Chromosomal localization of the mouse homolog of the Huntington's disease linked G8 (D4S10) marker
The human DNA probe G8 defines D4S10, a polymorphic locus tightly linked to the Huntington's disease gene on human chromosome 4. A subclone of G8, pSC33, showed significant cross-hybridization to discrete restriction fragments in total genomic mouse DNA. The probe detected restriction fragment...
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Veröffentlicht in: | DNA (New York, N.Y.) N.Y.), 1987-10, Vol.6 (5), p.401-407 |
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Sprache: | eng |
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Zusammenfassung: | The human DNA probe G8 defines D4S10, a polymorphic locus tightly linked to the Huntington's disease gene on human chromosome 4. A subclone of G8, pSC33, showed significant cross-hybridization to discrete restriction fragments in total genomic mouse DNA. The probe detected restriction fragment length polymorphisms (RFLPs) with the enzymes Taq I and Msp I, permitting chromosomal localization of the mouse G8 homolog by linkage analysis using three sets of recombinant inbred mouse strains: BXH, BXD, and AKXD. The mouse locus was mapped to the central region of chromosome 11 at 1 centiMorgan from the SPARC gene, a locus whose human counterpart is on human chromosome 5. |
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ISSN: | 0198-0238 |
DOI: | 10.1089/dna.1987.6.401 |