# The intracellular domains of the DSL ligands Serrate and Delta provide different activities

**Authors:** Ekaterina Seib, Maya Schmid, Hideyuki Shimizu, Tobias Troost, Sunday Faith Oyelere, Biswajit Chakraborty, Martin Baron, Thomas Klein

PMC · DOI: 10.1186/s12964-025-02472-w · Cell Communication and Signaling : CCS · 2025-10-31

## TL;DR

This study shows that the intracellular domains of Serrate and Delta ligands in the Notch signaling pathway have different roles in endocytosis and signaling.

## Contribution

The study reveals that Serrate's signaling activity depends entirely on Mib1-dependent ubiquitylation, unlike Delta.

## Key findings

- Serrate's lysine residues are essential for Mib1-mediated endocytosis and signaling.
- A minimum of five conserved lysines in Serrate's ICD are required for signaling.
- Adding a sixth lysine restores bulk endocytosis but not signaling activity.

## Abstract

Endocytosis of the ligands is a central requirement for the correct activation of the Notch-signalling pathway. It is initiated by E3-ligase mediated ubiquitylation (ubi) of the intracellular domain (ICD) of the ligands on lysine (K). In Drosophila, two ligands are present, termed Serrate (Ser) and Delta (Dl). They are ubiquitylated by the E3-ligases Mindbomb1 (Mib1) and Neuralized (Neur). Here, we show that the ICDs of Dl and Ser have different activities. We characterised the properties of the Ser-ICD and focused on the meaning of its Ks for ubi and signalling activity. For this purpose, we generated a variant in which all Ks of its ICD are replaced by the structurally similar arginine (R), termed SerK2R. Its analysis revealed that, in contrast to Dl, the Ks are essential for the endocytosis and degradation of Ser by Mib1. Moreover, whereas Dl possesses an ubi- and Mib1-independent signalling activity, Ser-signalling completely depends on Mib1-dependent ubi. We found that a minimum of five conserved Ks in the ICD are required for the Mib1-mediated activation of Ser and that the importance of the individual Ks differs. These core Ks appear to preferentially channel Ser into a rare signalling-relevant endocytosis pathway. Remarkably, the addition of a sixth K largely restores also bulk endocytosis, which is irrelevant for signalling. Thus, at least 6 of the 10 Ks of the ICD are required for the complete activity/behaviour of Ser.

The online version contains supplementary material available at 10.1186/s12964-025-02472-w.

## Linked entities

- **Genes:** SRRT (serrate, RNA effector molecule) [NCBI Gene 51593], PSMB6 (proteasome 20S subunit beta 6) [NCBI Gene 5694], MIB1 (MIB E3 ubiquitin protein ligase 1) [NCBI Gene 57534], neur (E3 ubiquitin-protein ligase neur) [NCBI Gene 5567387], neur (neuralized) [NCBI Gene 41085]
- **Proteins:** Notch (neurogenic locus notch homolog), EDAR (ectodysplasin A receptor)
- **Species:** Drosophila (taxon 7215)

## Full-text entities

- **Chemicals:** Serrate (-)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12577249/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12577249/full.md

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Source: https://tomesphere.com/paper/PMC12577249