FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
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Ribeiro, V., Da Costa, M., Dardalhon-Cuménal, D., Dupont, C.A., Gibert, J.M., Mouchel-Vielh, E., Thomassin, H., Randsholt, N.B., Debat, V., Peronnet, F. (2026). Genome-wide screen for deficiencies modifying Cyclin G-induced developmental instability in Drosophila melanogaster.  Genetics 232(3): iyaf278.
FlyBase ID
FBrf0264838
Publication Type
Research paper
Abstract
Despite long-lasting interest and research efforts, the genetic bases of developmental stability-the robustness to developmental noise-and its commonly used estimator, fluctuating asymmetry (FA), remain poorly understood. The Drosophila melanogaster Cyclin G gene (CycG) encodes a transcriptional cyclin that regulates growth and the cell cycle. Over-expression of a potentially more stable isoform of the protein (deletion of a PEST-rich domain, hereafter called CycGΔP) induces extreme wing size and shape FA (i.e. high developmental noise), indicating a major disruption of developmental stability. Previous attempts to identify the genetic bases of FA have been impeded by the constitutively low level of developmental noise, limiting the power to detect any effect. Here, we leverage the extreme developmental instability induced by overexpression of CycGΔP to explore the genetic bases of FA: we perform a genome-wide screen for deficiencies that enhance or reduce CycGΔP-induced wing FA. 495 deficiencies uncovering 90% of the euchromatic genome were combined with a recombinant chromosome expressing CycGΔP. We identified 13 and 16 deficiencies that respectively enhance and decrease FA. Analysis of mutants for some genes located in these deficiencies shows that Cyclin G ensures homogeneous growth of organs in synergy with the major morphogens of the wing, Dpp and Wg, as well as the Hippo and InR/TOR pathways. They also reveal that CycGΔP-induced FA involves Larp, a potential direct interactor of Cyclin G that regulates translation at the mitochondrial membrane. This opens up new research perspectives for understanding developmental stability, suggesting a significant role for mitochondrial activity.
PubMed ID
PubMed Central ID
PMC13016881 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Genetics
    Title
    Genetics
    Publication Year
    1916-
    ISBN/ISSN
    0016-6731
    Data From Reference