FB2026_02 , released June 18, 2026
FB2026_02 , released June 18, 2026
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Citation
Stasiv, Y., Kuzin, B., Regulski, M., Tully, T., Enikolopov, G. (2004). Regulation of multimers via truncated isoforms: a novel mechanism to control nitric-oxide signaling.  Genes Dev. 18(15): 1812--1823.
FlyBase ID
FBrf0179455
Publication Type
Research paper
Abstract
Nitric oxide (NO) is an essential regulator of Drosophila development and physiology. We describe a novel mode of regulation of NO synthase (NOS) function that uses endogenously produced truncated protein isoforms of Drosophila NOS (DNOS). These isoforms inhibit NOS enzymatic activity in vitro and in vivo, reflecting their ability to form complexes with the full-length DNOS protein (DNOS1). Truncated isoforms suppress the antiproliferative action of DNOS1 in the eye imaginal disc by impacting the retinoblastoma-dependent pathway, yielding hyperproliferative phenotypes in pupae and adult flies. Our results indicate that endogenous products of the dNOS locus act as dominant negative regulators of NOS activity during Drosophila development.
PubMed ID
PubMed Central ID
PMC517402 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Genes Dev.
    Title
    Genes & Development
    Publication Year
    1987-
    ISBN/ISSN
    0890-9369
    Data From Reference
    Alleles (6)
    Genes (6)
    Experimental Tools (2)
    Transgenic Constructs (6)