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PMID: 2945430 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A cell hybrid and recombinant DNA library that facilitate identification of polymorphic loci in the vicinity of the Huntington disease gene.

American journal of human genetics ·Vol. 39 ·No. 3 ·1986-09-00 ·Pages 397-403

Wasmuth JJ, Carlock LR, Smith B, Immken LL

Abstract

Somatic cell hybrids were selected that retain a derivative chromosome 5 from an individual in which the p15.1-pter segment of chromosome 5 is replaced with the p15.1-pter segment of chromosome 4. Hybrids that retain this derivative chromosome exclusively were found to be positive for G8, a DNA marker closely linked to the Huntington disease gene on chromosome 4p. From one such hybrid, a segregant was isolated that had deleted the entire q arm of the derivative chromosome but retained the p arm intact as its only detectable human DNA. A complete recombinant DNA library was prepared from this cell line, and the inserts in approximately 1/3 of the recombinant phage with human DNA were shown to be derived from 4pter-4p15.1, which represents only approximately 1% of the total human genome. The cell hybrid and DNA library represent a rapid and efficient means to identify and isolate many polymorphic DNA markers close to and flanking the Huntington disease gene.

MeSH Terms
Animals Chromosome Banding Chromosomes, Human, Pair 4 Cricetinae Cricetulus DNA, Recombinant Genetic Linkage Genetic Markers Humans Huntington Disease/genetics Hybrid Cells Karyotyping Polymorphism, Genetic
Chemicals
DNA, Recombinant Genetic Markers
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wasmuth J J
Carlock L R
Smith B
Immken L L
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14 references, click to expand
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Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
1986-09-00
Pages
397-403
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC1683957
Subset
IM
Grants
NIGMS NIH HHS · GM-25339 · United States
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