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DOI 10.1002/humu.24492

Медицинская библиотека · Human mutation · 2022

Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.

Suga Akiko, Yoshitake Kazutoshi, Minematsu Naoko, Tsunoda Kazushige, Fujinami Kaoru, Miyake Yozo, Kuniyoshi Kazuki, Hayashi Takaaki, Mizobuchi Kei, Ueno Shinji, Terasaki Hiroko, Kominami Taro, Nao-I Nobuhisa, Mawatari Go, Mizota Atsushi, Shinoda Kei, Kondo Mineo, Kato Kumiko, Sekiryu Tetsuju, Nakamura Makoto, Kusuhara Sentaro, Yamamoto Hiroyuki, Yamamoto Shuji, Mochizuki Kiyofumi, Kondo Hiroyuki, Matsushita Itsuka, Kameya Shuhei, Fukuchi Takeo, Hatase Tetsuhisa, Horiguchi Masayuki, Shimada Yoshiaki, Tanikawa Atsuhiro, Yamamoto Shuichi, Miura Gen, Ito Nana, Murakami Akira, Fujimaki Takuro, Hotta Yoshihiro, Tanaka Koji, Iwata Takeshi

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Аннотация

Inherited retinal diseases (IRDs) comprise a phenotypically and genetically heterogeneous group of ocular disorders that cause visual loss via progressive retinal degeneration. Here, we report the genetic characterization of 1210 IRD pedigrees enrolled through the Japan Eye Genetic Consortium and analyzed by whole exome sequencing. The most common phenotype was retinitis pigmentosa (RP, 43%), followed by macular dystrophy/cone- or cone-rod dystrophy (MD/CORD, 13%). In total, 67 causal genes were identified in 37% (448/1210) of the pedigrees. The first and second most frequently mutated genes were EYS and RP1, associated primarily with autosomal recessive (ar) RP, and RP and arMD/CORD, respectively. Examinations of variant frequency in total and by phenotype showed high accountability of a frequent EYS missense variant (c.2528G>A). In addition to the two known EYS founder mutations (c.4957dupA and c.8805C>G) of arRP, we observed a frequent RP1 variant (c.5797C>T) in patients with arMD/CORD.

Для цитирования: Suga Akiko, Yoshitake Kazutoshi, Minematsu Naoko, Tsunoda Kazushige, Fujinami Kaoru, Miyake Yozo, Kuniyoshi Kazuki, Hayashi Takaaki, Mizobuchi Kei, Ueno Shinji, Terasaki Hiroko, Kominami Taro, Nao-I Nobuhisa, Mawatari Go, Mizota Atsushi, Shinoda Kei, Kondo Mineo, Kato Kumiko, Sekiryu Tetsuju, Nakamura Makoto, Kusuhara Sentaro, Yamamoto Hiroyuki, Yamamoto Shuji, Mochizuki Kiyofumi, Kondo Hiroyuki, Matsushita Itsuka, Kameya Shuhei, Fukuchi Takeo, Hatase Tetsuhisa, Horiguchi Masayuki, Shimada Yoshiaki, Tanikawa Atsuhiro, Yamamoto Shuichi, Miura Gen, Ito Nana, Murakami Akira, Fujimaki Takuro, Hotta Yoshihiro, Tanaka Koji, Iwata Takeshi. Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.. Human mutation. 2022. DOI: 10.1002/humu.24492.

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