A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Dmel\P{GT1}roboBG01092 Insertion

General Information
Symbol Dmel\P{GT1}roboBG01092 Species D. melanogaster
Name FlyBase ID FBti0018081
Feature type transposable_element_insertion_site
Description
Inserted element P{GT1} Expression data
Affected gene(s) robo Viability / fertility viable, fertile
Causes allele(s) roboBG01092 Stock availability 1 publicly available
LINE ID BG01092
Genomic Location
Chromosomal location 2R ( 59A3 ) Sequence location 2R:18,588,259..18,588,259
Map ( GBrowse ) detailed view FBti0018081 FBti0028215 FBti0040285 FBti0100825 FBti0106564 FBti0046252 FBti0045622 FBti0041572
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Description
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FB2012_01
FB2011_10
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Chromosome (arm)
Sequence Location
2R:18,588,259..18,588,259
Orientation
Cytological location
(computed by FlyBase)
59A3 ( inferred by FlyBase from sequence location )
Cytological location
(reported)
58F6 (reported as inferred from sequence location)
Comments concerning
location
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Flanking sequence
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Construct P{GT1}
Location-dependent
role
Size 8.447, 8.447Kb
Associated alleles
Molecular map
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Insertion may
affect gene
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Causes alleles
Lethality
References
Sterility
References
hide Phenotype Manifest In
commissure
longitudinal connective
macrochaeta
midline crossing tract
presumptive embryonic/larval central nervous system
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Statement
Reference
robo[BG01092] homozygous flies show a consistent and significant shortening of the period of the behavioural rhythm compared to wild-type controls under free-running conditions. Heterozygous robo[BG01092] mutants exhibit largely normal behavioural rhythms. robo[BG01092] mutant flies exhibit a similar avoidance response to benzaldehyde as in wild-type. robo[BG01092] mutants display normal eclosion behaviour. Homozygous robo[BG01092] mutants exhibit axon guidance defects. The overall pattern of the CNS axon scaffold is fairly normal; the longitudinal axon tracts as well as the anterior and posterior commissures are spaced normally and usually have normal thickness. The main defect observed is related to the anterior defasciculation of the longitudinal tracts, whereby in certain segments up to five axonal bundles can be observed. in addition, commissural bundles in some segments appear slightly abnormal and wander between commissures, extending their projections along and over the midline instead of projecting towards the contralateral side, resulting in a distinct phenotype. Quantification reveals that the most prominent defect in robo[BG01092] individuals is the defasciculation of longitudinal axon bundles. robo[BG01092] responds to a light pulse during the early night (ZT 15) with an approximate 3hr delay, as in wild-type, although the phase shift in mutant flies is larger than in wild-type. After ZT 21, the magnitude of the hase respose is slightly smaller in robo[BG01092] individuals compared to wild-type. After 10 days under synchronizing temperature cycles (25-20[o]C, where the warmer temperatures are reminiscent of the light period), where robo[BG01092] flies disply close to 24hr rhythms under temperature entrainment, as wild-type, the endogenous free-running period is significantly shorter in robo[BG01092] homozygotes than in wild-type controls robo[BG01092] mutants display a similar morning anticipation as wild-type in a 12hr LD regime. However the anticipation of the evening transition starts at least half an hour earlier than in wild-type controls, consistent with the shorter periodicity in the activity rhythms in free-running conditions. Small LNv neurons are mislocalised in roughly half of the robo[BG01092] brain hemispheres analysed. Misplaced neurons are located in the dorsal protocerebrum and occasionally found next to the large LNvs. Supernumerary cells are not detected in pdf-positive clusters robo[BG01092] brains. Subtly altered axon trajectories are found in a high proportion of the dissected robo[BG01092] brains. The axon bundle running along the posterio optic tract does not run in the same way in robo[BG01092] brains as in wild-type. To quantify this difference the angle between the initial turn of the axon fibre and a base line with the same origin that reaches to an intermediate point in the posterior optic tract just on top of the esophageal foramen at the midline. Using this assay, wild-type brains tend to display \'negative\' angles, while most robo[BG01092] brains exhibit \'positive\' angles. robo[BG01092] brains show no apparent difference in the trajectory of photoreceptor axons at the level of the optic lobe. robo[BG01092] is homozygous viable. robo[BG01092]/robo[1] transheterozygotes exhibit ectopic midline crossing.
robo[BG01092] Pdf[01] double mutants exhibit a lengthening of the free-running period in a dose-dependent manner. Introducing a copy of robo[BG01092] into Pdf[01] mutants gives rise to >80% rhythmic individuals. The average activity plot of robo[BG01092] Pdf[01] flies shows a modest increase in the activity ~1hr before the lights-on transition, indicating that the morning anticipation is rescued even in the absence of Pdf neuropeptide. robo[BG01092] Pdf[01] double mutants show a significantly lengthened period of locomotor activity. Transheterozygous robo[BG01092] Pdf[01] flies display wild-type period and rhythmicity.
Homozygous males and females show a significant increase in starvation resistance compared to controls.
Mutants exhibit a quantitative gain of bristles.
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Reporter Expression
Additional Information
Statement
Reference
Marker for
Reflects
expression of
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Line ID
Origin as a multiple insertion line
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Aberration
Balancer
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Bloomington
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Reported As
Symbol Synonym
P{GT1}roboBG01092
Secondary FlyBase IDs
hide References ( 7 )
Research paper
Berni et al., 2008, Europ. J. Neurosci. 27(2): 396--407
The axon-guidance roundabout gene alters the pace of the Drosophila circadian clock. [FBrf0202846]
Bellen et al., 2004, Genetics 167(2): 761--781
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes. [FBrf0179132]
Harbison et al., 2004, Genetics 166(4): 1807--1823
Quantitative trait loci affecting starvation resistance in Drosophila melanogaster. [FBrf0174696]
Norga et al., 2003, Curr. Biol. 13(16): 1388--1397
Quantitative analysis of bristle number in Drosophila mutants identifies genes involved in neural development. [FBrf0162000]
Personal communication to FlyBase
Lukacsovich and Asztalos, 1999.7.15, Dual tagging gene-trap of novel genes in Drosophila melanogaster.
Dual tagging gene-trap of novel genes in Drosophila melanogaster. [FBrf0108534]
FlyBase analysis
FlyBase, 1992-, FlyBase curation
FlyBase curation. [FBrf0105495]
Computer file
Gene Disruption Project members, 2001-, [title not yet available]
[title not yet available] [FBrf0132177]