A cell type-specific approach to elucidate the role of miR-96 in inner ear hair cells.

Mir96Dmdo RNA-seq diminuendo hair cell inner ear miR-96 miRNA supporting cell

Journal

Frontiers in audiology and otology
ISSN: 2813-6055
Titre abrégé: Front Audiol Otol
Pays: Switzerland
ID NLM: 9918787485606676

Informations de publication

Date de publication:
2024
Historique:
medline: 3 6 2024
pubmed: 3 6 2024
entrez: 3 6 2024
Statut: ppublish

Résumé

Mutations in microRNA-96 (miR-96), a microRNA expressed within the hair cells (HCs) of the inner ear, result in progressive hearing loss in both mouse models and humans. In this study, we present the first HC-specific RNA-sequencing (RNA-seq) dataset from newborn Bulk RNA-seq was performed on HCs of newborn We identify 215 upregulated and 428 downregulated genes in the HCs of the Our data further support a role for miR-96 in HC development, possibly as a repressor of supporting cell transcriptional programs in HCs. The HC-specific

Identifiants

pubmed: 38826689
doi: 10.3389/fauot.2024.1400576
pmc: PMC11141775
pii:
doi:

Types de publication

Journal Article

Langues

eng

Déclaration de conflit d'intérêts

Conflict of interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Kathleen Gwilliam (K)

Section on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, United States.

Michal Sperber (M)

Department of Human Molecular Genetics and Biochemistry, Tel Aviv University School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Katherine Perry (K)

Department of Otorhinolaryngology Head and Neck Surgery, University of Maryland School of Medicine, Baltimore, MD, United States.

Kevin P Rose (KP)

Section on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, United States.

Laura Ginsberg (L)

Department of Otorhinolaryngology Head and Neck Surgery, University of Maryland School of Medicine, Baltimore, MD, United States.

Nikhil Paladugu (N)

Department of Otorhinolaryngology Head and Neck Surgery, University of Maryland School of Medicine, Baltimore, MD, United States.

Yang Song (Y)

Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, United States.

Beatrice Milon (B)

Section on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, United States.

Ran Elkon (R)

Department of Human Molecular Genetics and Biochemistry, Tel Aviv University School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Ronna Hertzano (R)

Section on Omics and Translational Science of Hearing, Neurotology Branch, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD, United States.
Department of Otorhinolaryngology Head and Neck Surgery, University of Maryland School of Medicine, Baltimore, MD, United States.
Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, MD, United States.

Classifications MeSH