The Drosophila maternal-effect gene abnormal oocyte (ao) does not repress histone gene expression.
Risa Takenaka, Eric H Albanese, Sierra M Simmerman, Shilpi Verghese, Mandalay A E Maddox, Aida Flor de la Cruz, Janet M Young, Casey A Schmidt, Leila E Rieder, Harmit S Malik
Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1citing papers in PubMed
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1 · What the graph read from it
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Risa TakenakaMolecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA 98195, United States.ORCID 0000-0003-2177-6759
Eric H AlbaneseDepartment of Biology, Emory University, Atlanta, GA 30322, United States.
Sierra M SimmermanDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, United States.
Shilpi VergheseDepartment of Biology, Emory University, Atlanta, GA 30322, United States.
Mandalay A E MaddoxBiology Department, Lafayette College, Easton, PA 18042, United States.
Aida Flor de la CruzDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, United States.
Janet M YoungDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, United States.
Casey A SchmidtDepartment of Biology, Emory University, Atlanta, GA 30322, United States.
Leila E RiederDepartment of Biology, Emory University, Atlanta, GA 30322, United States.ORCID 0000-0001-9851-0145
Harmit S MalikDivision of Basic Sciences, Fred Hutchinson Cancer Center, Seattle, WA 98109, United States.ORCID 0000-0001-6005-0016
Funding
IRACDA Fellowships in Research and Science Training (FIRST)K12GM000680 · NIGMS · EMORY UNIVERSITY · PI BROWN, LOU ANN S, MCCARTY, NAEL A · 2000 to 2024
$41.2M
TRAINING IN MOLECULAR AND CELLULAR BIOLOGYT32GM007270 · NIGMS · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2020
$21.0M
DROSOPHILA GENOMICS RESOURCE CENTERP40OD010949 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Andrew Zelhof · 2012 to 2026
$9.4M
FlyBase: A Drosophila Genomic and Genetic DatabaseU24HG013300 · NHGRI · HARVARD UNIVERSITY · PI NORBERT PERRIMON · 2024 to 2026
$6.2M
Genetic Conflict Shapes Centromeres and HeterochromatinR01GM074108 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MALIK, HARMIT S. · 2005 to 2022
$6.1M
Developmental Regulation of Nuclear DomainsR35GM142724 · NIGMS · EMORY UNIVERSITY · PI Leila Elizabeth Rieder · 2021 to 2026
$2.6M
Mechanisms of Nuclear Body Formation in the Early EmbryoR00HD092625 · NICHD · EMORY UNIVERSITY · PI RIEDER, LEILA ELIZABETH · 2019 to 2021
$640k
Defining the molecular interactions that drive histone locus body formation and functionF32GM140778 · NIGMS · EMORY UNIVERSITY · PI SCHMIDT, CASEY ALEXANDRA · 2022 to 2022
The abnormal oocyte (ao) gene of Drosophila melanogaster is a maternal-effect lethal gene previously identified as encoding a transcriptional regulator of core histones. However, background genetic mutations in existing ao mutant strains could compromise their utility in manipulating histone levels. To distinguish the true ao phenotype from background effects, we created 2 new ao reagents: a CRISPR/Cas9-mediated knockout of the ao allele for genetic and molecular analyses and an epitope-tagged ao allele for cytological experiments. Using these reagents, we confirm previous findings that loss of ao causes maternal-effect lethality, which can be rescued by either a decrease in the histone gene copy number or by Y chromosome heterochromatin. Our data indicate that ao genetically interacts with the heterochromatin, as previously suggested. However, contrary to a prior study, we detected neither Ao localization to histone genes nor ao repression of core histone transcript levels. Thus, the molecular basis for ao-associated maternal-effect lethality remains unknown.
Indexed as
Drosophila melanogasterDrosophila ProteinsHistonesAnimalsCRISPR-Cas SystemsFemaleGenes, LethalHeterochromatinOocytesDrosophila ProteinsHeterochromatinHistonesabnormal oocyteDET1embryonic lethalityheterochromatinhistone locus body
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