Literature DB >> 19657184

Expression of cochlin mRNA splice variants in the inner ear.

Kuwon Sekine1, Tetsuo Ikezono, Tomohiro Matsumura, Susumu Shindo, Atsushi Watanabe, Lishu Li, Ruby Pawankar, Takeshi Nishino, Toshiaki Yagi.   

Abstract

Proteomic analysis of inner ear proteins revealed unique properties of cochlin, encoded by the COCH gene. We detected 3 cochlin isoforms, p63s, p44s and p40s, in the inner ear tissue and a short 16-kDa isoform, cochlin-tomoprotein (CTP), in the perilymph. The role of the cochlin isoforms has not been elucidated. To improve our understanding of the mechanism of cochlin isoform expression, we investigated rat cochlin mRNA expression in the inner ear and other organs. We performed RNA-ligation-mediated amplification of cDNA ends (RLM-RACE) using RNA isolated from the inner ear and spleen of rats, which are known to express abundant cochlin mRNA. We also examined the expression profile of full-length cochlin mRNA by nested RT-PCR in the cerebrum, cerebellum/brain stem, eye, inner ear, thyroid gland, thymus gland, lung, heart, liver, spleen, adrenal gland, kidney and blood. We verified CTP expression in rat perilymph by Western blot. By RLM-RACE, alternately spliced variants of cochlin mRNA with 3 different lengths were detected (2442, 2008 and 724 bp). The two longer mRNAs encode full-length cochlin with different polyadenylation signals in the 3'-untranslated region, which are expressed both in the ear and spleen. The short variant encodes the limulus factor C, cochlin, late gestation lung protein (LCCL) domain and the N-terminal sequence of the von Willebrand factor A (vWFA1) domain, and this variant was detected only in the ear. All 3 variants have the same transcriptional start site. By RT-PCR, we found that full-length cochlin was expressed in all organs examined, with a splice variant in the heart. By Western blot, we detected short isoforms (11-17 kDa) in the perilymph. Cochlin isoform formation is regulated, at least in part, by alternative splicing at the transcriptional level. The short mRNA was detected only in the inner ear, and this variant may provide a clue to understanding the formation and function of cochlin isoforms. Copyright 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19657184     DOI: 10.1159/000231634

Source DB:  PubMed          Journal:  Audiol Neurootol        ISSN: 1420-3030            Impact factor:   1.854


  4 in total

1.  A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.

Authors:  Michael S Hildebrand; Luke Gandolfo; A Eliot Shearer; Jennifer A Webster; Maren Jensen; William J Kimberling; Dietrich Stephan; Patrick L M Huygen; Richard J H Smith; Melanie Bahlo
Journal:  Laryngoscope       Date:  2010-12       Impact factor: 3.325

2.  Cochlin expression in vestibular endorgans obtained from patients with Meniere's disease.

Authors:  Audrey P Calzada; Ivan A Lopez; Luis Beltran Parrazal; Akira Ishiyama; Gail Ishiyama
Journal:  Cell Tissue Res       Date:  2012-09-20       Impact factor: 5.249

3.  COCH transgene expression in cultured human trabecular meshwork cells and its effect on outflow facility in monkey organ cultured anterior segments.

Authors:  Eun Suk Lee; B'ann T Gabelt; Jennifer A Faralli; Donna M Peters; Curtis R Brandt; Paul L Kaufman; Sanjoy K Bhattacharya
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-11-20       Impact factor: 4.799

4.  Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in Usher syndrome type 1F.

Authors:  Mark R Chance; Jinsook Chang; Shuqing Liu; Giridharan Gokulrangan; Daniel H-C Chen; Aaron Lindsay; Ruishuang Geng; Qing Y Zheng; Kumar Alagramam
Journal:  Hum Mol Genet       Date:  2010-01-22       Impact factor: 6.150

  4 in total

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