Insertion of a copia element into the second intron.
copia insertion into intron 2.
copia insertion in the second intron.
Antiparallel blood insertion into intron 2.
Insertion of a copia element in the second intron, in parallel orientation.
copia insertion into the second intervening sequence.
5.2kb parallel copia insertion into the second intron.
Insertion of a copia element.
Parallel copia-element insertion in second intron.
Insertion of copia element.
copia insertion into an intron.
copia insertion in second chromosome.
Insertion of copia element into the second intron.
Insertion of a copia element within the small intron.
The wa allele of the white locus has been cloned by retrieving previously cloned segments carrying a copy of the transposable element copia together with contiguous sequences (Bingham, Levis and Rubin, 1981; Gehring and Paro, 1980). Bingham and Judd (1981) have shown that copia homology is tightly linked to the site of wa, copia being located at coordinate 0.0 on the physical map of the white locus (Levis, Bingham and Rubin, 1982; Levis, O'Hare and Rubin, 1984) and inserted in the small second intron (Pirrotta and Brockl, 1984). The size of the copia insertion is 5 kb. A small amount of the normal 2.6 kb white transcript is also found in wa mutants. su(wa), which darkens the eyes of wa flies, results in a higher level of the 2.6 kb transcript, while su(f), which decreases the amount of pigment, results in a lower level of this transcript. Partial revertants of wa have been sequenced and found to retain one LTR of copia (Carbonare and Gehring, 1985; Mount et al., 1988; Zachar, Davison, Garza and Bingham, 1985b). 5.0 kb copia insertion map site (kb): 0 (by definition)
Insertion of a 5.0 kb copia-element at map position 0.0 relative to the transcription start site of w.
copia insertion at coordinate 0, using coordinate system of FBrf0038648 where coordinate 0 is the copia insert of wa.
wa adults exhibit decreased short term memory in one-trail olfactory associative learning protocol.
wa mutant flies have orange eyes.
Homozygotes have dull orange eyes with only 3% red pigment (compared to 100% pigment in wild type).
Shows slight hyper dosage compensation.
Modified by z mutations.
Homozygous males are darker than homozygous females. Triple X metafemale individuals homozygous for wa exhibit dosage compensation of pigment levels.
Eye colour: orange.
Eye colour: yellow-orange. wa is slightly dosage overcompensated in males conferring slightly more eye pigment.
Strong response to E(wa).
Enhanced by duplications of Doa+.
Eye colour: orange-brown.
A wa optic disk transplanted into a wild-type host shows autonomous eye color development.
wa has abnormal eye color phenotype, enhanceable by Dp(2;2)Pdup-3/+
wa has abnormal eye color phenotype, enhanceable by Kr-h105208
wa has abnormal eye color phenotype, enhanceable by Kr-h110642
wa has abnormal eye color phenotype, enhanceable by mw2a
wa has abnormal eye color phenotype, enhanceable by mw1
wa has abnormal eye color phenotype, non-enhanceable by Nacαhs.PF
wa has abnormal eye color phenotype, suppressible by Df(2R)Pdel-1/+
wa has abnormal eye color phenotype, suppressible by Pcf11EMS2/Inr-a[+]
wa has abnormal eye color phenotype, suppressible by Df(2R)vg135/+
wa has abnormal eye color phenotype, suppressible by ox[+]/ox1
wa has abnormal eye color | recessive phenotype, suppressible by Rga[+]/Rga03834
wa has abnormal eye color | recessive phenotype, suppressible by Low1
wa has visible | adult stage phenotype, non-suppressible by wocD1
wa has abnormal eye color phenotype, non-suppressible by Nacαhs.PF
wa/we(g) is an enhancer of abnormal eye color phenotype of g53d
wa/we(g) is an enhancer of abnormal eye color phenotype of g2
wa/we(g) is an enhancer of abnormal eye color phenotype of g50e
Low1, wa, z1 has abnormal eye color phenotype
su(f)4, wa has abnormal eye color phenotype
su(f)4/su(f)1, wa has abnormal eye color phenotype
rb66a, wa has abnormal eye color phenotype
v1, wa has abnormal eye color | dominant phenotype
wa has eye phenotype, enhanceable by Dp(2;2)Pdup-3/+
wa has pigment cell phenotype, enhanceable by Kr-h105208
wa has pigment cell phenotype, enhanceable by Kr-h110642
sgl05007, wa has pigment cell phenotype, enhanceable by hh2
sgl05007, wa has pigment cell phenotype, enhanceable by hhAC
wa has phenotype, enhanceable by Ts(YLt;2Rt)L52+Ts(YLt;2Lt)R15
wa has phenotype, enhanceable by Ts(YSt;2Lt)B110+Ts(YSt;2Rt)R15
wa has phenotype, enhanceable by Ts(YLt;2Rt)G10+Ts(YLt;2Lt)R155
wa has phenotype, enhanceable by Ts(YLt;2Rt)A24+Ts(YLt;2Lt)B107
wa has phenotype, enhanceable by Ts(YSt;2Rt)B107+Ts(YLt;2Lt)L110
wa has phenotype, enhanceable by Ts(YLt;2Lt)R14+Ts(YSt;2Rt)L110
wa has phenotype, enhanceable by Ts(YSt;2Rt)L107+Ts(YSt;2Lt)P59
wa has phenotype, enhanceable by Ts(YSt;3Rt)B141+Ts(YSt;3Lt)G122
wa has phenotype, enhanceable by Ts(YLt;3Lt)A31+Ts(YLt;3Rt)G122
wa has phenotype, enhanceable by Ts(YSt;3Rt)L131+Ts(YSt;3Lt)R153
wa has phenotype, enhanceable by Ts(YLt;3Lt)B116+Ts(YLt;3Rt)G48
wa has phenotype, enhanceable by Ts(YSt;3Rt)G73+Ts(YSt;3Lt)R128
wa has phenotype, enhanceable by Ts(YLt;3Rt)R128
wa has phenotype, enhanceable by E(wa)706E706
wa has phenotype, enhanceable by E(wa)709E709
wa has phenotype, enhanceable by E(wa)736E736
wa has phenotype, enhanceable by E(wa)757E757
wa has phenotype, enhanceable by E(wa)761E761
wa has phenotype, enhanceable by E(wa)818E818
wa has pigment cell phenotype, enhanceable by mw2a
wa has pigment cell phenotype, enhanceable by mw1
wa has phenotype, non-enhanceable by Kr-h105208rev
wa has phenotype, non-enhanceable by Ts(YLt;2Lt)G120
wa has phenotype, non-enhanceable by Ts(YSt;2Rt)G146+Ts(2Lt;4Lt)J96+Ts(YSt;4Rt)J96
wa has phenotype, non-enhanceable by Ts(YLt;2Lt)H52+Ts(YLt;2Rt)J96
wa has phenotype, non-enhanceable by Ts(YLt;2Rt)B110+Ts(YSt;2Lt)D20
wa has phenotype, non-enhanceable by Ts(YLt;2Rt)D20+Ts(YSt;2Lt)G10
wa has phenotype, non-enhanceable by Ts(YSt;2Lt)L23+Ts(YSt;2Rt)R155
wa has phenotype, non-enhanceable by Ts(YSt;2Lt)A24+Ts(YLt;2Rt)L23
wa has phenotype, non-enhanceable by Ts(YSt;2Lt)H149+Ts(YSt;2Rt)R14
wa has phenotype, non-enhanceable by Dp(2;Y)J64
wa has phenotype, non-enhanceable by Ts(YLt;2Rt)B202
wa has phenotype, non-enhanceable by Ts(YLt;3Lt)B141
wa has phenotype, non-enhanceable by Ts(Y;3Rt)J1+Ts(YSt;3Lt)L132
wa has phenotype, non-enhanceable by Ts(YSt;2Rt)H52+Ts(YSt;2Lt)L52
wa has phenotype, non-enhanceable by Ts(Y;3Lt)J1+Ts(YSt;3Rt)J162
wa has phenotype, non-enhanceable by Ts(YSt;3Lt)B93+Ts(YSt;3Rt)B116
wa has phenotype, non-enhanceable by Ts(YLt;3Rt)B93+Ts(YLt;3Lt)D100
wa has phenotype, non-enhanceable by Ts(YLt;3Rt)B93+Ts(YLt;3Lt)G73
wa has phenotype, non-enhanceable by mod(mdg4)ul
wa has eye phenotype, suppressible by Df(2R)Pdel-1/+
sgl05007, wa has pigment cell phenotype, suppressible by wg1
sgl05007, wa has pigment cell phenotype, suppressible by wgP
wa has pigment cell phenotype, suppressible by RpLP001544
wa has pigment cell phenotype, suppressible by Rga[+]/Rga03834
wa has pigment cell phenotype, suppressible by Low1
wa has phenotype, suppressible by Ts(YLt;2Rt)H149+Ts(YLt;2Lt)L107
wa has phenotype, suppressible by Ts(YSt;3Rt)A31+Ts(YSt;3Lt)D228
wa has phenotype, suppressible by Ts(YSt;3Lt)G48+Ts(YSt;3Rt)R36
wa has phenotype, suppressible by E(wa)705E705
wa has phenotype, suppressible by E(wa)829E829
wa has phenotype, suppressible by su(wa)unspecified
wa has phenotype, non-suppressible by Ts(YLt;2Lt)G120
wa has phenotype, non-suppressible by Ts(YLt;2Rt)B202
wa has phenotype, non-suppressible by Ts(YLt;3Lt)B141
wa has phenotype, non-suppressible by Ts(Y;3Rt)J1+Ts(YSt;3Lt)L132
wa has phenotype, non-suppressible by Ts(YSt;2Rt)H52+Ts(YSt;2Lt)L52
wa has phenotype, non-suppressible by Ts(Y;3Lt)J1+Ts(YSt;3Rt)J162
wa has phenotype, non-suppressible by Ts(YSt;3Lt)B93+Ts(YSt;3Rt)B116
wa has phenotype, non-suppressible by Ts(YLt;3Rt)B93+Ts(YLt;3Lt)D100
wa has phenotype, non-suppressible by Ts(YLt;3Rt)B93+Ts(YLt;3Lt)G73
wa has phenotype, non-suppressible by Ts(YSt;2Rt)G146+Ts(2Lt;4Lt)J96+Ts(YSt;4Rt)J96
wa has phenotype, non-suppressible by Ts(YLt;2Lt)H52+Ts(YLt;2Rt)J96
wa has phenotype, non-suppressible by Ts(YLt;2Rt)B110+Ts(YSt;2Lt)D20
wa has phenotype, non-suppressible by Ts(YLt;2Rt)D20+Ts(YSt;2Lt)G10
wa has phenotype, non-suppressible by Ts(YSt;2Lt)L23+Ts(YSt;2Rt)R155
wa has phenotype, non-suppressible by Ts(YSt;2Lt)A24+Ts(YLt;2Rt)L23
wa has phenotype, non-suppressible by Ts(YSt;2Lt)H149+Ts(YSt;2Rt)R14
wa has phenotype, non-suppressible by Dp(2;Y)J64
wa has phenotype, non-suppressible by mod(mdg4)ul
wa/we(g) is an enhancer of pigment cell phenotype of g53d
wa/we(g) is an enhancer of pigment cell phenotype of g2
wa/we(g) is an enhancer of pigment cell phenotype of g50e
sgl05007, wa has pigment cell phenotype
Low1, wa, z1 has pigment cell phenotype
In(3)Msu1/+, wa has pigment cell phenotype
In(3)Msu2/+, wa has pigment cell phenotype
Bpt1, Nfa-g, wa has larval brain phenotype
Bpt1, Nfa-g, wa has adult optic lobe phenotype
su(f)4, wa has pigment cell phenotype
su(f)4/su(f)1, wa has pigment cell phenotype
su(f)1, wa has pigment cell phenotype
rb66a, wa has pigment cell phenotype
The addition of Inr-aEMS2/+ or Df(2R)Pdel-1/+ darkens the eye colour of wa flies.
The addition of Dp(2;2)Pdup-3/+ lightens the eye colour of wa flies.
Eye colour: the eye pigmentation level of wa flies is not affected by BEAF-32AB-KO.
Flies with a wa/we(g) mutant genotype enhance the eye colour defective phenotype of g2, g50e and g53d homozygous mutants leading to a greater reduction of red pigment in the eye. wa, g53d male mutants have lower amounts of pigment in the eye than wa single mutants, leading to a change in eye colour from dull orange-red to completely white.
wa shows an interaction with Df(2R)68-1, Df(2R)86-1, Df(2R)38-1, Df(2R)44-2, Df(2R)12-1, Df(2R)107-2 and Df(2R)157-1.
Eye phenotype is suppressed by Ufo1.
Eye colour: lighter than either mutation alone with z1.
Heterozygote with homozygous v1 has slightly lighter eye colour than wild-type.
Huestis, 1923.
Placed on the genetic map of w to the right of wbf and the left of wch. Deficiencies and duplications for wa can be produced as a result of nonhomologous exchanges within the w region.
waM allele derived as partial revertant of wa.
The copia element itself, not simply the physical interruption of the w gene, is essential for the wa phenotype and its response to the genetic modifiers su(wa), su(f), or E(wa).
The effect of combining any two mutations that modify the expression of wa is additive. If mutations at two loci suppressing wa, such as Doa and su(wa), are combined then the double mutant is darker (more wild type) than either mutation alone. The opposite applies to two mutations enhancing wa, such as mw and E(wa). A combination of suppressor and enhancer yields a colour similar to the original wa phenotype depending on their relative strengths.
The distribution of ry protein in the tissues of the adult fly is altered in this mutant.
copia element requires distant upstream sequences for polyadenylation. Dominant modifiers of wa pigmentation level have been isolated in an EMS screen.
Dosage compensation allele.
wa57i allele derived as partial revertant of wa.
Modulation of wa by Inr-b1 is at the level of transcription of the copia element.
Dosage compensation is not affected by su(Hw)V.