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通过脉冲场凝胶电泳从含ETS2的唐氏综合征染色体区域分离出的新的21号染色体DNA标记。

New chromosome 21 DNA markers isolated by pulsed field gel electrophoresis from an ETS2-containing Down syndrome chromosomal region.

作者信息

Yaspo M L, Crété N, Chettouh Z, Blouin J L, Rahmani Z, Stehelin D, Sinet P M, Créau-Goldberg N, Delabar J M

机构信息

Laboratoire de Biochimie-Génétique URA 1335 CNRS, Hôpital Necker, Paris, France.

出版信息

Hum Genet. 1992 Dec;90(4):427-34. doi: 10.1007/BF00220472.

Abstract

To generate new chromosome 21 markers in a region that is critical for the pathogenesis of Down syndrome (D21S55-MX1), we used pulsed field gel electrophoresis (PFGE) to isolate a 600-kb NruI DNA fragment from the WA17 hybrid cell line, which has retained chromosome 21 as the only human material. This fragment, which contains the oncogene ETS2, was used to construct a partial genomic library. Among the 14 unique sequences that were isolated, 3 were polymorphic markers and contained sequences that are conserved in mammals. Five of these markers mapped on the ETS2-containing NruI fragment and allowed us to define an 800-kb high-resolution PFGE map.

摘要

为了在对唐氏综合征(D21S55-MX1)发病机制至关重要的区域生成新的21号染色体标记,我们使用脉冲场凝胶电泳(PFGE)从WA17杂交细胞系中分离出一个600 kb的NruI DNA片段,该细胞系仅保留了21号染色体作为唯一的人类物质。这个包含癌基因ETS2的片段被用于构建一个部分基因组文库。在分离出的14个独特序列中,有3个是多态性标记,并且包含在哺乳动物中保守的序列。其中5个标记定位在包含ETS2的NruI片段上,使我们能够定义一个800 kb的高分辨率PFGE图谱。

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