共查询到16条相似文献,搜索用时 22 毫秒
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欧炯文 申滨 邹浪萍 赵丽萍 赵永和OU Jiong-Wen SHEN Bin ZHOU Lang-Ping ZHAO Li-Ping ZHAO Yong-He 《遗传》1996,18(3):29-29
DistributionandGeneFrequcnciesofEAP,ADAandAK1intheMiaoEthnicGroupofYunnan,ChinaouJiongwenShenBinZhouLangpingZhaoLipingZhaoYonghe(DepartmentofForensicMedicine,KunmingMedicalCollege,Kunming650031)我们对居住于云南的苗族人红细胞EAP、ADA和AK1的分布进行了调查。138例苗族人血样采自云南省屏边苗族自治县民族小学的学生,各取措梢血少许,涂于干净纱布上自然晾干,制成血痕样品,低温干燥保存。按文献[3]所述方法对样品进行EAP-AK1同步电泳分型检测,对所得数据进行统计处理。本次调查所检测的EAP、ADA… 相似文献
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对畲族血浆组特异性成分、红细胞磷酸葡萄糖变位酶1(PGM1)、酶性磷酸酶(AcP1)、6-磷酸葡萄糖酸氢酶(6-PGD)、腺苷脱氨酶(ADA0、腺苷酸激酶(AK1)的遗传多态性进行了研究。Gc与PGM1是用薄层聚丙烯酰胺凝胶等电聚集分析的,AcP1、6-PGD、ADA及AD1是用淀粉凝胶电泳分析的。各基因座的基因频率分别为Gc1F0.4722、Ge1S0.2421、Gc20.2738;PGM11A 相似文献
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对畲族血浆组特异性成分(Gc)、红细胞磷酸葡萄糖变位酶1(PGM1)、酸性磷酸酶(AcP1)、6-磷酸葡萄糖酸脱氢酶(6-PGD)、腺苷脱氨酶(ADA)、腺苷酸激酶(AK1)的遗传多态性进行了研究。Gc与PGM1是用薄层聚丙烯酰胺凝胶等电聚焦分析的,AcP1、6-PGD、ADA及AK1是用淀粉凝胶电泳分析的。各基因座的基因频率分别为Gc*1F0.4722、Gc*1S0.2421、Gc*20.2738;PGM1*1A0.5357、PGM1*1B0.1627、PGM1*2A0.1587、PGM1*2B0.1429;AcP*1A0.1825、AcP1*B0.8175;6-PGD*A0.9683、6-PGD*B0.0278;ADA*10.9881、ADA*20.0119;AK1*11.0000。畲族Gc、PGM1、AcP1、6-PGD和ADA基因为多态,而AK1基因为单态。发现1例带有6-PGD*R和3例带有Gc*1A2变异等位基因的个体,其中Gc*1A2基因频率为0.0119,达到多态水平。 相似文献
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中国20个民族中PGM_1及其亚型EsD、GLO1、AK、ADA和6-PGD酶型分布调查 总被引:2,自引:0,他引:2
调查了汉族、鄂伦春、赫哲、朝鲜、蒙古、羌、土家、苗、侗、畲、壮、纳西、傈僳、白、彝、景颇、哈尼、傣、维吾尔和塔吉克等20个民族的PGM_1及其亚型,EsD、GLO_1、AK、ADA和6-PGD等酶型的分布及基因频率。PGM_1及其亚型、EsD和GLO_1在中国各民族中是分布较好的,个人识别能力较高的酶。有12个民族查出有PQM_1~6基因,壮族的频率最高,PGM_1 6-1表型达4.15%。对在4174份血样中所检出的带有PGM_1~6基因的68份血样做亚型分析,在凝胶上PGM_1~6谱带均在同一位置上。EsD_1基因频率的总趋向是北方各民族高于南方。哈尼、傈僳、傣、纳西、畲、壮、侗和苗等民族EsD2-2表型达15%以上,哈尼族高达32.4%。GLO1~1基因频率塔吉克和维吾尔族为0.2927和0.2112,羌族为0.0583,其它各族在0.0714—0.1527。各民族AK~1、ADA和6-PGD~(?)基因频率均甚高。 相似文献
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为研究中国南方汉族人群核苷酸修复基因hMTH1遗传多态性,应用聚合酶链反应-单链构象多态性技术检测172名健康人外周血白细胞hMTH1基因启动子及全部5个外显子多态性,并进行DNA测序。结果发现hMTH1基因启动子及外显子1序列保守,未见突变;外显子2第73位碱基存在T→C杂合型突变,基因型TT和TC频率分别为93.02%、6.98%,等位基因T和C频率分别为96.51%、3.49%;外显子3第45位遗传密码存在T→C杂合型突变,基因型TT和TC频率分别为95.35%、4.65%,等位基因T和C频率分别为97.67%、2.33%,该多态性为首次发现;外显子4第83位遗传密码存在G→A杂合型突变,基因型GG和GA频率分别为89.53%、10.47%,等位基因G和A频率分别为94.77%、5.23%;外显子5第119位氨基酸遗传密码存在C→T杂合型突变,基因型CC和CT频率分别为95.93%、4.07%,等位基因C和T频率分别为97.97%、2.03%。Abstract: In order to study the genetic polymorphisms of nucleotide repair gene hMTH1 in southern Chinese Han population, the polymorphisms of the gene’s promoter and its five exons among peripheral blood lymphocytes of 172 Chinese Han people were analyzed with polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and DNA sequencing. The sequences of the promoter and exon 1 of hMTH1 gene were conserved. A T to C polymorphism was detected at the 73th base in exon2. The genotype frequencies of TT and TC were 93.02% and 6.98%, respectively. The allelic frequencies of T and C were 96.51% and 3.49%, respectively. A T to C polymorphism was detected at codon 45 in exon3, which was first reported. The genotype frequencies of TT and TC were 95.35% and 4.65%, respectively. The allelic frequencies of T and C were 97.67% and 2.33%, respectively. A G to A polymorphism was detected at codon 83 in exon4. The genotype frequencies of GG and GA were 89.53% and 10.47%, respectively. The allelic frequencies of G and A were 94.77% and 5.23%, respectively. A C to T polymorphism was detected at codon 119 in exon5. The genotype frequencies of CC and CT were 95.93% and 4.07%, respectively. The allelic frequencies of C and T were 97.97% and 2.03%, respectively. 相似文献
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