Zhang Q, Mao W, Ma Q, Zeng R, Wu L, Wu D, Chen Y
Zhongshan Ophthalmic Center, Sun Yat-sen University of Medical Sciences, Guangzhou, China.
Yan Ke Xue Bao. 1990 Dec;6(3-4):51-7.
Applying recombinant DNA techniques, the structures of red pigment gene (RPG) and green pigment gene (GPG) were analyzed for 43 patients with protan or deutan (including 3 females), 4 normal relatives and 3 carriers out of 3 families, as well as 11 normal controls. Abnormality of RPG was detected in all 19 protan and that of GPG was found in 14 out of 24 deutan. In about 80% (32/40) of protan and deutan the changing of exon 5 for RPG or GPG was discovered. In protan the normal RPG was replaced by a 5' red -3' green hybrid gene. Some of the deutan had no GPG, some had 5' green -3' red hybrid gene with or without GPG. Furthermore, the exon 5 of RPG and GPG was amplified by polymerase chain reaction (PCR) and further analyzed by Rsa I digestion. The results for PCR are identical to that of Southern blot hybridization.
应用重组DNA技术,对43例红色盲或绿色盲患者(包括3名女性)、4名正常亲属、3个家庭中的3名携带者以及11名正常对照者的红色素基因(RPG)和绿色素基因(GPG)结构进行了分析。在所有19例红色盲患者中均检测到RPG异常,在24例绿色盲患者中有14例发现GPG异常。在约80%(32/40)的红色盲和绿色盲患者中发现RPG或GPG的第5外显子发生改变。在红色盲患者中,正常的RPG被一个5'红 - 3'绿的杂交基因所取代。部分绿色盲患者没有GPG,部分患者有5'绿 - 3'红的杂交基因,有或没有GPG。此外,通过聚合酶链反应(PCR)扩增RPG和GPG的第5外显子,并通过Rsa I酶切进一步分析。PCR结果与Southern印迹杂交结果一致。