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PMID: 2576211 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Recombination events suggest potential sites for the Huntington's disease gene.

Neuron ·Vol. 3 ·No. 2 ·1989-08-00 ·Pages 183-90

MacDonald ME, Haines JL, Zimmer M, Cheng SV, Youngman S, Whaley WL, Wexler N, Bucan M, Allitto BA, Smith B

Abstract

The Huntington's disease gene (HD) maps distal to the D4S10 marker in the terminal 4p16.3 subband of chromosome 4. Directed cloning has provided several DNA segments that have been grouped into three clusters on a physical map of approximately 5 X 10(6) bp in 4p16.3. We have typed RFLPs in both reference and HD pedigrees to produce a fine-structure genetic map that establishes the relative order of the clusters and further narrows the target area containing the HD gene. Despite the large number of meiotic events examined, the HD gene cannot be positioned relative to the most distal cluster. One recombination event with HD suggests that the terminal-most markers flank the disease gene; two others favor a telomeric location for the defect. Efforts to isolate the HD gene must be divided between these two distinct intervals until additional genetic data resolve the apparent contradiction in localization.

MeSH Terms
Cell Line Chromosome Mapping Chromosomes, Human, Pair 4/ultrastructure Genes/genetics Genetic Linkage Genetic Markers Humans Huntington Disease/genetics Mutation Pedigree Polymorphism, Restriction Fragment Length Recombination, Genetic
Chemicals
Genetic Markers
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
MacDonald M E
Neurogenetics Laboratory, Massachusetts General Hospital, Boston 02114.
Haines J L
Zimmer M
Cheng S V
Youngman S
Whaley W L
Wexler N
Bucan M
Allitto B A
Smith B
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1989-08-00
Pages
183-90
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NINDS NIH HHS · NS16367 · United States
NINDS NIH HHS · NS20012 · United States
NINDS NIH HHS · NS22031 · United States
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