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Linear order of new and established DNA markers around the fragile site at Xq27.3

Identifieur interne : 001C72 ( Istex/Curation ); précédent : 001C71; suivant : 001C73

Linear order of new and established DNA markers around the fragile site at Xq27.3

Auteurs : M. C. Hirst [Royaume-Uni] ; A. Roche [Royaume-Uni] ; T. J. Flint [Royaume-Uni] ; R. N. Mackinnon [Royaume-Uni] ; J. H. D. Bassett [Royaume-Uni] ; Y. Nakahori [Royaume-Uni] ; J. E. V. Watson [Royaume-Uni] ; M. V. Bell [Royaume-Uni] ; M. N. Patterson [Royaume-Uni] ; Y. Boyd [Royaume-Uni] ; N. S. T. Thomas [Royaume-Uni] ; S. J. L. Knight [Royaume-Uni] ; S. T. Warren [États-Unis] ; M. Hors-Cayla [France] ; M. Schmidt [Australie] ; G. R. Sutherland [Australie] ; K. E. Davies [Royaume-Uni]

Source :

RBID : ISTEX:972B102FB12AA5CF605C8E69FDA938F694848B88

English descriptors

Abstract

Abstract: We have used recombinant clones derived from microdissection of the fragile X region to characterize breakpoints around the fragile site at Xq27.3. So far, no microdissection markers derived from Xq28 material have been found, thus allowing a rapid screening for clones surrounding the fragile site by their presence in a somatic cell hybrid containing Xq27.2-Xqter. A total of 43 new DNA markers from Xq27 have been sublocalized within this chromosome band. Of these new DNA markers, 5 lie in an interval defined as containing the fragile X region. The saturation of Xq27 with DNA markers by microdissection demonstrates the power of this technique and provides the resources for generating a complete physical map of the region.

Url:
DOI: 10.1016/0888-7543(91)90506-A

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ISTEX:972B102FB12AA5CF605C8E69FDA938F694848B88

Le document en format XML

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<name sortKey="Schmidt, M" sort="Schmidt, M" uniqKey="Schmidt M" first="M." last="Schmidt">M. Schmidt</name>
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<name sortKey="Davies, K E" sort="Davies, K E" uniqKey="Davies K" first="K. E." last="Davies">K. E. Davies</name>
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<term>Amer</term>
<term>Breakpoint</term>
<term>Breakpoints</term>
<term>Cell lines</term>
<term>Chromosome</term>
<term>Clone</term>
<term>Cosmid</term>
<term>Fragile</term>
<term>Fragile site</term>
<term>Genet</term>
<term>Hirst</term>
<term>Hybrid</term>
<term>Hybrid breakpoints</term>
<term>Hybridization</term>
<term>Ledbetter</term>
<term>Localization</term>
<term>Locus</term>
<term>Mackinnon</term>
<term>Marker</term>
<term>Mental retardation</term>
<term>Microclone</term>
<term>Microclones</term>
<term>Microdissection</term>
<term>Microdissection library</term>
<term>Mutation</term>
<term>Nucleic acids</term>
<term>Physical mapping</term>
<term>Polymerase</term>
<term>Polymerase chain reaction</term>
<term>Rapid isolation</term>
<term>Somatic</term>
<term>Somatic cell</term>
<term>Somatic cell hybrids</term>
<term>Suthers</term>
<term>Xqter</term>
<term>Xqter content</term>
</keywords>
<keywords scheme="Teeft" xml:lang="en">
<term>Amer</term>
<term>Breakpoint</term>
<term>Breakpoints</term>
<term>Cell lines</term>
<term>Chromosome</term>
<term>Clone</term>
<term>Cosmid</term>
<term>Fragile</term>
<term>Fragile site</term>
<term>Genet</term>
<term>Hirst</term>
<term>Hybrid</term>
<term>Hybrid breakpoints</term>
<term>Hybridization</term>
<term>Ledbetter</term>
<term>Localization</term>
<term>Locus</term>
<term>Mackinnon</term>
<term>Marker</term>
<term>Mental retardation</term>
<term>Microclone</term>
<term>Microclones</term>
<term>Microdissection</term>
<term>Microdissection library</term>
<term>Mutation</term>
<term>Nucleic acids</term>
<term>Physical mapping</term>
<term>Polymerase</term>
<term>Polymerase chain reaction</term>
<term>Rapid isolation</term>
<term>Somatic</term>
<term>Somatic cell</term>
<term>Somatic cell hybrids</term>
<term>Suthers</term>
<term>Xqter</term>
<term>Xqter content</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: We have used recombinant clones derived from microdissection of the fragile X region to characterize breakpoints around the fragile site at Xq27.3. So far, no microdissection markers derived from Xq28 material have been found, thus allowing a rapid screening for clones surrounding the fragile site by their presence in a somatic cell hybrid containing Xq27.2-Xqter. A total of 43 new DNA markers from Xq27 have been sublocalized within this chromosome band. Of these new DNA markers, 5 lie in an interval defined as containing the fragile X region. The saturation of Xq27 with DNA markers by microdissection demonstrates the power of this technique and provides the resources for generating a complete physical map of the region.</div>
</front>
</TEI>
</record>

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