Literature DB >> 20648058

Gene expression associated with the onset of hearing detected by differential display in rat organ of Corti.

Ellen Reisinger1, David Meintrup, Dominik Oliver, Bernd Fakler.   

Abstract

The exquisite performance of the mammalian hearing organ results from a finely orchestrated array of cell types, and their highly specialized functions are determined by their gene expression profile. In rodents, this profile is established mainly during the first 2 weeks of postnatal maturation. In this paper, we used the differential display technique on the rat organ of Corti to uncover transcripts upregulated in expression between postnatal stages P0 and P14. A total of 176 different genes were identified, the mRNA amount of which increased during early postnatal development. The transcripts code for proteins serving a broad spectrum of cellular functions including intracellular signaling, control of growth/differentiation, regulation of protein synthesis/degradation/modification, metabolism and synaptic function. In addition, the set of upregulated transcripts contained several proteins of yet unknown function, as well as hypothetical proteins and so far unknown mRNA sequences. Thus, this study unravels the broad and specific transcription program that operates the maturation of the mammalian hearing organ. Further, as 49 of the genes found here map to at least one unspecified deafness locus, our study provides candidate genes for these and novel deafness loci.

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Year:  2010        PMID: 20648058      PMCID: PMC3002860          DOI: 10.1038/ejhg.2010.111

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  38 in total

Review 1.  Molecular genetics of hearing loss.

Authors:  C Petit; J Levilliers; J P Hardelin
Journal:  Annu Rev Genet       Date:  2001       Impact factor: 16.830

2.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

Authors:  K J Livak; T D Schmittgen
Journal:  Methods       Date:  2001-12       Impact factor: 3.608

3.  Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.

Authors:  Z M Ahmed; S Riazuddin; S L Bernstein; Z Ahmed; S Khan; A J Griffith; R J Morell; T B Friedman; S Riazuddin; E R Wilcox
Journal:  Am J Hum Genet       Date:  2001-06-07       Impact factor: 11.025

4.  Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

Authors:  K N Alagramam; H Yuan; M H Kuehn; C L Murcia; S Wayne; C R Srisailpathy; R B Lowry; R Knaus; L Van Laer; F P Bernier; S Schwartz; C Lee; C C Morton; R F Mullins; A Ramesh; G Van Camp; G S Hageman; R P Woychik; R J Smith; G S Hagemen
Journal:  Hum Mol Genet       Date:  2001-08-01       Impact factor: 6.150

5.  Longitudinal gradients of KCNQ4 expression in spiral ganglion and cochlear hair cells correlate with progressive hearing loss in DFNA2.

Authors:  K W Beisel; N C Nelson; D C Delimont; B Fritzsch
Journal:  Brain Res Mol Brain Res       Date:  2000-10-20

6.  Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin.

Authors:  Thomas Weber; Ulrike Zimmermann; Harald Winter; Andreas Mack; Iris Köpschall; Karin Rohbock; Hans-Peter Zenner; Marlies Knipper
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-26       Impact factor: 11.205

7.  Genomic characterization and expression of mouse prestin, the motor protein of outer hair cells.

Authors:  Jing Zheng; Kevin B Long; Keiji B Matsuda; Laird D Madison; Allen D Ryan; Peter D Dallos
Journal:  Mamm Genome       Date:  2003-02       Impact factor: 2.957

8.  Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.

Authors:  Dominique Weil; Aziz El-Amraoui; Saber Masmoudi; Mirna Mustapha; Yoshiaki Kikkawa; Sophie Lainé; Sedigheh Delmaghani; Avital Adato; Sellama Nadifi; Zeineb Ben Zina; Christian Hamel; Andreas Gal; Hammadi Ayadi; Hiromichi Yonekawa; Christine Petit
Journal:  Hum Mol Genet       Date:  2003-03-01       Impact factor: 6.150

9.  Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.

Authors:  Xue Zhong Liu; Xiao Mei Ouyang; Xia Juan Xia; Jing Zheng; Arti Pandya; Fang Li; Li Lin Du; Katherine O Welch; Christine Petit; Richard J H Smith; Bradley T Webb; Denise Yan; Kathleen S Arnos; David Corey; Peter Dallos; Walter E Nance; Zheng Yi Chen
Journal:  Hum Mol Genet       Date:  2003-05-15       Impact factor: 6.150

Review 10.  Hearing loss: mechanisms revealed by genetics and cell biology.

Authors:  Amiel A Dror; Karen B Avraham
Journal:  Annu Rev Genet       Date:  2009       Impact factor: 16.830

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  1 in total

1.  Atoh1 directs the formation of sensory mosaics and induces cell proliferation in the postnatal mammalian cochlea in vivo.

Authors:  Michael C Kelly; Qing Chang; Alex Pan; Xi Lin; Ping Chen
Journal:  J Neurosci       Date:  2012-05-09       Impact factor: 6.167

  1 in total

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