Aberration Dmel\Df(2R)gsb
| General Information | |||
|---|---|---|---|
| Symbol | Dmel\Df(2R)gsb | Species | D. melanogaster |
| Name | FlyBase ID | FBab0001966 | |
| Feature type | chromosomal_deletion | ||
| Also Known As | Df(2R)IIX62, Df(2R)gsbIIX62 | ||
| Computed Breakpoints include | 60E9;60F1 | ||
| Deleted segment | 60E9--60F1 | ||
| Sequence coordinates | |||
| Member of large scale dataset(s) | |||
Recent Updates
|
|||
| Description |
What does this section display?
This section contains items that were added to this record for each release.
It currently only tracks new links between this FlyBase report and other
FlyBase data classes (e.g. genes, references, stocks) or controlled
vocabulary terms (e.g. GO, anatomy terms).
What does this section not display?
This section does not currently display links that were removed or gene model changes.
|
||
| Update Feed |
Click the icon below to subscribe to this FlyBase record and receive updates automatically through your
feed reader.
|
||
| 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 Aberration
| |||
| Cytological Order | |||
| Progenitor | |||
| Mutagen | |||
| Class of aberration (relative to progenitor) | |||
| Breakpoints | 60E9-60E10;60F1-60F2 60E9;60F1 | ||
| Causes alleles | |||
| Carries alleles | |||
| Transposon Insertions | |||
| Formalized genetic data | bk1 hits zip << Tkr << bk2 << Kr | ||
| Genetic mapping information | |||
| Comments | Deficiency breakpoint within the zip locus. Proximal breakpoint at -55 to -49 kb and distal breakpoint at +40 to +42.5 kb (Cote et al., 1987), with the proximal breakpoint of Df(2R)SB1 approximately at 0. | ||
Comments on Cytology
| |||
Ref: Nusslein-Volhard et al., 1984, Roux Arch. dev. Biol. 193: 267--282 Left limit of break 1 from polytene analysis (FBrf0046110) Right limit of break 1 from inclusion of zip (FBrf0045941) Left limit of break 2 from inclusion of Tkr (FBrf0046110) Right limit of break 2 from polytene analysis (FBrf0046110) | |||
Sequence Crossreferences
| |||
| DDBJ
/
EMBL / GenBank | DNA sequence Protein sequence Name | ||
Gene Deletion & Duplication Data
| |||
Genes Deleted / Disrupted
| |||
| Complementation Data | |||
| Completely deleted / disrupted | |||
| Partially deleted / disrupted | |||
| Molecular Data | |||
Genes NOT Deleted / Disrupted
| |||
| Complementation Data | |||
| Molecular Data | |||
Genes Duplicated
| |||
| Complementation Data | |||
| Molecular Data | |||
Genes NOT Duplicated
| |||
| Complementation Data | |||
| Molecular Data | |||
Related Comments
| |||
Phenotypic Data
| |||
| In combination with other aberrations | Ecol\lacZY72 staining of Df(2R)gsb/Df(2R)Kr10 mutants suggests aCC and pCC neurons are not duplicated (contrary to results of FBrf0049834). Df(2R)gsb/Df(2R)Kr10 mutants exhibit duplicated RP2 neurons and lack U and CQ neurons, phenotype can be rescued by gsb+t20.1 (though rescue of U and CQ neurons is incomplete). Posterior commissures are missing or reduced, phenotype varies between segments but no segment is wild type. No effect on In(1)wm4h position-effect variegation. Df(2R)gsb/Df(2R)SB1 embryos express gsb but not zip (Cote et al., 1987). | ||
| NOT in combination with other aberrations | In the embryonic motor system of mutant animals exhibit frequently fused ISN and SN nerve roots but the respective dendritic fields do not appear to intermingle. Mutant embryos show an increase in apoptotic nuclei in the anterior portion of the segment similar to that seen in wgl-12 and arm8, though the increase in cell death is restricted to the ventral and ventrolateral surface of the embryo. There is also a slight in crease in cell death in the ventral en-expressing cells. Neuroblast NB5-2 is transformed into MP2. Cuticular phenotype is rescued by the construct P{gsb-prd}. Defective in gonad assembly. | ||
Stocks
( 2 ) | |||
| Bloomington | |||
| Kyoto | |||
Notes on Origin
| |||
| Discoverer | |||
Balancer / Genotype Variants of the Aberration
| |||
Separable Components
| |||
Other Comments
| |||
The Df(2R)gsb chromosome may act as a dominant 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), but the eye colour phenotype in the presence of Df(2R)gsb overlaps the eye colour phenotype in a wild-type background so it cannot be unequivocally demonstrated that the deficiency chromosome uncovers a suppressor of telomeric silencing. In addition, any suppression is a false positive result (the suppressor is not within the bounds of the deficient region) because the region of the deficiency is covered by a combination of nonsuppressing deficiencies and deficiencies with suppressors that map to the 2L tip. Df(2R)ES1/Df(2R)gsb embryos fail to complete dorsal closure. Distal breakpoint maps to position +40 to +42.5 and the proximal breakpoint to position -55 to -49 on the map of the 60E9-F1 interval. | |||
Synonyms & Secondary IDs
( 10 ) | |||
| Reported As | |||
| Symbol Synonym | BL-2528 Df2R(gsb) Df(2R)11X62 Df(2R)gsb Df(2R)gsbIIX62 Df(2R)gsbIIX Df(2R)gsbzipper Df(2R)gspIIx62 Df(2R)IIX62 unnamed | ||
| Name Synonym | |||
| Secondary FlyBase IDs | |||
| |||
References
( 43 ) | |||
| Generate a list of | |||
| List References by type |
| ||
Recent research papers ( 1 ) | |||
| |||
Recent reviews (0)
| |||
| All reviews listed in FlyBase were published before 2011 | |||
Recent Updates