# Comprehensive comparative analysis of the effects of temperature on the Notch signaling response in vivo

**Authors:** Nimmy S. John, Kah Seng Tang, Michelle A. Urman, ChangHwan Lee

PMC · DOI: 10.1242/bio.062031 · Biology Open · 2025-10-15

## TL;DR

This study shows that Notch signaling in stem cells is largely unaffected by temperature changes, suggesting built-in compensatory mechanisms.

## Contribution

The study provides a comprehensive analysis of temperature effects on Notch signaling using direct readouts at multiple biological levels.

## Key findings

- Notch activation remains stable across temperatures, indicating compensatory mechanisms.
- Notch transcriptional activity increases with higher temperatures at the chromosomal level.

## Abstract

Temperature is a critical factor that modulates cellular metabolism and stem cell regulation. Despite extensive studies, the influence of temperature on stem cell regulation via Notch signaling has been limited to studies relying on studies that involve indirect readouts to Notch activation. This study systematically analyzes the effects of temperature on the Notch signaling transcriptional response at the chromosomal, cellular, and tissue levels. Using complementary direct Notch readouts, we demonstrate that Notch activation remains largely unchanged across temperatures, suggesting the presence of temperature-compensatory mechanisms that maintain robust Notch activation. Notch transcriptional activity readouts, however, increased with temperature, indicating that elevated temperatures may enhance Notch transcriptional activity at the chromosomal level. These findings provide a comprehensive framework for understanding effects of temperature and offer new insights into the regulation of Notch signaling in stem cell biology.

Summary: Notch activation remains largely unchanged across temperatures, suggesting the presence of temperature-compensatory mechanisms that maintain robust Notch activation.

## Linked entities

- **Proteins:** Notch (neurogenic locus notch homolog)

## Full-text entities

- **Genes:** lin-12 (lin-12/Notch intracellular domain) [NCBI Gene 176282], lst-1 (Lateral signaling target 1 protein) [NCBI Gene 172948], lag-2 (Protein lag-2) [NCBI Gene 178755], sygl-1 (Ecdysone-induced protein 74EF) [NCBI Gene 173116], lag-1 (Suppressor of hairless protein homolog) [NCBI Gene 177373], let-858 (Pre-mRNA-splicing factor CWC22 homolog) [NCBI Gene 174689]
- **Diseases:** hypothermia (MESH:D007035), ATS (MESH:D009371)
- **Chemicals:** PBS (MESH:D007854), levamisole (MESH:D007978), hypochlorite (MESH:D006997), Tween-20 (MESH:D011136), Ethanol (MESH:D000431), PMC (MESH:C008859), DAPI (-), formaldehyde (MESH:D005557), N2 (MESH:D009584)
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227], Caenorhabditis elegans (species) [taxon 6239], C. elegans [taxon 328850], Gallus gallus (bantam, species) [taxon 9031]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12570151/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12570151/full.md

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Source: https://tomesphere.com/paper/PMC12570151