Analysis of myocilin gene mutations in Japanese patients with normal tension glaucoma and primary open-angle glaucoma

The myocilin gene was identified as a gene (MYOC) that caused primary open- angle glaucoma (POAG). Although a normal tension glaucoma (NTG) patient wit h the myocilin gene mutation was previously reported, no study using large numbers of patients with NTG has been reported. Single-strand conformation polymorphism analysis and subsequent sequence analysis were performed for g enotyping the myocilin gene in 114 unrelated Japanese patients with NTG. On e hundred and nineteen patients with POAG and 100 control subjects without glaucoma were studied as reference subjects. Five amino acid sequence chang es of the myocilin were identified: Arg46Stop tone NTG), Arg76Lys (four NTG , 10 POAG, seven control), Arg158Gln tone NTG, one POAG, one control) found in only Japanese, Asp208Glu (four NTG, three POAG, one control), Pro481Ser tone control). Pro481Ser was novel. Arg76Lys always occurred with 1-83 fro m G to A in the promoter as it was reported in Chinese. Although some Japan ese patients with NTG had sequence changes of the myocilin gene, there were no apparent specific mutations in patients with NTG.