FB2025_01 , released February 20, 2025
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Citation
Ihara, M., Furutani, S., Shigetou, S., Shimada, S., Niki, K., Komori, Y., Kamiya, M., Koizumi, W., Magara, L., Hikida, M., Noguchi, A., Okuhara, D., Yoshinari, Y., Kondo, S., Tanimoto, H., Niwa, R., Sattelle, D.B., Matsuda, K. (2020). Cofactor-enabled functional expression of fruit fly, honeybee, and bumblebee nicotinic receptors reveals picomolar neonicotinoid actions.  Proc. Natl. Acad. Sci. U.S.A. 117(28): 16283--16291.
FlyBase ID
FBrf0246238
Publication Type
Research paper
Abstract
The difficulty of achieving robust functional expression of insect nicotinic acetylcholine receptors (nAChRs) has hampered our understanding of these important molecular targets of globally deployed neonicotinoid insecticides at a time when concerns have grown regarding the toxicity of this chemotype to insect pollinators. We show that thioredoxin-related transmembrane protein 3 (TMX3) is essential to enable robust expression in Xenopus laevis oocytes of honeybee (Apis mellifera) and bumblebee (Bombus terrestris) as well as fruit fly (Drosophila melanogaster) nAChR heteromers targeted by neonicotinoids and not hitherto robustly expressed. This has enabled the characterization of picomolar target site actions of neonicotinoids, findings important in understanding their toxicity.
PubMed ID
PubMed Central ID
PMC7368294 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Proc. Natl. Acad. Sci. U.S.A.
    Title
    Proceedings of the National Academy of Sciences of the United States of America
    Publication Year
    1915-
    ISBN/ISSN
    0027-8424
    Data From Reference