# Genetic mutations in GLP-1/Notch pathway reveal distinct mechanisms of Notch signaling in germline stem cell regulation

**Authors:** Nimmy S. John, Michelle A. Urman, Mahasin G. Mehmood, Vanessa Gentile, ChangHwan Lee

PMC · DOI: 10.1242/bio.062008 · Biology Open · 2026-02-09

## TL;DR

This study explores how different GLP-1/Notch mutations in C. elegans affect stem cell regulation, revealing distinct impacts on transcription and germline function.

## Contribution

The research introduces a systematic analysis of GLP-1 mutations, identifying domain-specific effects and predictive markers for germline function.

## Key findings

- NICD mutations reduce Notch transcriptional activation at cellular and germline levels but not at the chromosomal level.
- NECD mutations have minimal effects across all biological levels.
- Regression analyses show strong correlations between sygl-1 activation, mRNA production, and PZ size.

## Abstract

The Notch signaling pathway is crucial for germline stem cell (GSC) regulation in Caenorhabditis elegans, yet the molecular and biological consequences of GLP-1/Notch mutations remain poorly understood. This study systematically analyzes commonly used and pathological glp-1 loss- (lf) and gain-of-function (gf) mutations to investigate their effects on Notch activity at nascent transcript (ATS), mRNA, and germline levels. Using complementary direct readouts of Notch activation, including sygl-1 activation sites, mRNA levels, and germline functional assays of the Notch-responsive GSC pool and progenitor zone (PZ), we demonstrate that the severity of glp-1 mutations is dependent on their position within the GLP-1 protein. Among the commonly used glp-1 alleles we examined, NICD mutations reduced Notch transcriptional activation at cellular and germline levels while having little impact at the chromosomal (ATS) level, whereas partial lf NECD mutations have minimal effects across all biological levels. Furthermore, a series of regression analyses of sygl-1 activation, mRNA production, and PZ size reveal strong correlations, qualifying these readouts as predictive markers for germline function. These findings provide a comprehensive framework for understanding glp-1 mutation effects and offer new insights into the regulation of Notch signaling in stem cell biology.

Summary: Systematic single-molecule analysis of C. elegans GLP-1/Notch mutations reveals domain-specific effects on transcription, mRNA, and germline biology, establishing predictive markers linking transcriptional activity to stem cell regulation.

## Linked entities

- **Genes:** GCG (glucagon) [NCBI Gene 2641], sygl-1 (Ecdysone-induced protein 74EF) [NCBI Gene 173116]
- **Proteins:** GCG (glucagon), nicD (N-formylmaleamate deformylase), N (Notch)
- **Species:** Caenorhabditis elegans (taxon 6239)

## Full-text entities

- **Genes:** sygl-1 (Ecdysone-induced protein 74EF) [NCBI Gene 173116], glp-1 (glp-1/Notch intracellular domain) [NCBI Gene 176286], lin-12 (lin-12/Notch intracellular domain) [NCBI Gene 176282]
- **Species:** C. elegans [taxon 328850]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937919/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937919/full.md

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Source: https://tomesphere.com/paper/PMC12937919