Literature DB >> 20596040

Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes.

Hiroshi Nakanishi1, Masafumi Ohtsubo, Satoshi Iwasaki, Yoshihiro Hotta, Kunihiro Mizuta, Hiroyuki Mineta, Shinsei Minoshima.   

Abstract

mRNA is an important tool to study the effects of particular mutations on the mode of splicing and transcripts. However, it is often difficult to isolate mRNA because the organ or tissue in which the gene is expressed cannot be sampled. We previously identified two probable splicing mutations (c.6485+5G>A and c.8559-2A>G) during the mutation analysis of USH2A in Japanese Usher syndrome (USH) type 2 patients, but we could not observe their effects on splicing because the gene is expressed in only a few tissues/organs, and is not expressed in peripheral lymphocytes. In this study, we used hair roots as a source of mRNA of USH-causing genes, and successfully detected the expression of seven, except USH1C and CLRN1, of the nine USH-causing genes. We used RNA extracted from the hair roots of a patient who has both c.6485+5G>A and c.8559-2A>G mutations in USH2A in a compound heterozygous state to observe the effects of these mutations on transcripts. Reverse-transcription PCR analysis revealed that c.6485+5G>A and c.8559-2A>G inactivated splice donor and splice acceptor sites, respectively, and caused skipping of exons. Thus, RNA extracted from hair roots is a potential powerful and convenient tool for the mutation analysis of USH-causing genes.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20596040     DOI: 10.1038/jhg.2010.83

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  6 in total

1.  The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients.

Authors:  Yang Zhao; Katsuhiro Hosono; Kimiko Suto; Chie Ishigami; Yuuki Arai; Akiko Hikoya; Yasuhiko Hirami; Masafumi Ohtsubo; Shinji Ueno; Hiroko Terasaki; Miho Sato; Hiroshi Nakanishi; Shiori Endo; Kunihiro Mizuta; Hiroyuki Mineta; Mineo Kondo; Masayo Takahashi; Shinsei Minoshima; Yoshihiro Hotta
Journal:  J Hum Genet       Date:  2014-07-31       Impact factor: 3.172

2.  Targeted next-generation sequencing reveals novel USH2A mutations associated with diverse disease phenotypes: implications for clinical and molecular diagnosis.

Authors:  Xue Chen; Xunlun Sheng; Xiaoxing Liu; Huiping Li; Yani Liu; Weining Rong; Shaoping Ha; Wenzhou Liu; Xiaoli Kang; Kanxing Zhao; Chen Zhao
Journal:  PLoS One       Date:  2014-08-18       Impact factor: 3.240

3.  Novel deletions involving the USH2A gene in patients with Usher syndrome and retinitis pigmentosa.

Authors:  Gema García-García; Elena Aller; Teresa Jaijo; Maria J Aparisi; Lise Larrieu; Valérie Faugère; Fiona Blanco-Kelly; Carmen Ayuso; Anne-Francoise Roux; José M Millán
Journal:  Mol Vis       Date:  2014-09-25       Impact factor: 2.367

4.  A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report.

Authors:  Shanling Liu; Jing Wang; Cong Zhou; Yuanyuan Xiao; Hanbing Xie
Journal:  BMC Med Genomics       Date:  2021-08-10       Impact factor: 3.063

5.  Global spectrum of USH2A mutation in inherited retinal dystrophies: Prompt message for development of base editing therapy.

Authors:  Bing-Nan Su; Ren-Juan Shen; Zhuo-Lin Liu; Yang Li; Zi-Bing Jin
Journal:  Front Aging Neurosci       Date:  2022-08-10       Impact factor: 5.702

6.  Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing.

Authors:  Heather B Steele-Stallard; Polona Le Quesne Stabej; Eva Lenassi; Linda M Luxon; Mireille Claustres; Anne-Francoise Roux; Andrew R Webster; Maria Bitner-Glindzicz
Journal:  Orphanet J Rare Dis       Date:  2013-08-08       Impact factor: 4.123

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.