FB2024_03 , released June 25, 2024
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Citation
Galeone, A., Han, S.Y., Huang, C., Hosomi, A., Suzuki, T., Jafar-Nejad, H. (2017). Tissue-specific regulation of BMP signaling by Drosophila N-glycanase 1.  eLife 6(): e27612.
FlyBase ID
FBrf0236685
Publication Type
Research paper
Abstract
Mutations in the human N-glycanase 1 (NGLY1) cause a rare, multisystem congenital disorder with global developmental delay. However, the mechanisms by which NGLY1 and its homologs regulate embryonic development are not known. Here we show that Drosophila Pngl encodes an N-glycanase and exhibits a high degree of functional conservation with human NGLY1. Loss of Pngl results in developmental midgut defects reminiscent of midgut-specific loss of BMP signaling. Pngl mutant larvae also exhibit a severe midgut clearance defect, which cannot be fully explained by impaired BMP signaling. Genetic experiments indicate that Pngl is primarily required in the mesoderm during Drosophila development. Loss of Pngl results in a severe decrease in the level of Dpp homodimers and abolishes BMP autoregulation in the visceral mesoderm mediated by Dpp and Tkv homodimers. Thus, our studies uncover a novel mechanism for the tissue-specific regulation of an evolutionarily conserved signaling pathway by an N-glycanase enzyme.
PubMed ID
PubMed Central ID
PMC5599231 (PMC) (EuropePMC)
Related Publication(s)
Note

Signaling: Enzymatic insights into an inherited genetic disorder.
Zhang and Ten Hagen, 2017, eLife 6: e31127 [FBrf0239536]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    eLife
    Title
    eLife
    ISBN/ISSN
    2050-084X
    Data From Reference