Literature DB >> 19645628

Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians.

Byung Yoon Choi1, Andrew K Stewart, Katherine K Nishimura, Won Jae Cha, Moon-Woo Seong, Sung Sup Park, Seung Won Kim, Yang Sook Chun, Jong Woo Chung, Shi-Nae Park, Sun O Chang, Chong-Sun Kim, Seth L Alper, Andrew J Griffith, Seung-Ha Oh.   

Abstract

CONTEXT: Enlargement of the vestibular aqueduct (EVA) is a commonly detected inner ear anomaly related to hearing loss and often associated with mutations of SLC26A4 encoding pendrin, a transmembrane exchanger of Cl(-), I(-), and HCO(3)(-). Here we describe the phenotypes of 27 Korean EVA subjects and their SLC26A4 genotypes determined by bidirectional nucleotide sequencing.
RESULTS: The detected variants include two novel missense substitutions (p.V138L and p.P542R). We characterized the ability of p.V138L and p.P542R pendrin products to traffic to the plasma membrane in COS-7 cells and to transport Cl(-), I(-), and HCO(3)(-) in Xenopus oocytes. The results indicate that p.P542R is a benign polymorphic variant, whereas p.V138L is a pathogenic mutation. Since this and other studies of East Asian EVA cohorts show that the majority of SLC26A4 mutations affect either or both of two amplicons (exons 7-8 and 19), we developed a hierarchical protocol that integrates direct sequencing with denaturing high-performance liquid chromatography analyses for detection of SLC26A4 mutations in these populations. We validated the cost efficiency of the integrated protocol by a simulated screen of published East Asian EVA cohorts with known SLC26A4 genotypes.
CONCLUSIONS: Our study further defines the spectrum of SLC26A4 mutations among East Asians and demonstrates a rapid and efficient protocol for their detection.

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Year:  2009        PMID: 19645628      PMCID: PMC2953255          DOI: 10.1089/gtmb.2009.0054

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  41 in total

1.  Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion.

Authors:  I E Royaux; S M Wall; L P Karniski; L A Everett; K Suzuki; M A Knepper; E D Green
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-27       Impact factor: 11.205

2.  Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells.

Authors:  I E Royaux; K Suzuki; A Mori; R Katoh; L A Everett; L D Kohn; E D Green
Journal:  Endocrinology       Date:  2000-02       Impact factor: 4.736

3.  Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.

Authors:  Guntram Borck; Christian Roth; Ursula Martiné; Gabriele Wildhardt; Joachim Pohlenz
Journal:  J Clin Endocrinol Metab       Date:  2003-06       Impact factor: 5.958

4.  Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome.

Authors:  Pnina Rotman-Pikielny; Koret Hirschberg; Padma Maruvada; Koichi Suzuki; Ines E Royaux; Eric D Green; Leonard D Kohn; Jennifer Lippincott-Schwartz; Paul M Yen
Journal:  Hum Mol Genet       Date:  2002-10-01       Impact factor: 6.150

5.  Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene: correlation between sulfate transport activity and chondrodysplasia phenotype.

Authors:  L P Karniski
Journal:  Hum Mol Genet       Date:  2001-07-01       Impact factor: 6.150

6.  Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations.

Authors:  C Campbell; R A Cucci; S Prasad; G E Green; J B Edeal; C E Galer; L P Karniski; V C Sheffield; R J Smith
Journal:  Hum Mutat       Date:  2001-05       Impact factor: 4.878

7.  Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.

Authors:  H-J Park; S Shaukat; X-Z Liu; S H Hahn; S Naz; M Ghosh; H-N Kim; S-K Moon; S Abe; K Tukamoto; S Riazuddin; M Kabra; R Erdenetungalag; J Radnaabazar; S Khan; A Pandya; S-I Usami; W E Nance; E R Wilcox; S Riazuddin; A J Griffith
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

8.  Prolactin regulation of the pendrin-iodide transporter in the mammary gland.

Authors:  James A Rillema; Melissa A Hill
Journal:  Am J Physiol Endocrinol Metab       Date:  2002-09-11       Impact factor: 4.310

9.  Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome.

Authors:  Julie P Taylor; Russell A Metcalfe; Philip F Watson; Anthony P Weetman; Richard C Trembath
Journal:  J Clin Endocrinol Metab       Date:  2002-04       Impact factor: 5.958

10.  Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

Authors:  Byung Yoon Choi; Andrew K Stewart; Anne C Madeo; Shannon P Pryor; Suzanne Lenhard; Rick Kittles; David Eisenman; H Jeffrey Kim; John Niparko; James Thomsen; Kathleen S Arnos; Walter E Nance; Kelly A King; Christopher K Zalewski; Carmen C Brewer; Thomas Shawker; James C Reynolds; John A Butman; Lawrence P Karniski; Seth L Alper; Andrew J Griffith
Journal:  Hum Mutat       Date:  2009-04       Impact factor: 4.878

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  9 in total

1.  Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.

Authors:  Shasha Huang; Dongyi Han; Yongyi Yuan; Guojian Wang; Dongyang Kang; Xin Zhang; Xiaofei Yan; Xiaoxiao Meng; Min Dong; Pu Dai
Journal:  J Transl Med       Date:  2011-09-30       Impact factor: 5.531

Review 2.  Transcriptional regulation of the pendrin gene.

Authors:  Julia Rozenfeld; Edna Efrati; Lior Adler; Osnat Tal; Stephen L Carrithers; Seth L Alper; Israel Zelikovic
Journal:  Cell Physiol Biochem       Date:  2011-11-16

Review 3.  Application of next generation sequencing upon the molecular genetic diagnosis of deafness.

Authors:  Byung Yoon Choi; Bong Jik Kim
Journal:  Korean J Audiol       Date:  2012-04-30

4.  Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans.

Authors:  Kyu-Hee Han; Ah Reum Kim; Min Young Kim; Soyeon Ahn; Seung-Ha Oh; Ju Hun Song; Byung Yoon Choi
Journal:  PLoS One       Date:  2016-09-01       Impact factor: 3.240

5.  Functional Testing of SLC26A4 Variants-Clinical and Molecular Analysis of a Cohort with Enlarged Vestibular Aqueduct from Austria.

Authors:  Sebastian Roesch; Emanuele Bernardinelli; Charity Nofziger; Miklós Tóth; Wolfgang Patsch; Gerd Rasp; Markus Paulmichl; Silvia Dossena
Journal:  Int J Mol Sci       Date:  2018-01-10       Impact factor: 5.923

6.  Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects.

Authors:  Renata Watanabe Nonose; Karina Lezirovitz; Maria Teresa Balester de Mello Auricchio; Ana Carla Batissoco; Guilherme Lopes Yamamoto; Regina Célia Mingroni-Netto
Journal:  BMC Med Genet       Date:  2018-05-08       Impact factor: 2.103

7.  Rapid Genetic Diagnosis for Okinawan Patients with Enlarged Vestibular Aqueduct Using Single-Stranded Tag Hybridization Chromatographic Printed-Array Strip.

Authors:  Akira Ganaha; Eiji Hishinuma; Tadashi Kaname; Masahiro Hiratsuka; Shunsuke Kondo; Tetsuya Tono
Journal:  J Clin Med       Date:  2022-02-19       Impact factor: 4.241

8.  Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.

Authors:  Yi Jiang; Shasha Huang; Tao Deng; Lihua Wu; Juan Chen; Dongyang Kang; Xiufeng Xu; Ruiyu Li; Dongyi Han; Pu Dai
Journal:  PLoS One       Date:  2015-08-07       Impact factor: 3.240

9.  An effective screening strategy for deafness in combination with a next-generation sequencing platform: a consecutive analysis.

Authors:  Naoko Sakuma; Hideaki Moteki; Masahiro Takahashi; Shin-ya Nishio; Yasuhiro Arai; Yukiko Yamashita; Nobuhiko Oridate; Shin-ichi Usami
Journal:  J Hum Genet       Date:  2016-01-14       Impact factor: 3.172

  9 in total

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