Allele Dmel\Med1
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Med1 | Species | D. melanogaster |
| Name | FlyBase ID | FBal0011292 | |
| Feature type | allele | Created / Updated | 2006-08-22/2006-08-22 |
| Associated gene | Dmel\Med | ||
| Allele class | |||
| Mutagen | ethyl methanesulfonate | ||
Nature of the Allele
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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 Amino acid replacement: Q283@. | ||
| Assay mode | |||
| Cytology | Polytene chromosomes apparently normal. | ||
Phenotypic Data
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Phenotypic Class
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Phenotype Manifest In
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larval head & embryo | |||
Detailed Description
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Statement Reference imaginal discs missing weak effect on mitotic chromosome condensation Homozygous larvae contain rudimentary imaginal discs, but disc primordia do not grow during larval development; testes and ovaries smaller than normal and cell number in central nervous system reduced. Mutant gonads do not survive metamorphosis when implanted into wild-type larvae. Homozygous cuticular clones appear to develop normally, but with reduced frequency and size compared to control clones. Mutant larvae support growth of implanted wild-type discs. Normal gene product postulated to be required for cell proliferation; survival of somatic epidermal clones attributed to perdurance. Larval ganglion mitoses exhibit weak effect on chromosome condensation as well as chromosome breakage (Gatti and Baker, 1989); Imaginal discs of homozygous larvae are missing or degenerate. Defects in the cell cycle: few or no dividing cells and affects chromosome condensation. Late larval early pupal lethality. Reduction in the number of mitosis in the larval brain (FBrf0049822). Embryos lacking maternal and zygotic Med function (Med1/Med25 embryos derived from females with homozygous Med1 germ line clones) show loss of dorsal tissue, expansion of the lateral denticle bands into dorsal regions and severe head defects. The phenotype is partially paternally rescuable. Homozygous clones in the eye are only seen at the margins of the eye, most commonly at the posterior margin, and result in loss of eye tissue. Mutant stage 17 embryos do not show significant defects in the location or formation of the tracheal dorsal trunk branch, dorsal branch 10, spiracular branch 10 or the posterior spiracle. Med1 zygotic mutant embryos occasionally have dorsal defects. | |||
Interactions
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Phenotypic Class
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NOT Enhanced by | |||
Statement Reference | |||
Suppressor of | |||
Statement Reference | |||
Other | |||
Statement Reference | |||
Phenotype Manifest In
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Enhancer of | |||
Statement Reference | |||
Suppressor of | |||
Statement Reference Med[+]/Med1 is a suppressor of wing | posterior phenotype of Scer\GAL4en-e16E, saxQ263D.Scer\UAS.cDa Med[+]/Med1 is a suppressor of wing vein | ectopic phenotype of Scer\GAL4en-e16E, saxQ263D.Scer\UAS.cDa | |||
Additional Comments
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Genetic Interactions
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Statement Reference Maternal lethal interaction with dpphr4 is due to a loss of dorsal-most fates in the embryos, demonstrated by loss of amnioserosa cells. Slightly suppresses the wing phenotype produced by tkvSC143. Shows a dominant maternal effect interaction with dpp; when Med1/+ females are crossed to dpphr27/+ males, all progeny carrying dpphr27 die. This lethality is rescued by MedUbi-p63E.PD also partly by MadUbi-p63E.T:Hsap\MYC. | |||
Xenogenetic Interactions
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Statement Reference | |||
Complementation & Rescue Data
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| Fails to complement | |||
| Comments | |||
Stocks
( 1 ) | |||
| Bloomington | |||
Notes on Origin
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| Discoverer | |||
Synonyms & Secondary IDs
( 4 ) | |||
| Reported As | |||
| Symbol Synonym | l(3)12m137 l(3)SG701 med1 Med1 | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
References
( 14 ) | |||
| Research paper |
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| Personal communication to FlyBase |
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Nature of the Allele