FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Hodkinson, L.J., Smith, C., Comstra, H.S., Ajani, B.A., Albanese, E.H., Arsalan, K., Daisson, A.P., Forrest, K.B., Fox, E.H., Guerette, M.R., Khan, S., Koenig, M.P., Lam, S., Lewandowski, A.S., Mahoney, L.J., Manai, N., Miglay, J., Miller, B.A., Milloway, O., Ngo, N., Ngo, V.D., Oey, N.F., Punjani, T.A., SiMa, H., Zeng, H., Schmidt, C.A., Rieder, L.E. (2023). A bioinformatics screen reveals hox and chromatin remodeling factors at the Drosophila histone locus.  BMC Genom Data 24(1): 54.
FlyBase ID
FBrf0257619
Publication Type
Research paper
Abstract
Cells orchestrate histone biogenesis with strict temporal and quantitative control. To efficiently regulate histone biogenesis, the repetitive Drosophila melanogaster replication-dependent histone genes are arrayed and clustered at a single locus. Regulatory factors concentrate in a nuclear body known as the histone locus body (HLB), which forms around the locus. Historically, HLB factors are largely discovered by chance, and few are known to interact directly with DNA. It is therefore unclear how the histone genes are specifically targeted for unique and coordinated regulation. To expand the list of known HLB factors, we performed a candidate-based screen by mapping 30 publicly available ChIP datasets of 27 unique factors to the Drosophila histone gene array. We identified novel transcription factor candidates, including the Drosophila Hox proteins Ultrabithorax (Ubx), Abdominal-A (Abd-A), and Abdominal-B (Abd-B), suggesting a new pathway for these factors in influencing body plan morphogenesis. Additionally, we identified six other factors that target the histone gene array: JIL-1, hormone-like receptor 78 (Hr78), the long isoform of female sterile homeotic (1) (fs(1)h) as well as the general transcription factors TBP associated factor 1 (TAF-1), Transcription Factor IIB (TFIIB), and Transcription Factor IIF (TFIIF). Our foundational screen provides several candidates for future studies into factors that may influence histone biogenesis. Further, our study emphasizes the powerful reservoir of publicly available datasets, which can be mined as a primary screening technique.
PubMed ID
PubMed Central ID
PMC10515271 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    BMC Genom Data
    Title
    BMC genomic data
    ISBN/ISSN
    2730-6844
    Data From Reference
    Genes (17)
    Cell Lines (3)