Literature DB >> 2576211

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

M E MacDonald1, J L Haines, M Zimmer, S V Cheng, S Youngman, W L Whaley, N Wexler, M Bucan, B A Allitto, B Smith.   

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.

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Year:  1989        PMID: 2576211     DOI: 10.1016/0896-6273(89)90031-7

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  27 in total

1.  Structural and transcriptional analysis of a human subtelomeric repeat.

Authors:  J F Cheng; C L Smith; C R Cantor
Journal:  Nucleic Acids Res       Date:  1991-01-11       Impact factor: 16.971

2.  Evidence for linkage disequilibrium between D16S94 and the adult onset polycystic kidney disease (PKD1) gene.

Authors:  S E Pound; A D Carothers; P M Pignatelli; A M Macnicol; M L Watson; A F Wright
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

3.  Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

Authors:  K A Mills; K H Buetow; Y Xu; T M Ritty; K D Mathews; S E Bodrug; C Wijmenga; I Balazs; J C Murray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

4.  The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).

Authors:  M Upadhyaya; P Lunt; M Sarfarazi; W Broadhead; J Farnham; P S Harper
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

5.  The end in sight for Huntington disease?

Authors:  C Pritchard; D R Cox; R M Myers
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

6.  Influence of aberrant observations on high-resolution linkage analysis outcomes.

Authors:  K H Buetow
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

7.  Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.

Authors:  Jong-Min Lee; Tammy Gillis; Jayalakshmi Srinidhi Mysore; Eliana Marisa Ramos; Richard H Myers; Michael R Hayden; Patrick J Morrison; Martha Nance; Christopher A Ross; Russell L Margolis; Ferdinando Squitieri; Annamaria Griguoli; Stefano Di Donato; Estrella Gomez-Tortosa; Carmen Ayuso; Oksana Suchowersky; Ronald J Trent; Elizabeth McCusker; Andrea Novelletto; Marina Frontali; Randi Jones; Tetsuo Ashizawa; Samuel Frank; Marie-Helene Saint-Hilaire; Steven M Hersch; Herminia D Rosas; Diane Lucente; Madaline B Harrison; Andrea Zanko; Ruth K Abramson; Karen Marder; Jorge Sequeiros; Marcy E MacDonald; James F Gusella
Journal:  Am J Hum Genet       Date:  2012-03-01       Impact factor: 11.025

8.  Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)

Authors:  J Yaouanq; M Perichon; M Chorney; P Pontarotti; A Le Treut; A el Kahloun; V Mauvieux; M Blayau; A M Jouanolle; B Chauvel
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

9.  Recombination of 4p16 DNA markers in an unusual family with Huntington disease.

Authors:  C Pritchard; N Zhu; J Zuo; L Bull; M A Pericak-Vance; J M Vance; A D Roses; A Milatovich; U Francke; D R Cox
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

10.  Huntington disease in Finland: a molecular and genealogical study.

Authors:  E Ikonen; J Ignatius; R Norio; J Palo; L Peltonen
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

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