Literature DB >> 8213815

A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD).

S T Winokur1, B Schutte, B Weiffenbach, S S Washington, D McElligott, A Chakravarti, J H Wasmuth, M R Altherr.   

Abstract

A physical map of 4q35 was constructed through radiation hybrid analysis of 134 clones generated from the cell line HHW416, a chromosome 4-only human-hamster somatic cell hybrid. This subtelomeric region contains the as-yet-unidentified gene responsible for facioscapulohumeral muscular dystrophy. The most likely order of 15 loci within 4q35 was determined. The loci ordered on this radiation hybrid map include both genes and polymorphic loci, as well as monomorphic loci which cannot be placed on a genetic linkage map. The physical distance spanning these loci was estimated to be approximately 4.5 Mb, by using a kilobase/centiray conversion factor derived from 4p16.3 marker analysis through the same set of radiation hybrids. The comparison of this physical map to establish genetic maps suggests that this region is smaller than initially estimated and that recombination rates are increased near the telomere.

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Year:  1993        PMID: 8213815      PMCID: PMC1682402     

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


  32 in total

1.  Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5.

Authors:  J Overhauser; U Bengtsson; J McMahon; J Ulm; M G Butler; L Santiago; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

2.  A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressed.

Authors:  K Li; C K Warner; J A Hodge; S Minoshima; J Kudoh; R Fukuyama; M Maekawa; Y Shimizu; N Shimizu; D C Wallace
Journal:  J Biol Chem       Date:  1989-08-25       Impact factor: 5.157

3.  Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4[HGM provisional no. D4S139].

Authors:  E C Milner; C L Lotshaw; K Willems van Dijk; P Charmley; P Concannon; H W Schroeder
Journal:  Nucleic Acids Res       Date:  1989-05-25       Impact factor: 16.971

4.  Frequent recombination is observed in the distal end of the long arm of chromosome 14.

Authors:  Y Nakamura; M Lathrop; P O'Connell; M Leppert; M I Kamboh; J M Lalouel; R White
Journal:  Genomics       Date:  1989-01       Impact factor: 5.736

5.  Organization of the gene for human factor XI.

Authors:  R Asakai; E W Davie; D W Chung
Journal:  Biochemistry       Date:  1987-11-17       Impact factor: 3.162

6.  Isolation of a novel mildly repetitive DNA sequence that is predominantly located at the terminus of the short arm of chromosome 4 near the Huntington disease gene.

Authors:  M R Altherr; B Smith; M E MacDonald; L Hall; J J Wasmuth
Journal:  Genomics       Date:  1989-10       Impact factor: 5.736

7.  Genetic counterselective procedure to isolate interspecific cell hybrids containing single human chromosomes: construction of cell hybrids and recombinant DNA libraries specific for human chromosomes 3 and 4.

Authors:  L R Carlock; D Smith; J J Wasmuth
Journal:  Somat Cell Mol Genet       Date:  1986-03

8.  Nucleotide sequence of a cDNA for a member of the human 90-kDa heat-shock protein family.

Authors:  N F Rebbe; J Ware; R M Bertina; P Modrich; D W Stafford
Journal:  Gene       Date:  1987       Impact factor: 3.688

9.  Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination events.

Authors:  B Weiffenbach; J Dubois; D Storvick; R Tawil; S J Jacobsen; J Gilbert; C Wijmenga; J R Mendell; S Winokur; M R Altherr
Journal:  Nat Genet       Date:  1993-06       Impact factor: 38.330

10.  Structurally similar but functionally distinct factors, IRF-1 and IRF-2, bind to the same regulatory elements of IFN and IFN-inducible genes.

Authors:  H Harada; T Fujita; M Miyamoto; Y Kimura; M Maruyama; A Furia; T Miyata; T Taniguchi
Journal:  Cell       Date:  1989-08-25       Impact factor: 41.582

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  7 in total

1.  Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.

Authors:  R Tupler; L Barbierato; M Memmi; C A Sewry; D De Grandis; P Maraschio; L Tiepolo; A Ferlini
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

2.  Localization of the cell death genes CPP32 and Mch-2 to human chromosome 4q.

Authors:  J Nasir; J L Theilmann; V Chopra; A M Jones; D Walker; D M Rasper; J P Vaillancourt; J E Hewitt; D W Nicholson; M R Hayden
Journal:  Mamm Genome       Date:  1997-01       Impact factor: 2.957

Review 3.  Irradiation and fusion gene transfer.

Authors:  M A Walter; P N Goodfellow
Journal:  Mol Biotechnol       Date:  1995-04       Impact factor: 2.695

4.  The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

Authors:  S T Winokur; U Bengtsson; J Feddersen; K D Mathews; B Weiffenbach; H Bailey; R P Markovich; J C Murray; J J Wasmuth; M R Altherr
Journal:  Chromosome Res       Date:  1994-05       Impact factor: 5.239

5.  Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle.

Authors:  Dalila Laoudj-Chenivesse; Gilles Carnac; Catherine Bisbal; Gerald Hugon; Sandrine Bouillot; Claude Desnuelle; Yegor Vassetzky; Anne Fernandez
Journal:  J Mol Med (Berl)       Date:  2004-11-17       Impact factor: 4.599

6.  Actinin-associated LIM protein: identification of a domain interaction between PDZ and spectrin-like repeat motifs.

Authors:  H Xia; S T Winokur; W L Kuo; M R Altherr; D S Bredt
Journal:  J Cell Biol       Date:  1997-10-20       Impact factor: 10.539

7.  Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD).

Authors:  S Cacurri; G Deidda; N Piazzo; A Novelletto; I La Cesa; S Servidei; G Galluzzi; C Wijmenga; R R Frants; L Felicetti
Journal:  Hum Genet       Date:  1994-10       Impact factor: 4.132

  7 in total

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