Abstract

Fringes are glycosyltransferases that transfer a GlcNAc to O-fucose residues on Epidermal Growth Factor-like (EGF) repeats. Three Fringes exist in mammals: LUNATIC FRINGE (LFNG), MANIC FRINGE (MFNG), and RADICAL FRINGE (RFNG). Fringe modification of O-fucose on EGF repeats in the NOTCH1 (N1) extracellular domain modulates the activation of N1 signaling. Not all O-fucose residues of N1 are modified by all Fringes; some are modified by one or two Fringes and others not modified at all. The distinct effects on N1 activity depend on which Fringe is expressed in a cell. However, little data is available on the effect that more than one Fringe has on the modification of O-fucose residues and the resulting downstream consequence on Notch activation. Using mass spectral glycoproteomic site mapping and cell-based N1 signaling assays, we compared the effect of co-expression of N1 with one or more Fringes on modification of O-fucose and activation of N1 in three cell lines. Individual expression of each Fringe with N1 in the three cell lines revealed differences in modulation of the Notch pathway dependent on the presence of endogenous Fringes. Despite these cell-based differences, co-expression of several Fringes with N1 demonstrated a dominant effect of LFNG over MFNG or RFNG. MFNG and RFNG appeared to be co-dominant but strongly dependent on the ligands used to activate N1 and on the endogenous expression of Fringes. These results show a hierarchy of Fringe activity and indicate that the effect of MFNG and/or RFNG could be small in the presence of LFNG.

Highlights

  • Our first objective was to determine how co-expression of N1 with members of the Fringe family (LFNG, MANIC FRINGE (MFNG), or RADICAL FRINGE (RFNG)) modulates Notch signaling within three cell lines commonly used for Notch activation assays (NIH3T3, CHO, and U2OS)

  • We showed that LUNATIC FRINGE (LFNG) had a dominant effect over MFNG or RFNG on N1 activation by Delta-like 1 (DLL1) in cell-based N1 signaling assays

  • Using mass spectral glycoproteomic analysis, we demonstrated that this dominance was due to the ability of LFNG to more extensively modify O-fucose residues present on EGF8 and 12, both of which play a key role in the activation of N1 by DLL1

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. The Notch signaling pathway is essential for the regulation of developmental processes and for the maintenance of homeostasis in adult tissues [1]. This signaling pathway is initiated by interaction of Notch receptors with their canonical ligands Delta-like (DLL1 and 4) and JAGGED (JAG1 and 2) [2]. Four Notch receptors exist in mammals (NOTCH1-4)

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