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补体C6和C7基因的DNA多态性

DNA polymorphisms of the complement C6 and C7 genes.

作者信息

Fernie B A, Würzner R, Unsworth D J, Tuxworth R I, Hobart M J

机构信息

Molecular Immunopathology Unit, MRC Centre, Cambridge, U.K.

出版信息

Ann Hum Genet. 1995 Apr;59(2):163-81. doi: 10.1111/j.1469-1809.1995.tb00739.x.

Abstract

The linked C6 and C7 loci are rich in genetic markers, both at the protein and DNA levels. There are now seven common DNA polymorphisms distributed over about 300 kbp of chromosome 5p12-14. We report a new TaqI RFLP for C7 and a method for typing a C7 variant (T368S) hitherto known only from cDNA clones. We have re-investigated the published RFLPs to provide information on their frequency in North European Caucasian (predominantly British and Irish) subjects and have revised some of the published parameters, especially the sizes of polymorphic restriction fragments. Their precise locations within the genes are also reported: the three markers for C6 are in exon 3, intron 3 and adjacent to exon 17 and the four markers for C7 are in introns 15 and 13 and in exons 13 and 9. The gene frequencies of the second commonest allele of all seven markers lie in the range 0.2 to 0.37, except C6 A/B in the Japanese, where the frequencies of both common alleles are about 0.45. We have estimated the gene frequencies for the DNA polymorphisms which correlate with C7 M/N phenotype and for the C6 A/B phenotype and find them to be the same as the phenotypic estimates in Caucasians and in the Japanese respectively. The markers provide the possibility of defining 128 haplotypes, many (28) of which have been observed. Allelic associations in these genes are generally surprisingly weak.

摘要

相连的C6和C7基因座在蛋白质和DNA水平上都富含遗传标记。现在有7种常见的DNA多态性分布在5号染色体p12 - 14区域约300千碱基对的范围内。我们报告了一种新的C7的TaqI限制性片段长度多态性(RFLP)以及一种对迄今仅从cDNA克隆中得知的C7变体(T368S)进行分型的方法。我们重新研究了已发表的RFLP,以提供其在北欧白种人(主要是英国人和爱尔兰人)中的频率信息,并修订了一些已发表的参数,特别是多态性限制性片段的大小。还报告了它们在基因内的确切位置:C6的三个标记位于外显子3、内含子3以及外显子17附近,C7的四个标记位于内含子15和13以及外显子13和9中。除了日本人中C6 A/B的情况,所有七个标记的第二常见等位基因的基因频率在0.2至0.37的范围内,在日本人中,两个常见等位基因的频率约为0.45。我们估计了与C7 M/N表型相关的DNA多态性以及C6 A/B表型的基因频率,发现它们分别与白种人和日本人中的表型估计值相同。这些标记提供了定义128种单倍型的可能性,其中许多(28种)已经被观察到。这些基因中的等位基因关联通常弱得出奇。

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