# Independent Mutations in the LRP2 Gene Mediating Telescope Eyes and Celestial Eyes in Goldfish

**Authors:** Rongni Li, Bo Zhang, Yansheng Sun, Jingyi Li

PMC · DOI: 10.3390/ijms262110625 · International Journal of Molecular Sciences · 2025-10-31

## TL;DR

This study identifies mutations in the LRP2 gene that cause eye deformities in goldfish, offering insights into evolutionary and disease-related eye development.

## Contribution

The study identifies a novel mutation in the LRP2 gene linked to celestial eye deformities in goldfish for the first time.

## Key findings

- A premature stop codon in Exon 38 of the LRP2 gene is associated with celestial eye deformities in goldfish.
- Fatty acid metabolism and keratocyte-related functions are inhibited in celestial eye goldfish eyeballs.
- Inflammatory reactions and extracellular matrix secretions are increased in celestial eye goldfish.

## Abstract

After intensive artificial selection, the development of celestial eyes in goldfish involves the eyeballs protuberating and turning upwards. Thus, the celestial eye goldfish is an excellent model for both evolutionary and human ocular disease studies. Here, two mapping populations of goldfish with segregating eye phenotypes in the offspring were constructed. Through whole-genome sequencing and RNA-seq for eyeball samples, a premature stop codon in Exon 38 of the LRP2 gene was identified as the top candidate mutation for the celestial eye in goldfish. Fatty acid metabolism and epidermal cells, especially keratocyte-related functions, were inhibited in the eyeballs of celestial eye goldfish, while inflammatory reactions and extracellular matrix secretions were stimulated. These results suggest the dysfunction of the cornea in the celestial eye goldfish, and the same for the retina, which could be the results of the truncated LRP2 protein. In addition, the same gene, LRP2, is in charge of similar phenotypes (celestial eye and telescope eye) in goldfish, but these phenotypes have no shared mutations. In conclusion, the candidate mutation for the celestial eye in goldfish was identified by this study for the first time, and parallel evolutions of similar phenotypes at the molecular level under artificial selection were observed. These findings provide insights into the developmental and evolutionary processes of morphological changes in the eyes of goldfish.

## Linked entities

- **Genes:** LRP2 (LDL receptor related protein 2) [NCBI Gene 4036]

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), ocular disease (MESH:D005128)
- **Chemicals:** Fatty acid (MESH:D005227)
- **Species:** Homo sapiens (human, species) [taxon 9606], Carassius auratus (goldfish, species) [taxon 7957]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12608239/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12608239/full.md

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Source: https://tomesphere.com/paper/PMC12608239