# Tekt3 Safeguards Proper Functions and Morphology of Neuromast Hair Bundles

**Authors:** Dongmei Su, Sirun Lu, Ling Zheng, Dong Liu

PMC · DOI: 10.3390/ijms26073115 · International Journal of Molecular Sciences · 2025-03-28

## TL;DR

This study shows that Tekt3 is important for the structure and function of hair cells in zebrafish and mice, especially in non-hearing-related cells.

## Contribution

The study identifies Tekt3's role in maintaining neuromast hair bundle morphology and function in zebrafish and mice.

## Key findings

- Tekt3 is expressed in neuromast and utricular hair cells but not in saccule or crista.
- Tekt3 mutant neuromast hair cells show kinocilia defects and impaired function.
- Wild-type tekt3 mRNA rescues the functional defects in tekt3 mutants.

## Abstract

The inner ear and/or lateral line are responsible for hearing and balance of vertebrate. The otic sensory hair cells (HCs) employ cilium organelles, namely stereocilia and/or kinocilia, to mediate mechanical stimuli to electrical signal transition. Tektins (Tekts) are known as the cilium microtubule stabilizer and inner-space filler, and four Tekt(1-4)-encoding genes are identified in zebrafish HCs, but the subcellular location of Tekts in HCs remains unknown. In the present study, we first found that tekt3 is expressed in the inner ear and lateral line neuromast. Antibody staining revealed that Tekt3 is present in neuromast and utricular HCs. It is absent in the saccule, the authentic hearing end-organ of zebrafish and the crista of semi-circular canals. Furthermore, Tekt3 were enriched at the apical side of neuromast and utricular HCs, mainly in the cytosol. Similar subcellular distribution of Tekt3 was also evident in the outer HCs of mature mouse cochlea, which are not directly linked to the hearing sense. However, only neuromast HCs exerted morphological defect of kinocilia in tekt3 mutant. The disrupted or distorted HC kinocilia of mutant neuromast ultimately resulted in slower vital dye intake, delayed HC regeneration after neomycin treatment, and reduced startle response to vibration stimulation. All functional defects of tekt3 mutant were largely rescued by wild-type tekt3 mRNA. Our study thus suggests that zebrafish Tekt3 maintains the integrity and function of neuromast kinocilia to against surrounding and persistent low-frequency noises, perhaps via the intracellular distribution of Tekt3. Nevertheless, TEKT3/Tekt3 could be used to clarify HC sub-types in both zebrafish and mice, to highlight the non-hearing HCs.

## Linked entities

- **Genes:** TEKT3 (tektin 3) [NCBI Gene 64518]
- **Proteins:** TEKT3 (tektin 3), TEKT3 (tektin 3)
- **Species:** Danio rerio (taxon 7955), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** tekt3 (tektin 3) [NCBI Gene 572368]
- **Diseases:** startle (MESH:D016750)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Danio rerio (leopard danio, species) [taxon 7955]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11989051/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC11989051/full.md

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Source: https://tomesphere.com/paper/PMC11989051