Aberration Dmel\Df(2L)al
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2L)al | Species | D. melanogaster |
| Name | Deficiency (2L) aristaless | FlyBase ID | FBab0001692 |
| Feature type | chromosomal_deletion | ||
| Computed Breakpoints include | 21C1;21C7 | ||
| Deleted segment | 21C1--21C7 | ||
| Map ( GBrowse ) |
ErrorNo matching regions found. | ||
| Sequence coordinates | 2L:300,574..303,911 [+] (Df(2L)al:bk1) | ||
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| Description |
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| FB2012_01 |
References
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| FB2011_10 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Nature of the Aberration
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| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 21B7--21B8;[] 21B8-21C1;21C7-21C8 21B8-21C1;21C8-21D1 21C1;21C7 21C1;21C8 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | U2af38 << bk1 << fs(2)al << bk2 << lwr | ||
| Genetic mapping information | |||
| Comments | Breakpoint(s) molecularly mapped | ||
Comments on Cytology
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The distal breakpoint of Df(2L)al is about 300kb from the telomere. Pi3K21B probably overlaps the distal breakpoint. Left breakpoint is just before 21C1-21C2, right breakpoint is just before 21D1-21D2. Left limit of break 1 from polytene analysis (FBrf0031322) Right limit of break 1 from inclusion of al (FBrf0006343) Left limit of break 2 from polytene analysis (FBrf0047732) Right limit of break 2 from polytene analysis (FBrf0098232) | |||
Sequence Crossreferences
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| DDBJ
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EMBL / GenBank | DNA sequence Protein sequence Name | ||
Gene Deletion & Duplication Data
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Genes Deleted / Disrupted
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| Complementation Data | |||
| Completely deleted / disrupted | |||
| Molecular Data | |||
Genes NOT Deleted / Disrupted
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| Complementation Data | |||
| Molecular Data | |||
Genes Duplicated
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| Complementation Data | |||
| Molecular Data | |||
Genes NOT Duplicated
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| Complementation Data | |||
| Molecular Data | |||
Related Comments
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Stated to delete or disrupt ds. Aspects of this conclusion subsequently challenged, see FBrf0125086. | |||
Phenotypic Data
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| In combination with other aberrations | Df(2L)al dominantly enhances the transformation of arista to leg phenotype seen in Df(2R)Dll-MP heterozygotes. No effect on In(1)wm4h position-effect variegation. Viable in combination with In(2LR)alv. Df(2L)al/In(2LR)al8 heterozygotes survive poorly; escapers have reduced aristae, broad thoraces, arched wings, incomplete veins and large eyes (Koroshkina and Golubovsky, 1978). | ||
| NOT in combination with other aberrations | The Df(2L)al chromosome acts as a dominant weak suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion). Wild-type clones made in the ovaries of a mutant female, are significantly larger than clones of heterozygous mutant cells. This size difference is greater in clones initiated at 48 hours after egg laying (AEL) than 2 hours AEL. Homozygous Df(2L)al mutants show an increase in cardial and pericardial cells during embryonic development. Df(2L)al in combination with a pair of introgressions from D.simulans spanning 30F1-31E7 to 35D7-36A14 Dsim\Int(2L)S and 21A1 to 22D1--23A2 Dsim\Int(2L)D Dsim\Int(2L)D produces fertile male flies. These flies are female sterile. Macrophages in homozygotes remain very small and round with a much lower phagocytic index (PI) for apoptotic corpses than wild type (0.26 compared to 3.96). Heterozygotes show a PI of about 1.5. No second site non-complementing phenotype with zipEbr and zipmhc-c6.1. Shows no maternal enhancement of dpphr4. Does not act as a dominant suppressor of Nnd-1. Strong enhancer of B. Midgut development of mutant embryos is wild type. Maternal hemizygosity for Df(2L)al significantly increases post-fertilization embryonic mortality. Paternal hemizygosity has no effect. Homozygous embryos do not complete head involution and tracheae are disconnected. Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2. Homozygous lethal. Heterozygotes have an extreme Minute phenotype with rough eyes. Homozygous lethal heterozygous Minute phenotype | ||
Stocks
( 4 ) | |||
| Bloomington | |||
| Kyoto | |||
Notes on Origin
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| Discoverer | E.B. Lewis, 1940. | ||
Balancer / Genotype Variants of the Aberration
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Separable Components
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Other Comments
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Synonyms & Secondary IDs
( 6 ) | |||
| Reported As | |||
| Symbol Synonym | Df(2L)a1 Df(2L)al Dfal M(2)21C | ||
| Name Synonym | Deficiency (2L) aristaless | ||
| Secondary FlyBase IDs | |||
References
( 74 ) | |||
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Recent research papers ( 1 ) | |||
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Recent reviews (0)
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| All reviews listed in FlyBase were published before 2010 | |||
Recent Updates