhanceable by sfl[+]/sflunspecified
dally06464 has embryonic epidermis | germline clone phenotype, enhanceable by sfl[+]/sflunspecified
dally06464 has eye phenotype, enhanceable by dppd-blk/dpp[+]
dally06464 has eye phenotype, enhanceable by dppd14/dpp[+]
dally06464 has antenna phenotype, enhanceable by dppd14/dpp[+]
dally06464 has genitalia phenotype, enhanceable by dppd14/dpp[+]
dally06464 has antenna phenotype, non-enhanceable by Df(2R)59AB/+
dally06464 has genitalia phenotype, non-enhanceable by Df(2R)59AB/+
dally06464 has ommatidium phenotype, non-enhanceable by Df(2R)59AB/+
dally06464 has wing vein L5 phenotype, non-enhanceable by Df(2R)59AB/+
dally06464 has genitalia phenotype, non-enhanceable by CycA[+]/CycAunspecified
dally80/dally06464 has ovary | larval stage phenotype, suppressible by Scer\GAL4C587/dppUAS.cUa.GFP
dally80/dally06464 has ovary | larval stage phenotype, suppressible by Scer\GAL4nanos.PG/KrUASz.Tag:HA
dally06464 has antenna phenotype, suppressible by CycA3/CycA[+]
dally06464 has antenna phenotype, suppressible by CycA[+]/CycA5
dally06464 has lamina anlage & mitotic cell cycle phenotype, suppressible by CycA3/CycA[+]
dally06464 has ommatidium phenotype, suppressible by CycA3/CycA[+]
dally06464 has ommatidium phenotype, suppressible by CycA[+]/CycA5
dally06464 has wing vein L5 phenotype, suppressible by CycA3/CycA[+]
dally06464 has wing vein L5 phenotype, suppressible by CycA[+]/CycA5
dally06464 has wing phenotype, suppressible by armact.UAS/Scer\GAL4bbg-C96
dally06464 has wing margin bristle phenotype, suppressible by armact.UAS/Scer\GAL4bbg-C96
dallygem/dally06464 has genitalia phenotype, suppressible by wg[+]/wgl-17
dally06464 has wing phenotype, suppressible by dppd14/dpp[+]
dally06464 has antenna phenotype, non-suppressible by Df(2R)59AB/+
dally06464 has genitalia phenotype, non-suppressible by CycA[+]/CycAunspecified
dally06464 has genitalia phenotype, non-suppressible by Df(2R)59AB/+
dally06464 has lamina anlage & mitotic cell cycle phenotype, non-suppressible by Df(2R)59AB/+
dally06464 has lamina anlage & mitotic cell cycle phenotype, non-suppressible by stg2/stg[+]
dally06464 has ommatidium phenotype, non-suppressible by Df(2R)59AB/+
dally06464 has wing vein L5 phenotype, non-suppressible by Df(2R)59AB/+
dally06464 is an enhancer of wing phenotype of Scer\GAL4bbg-C96, fz2UAS.N
dally06464 is an enhancer of wing margin bristle phenotype of Scer\GAL4bbg-C96, fz2UAS.N
dally06464 is a non-enhancer of anterior fascicle & axon | ectopic phenotype of Larbypass
dally[+]/dally06464 is a non-enhancer of wing vein phenotype of sogEP7
dally[+]/dally06464 is a non-enhancer of wing vein phenotype of sogEP11
dally06464 is a suppressor of phenotype of wgPE2
dally06464 is a suppressor of wing phenotype of Scer\GAL469B, fz2UAS.cCa
dally[+]/dally06464 is a non-suppressor of wing vein phenotype of sogEP7
dally[+]/dally06464 is a non-suppressor of wing vein phenotype of sogEP11
Scer\GAL4nanos.PG, dally80/dally06464, tllUAS.ORF.GW.Tag:HA has ovary | larval stage phenotype
KrKK105429, Scer\GAL4nanos.PG, dally80/dally06464 has ovary | larval stage phenotype
Scer\GAL4tj.PU, dally80/dally06464, tslUAS.cSa has ovary | larval stage phenotype
dally[+]/dally06464, dppd-blk has eye phenotype
dally[+]/dally06464, dppd12 has eye phenotype
dally[+]/dally06464, dppd12 has antenna phenotype
dally[+]/dally06464, dppd5 has eye phenotype
dally[+]/dally06464, dppd5 has antenna phenotype
The dally06464 mutation does not increase the frequency of the Larbypass ISNb bypass phenotype.
The lethality seen in dally06464 homozygotes is reduced if they are also heterozygous for CycA5. The penetrance of the eye, antenna and wing defects seen in dally06464 homozygotes is reduced if they are also heterozygous for CycA5. The lethality seen in dally06464 homozygotes is completely suppressed if they are also heterozygous for CycA3. The penetrance of the eye, antenna and wing defects seen in dally06464 homozygotes is reduced if they are also heterozygous for CycA3. The severity of the dally06464 eye defects are also reduced in the double mutants. The ability of dally06464 lamina precursor neurons to enter a second division cycle is largely restored if they are also carrying CycA3. Df(2R)59AB has no effect on the divisions of dally06464 lamina precursor neurons. One copy of stg2 does not rescue the second division in dally06464 lamina precursor neurons and appears to expand the first G2/M domain of lamina precursor neuron division.
The addition of wgl-17 to dallygem/dally06464 flies, leads to enhancement of the posterior supraalar bristle phenotype seen in dallygem/dally06464 flies alone: 30% of flies have the phenotype, rather than 1%. The addition of put10460 to dallygem/dally06464 flies, leads to enhancement of the anterior dorsocentral bristle phenotype seen in dallygem/dally06464 flies alone: 90% of flies have the phenotype, rather than 24%. The posterior supraalar bristle phenotype is also enhanced by the addition of put10460. All flies have the phenotype, rather than 86%.
Homozygous embryos derived from dally06464 germline clones show weak segment polarity defects (8% penetrance). More severe defects are detected in embryos where the maternal sfl message is also eliminated (14% penetrance). The segment polarity phenotype seen in embryos derived from dally06464 germline clones is enhanced if zygotic wg is reduced by half. Penetrance is increased from 8% to 16%. Wings on wgl-8/+; dally06464/dally06464 animals show a stronger wing notch phenotype than dally06464/dally06464 alone at a higher penetrance (3% to 8%). dally06464/dally06464 strongly enhances the fully penetrant mild wing margin defect see when ectopic expression of fz2Scer\UAS.N at the presumptive wing margin is driven by Scer\GAL4C96. The wing margin phenotype seen in dally06464/dally06464, is fully suppressed by ectopic expression of armact.Scer\UAS driven by Scer\GAL4C96. The ectopic bristle phenotype seen when fz2Scer\UAS.cCa is driven uniformly in the wing pouch by Scer\GAL469B is strikingly reduced in fz2Scer\UAS.cCa, dally06464/Scer\GAL469B, dally06464 flies.
The abnormal genitalia phenotype of dally06464/dallygem flies is dominantly suppressed (down to less than 10% penetrance) by wgl-17.
Flies heterozygous for both dally06464 and dppd-blk show eye abnormalities never observed in flies heterozygous for dally06464 or dppd-blk alone. dally06464 homozygotes show a slight reduction in the eye which is more severe when they are also heterozygous for dppd-blk. The penetrance and expressivity of eye, antenna and genitalia defects seen in dally06464 homozygotes is increased if they are also heterozygous for dppd14. The wing defects seen in dally06464 homozygotes are suppressed if they are also heterozygous for dppd14. The penetrance of eye, antenna and genitalia defects seen in dally06464 homozygotes is decreased if they are carrying three copies of dpp+. The wing defects seen in dally06464 homozygotes are enhanced if they are carrying three copies of dpp+.
dally80/dally06464 is rescued by Scer\GAL4C587/dallyUAS.cUa
dally80/dally06464 is rescued by dallyUAS.cUa/Scer\GAL4tj.PU
dally80/dally06464 is not rescued by Scer\GAL4nanos.PG/dallyUAS.cUa
A. Spradling.
Separable from: l(3)87Df06464. Evidence suggests that the "l(3)06464" line contains 2 P{PZ} insertions; one at 87D in l(3)87Df (P{PZ}l(3)87Df06464) corresponding to the site of the flanking sequence AQ073333, and one at 66E (P{PZ}dally06464) which causes a mutation in dally.
Complements: l(3)0162901629. Complements: l(3)0626406264. Complements: mRpL1210534. Complements: mRpL12j4B2. Complements: l(3)neo141. Complements: mRpL12rL424. Complements: l(3)s2383s2383.
Reversion of the P-element insertion provides evidence that the insertion is responsible for the mutant phenotype.