Literature DB >> 1350884

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

C Pritchard1, N Zhu, J Zuo, L Bull, M A Pericak-Vance, J M Vance, A D Roses, A Milatovich, U Francke, D R Cox.   

Abstract

The Huntington disease (HD) mutation has been localized to human chromosome 4p16, in a 6-Mb region between the D4S10 locus and the 4p telomere. In a report by Robbins et al., a family was identified in which an affected individual failed to inherit three alleles within the 6-Mb region originating from the parental HD chromosome. To explain these results, it was suggested that the HD locus (HD) lies close to the telomere and that a recombination event took place between HD and the most telomeric marker examined, D4S90. As a test of this telomere hypothesis, we examined six members of this family, five of whom are affected with HD, for the segregation of 12 polymorphic markers from 4p16, including D4S169, which lies within 80 kb of the 4p telomere. We separated, in somatic cell hybrids, the chromosomes 4 from each family member, to determine the phase of marker alleles on each chromosome. We excluded nonpaternity by performing DNA fingerprint analyses on all six family members, and we found no evidence for chromosomal rearrangements when we used high-resolution karyotype analysis. We found that two affected siblings, including one of the patients originally described by Robbins et al., inherited alleles from the non-HD chromosome 4 of their affected parents, throughout the 6-Mb region. We found that a third affected sibling, also studied by Robbins et al., inherited alleles from the HD chromosome 4 of the affected parent, throughout the 6-Mb region. Finally, we found that a fourth sibling, who is likely affected with HD, has both a recombination event within the 6-Mb region and an additional recombination event in a more centromeric region of the short arm of chromosome 4. Our results argue against a telomeric location for HD and suggest that the HD mutation in this family is either associated with DNA predisposed to double recombination and/or gene conversion within the 6-Mb region or is in a gene that is outside this region and that is different from that mutated in most other families with HD.

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Year:  1992        PMID: 1350884      PMCID: PMC1682573     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  34 in total

1.  Dinucleotide repeat polymorphism located at D4S169.

Authors:  C Pritchard; D R Cox; R M Myers
Journal:  Nucleic Acids Res       Date:  1991-11-25       Impact factor: 16.971

2.  Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation.

Authors:  M Bućan; M Zimmer; W L Whaley; A Poustka; S Youngman; B A Allitto; E Ormondroyd; B Smith; T M Pohl; M MacDonald
Journal:  Genomics       Date:  1990-01       Impact factor: 5.736

3.  Linkage disequilibrium in Huntington's disease: an improved localisation for the gene.

Authors:  R G Snell; L P Lazarou; S Youngman; O W Quarrell; J J Wasmuth; D J Shaw; P S Harper
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

4.  Linkage disequilibrium and modification of risk for Huntington disease.

Authors:  S Adam; J Theilmann; K Buetow; A Hedrick; C Collins; B Weber; M Huggins; M Hayden
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

5.  A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.

Authors:  K H Buetow; R Shiang; P Yang; Y Nakamura; G M Lathrop; R White; J J Wasmuth; S Wood; L D Berdahl; N J Leysens
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

6.  A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients.

Authors:  C Pritchard; D Casher; L Bull; D R Cox; R M Myers
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

7.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

8.  Defined physical limits of the Huntington disease gene candidate region.

Authors:  G P Bates; M E MacDonald; S Baxendale; S Youngman; C Lin; W L Whaley; J J Wasmuth; J F Gusella; H Lehrach
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

9.  Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid.

Authors:  D R Cox; C A Pritchard; E Uglum; D Casher; J Kobori; R M Myers
Journal:  Genomics       Date:  1989-04       Impact factor: 5.736

10.  Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.

Authors:  C Robbins; J Theilmann; S Youngman; J Haines; M J Altherr; P S Harper; C Payne; A Junker; J Wasmuth; M R Hayden
Journal:  Am J Hum Genet       Date:  1989-03       Impact factor: 11.025

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  5 in total

1.  Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes.

Authors:  Sandra Martins; Christopher E Pearson; Paula Coutinho; Sylvie Provost; António Amorim; Marie-Pierre Dubé; Jorge Sequeiros; Guy A Rouleau
Journal:  Hum Genet       Date:  2014-07-16       Impact factor: 4.132

2.  Single and coincident intragenic mutations attributable to gene conversion in a human cell line.

Authors:  C R Giver; A J Grosovsky
Journal:  Genetics       Date:  1997-08       Impact factor: 4.562

3.  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

4.  Huntington disease without CAG expansion: phenocopies or errors in assignment?

Authors:  S E Andrew; Y P Goldberg; B Kremer; F Squitieri; J Theilmann; J Zeisler; H Telenius; S Adam; E Almquist; M Anvret
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

5.  Allele frequencies and linkage disequilibrium of polymorphic DNA markers of the Huntington disease region in the German population.

Authors:  U Thies; B Bockel; B Gerdes; K Schröder
Journal:  Hum Genet       Date:  1993-12       Impact factor: 4.132

  5 in total

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