A Database of Drosophila Genes & Genomes

FB2008_07, released August 8, 2008
 

Allele Dmel\AntpNs

General Information
SymbolDmel\AntpNsSpeciesD. melanogaster
NameNasobemiaFlyBase IDFBal0000587
Feature typealleleCreated / Updated2006-05-14/2006-05-14
Associated geneDmel\Antp
Allele classneomorph, gain of function
Mutagenspontaneous
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Allele class
Mutagen
Mapped Features and Mutations
Type
Symbol & Location
Additional Notes
References
 
 
 
 
Associated Sequence Data
DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
      Progenitor genotype
      Nature of the lesion
      Statement
      Reference
      Insertion of an 8kb roo element at map position +128.
      25kb duplication of the exon 3 region with a roo transposon separating the duplicated sequences.
      Internal 25kb partial duplication from position 46 to 71 and a complex insertion of more than 40kb including two roo elements. Truncated roo element has inserted at position 71 within intron sequences in opposite transcriptional orientation. The 5' half of a roo element has inserted at position 46 in opposite transcriptional orientation. The duplication gives the gene three promoters, P1, P2A and P2B. Dominant mutant phenotype due to ectopic expression from promoter Antp P2A.
      Assay mode
      Caused by insertion
      Cytology
      Polytene chromosomes normal.
       
      Polytene chromosomes normal.
      Polytene chromosomes normal.
      hide Phenotypic Data
      hide Phenotypic Class
      hide Phenotype Manifest In
       
       
      hide Detailed Description
      Statement
      Reference
      In extreme cases, AntpNs/+ forms, in place of an antenna, a complete leg that includes sternopleura, coxa, trochanter, femur, tibia, and tarsus. Antennal leg has no sex comb in male, and bristle pattern is that of a middle leg. Eyes smaller; whole head tends to be malformed. AntpNs ssa/+ ssa indistinguishable from AntpNs/+. AntpNs/AntpB viable; phenotype like extreme AntpNs/+. Expression variable but penetrance complete. RK1.
       
      Antenna are leg-like.
      Transformation of antenna to prothoracic leg identity.
      Antennae to leg transformation.
      Transformation of head to thoracic tissue.
      Partial transformation of antennae into legs. Flies exhibit diminished chemosensory jump behaviour to ethyl acetate but no change in the jump response to a visual stimulus.
      AntpNs derepresses the Antp P2 promoter in the eye-antennal disc. The penetrance of antennae to leg transformations of AntpNs mutations is greatly reduced in brm1 heterozygotes.
      A viable dominant leg to antenna transformation.
      96-99% of heterozygotes show differentiation of leg structures in the antennae.
      Antenna to leg transformation. Heterozygotes exhibit reduced compound eye and ommatidia are replaced by micro- and macrochaetae.
      96% of heterozygous flies show transformation of antenna to leg.
      95% of mutant flies show an antenna to leg transformation.
      Heterozygotes show transformation of antenna to leg.
      Only 15% of heterozygotes show normal arista development.
      AntpNs/+ mutants show ectopic transformation of antennae into leg tissue.
      Heterozygotes lack the arista, but appear to have normal maxillary palps. The locomotor activity of heterozygous flies in an open field arena is not significantly different from that of wild-type flies.
      hide Interactions
      hide Phenotypic Class
      hideEnhanced by
      Statement
      Reference
      AntpNs has visible phenotype, enhanceable by tsh17
      AntpNs, Pc2 has visible | homeotic phenotype, enhanceable by Pcl[+]/Pcl18
      hideSuppressed by
      Statement
      Reference
      AntpNs has visible | dominant phenotype, suppressible by mor1
      AntpNs has visible | dominant phenotype, suppressible by mor2
      AntpNs has visible | dominant phenotype, suppressible | partially by Snr1R3
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by brm1/brm[+]
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by mor[+]/mor1
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by mor2/mor[+]
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by osa1/osa[+]
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by osa2/osa[+]
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by osa[+]/osa3
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by osa[+]/osa4
      AntpNs, Pc2 has visible | homeotic phenotype, suppressible by trxE3/trx[+]
      AntpNs has visible | dominant phenotype, suppressible | partially by Gug[+]/Gug1757
      AntpNs has visible | dominant phenotype, suppressible | partially by Gug3333/Gug[+]
      AntpNs has visible | dominant phenotype, suppressible | partially by Gug519/Gug[+]
      AntpNs has visible | homeotic phenotype, suppressible by osa2
      AntpNs has visible | homeotic phenotype, suppressible | partially by Df(2R)ED3921
      AntpNs has visible phenotype, suppressible | partially by Df(3L)vin2/+
      AntpNs has visible phenotype, suppressible | partially by tna[+]/tnarI075
      AntpNs has visible phenotype, suppressible | partially by tna[+]/tna1
      AntpNs has visible | homeotic | dominant phenotype, suppressible by osa1/osa[+]
      AntpNs has visible | homeotic | dominant phenotype, suppressible by osa2/osa[+]
      hideNOT suppressed by
      Statement
      Reference
      AntpNs has visible | dominant phenotype, non-suppressible by Gug2295/Gug[+]
      hideOther
      Statement
      Reference
      hide Phenotype Manifest In
      hideEnhanced by
      Statement
      Reference
      AntpNs has phenotype, enhanceable by d1
      AntpNs has ommatidium phenotype, enhanceable by tsh17
      AntpNs has eye phenotype, enhanceable by tsh17
      AntpNs has phenotype, enhanceable by al1
      AntpNs, Pc2 has antenna phenotype, enhanceable by Pcl[+]/Pcl18
      AntpNs has phenotype, enhanceable by ash211
      AntpNs has phenotype, enhanceable by ash212
      AntpNs has phenotype, enhanceable by ash218
      AntpNs has phenotype, enhanceable by ash21
      AntpNs has phenotype, enhanceable by ash22
      AntpNs has phenotype, enhanceable by ash24
      AntpNs has phenotype, enhanceable by ash29
      hideSuppressed by
      Statement
      Reference
      AntpNs has antenna phenotype, suppressible by mor1
      AntpNs has antenna phenotype, suppressible by mor2
      AntpNs has antenna phenotype, suppressible | partially by Snr1R3
      AntpNs has leg | ectopic phenotype, suppressible | partially by Snr1R3
      AntpNs, Pc2 has antenna phenotype, suppressible by brm1/brm[+]
      AntpNs, Pc2 has antenna phenotype, suppressible by mor[+]/mor1
      AntpNs, Pc2 has antenna phenotype, suppressible by mor2/mor[+]
      AntpNs, Pc2 has antenna phenotype, suppressible by osa1/osa[+]
      AntpNs, Pc2 has antenna phenotype, suppressible by osa2/osa[+]
      AntpNs, Pc2 has antenna phenotype, suppressible by osa[+]/osa3
      AntpNs, Pc2 has antenna phenotype, suppressible by osa[+]/osa4
      AntpNs, Pc2 has antenna phenotype, suppressible by trxE3/trx[+]
      AntpNs has arista phenotype, suppressible | partially by Gug[+]/Gug1757
      AntpNs has arista phenotype, suppressible | partially by Gug3333/Gug[+]
      AntpNs has arista phenotype, suppressible | partially by Gug519/Gug[+]
      AntpNs has antenna phenotype, suppressible by osa2
      AntpNs has leg | ectopic phenotype, suppressible by osa2
      AntpNs has antenna phenotype, suppressible | partially by Df(2R)ED3921
      AntpNs has leg | ectopic phenotype, suppressible | partially by Df(2R)ED3921
      AntpNs has phenotype, suppressible by skd2
      AntpNs has antenna phenotype, suppressible | partially by Df(3L)vin2/+
      AntpNs has leg | ectopic phenotype, suppressible | partially by Df(3L)vin2/+
      AntpNs has antenna phenotype, suppressible | partially by tna[+]/tnarI075
      AntpNs has leg | ectopic phenotype, suppressible | partially by tna[+]/tnarI075
      AntpNs has antenna phenotype, suppressible | partially by tna[+]/tna1
      AntpNs has leg | ectopic phenotype, suppressible | partially by tna[+]/tna1
      AntpNs has antenna phenotype, suppressible by osa1/osa[+]
      AntpNs has leg | ectopic phenotype, suppressible by osa1/osa[+]
      AntpNs has antenna phenotype, suppressible by osa2/osa[+]
      AntpNs has leg | ectopic phenotype, suppressible by osa2/osa[+]
      hideNOT suppressed by
      Statement
      Reference
      AntpNs has arista phenotype, non-suppressible by Gug2295/Gug[+]
      hideOther
      Statement
      Reference
      hide Additional Comments
      hide Genetic Interactions
      Statement
      Reference
      Suppressed by brm1.
      ash2 alleles affect the expressivity or penetrance of the antenna to leg transformation. ash21, ash29, ash211, ash212 and ash218 enhance the transformation phenotype, ash22 and ash24 suppress the transformation phenotype.
      The penetrance of AntpNs/+ phenotype is greatly reduced if the flies are also heterozygous for mor1 or mor2.
      Eye phenotype is enhanced in a tsh17 mutant background.
      obk1, Antp73b (or AntpNs), hthdtl-S142204 triple mutants produce biramous antenna/legs in place of single antennae.
      The AntpNs/+ antenna to leg transformation is suppressed about 50% by Snr1R3.
      The mutant arista phenotype seen in AntpNs/+ adults is partially suppressed if they are also heterozygous for Gug519 (36% of flies have normal arista development), Gug1757 (26% of flies have normal arista development) or Gug3333 (28% of flies have normal arista development), but is unaffected if they are also heterozygous for Gug2295.
      The Df(2R)ED3921 deficiency causes a 21% suppression of the AntpNs homeotic transformation. The osa2 mutation suppresses this phenotype by 87%.
      hide Xenogenetic Interactions
      Statement
      Reference
      hide Complementation & Rescue Data
      Complements
       
      Comments
      hide Stocks ( 2 )
      Bloomington
      2235
      Kyoto
      106749
      hide Notes on Origin
      Discoverer
      Gehring.
      hide Comments
      Etymology: W. Gehring believed this variant to be a separate locus from Antp and named it "Nasobemia" after Morgenstern's mythological creature that walked on its nose.
      Etymology: mutation is named "Nasobemia" after an imaginary animal that can walk on its nose in a poem by Christian Morgenstern; mutant flies show transformation of antenna to leg.
      hide Synonyms & Secondary IDs ( 4 )
      Reported As
      Symbol Synonym
      AntpNs
       
      Ns
       
      Name Synonym
      Secondary FlyBase IDs
        hide References ( 29 )
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        hide Recent research papers ( 2 )
        Liu et al., 2007, Genetics 175(3): 1197--1212
        Exploratory activity in Drosophila requires the kurtz nonvisual arrestin. [FBrf0200160]
        Ragab et al., 2006, Genetics 172(2): 1069--1078
        High mobility group proteins HMGD and HMGZ interact genetically with the Brahma chromatin remodeling complex in Drosophila. [FBrf0190761]