ArticleEMBO reports2025
Neuralized-like proteins differentially activate Notch ligands.
Article in EMBO reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Aryl hydrocarbon receptor deficiency triggers the activation of γδT17 cells to exacerbate autoimmune inflammation.Science advances · 2026Article
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8 authors.
Funding
Abstract
Notch signalling is a major signalling pathway coordinating cellular processes between neighbouring animal cells. In Drosophila, two E3 ubiquitin ligases, Neuralized (Neur) and Mindbomb1 (Mib1), regulate Notch ligand activation and are essential for development. However, the mammalian orthologs of Neur, Neuralized-like (NEURL) 1 and 1B, appear to be dispensable for development, as double knock-out mice show no overt developmental defects. Thus, it is unclear if and how NEURL proteins regulate the mammalian Notch ligands. To address this question, we examined NEURL proteins' ability to activate Notch ligands in a humanized Drosophila model and mammalian cell culture. We found that, unlike MIB1, NEURL proteins activate Notch only with a subset of mammalian ligands, which contain a Neuralized binding motif. This motif has the consensus sequence NxxN and is present only in Notch ligands DLL1 and JAG1, but not in DLL4 and JAG2. Thus, our results reveal a differential regulatory mechanism of Notch activation in mammals, which can potentially explain the limited role of NEURL proteins in mammalian development and homeostasis.
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