New chromosome 21 DNA markers isolated by pulsed field gel electrophoresis from an ETS2-containing Down syndrome chromosomal region |
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Authors: | Marie-Laure Yaspo Nathalie Crété Zoubida Chettouh Jean-Louis Blouin Zohra Rahmani Dominique Stehelin Pierre-Marie Sinet Nicole Créau-Goldberg Jean-Maurice Delabar |
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Affiliation: | (1) Laboratoire de Biochimie-Génétique URA 1335 CNRS, Hôpital Necker, 149, Rue de Sèvres, F-75743 Paris Cedex 15, France;(2) U 186 INSERM, Institut Pasteur, 1, Rue du Docteur Calmette, F-59019 Lille Cedex, France;(3) U 173 INSERM, Hôpital Necker, 149, Rue de Sèvres, F-75743 Paris Cedex 15, France |
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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. |
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