Objective.To identify and evaluate mutations in the RP1 gene among Chinese patients with retinitis pigmentosa(RP).Methods.Leukocyte DNA of 92 RP patients were collected in Hong Kong.Sequence changes of the entire codi...Objective.To identify and evaluate mutations in the RP1 gene among Chinese patients with retinitis pigmentosa(RP).Methods.Leukocyte DNA of 92 RP patients were collected in Hong Kong.Sequence changes of the entire coding region of the RP1 gene were examined using PCR,conformation sensitive gel electrophoresis and DNA sequencing.Results.In total,1 nonsense mutation and 1 nonsense variant as well as 10 missense alterations were identified in the RP1 gene,among which,Arg 677 Ter was found in 1 RP patient and another nonsense variant,Arg 1933Ter ,was identified in 3 normal individuals and 1 patient with Stargardt's disease,suggesting its nonpatogenicity,Arg667 Ter is expected to lead to large disruptions of the encoded protein.Couclusions.The nonpathogenicity of Arg 1933 Ter indicates that the C-terminal 224 residues of RP1 protein may be not critical for RP1.The most C-terminal truncation previously reported was due to Tyr1053(1-bp del) and occurred in RP patients.Thus RP can be caused by reduction in the level of the region of RP1 protein after condon 1052 but before 1933.T o ascertain such a proposition,genotypes of more RP patients may reveal more RP cousative mutations and more sequence alterations different than those of other ethnic groups.展开更多
文摘Objective.To identify and evaluate mutations in the RP1 gene among Chinese patients with retinitis pigmentosa(RP).Methods.Leukocyte DNA of 92 RP patients were collected in Hong Kong.Sequence changes of the entire coding region of the RP1 gene were examined using PCR,conformation sensitive gel electrophoresis and DNA sequencing.Results.In total,1 nonsense mutation and 1 nonsense variant as well as 10 missense alterations were identified in the RP1 gene,among which,Arg 677 Ter was found in 1 RP patient and another nonsense variant,Arg 1933Ter ,was identified in 3 normal individuals and 1 patient with Stargardt's disease,suggesting its nonpatogenicity,Arg667 Ter is expected to lead to large disruptions of the encoded protein.Couclusions.The nonpathogenicity of Arg 1933 Ter indicates that the C-terminal 224 residues of RP1 protein may be not critical for RP1.The most C-terminal truncation previously reported was due to Tyr1053(1-bp del) and occurred in RP patients.Thus RP can be caused by reduction in the level of the region of RP1 protein after condon 1052 but before 1933.T o ascertain such a proposition,genotypes of more RP patients may reveal more RP cousative mutations and more sequence alterations different than those of other ethnic groups.
