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通过选择性扩增和直接测序对人类α珠蛋白突变进行基因座定位。

Locus assignment of human alpha globin mutations by selective amplification and direct sequencing.

作者信息

Dodé C, Rochette J, Krishnamoorthy R

机构信息

ICGM, INSERM U 129, CHU Cochin Port-Royal, Paris, France.

出版信息

Br J Haematol. 1990 Oct;76(2):275-81. doi: 10.1111/j.1365-2141.1990.tb07884.x.

Abstract

We describe a simple approach for molecular characterization and locus assignment of structural mutants by direct sequencing of enzymatically amplified DNA selective to alpha 1 and alpha 2 globin gene regions. Nucleotide substitution of two structural variants (Stanleyville II alpha 2(78Lys) and J Mexico alpha 2(54Glu) were determined and their encoding loci were specified. The amplified segment encompasses sequences upstream of the CAAT box to downstream of the Poly(A) addition signal. Hence all of the alpha globin structural variants and most of the nondeletion alpha thalassaemic mutants should be characterizable by this approach.

摘要

我们描述了一种通过对α1和α2珠蛋白基因区域选择性酶促扩增的DNA进行直接测序,来对结构突变体进行分子特征分析和基因座定位的简单方法。确定了两种结构变异体(斯坦利维尔II型α2(78Lys)和J墨西哥型α2(54Glu))的核苷酸取代情况,并指定了它们的编码基因座。扩增片段涵盖了CAAT框上游至聚腺苷酸添加信号下游的序列。因此,所有的α珠蛋白结构变异体和大多数非缺失型α地中海贫血突变体都应该可以通过这种方法进行特征分析。

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