PLoS ONE (Jan 2014)

Whole exome analysis identifies frequent CNGA1 mutations in Japanese population with autosomal recessive retinitis pigmentosa.

  • Satoshi Katagiri,
  • Masakazu Akahori,
  • Yuri Sergeev,
  • Kazutoshi Yoshitake,
  • Kazuho Ikeo,
  • Masaaki Furuno,
  • Takaaki Hayashi,
  • Mineo Kondo,
  • Shinji Ueno,
  • Kazushige Tsunoda,
  • Kei Shinoda,
  • Kazuki Kuniyoshi,
  • Yohinori Tsurusaki,
  • Naomichi Matsumoto,
  • Hiroshi Tsuneoka,
  • Takeshi Iwata

DOI
https://doi.org/10.1371/journal.pone.0108721
Journal volume & issue
Vol. 9, no. 9
p. e108721

Abstract

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OBJECTIVE:The purpose of this study was to investigate frequent disease-causing gene mutations in autosomal recessive retinitis pigmentosa (arRP) in the Japanese population. METHODS:In total, 99 Japanese patients with non-syndromic and unrelated arRP or sporadic RP (spRP) were recruited in this study and ophthalmic examinations were conducted for the diagnosis of RP. Among these patients, whole exome sequencing analysis of 30 RP patients and direct sequencing screening of all CNGA1 exons of the other 69 RP patients were performed. RESULTS:Whole exome sequencing of 30 arRP/spRP patients identified disease-causing gene mutations of CNGA1 (four patients), EYS (three patients) and SAG (one patient) in eight patients and potential disease-causing gene variants of USH2A (two patients), EYS (one patient), TULP1 (one patient) and C2orf71 (one patient) in five patients. Screening of an additional 69 arRP/spRP patients for the CNGA1 gene mutation revealed one patient with a homozygous mutation. CONCLUSIONS:This is the first identification of CNGA1 mutations in arRP Japanese patients. The frequency of CNGA1 gene mutation was 5.1% (5/99 patients). CNGA1 mutations are one of the most frequent arRP-causing mutations in Japanese patients.