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[马里埃尔共和国人口中遗传性病理学的多样性及其在遗传性疾病基因频率方面的差异]

[Diversity of hereditary pathology in the population of Marii El Republic and its differentiation with respect to gene frequencies for hereditary diseases].

作者信息

Ginter E K, Mamedova R A, Kozlova S I, Galkina V A, Moshkina I S, Rudenskaia G E, Khlebnikova O V, Nurbaev S D, Balanovskaia E V, Rassanov V P

机构信息

Research Center for Medical Genetics, Russian Academy of Medical Sciences, Moscow, Russia.

出版信息

Genetika. 1998 Jul;34(7):963-72.

PMID:9749338
Abstract

The diversity of Mendelian hereditary pathology was studied in Marii El Republic. In total, 276,900 subjects, including 171,151 Maris and 88,714 Russians, living in seven raions (districts) were studied. Fifty-five autosomal dominant disease entities were found, with more than ten diseases having a frequency of 1:50,000 people or higher. In Maris, autosomal recessive hypotrichosis was observed at a relatively high frequency (1:15,337); this disease was not revealed in the Russian population studied earlier. Conversely, no phenylketonuria (PKU) was found in Maris, while it was a relatively common autosomal recessive disease in Russians. Regarding autosomal dominant pathology, 76 disease entities were revealed, with 21 diseases being observed at a frequency of at least 1:50,000. Ten X-linked diseases were found. The numbers of both autosomal recessive and autosomal dominant diseases exhibited a linear relationship with the number of subjects examined. The genetic structure of the Mari population was studied on the basis of data on the genes of recessive diseases. A matrix of Nei's genetic distances was calculated from the frequencies of 45 recessive diseases found in the seven districts studied. The average genetic distance calculated for the 45 loci of autosomal recessive diseases was 0.006175 x 10(-3). Similarly, matrix of genetic distances for five Mari populations was obtained (Medvedevskii and Zvenigovskii raions were not included) based on a total of 32 allelic frequencies for ten polymorphic immune and biochemical loci. The average genetic distance calculated from the ten polymorphic loci was 0.001930, i.e., 2.5 orders of magnitude greater than the average genetic distance for recessive diseases. The matrices of genetic distances for the five Mari populations calculated from the gene frequencies for recessive diseases and for the ten polymorphic systems were largely similar to each other. Thus, the main elements of the genetic structure of the Mari population can be estimated on the basis of gene frequencies for hereditary diseases. In this case, the characteristics of individual populations, which are more or less isolated, and of their interaction are the same as in the case of studying genetic structure with the use of polymorphic biological markers.

摘要

在马里埃尔共和国对孟德尔遗传病理学的多样性进行了研究。总共对居住在七个区的276,900名受试者进行了研究,其中包括171,151名马里人以及88,714名俄罗斯人。发现了55种常染色体显性疾病实体,其中十多种疾病的发病率为1:50,000或更高。在马里人中,常染色体隐性少毛症的发病率相对较高(1:15,337);在先前研究的俄罗斯人群中未发现这种疾病。相反,在马里人中未发现苯丙酮尿症(PKU),而在俄罗斯人中这是一种相对常见的常染色体隐性疾病。关于常染色体显性病理学,发现了76种疾病实体,其中21种疾病的发病率至少为1:50,000。发现了10种X连锁疾病。常染色体隐性疾病和常染色体显性疾病的数量均与检查的受试者数量呈线性关系。根据隐性疾病基因的数据研究了马里人群的遗传结构。从在研究的七个区中发现的45种隐性疾病的基因频率计算出内氏遗传距离矩阵。常染色体隐性疾病的45个基因座的平均遗传距离计算为0.006175×10⁻³。同样,基于十个多态性免疫和生化基因座的总共32个等位基因频率,获得了五个马里人群的遗传距离矩阵(未包括梅德韦杰夫斯基区和兹韦尼戈夫斯基区)。从十个多态性基因座计算出的平均遗传距离为0.001930,即比隐性疾病的平均遗传距离大2.5个数量级。从隐性疾病的基因频率和十个多态性系统计算出的五个马里人群的遗传距离矩阵彼此大致相似。因此,可以根据遗传性疾病的基因频率来估计马里人群遗传结构的主要要素。在这种情况下,或多或少隔离的各个群体的特征及其相互作用与使用多态性生物标记研究遗传结构的情况相同。

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