Pathological mechanisms and candidate therapeutic approaches in the hearing loss of mice carrying human MIR96 mutations.

Autor: Lewis MA; Wolfson Sensory, Pain and Regeneration Centre, King's College London, Guy's Campus, London, SE1 1UL, UK. morag.lewis@kcl.ac.uk., Lachgar-Ruiz M; Wolfson Sensory, Pain and Regeneration Centre, King's College London, Guy's Campus, London, SE1 1UL, UK., Di Domenico F; Wolfson Sensory, Pain and Regeneration Centre, King's College London, Guy's Campus, London, SE1 1UL, UK., Duddy G; Wellcome Sanger Institute, Hinxton, CB10 1SA, UK., Chen J; Wolfson Sensory, Pain and Regeneration Centre, King's College London, Guy's Campus, London, SE1 1UL, UK., Fernandez S; Servicio de Genética, Hospital Universitario Ramón y Cajal, IRYCIS and Biomedical Network Research Centre On Rare Diseases (CIBERER), Km 9.100, Madrid, 28034, Spain., Morin M; Servicio de Genética, Hospital Universitario Ramón y Cajal, IRYCIS and Biomedical Network Research Centre On Rare Diseases (CIBERER), Km 9.100, Madrid, 28034, Spain., Williams G; Wolfson Sensory, Pain and Regeneration Centre, King's College London, Guy's Campus, London, SE1 1UL, UK., Moreno Pelayo MA; Servicio de Genética, Hospital Universitario Ramón y Cajal, IRYCIS and Biomedical Network Research Centre On Rare Diseases (CIBERER), Km 9.100, Madrid, 28034, Spain., Steel KP; Wolfson Sensory, Pain and Regeneration Centre, King's College London, Guy's Campus, London, SE1 1UL, UK.
Jazyk: angličtina
Zdroj: Genome medicine [Genome Med] 2024 Oct 21; Vol. 16 (1), pp. 121. Date of Electronic Publication: 2024 Oct 21.
DOI: 10.1186/s13073-024-01394-5
Abstrakt: Background: Progressive hearing loss is a common problem in the human population with no effective therapeutics currently available. However, it has a strong genetic contribution, and investigating the genes and regulatory interactions underlying hearing loss offers the possibility of identifying therapeutic candidates. Mutations in regulatory genes are particularly useful for this, and an example is the microRNA miR-96, a post-transcriptional regulator which controls hair cell maturation. Mice and humans carrying mutations in miR-96 all exhibit hearing impairment, in homozygosis if not in heterozygosis, but different mutations result in different physiological, structural and transcriptional phenotypes.
Methods: Here we present our characterisation of two lines of mice carrying different human mutations knocked-in to Mir96. We have carried out auditory brainstem response tests to examine their hearing with age and after noise exposure and have used confocal and scanning electron microscopy to examine the ultrastructure of the organ of Corti and hair cell synapses. Bulk RNA-seq was carried out on the organs of Corti of postnatal mice, followed by bioinformatic analyses to identify candidate targets.
Results: While mice homozygous for either mutation are profoundly deaf from 2 weeks old, the heterozygous phenotypes differ markedly, with only one mutation resulting in hearing impairment in heterozygosis. Investigations of the structural phenotype showed that one mutation appears to lead to synaptic defects, while the other has a much more severe effect on the hair cell stereociliary bundles. Transcriptome analyses revealed a wide range of misregulated genes in both mutants which were notably dissimilar. We used the transcriptome analyses to investigate candidate therapeutics, and tested one, finding that it delayed the progression of hearing loss in heterozygous mice.
Conclusions: Our work adds further support for the importance of the gain of novel targets in microRNA mutants and offers a proof of concept for the identification of pharmacological interventions to maintain hearing.
(© 2024. The Author(s).)
Databáze: MEDLINE
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