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来自不同人群的有和没有家族性高胆固醇血症的受试者中低密度脂蛋白受体基因位点的多态性单倍型和重组率。

Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations.

作者信息

Miserez A R, Schuster H, Chiodetti N, Keller U

机构信息

Department of Research, University Hospital, Basel, Switzerland.

出版信息

Am J Hum Genet. 1993 Apr;52(4):808-26.

Abstract

RFLPs at the low-density lipoprotein (LDL) receptor locus for TaqI, StuI, HincII, AvaII, ApaLI (5' and 3'), PvuII, and NcoI were studied in Swiss and German families with familial hypercholesterolemia (FH). A total of 1,104 LDL receptor alleles were analyzed using Southern blotting and new PCR-based techniques for detection of the TaqI, StuI, HincII, AvaII, NcoI RFLPs. Two hundred fifty-six independent haplotypes from 368 individuals of 61 unrelated Swiss families, as well as 114 independent haplotypes from 184 subjects of 25 unrelated German families, were constructed. In 76 families, clinical diagnosis of FH was confirmed by cosegregation analysis. Of the 43 unique haplotypes consisting of seven RFLPs detected in the Swiss and Germans, only 9 were common in both population samples. Analysis of linkage disequilibrium revealed nonrandom associations between several of the investigated RFLPs. ApaLI (5'), NcoI, PvuII, TaqI, and AvaII or HincII were particularly informative (cumulative informativeness .85). Relative frequencies, heterozygosity indexes, and PICs of the RFLPs from the Swiss and Germans were compared with values calculated from reported haplotype data for Italians, Icelanders, North American Caucasians, South African Caucasians, and Japanese. Pairwise comparisons of population samples by common RFLPs demonstrated unexpected differences even between geographically adjacent populations (e.g., the Swiss and Germans). Furthermore, genetic distances from the Germans to the other Caucasians were larger than to the Japanese. An unexpected lack of correlation between linkage disequilibria and physical distances was detected for the German and Japanese data, possibly because of nonuniform recombination with excessively high rates between exon 13 and intron 15. Hence, the present study revealed a striking variety of polymorphic haplotypes and heterogeneity of RFLP frequencies and recombination rates among the seven population samples.

摘要

在瑞士和德国家庭中,对家族性高胆固醇血症(FH)患者低密度脂蛋白(LDL)受体基因座上的TaqI、StuI、HincII、AvaII、ApaLI(5'和3')、PvuII和NcoI限制性片段长度多态性(RFLP)进行了研究。使用Southern印迹法以及基于聚合酶链反应(PCR)的新技术对1104个LDL受体等位基因进行分析,以检测TaqI、StuI、HincII、AvaII、NcoI RFLP。构建了来自61个无亲缘关系的瑞士家庭的368名个体的256个独立单倍型,以及来自25个无亲缘关系的德国家庭的184名受试者的114个独立单倍型。在76个家庭中,通过共分离分析证实了FH的临床诊断。在瑞士人和德国人中检测到的由7种RFLP组成的43种独特单倍型中,只有9种在两个群体样本中是常见的。连锁不平衡分析显示,所研究的几种RFLP之间存在非随机关联。ApaLI(5')、NcoI、PvuII、TaqI以及AvaII或HincII的信息量特别大(累积信息量>0.85)。将瑞士人和德国人RFLP的相对频率、杂合度指数和多态信息含量(PIC)与根据意大利人、冰岛人、北美白种人、南非白种人和日本人报告的单倍型数据计算的值进行了比较。通过常见RFLP对群体样本进行成对比较,结果显示即使在地理上相邻的群体(如瑞士人和德国人)之间也存在意外差异。此外,德国人到其他白种人的遗传距离大于到日本人的遗传距离。在德国人和日本人的数据中,检测到连锁不平衡与物理距离之间意外缺乏相关性,这可能是由于外显子13和内含子15之间的重组率过高且不均匀所致。因此,本研究揭示了七个群体样本中多态单倍型的显著多样性以及RFLP频率和重组率的异质性。

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