A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Gene Dmel\Rex

General Information
SymbolDmel\RexSpeciesD. melanogaster
NameRibosomal exchangeAnnotation symbol
Feature typegeneFlyBase IDFBgn0003239
Gene Model StatusUnannotated Stock availability 1 publicly available
Genomic Location
Chromosome (arm)Recombination map1-66
Cytogenetic map20F1-h32Sequence location
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Automatically generated summary

See sections below for more information
The gene Ribosomal exchange is referred to in FlyBase by the symbol Dmel\Rex (FBgn0003239). It is a gene from Drosophila melanogaster. Its molecular function is unknown. The biological processes in which it is involved are not known. One allele is reported. No phenotypic data is available. It has no annotated transcripts. Gene has not been localized to the genome sequence.

hide Phenotypic Description from the Red Book (Lindsley & Zimm 1992)
Gene/Allele symbols may differ from current usage
Rex: Ribosomal exchange (L. Robbins)
Semi-dominant, maternal-effect locus which causes an early mitotic exchange between blocks of rDNA in 1 to 10% of the offspring of Rex-bearing females. Rex affects chromosomes with two separated, complete or partial ribosomal-DNA regions, such as YSX.YL or In(1)scS1Lsc4R. Chromosomes having separated blocks of heterochromatin that do not both include ribosomal genes, such as In(1)wm4, are insensitive. Affected chromosomes may pair in either spiral or hairpin configurations; the former results in loss of the intervening material (e.g., YbbRex, Dp(1;f)scS1Lsc4R, Dp(1;f)wm51bLwm4R), the latter in the inversion of that material (Dp(1;1)scS1Lsc4R, Dp(1;1)wm51bLwm4R) (Robbins and Swanson, 1988, Genetics 120: 1053-59). Exchanges usually occur early enough to yield whole-body recombinant genotypes, but a minority of events yield half-half mosaics. The exchange event generally results in partial deletion of rDNA (Robbins).
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FB2012_01
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FB2011_10
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FlyBase Computed Cytological Location
Cytogenetic map
Evidence for location
20F1-h32  
Left limit from recombination mapping relative to su(f) (FBrf0054128) Right limit from (method unavailable) (citation unavailable)  
Experimentally Determined Cytological Location
Cytogenetic map
Notes
References
Experimentally Determined Recombination Data
Location
1-66
 
Left of (cM)
Right of (cM)
Notes
Mapped by Rasooly.
 
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Annotated Transcripts
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FlyBase ID
RefSeq ID
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Annotated Polypeptides
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Allele
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Allele
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Allele of RexClassMutagenStocksKnown lesion
Rex11 --
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Allele of RexClassMutagenStocksKnown lesion
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Transgenic Constructs
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Type of insertions
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Rex allele
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Bloomington
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All of the cytological damage caused by Rex-induced recombination can be accounted for by damage to the rDNA and the rest of the genome, if it is at all sensitive to Rex, is far less sensitive than is the rDNA.
Rex is a genetically identified repeated element within the rDNA which has a semidominant maternal effect that promoter exchange within and between rDNA arrays in the first few embryonic mitoses. Genetic properties suggest the primary effect of Rex is rDNA-specific chromosome breakage that is resolved by recombination.
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GenomeRNAi - GenomeRNAi – A database for cell-based and in vivo RNAi phenotypes and reagents
hide Synonyms & Secondary IDs ( 3 )
Reported As
Symbol Synonym
Rex
 
Name Synonym
Ribosomal exchange
 
Secondary FlyBase IDs
hide References ( 13 )
Research paper
Robbins, 2000, Genetics 154(1): 13--26
Do-it-yourself statistics: a computer-assisted likelihood approach to analysis of data from genetic crosses. [FBrf0125172]
Robbins, 1996, Genetics 144(1): 109--115
Specificity of chromosome damage caused by the rex element of Drosophila melanogaster. [FBrf0089797]
Robbins and Pimpinelli, 1994, Genetics 138(2): 401--411
Chromosome damage and early developmental arrest caused by the Rex element of Drosophila melanogaster. [FBrf0076548]
Rasooly and Robbins, 1991, Genetics 129: 119--132
Rex and a suppressor of Rex are repeated neomorphic loci in the Drosophila melanogaster ribosomal DNA. [FBrf0054128]
Rasooly and Robbins, 1991, D. I. S. 70: 185--186
Mitotic instability of a P-element ribosomal cistron insertion. [FBrf0053581]
Robbins and Swanson, 1988, Genetics 120: 1053--1059
Rex-induced recombination implies bipolar organization of the ribosomal RNA genes of Drosophila melanogaster. [FBrf0048189]
Swanson, 1987, Genetics 115: 271--276
The responding site of the Rex locus of Drosophila melanogaster. [FBrf0046361]
Robbins, 1981, Genetics 99(34): 443--459
Genetically induced mitotic exchange in the heterochromatin of Drosophila melanogaster. [FBrf0036521]
Review
Gatti and Pimpinelli, 1992, A. Rev. Genet. 26: 239--275
Functional elements in Drosophila melanogaster heterochromatin. [FBrf0055232]
Robbins, 1992, Lindsley, Zimm, 1992: 585
Entry for Rex [FBrf0056735]
Williams and Robbins, 1992, Trends Genet. 8(10): 335--340
Molecular genetic analysis of Drosophila rDNA arrays. [FBrf0057721]
Abstract
Robbins et al., 2001, Europ. Dros. Res. Conf. 17: A3
Rex and the naked nucleolus organizer - characterization of some useful recombinant rDNA arrays. [FBrf0137879]
Thesis
Swanson, 1984, Ph.D. Thesis, Michigan State University, MI: vii + 106pp
Parameters of the Rex phenotype in Drosophila melanogaster. [FBrf0064875]