Allele Dmel\dppd12
| General Information | |||
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| Symbol | Dmel\dppd12 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0003009 | |
| Feature type | allele | Associated gene | Dmel\dpp |
| Also Known As | dpp12 | ||
| Allele class | hypomorphic allele - genetic evidence | ||
| Mutagen | X ray | ||
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Nature of the Allele
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| Allele class | |||
| Mutagen | |||
| Mutations Mapped to the Genome | |||
Type Location Additional Notes References | |||
| Associated Sequence Data | |||
| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
| UniProtKB/Swiss-Prot | |||
| UniProtKB/TrEMBL | |||
| Progenitor genotype | |||
| Nature of the lesion | Statement Reference Deletion of control elements. Disrupts 3' regions controlling disc expression. Alterations in the disk regulatory region of dpp gene. Breakpoint allele. | ||
| Caused by aberration | |||
| Cytology | |||
Phenotypic Data
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Phenotypic Class
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viable (with dppTgR46.1) | |||
Phenotype Manifest In
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capitellum (with dppd5) ommatidium (with dppd6) taste bristle (with dppd6) | |||
Detailed Description
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Statement Reference dppd6/dppd12 flies have a reduced number of ommatidia. The adults are weak, short-lived (live for 2-3 days) and have abnormalities in the wing, leg, antenna and external genitalia. The tarsal and meta-tarsal segments of all legs are abnormal in dppd6/dppd12 flies, due to loss of claws and fusion of the tarsal segments. The dorsal parts of the leg are sometimes ventralised. The tibia and femur are progressively less affected, while the trochanter and coxa are almost wild type. The number of sex comb bristles is generally higher than normal. dppd6/dppd12 flies have defects in the distal segments of the antenna. The arista is usually absent and a conical projection is present on the third segment (which presumably represents the fused 4th, 5th and 6th antennal segments). The leg and antennal discs of dppd6/dppd12 larvae are deformed. Most dppd6/dppd12 males completely lack external genitalia while some have abnormal external genitalia. There is little effect on the female genitalia. The external genitalia of dppd6/dppd12 and dppd8/dppd12 males are reduced to a small ring like structure. The external genitalia of dpp10638/dppd12 males are highly defective and the penis apparatus is less defective. dppd6/dppd12 and dpp10638/dppd12 females show duplication of the thorn bristles accompanied by an absence of long bristles. dppd8/dppd12 females show a complete duplication of the thorn bristles of the vaginal plate. Heterozygotes are phenotypically wild-type. Homozygous clones induced in first instar larvae produce abnormalities in the dorsal side of the leg. Pattern elements from the dorsal side are missing, and may or may not be replaced with a duplicate version of the remaining ventral part of the leg. Duplications are arranged as mirror images. Homozygous clones doubly mutant for dppd12 and wgl-17 show defects in both the ventral and dorsal sides of the leg. The frequency of duplications is reduced compared to the single mutant homozygous dppd12 or wgl-17 clones. dppd8/dppd12 dics wing pouch is small, almost no wing tissue remains, except structures for the proximal hinge region. The proximal costa remains in the anterior compartment and a reduced alula in the posterior. Partial rescue of the wing phenotype is achieved by tkvQ253D.Scer\UAS.cLa expression driven by Scer\GAL4dpp.blk1. Mutation partially suppresses the penetrance of the hhMrt phenotype. Heterozygotes with dppd5 have reduced wings. dppd5/dppd12 heterozygotes have reduced wings. Some dppd12 ptcG20/dppd5 ptc16 individuals eclose and show a partial rescue of the ptc phenotype (decrease in the numbers of bristles on the notum, legs and antennae and number of teeth in the male sex comb and a reduction in size of overgrown structures). A posterior clone runs along the antero-posterior boundary until it reaches a gap in wing vein 4 (a region sensitive to lack of dpp) where the border of the clone becomes irregular. Rudimentary imaginal discs. | |||
External Data
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| Linkouts | |||
Interactions
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Phenotypic Class
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Enhanced by | |||
Statement Reference | |||
Suppressed by | |||
Statement Reference | |||
Enhancer of | |||
Statement Reference | |||
NOT Enhancer of | |||
Statement Reference dppd12/dpp[+] is a non-enhancer of visible phenotype of I-2Scer\UAS.T:Zzzz\His6,T:Hsap\MYC, Scer\GAL4vg.PM, putScer\UAS.cMa | |||
Suppressor of | |||
Statement Reference dppd12 is a suppressor of increased cell number | somatic clone phenotype of BacA\p35Scer\UAS.cHa, Scer\GAL4tub.PU wgl-17/dppd12 is a suppressor of increased cell number | somatic clone phenotype of BacA\p35Scer\UAS.cHa, Scer\GAL4tub.PU | |||
NOT Suppressor of | |||
Statement Reference dppd12/dpp[+] is a non-suppressor of large body phenotype of Scer\GAL429BD, dallysec.Scer\UAS.T:Hsap\MYC dppd12/dpp[+] is a non-suppressor of visible phenotype of I-2Scer\UAS.T:Zzzz\His6,T:Hsap\MYC, Scer\GAL4vg.PM, putScer\UAS.cMa dppd12 is a non-suppressor of cell death defective | somatic clone phenotype of BacA\p35Scer\UAS.cHa, Scer\GAL4tub.PU dppd12 is a non-suppressor of planar polarity defective phenotype of Scer\GAL4hs.2sev, Tak1Scer\UAS.cMa wgl-17/dppd12 is a non-suppressor of cell death defective | somatic clone phenotype of BacA\p35Scer\UAS.cHa, Scer\GAL4tub.PU | |||
Other | |||
Statement Reference | |||
Phenotype Manifest In
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Enhanced by | |||
Statement Reference | |||
Suppressed by | |||
Statement Reference | |||
Enhancer of | |||
Statement Reference | |||
NOT Enhancer of | |||
Statement Reference dppd12/dpp[+] is a non-enhancer of wing phenotype of I-2Scer\UAS.T:Zzzz\His6,T:Hsap\MYC, Scer\GAL4vg.PM, putScer\UAS.cMa | |||
Suppressor of | |||
Statement Reference | |||
NOT Suppressor of | |||
Statement Reference dppd12/dpp[+] is a non-suppressor of wing phenotype of I-2Scer\UAS.T:Zzzz\His6,T:Hsap\MYC, Scer\GAL4vg.PM, putScer\UAS.cMa dppd12 is a non-suppressor of eye photoreceptor cell phenotype of Scer\GAL4hs.2sev, Tak1Scer\UAS.cMa | |||
Other | |||
Statement Reference | |||
Additional Comments
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Genetic Interactions
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Statement Reference The glial overmigration phenotype seen in spin[10403] eye discs is significantly suppressed if the animals are also heterozygous for dpp[d12]. sax[1]/+ enhances the trans-heterozygous dpp[d12] Df(2L)JS17 phenotype characterised by missing tarsal claws and abnormal wing venation. dppd12 heterozygosity does not reduce animal size when dallysec.Scer\UAS.T:Hsap\MYC is driven by Scer\GAL429BD. The small size of dppd-blk/dppd12 eye discs is partially rescued by eyaScer\UAS.cBa expressed under the control of Scer\GAL4dpp.blk1 and greater numbers of developing ommatidia are seen. The severity of the leg defects seen in dppd6/dppd16 flies is enhanced by B1. There is an overall shortening in length along the proximal-distal axis of the leg and complete or partial fusion or even total loss of tarsal segments. The tibia and femur are deformed, showing shortening, bulging and disorganised bristle patterns. The coxa and trochanter are not so strongly affected. The sex comb of the prothoracic leg, when present, is always duplicated in these flies. The antenna phenotype of dppd6/dppd16 flies is enhanced by B1; the arista, 4th and 5th segments are completely absent and the 2nd and 3rd segments are widened and deformed and have defects in the bristle pattern. B1 ; dppd6/dppd16 flies completely lack ommatidia. All B1 ; dppd6/dppd16 males completely lack external genitalia. The gbb4/gbb4 and gbb1/gbb4 phenotypes are dominantly enhanced by dppd12; there is a greater loss of wing vein L4, wing vein L2 and the anterior crossvein than in gbb single mutant flies. There is also loss of intervein tissue, especially between veins L2 and L3 and between veins L4 and L5, resulting in a reduction in the size of the wing. A gap at the distal end of vein L3 is seen in 3% of cases. A reduction in the loss of wing vein L5 is seen in these flies. Viability is reduced. gbb1 dppd12/gbb4 + flies show truncations and/or fusions of the distal-most tarsal segments of the male prothoracic leg. Flies heterozygous for both dally06464 and dppd12 show eye and antenna abnormalities. | |||
Xenogenetic Interactions
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Statement Reference X-ray irradiated wing disc clones expressing BacA\p35Scer\UAS.cHa under the control of Scer\GAL4tub in dppd12 mutants contain a mixture of two types of cell: `live' cells, which have not initiated apoptosis due to the irradiation, and `undead' cells (between 20 and 70% of the clone), which have initiated apoptosis, but have failed to complete programmed cell death. No such cells persist outside the clones in which BacA\p35Scer\UAS.cHa is expressed. X-ray irradiated wing disc clones expressing BacA\p35Scer\UAS.cHa under the control of Scer\GAL4tub in dppd12 wgl-17 mutants contain a mixture of two types of cell: `live' cells, which have not initiated apoptosis due to the irradiation, and `undead' cells (between 20 and 70% of the clone), which have initiated apoptosis, but have failed to complete programmed cell death. No such cells persist outside the clones in which BacA\p35Scer\UAS.cHa is expressed. Unlike BacA\p35Scer\UAS.cHa (Scer\GAL4tub) wing disc clones, neither BacA\p35Scer\UAS.cHa (Scer\GAL4tub) dppd12 nor BacA\p35Scer\UAS.cHa (Scer\GAL4tub) dppd12 wgl-17 clones appear to be associated with extra proliferation or growth after stress (such as X-ray irradiation). | |||
Complementation & Rescue Data
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| Rescued by | |||
| Partially rescued by | |||
| Not rescued by | |||
| Comments | Expression of dppαTub84B.PG in clones in the male terminalia in a dppd5/dppd12 background results in the recovery of terminal structures. The degree of recovery depends on the developmental stage at which the clone is induced. Recovery of terminal structures is accompanied by reduced penis apparatus duplications. The rescue is non-autonomous. dppScer\UAS.T.T:Avic\GFP-EGFP rescues the wing phenotype of dppd8/dppd12 flies when expressed under the control of Scer\GAL4dpp.blk1; wing size and pattern are almost normal except that ectopic vein material is seen near vein 3 and the spacing between veins 3 and 4 is slightly increased. Belongs to the disk-V class of alleles. Allele class: d-V | ||
Stocks
( 3 ) | |||
| Bloomington | 2070 | ||
| Kyoto | 106650 101482 | ||
Notes on Origin
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| Discoverer | |||
Comments
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Remove most or all of the imaginal disc function of dpp. Lacks disc function and retains shortvein function. dpp class V allele. | |||
External Crossreferences & Linkouts
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| Other Crossreferences | |||
| Linkouts | |||
Synonyms & Secondary IDs
( 5 ) | |||
| Reported As | |||
| Symbol Synonym | d12 Dpp12 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 65 ) | |||
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Recent research papers ( 2 ) | |||
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Recent Updates
External Crossreferences & Linkouts