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瑞典萨米人的血清补体(C3、BF、C4)类型

Serum complement (C3, BF, C4) types in Swedish Saamis.

作者信息

Beckman G, Beckman L, Sikström C

机构信息

Department of Medical Genetics, University of Umeå, Sweden.

出版信息

Hum Hered. 1993 Nov-Dec;43(6):362-5. doi: 10.1159/000154160.

Abstract

Serum complement (C3, BF, C4) types were examined in Swedish Saamis (Lapps). In agreement with previous studies, a very low frequency of the C3*F allele (0.033) was found. Compared to Swedes and other Caucasian populations, Swedish Saamis showed a significantly increased frequency of the BFS, C4A4 and C4B2 variants, and a lower frequency of C4 deficiency. BFS, C4A4 and C4B2 show haplotype associations and thus the frequency of the S-A4-B2 complotype is significantly increased among the Saamis. Although the serum complement constitution of the Saamis shows some similarity with that of Asiatic Mongoloid populations it is unlikely to be due to Asiatic ethnic influence. The marked genetic deviations of the Saamis from all other populations has often been interpreted as a result of the founder effect and genetic drift. In this particular case, however, immunogenetic adaptation appears to be a plausible alternative explanation for the deviations in genetic complement factors.

摘要

对瑞典萨米人(拉普人)的血清补体(C3、BF、C4)类型进行了检测。与之前的研究一致,发现C3*F等位基因的频率非常低(0.033)。与瑞典人和其他高加索人群相比,瑞典萨米人BFS、C4A4和C4B2变体的频率显著增加,C4缺乏的频率较低。BFS、C4A4和C4B2表现出单倍型关联,因此萨米人中S - A4 - B2复合体型的频率显著增加。尽管萨米人的血清补体构成与亚洲蒙古人种人群有一些相似之处,但不太可能是由于亚洲种族影响。萨米人与所有其他人群明显的基因偏差常被解释为奠基者效应和遗传漂变的结果。然而,在这种特殊情况下,免疫遗传适应似乎是基因补体因子偏差的一个合理的替代解释。

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