Journal article
Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and Perspective
Frontiers in genetics, Vol.9(MAY), pp.156-156
05/08/2018
DOI: 10.3389/fgene.2018.00156
PMCID: PMC5951964
PMID: 29868110
Abstract
The mammalian hearing organ is a regular array of two types of hair cells (HCs) surrounded by six types of supporting cells. Along the tonotopic axis, this conserved radial array of cell types shows longitudinal variations to enhance the tuning properties of basilar membrane. We present the current evidence supporting the hypothesis that quantitative local variations in gene expression profiles are responsible for local cell responses to global gene manipulations. With the advent of next generation sequencing and the unprecedented array of technologies offering high throughput analyses at the single cell level, transcriptomics will become a common tool to enhance our understanding of the inner ear. We provide an overview of the approaches and landmark studies undertaken to date to analyze single cell variations in the organ of Corti and discuss the current limitations. We next provide an overview of the complexity of known regulatory mechanisms in the inner ear. These mechanisms are tightly regulated temporally and spatially at the transcription, RNA-splicing, mRNA-regulation, and translation levels. Understanding the intricacies of regulatory mechanisms at play in the inner ear will require the use of complementary approaches, and most probably, a combinatorial strategy coupling transcriptomics, proteomics, and epigenomics technologies. We highlight how these data, in conjunction with recent insights into molecular cell transformation, can advance attempts to restore lost hair cells.
Details
- Title: Subtitle
- Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and Perspective
- Creators
- Kevin T Booth - Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, University of IowaHela Azaiez - Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, University of IowaIsrat Jahan - Department of Biology, University of IowaRichard J. H Smith - Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, University of IowaBernd Fritzsch - Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, University of Iowa
- Resource Type
- Journal article
- Publication Details
- Frontiers in genetics, Vol.9(MAY), pp.156-156
- DOI
- 10.3389/fgene.2018.00156
- PMID
- 29868110
- PMCID
- PMC5951964
- NLM abbreviation
- Front Genet
- ISSN
- 1664-8021
- eISSN
- 1664-8021
- Publisher
- Frontiers Media S.A
- Grant note
- IJ DC013655; RJS DC003544; DC002842; DC012049 / National Institute on Deafness and Other Communication Disorders
- Language
- English
- Date published
- 05/08/2018
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Biology; Craniofacial Anomalies Research Center; Otolaryngology; Internal Medicine
- Record Identifier
- 9984006361102771
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