A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Allele Dmel\amx1

General Information
SymbolDmel\amx1SpeciesD. melanogaster
NameFlyBase IDFBal0000504
Feature typealleleAssociated geneDmel\amx
Allele classamorphic allele - genetic evidence, hypomorphic allele - genetic evidence
MutagenX rayethyl methanesulfonate
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Description
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FB2013_03
FB2013_02
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Cytology
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Embryos from amx1/Df(1)10-70d females die and show the hypertrophy of the central nervous system characteristic of amx1/amx1 progeny.
Displays locomotor activity rhythm with an approximately 24h period.
Hyperplasia of replicating sensory precursors: due to an increased number of ectodermal cells being recruited as sensory precursor cells.
amx1 shows neural hypertrophy, a 2-5 fold increase in nau expressing cells per cluster relative to wild type.
Increase in SMCs per cluster in embryos lacking the maternal product.
Variable embryonic neurogenic phenotype.
Most homozygotes are indistinguishable from wild-type, but some flies have smaller eyes than normal with disarranged facets, giving a rough eye phenotype.
Eyes slightly reduced, narrower below; trident pattern stronger than in lz. Studies by Shannon (FBrf0023892) show that amx1 progeny and many amx1/+ progeny of amx1 mothers are embryonic lethals. Ovaries and egg production of amx1 females normal. General disorganization of early embryo with amx1/+ progeny of amx1 mothers less extreme than amx1 progeny (FBrf0025447) amx1/+ daughters show 0.2% survival; amx1/Dp(1;1)lz-2 show considerably higher survival (FBrf0040181); Lethal embryos exhibit hypertrophy of central nervous system at the expense of epidermal tissue (FBrf0037306; FBrf0040185). Similarly peripheral nervous elements, the sensilla, exhibit increased numbers and abnormal morphology; cells diverted from epidermal to neurological pathway (FBrf0045357). Embryonic phenotype locally rescuable by injections of ooplasm from wild-type or pcxunspecified ova during preblastoderm stages (FBrf0040181; FBrf0042361). lz/amx1 is wild type. Mosaics in amx1/+ daughters of +/+ or amx1/+ females show that ventral tissues are sensitive to reduced amx+ activity; no clones of amx1 tissue found in cuticle of amx1/+ daughters of amx1 mothers (FBrf0041016). RK2.
 
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amx1 has phenotype, non-suppressible by su(Hw)2
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No effect on the faf eye phenotype.
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Bloomington
Kyoto
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