Genetic Mapping and Phenotypic Characterization of the Drosophila AIFe04281 Allele Reveals Mutant Clone Loss in Mosaic Eyes

As part of the Fly-CURE consortium, a mutant allele of <i>Apoptosis inducing factor</i> ( <i>AIF</i> ) was characterized using complementation mapping, genomic sequencing, and mosaic phenotypic analysis to investigate its role in cell growth control in <i>Drosophila melanogaster</i> . The <i>AIF <sup>e04281</sup></i> mutation dramatically reduced homozygous mutant clone size and caused morphological defects in genetically mosaic eyes. Sequencing confirmed a transposon insertion that truncates the AIF protein preceding conserved domains essential for mitochondrial function and apoptosis. The observed clone loss indicates a cell-autonomous requirement for <i>AIF</i> and supports the use of <i>AIF <sup>e04281</sup></i> as a loss-of-function background for genetic modifier screens on chromosome arm 2L.

Publication Details

Journal
PubMed
Published
2025-09-16
DOI
https://doi.org/10.17912/micropub.biology.001854
Primary Topic
Mitochondrial Function and Pathology
Type
article
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0.00
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article

Genetic Mapping and Phenotypic Characterization of the Drosophila AIFe04281 Allele Reveals Mutant Clone Loss in Mosaic Eyes

PubMed
Mitochondrial Function and Pathology
article

Genetic Mapping and Phenotypic Characterization of the Drosophila AIFe04281 Allele Reveals Mutant Clone Loss in Mosaic Eyes

article en

Abstract

As part of the Fly-CURE consortium, a mutant allele of <i>Apoptosis inducing factor</i> ( <i>AIF</i> ) was characterized using complementation mapping, genomic sequencing, and mosaic phenotypic analysis to investigate its role in cell growth control in <i>Drosophila melanogaster</i> . The <i>AIF <sup>e04281</sup></i> mutation dramatically reduced homozygous mutant clone size and caused morphological defects in genetically mosaic eyes. Sequencing confirmed a transposon insertion that truncates the AIF protein preceding conserved domains essential for mitochondrial function and apoptosis. The observed clone loss indicates a cell-autonomous requirement for <i>AIF</i> and supports the use of <i>AIF <sup>e04281</sup></i> as a loss-of-function background for genetic modifier screens on chromosome arm 2L.

PubMedVol. 2025
Openalex Percentile: Top 41%
Mitochondrial Function and Pathology
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