Literature DB >> 1642243

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

K A Mills1, K H Buetow, Y Xu, T M Ritty, K D Mathews, S E Bodrug, C Wijmenga, I Balazs, J C Murray.   

Abstract

We have used a combination of classical RFLPs and PCR-based polymorphisms including CA repeats and single-strand conformation polymorphisms to generate a fine-structure genetic map of the distal long arm of chromosome 4q. This map is now genetically linked to the pre-existing anchor map of 4pter-4q31 and generates, for the first time, a complete linkage map of this chromosome. The map consists of 32 anchor loci placed with odds of greater than 1,000:1. The high-resolution map in the cytogenetic region surrounding 4q35 provides the order 4cen-D4S171-F11-D4S187-D4S163-D4S139-4q ter. When we used somatic cell hybrids from a t(X;4)(p21;q35) translocation, these five markers fell into three groups consistent with the genetic map-D4S171 and F11 in 4pter-4q35, D4S163 and D4S139 in 4q35-4qter, and D4S187 as a junction fragment between these two regions. These markers are in tight linkage to the gene for facioscapulo-humeral muscular dystrophy (FSHD) mapped to this region by several collaborating investigators and provide a framework for further detailed analysis of this region.

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Year:  1992        PMID: 1642243      PMCID: PMC1682692     

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


  32 in total

1.  Sequential tests for the detection of linkage.

Authors:  N E MORTON
Journal:  Am J Hum Genet       Date:  1955-09       Impact factor: 11.025

2.  Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4.

Authors:  Y Ning; J L Weber; A M Killary; D H Ledbetter; J R Smith; O M Pereira-Smith
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

3.  Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.

Authors:  M Sarfarazi; C Wijmenga; M Upadhyaya; B Weiffenbach; C Hyser; K Mathews; J Murray; J Gilbert; M Pericak-Vance; P Lunt
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

4.  A highly polymorphic VNTR locus on the long arm of chromosome 4.

Authors:  M R Altherr; J J Wasmuth; Y Nakamura; R White
Journal:  Nucleic Acids Res       Date:  1991-03-11       Impact factor: 16.971

5.  A detailed multipoint gene map of chromosome 1q.

Authors:  K H Buetow; D Nishimura; Y Nakamura; O Jiang; J C Murray
Journal:  Genomics       Date:  1990-09       Impact factor: 5.736

6.  DNA sequence polymorphisms in Alu repeats.

Authors:  M Orita; T Sekiya; K Hayashi
Journal:  Genomics       Date:  1990-10       Impact factor: 5.736

7.  The interpretation of lods in linkage analysis.

Authors:  J H Edwards
Journal:  Cytogenet Cell Genet       Date:  1976

8.  Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors:  Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal:  Science       Date:  1987-03-27       Impact factor: 47.728

9.  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

10.  Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophy.

Authors:  S E Bodrug; J J Holden; P N Ray; R G Worton
Journal:  EMBO J       Date:  1991-12       Impact factor: 11.598

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  15 in total

1.  Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.

Authors:  B Weiffenbach; R G Bagley; K Falls; J Dubois; C Hyser; D Storvick; P Schultz; J R Mendell; E C Milner; S J Jacobsen
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  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

3.  Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Authors:  K D Mathews; K A Mills; E P Bosch; V V Ionasescu; K R Wiles; K H Buetow; J C Murray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

4.  Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level.

Authors:  Rinse Klooster; Kirsten Straasheijm; Bharati Shah; Janet Sowden; Rune Frants; Charles Thornton; Rabi Tawil; Silvère van der Maarel
Journal:  Eur J Hum Genet       Date:  2009-10-07       Impact factor: 4.246

5.  New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?

Authors:  Mouna Barat-Houari; Karine Nguyen; Rafaëlle Bernard; Céline Fernandez; Catherine Vovan; Corinne Bareil; Philippe Khau Van Kien; Delphine Thorel; Sylvie Tuffery-Giraud; Francis Vasseur; Shahram Attarian; Jean Pouget; Anne Girardet; Nicolas Lévy; Mireille Claustres
Journal:  Eur J Hum Genet       Date:  2009-11-25       Impact factor: 4.246

6.  The incidence of mini- and micro-satellite repetitive DNA in the canine genome.

Authors:  J Rothuizen; J Wolfswinkel; J A Lenstra; R R Frants
Journal:  Theor Appl Genet       Date:  1994-10       Impact factor: 5.699

7.  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

8.  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).

Authors:  S T Winokur; B Schutte; B Weiffenbach; S S Washington; D McElligott; A Chakravarti; J H Wasmuth; M R Altherr
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

9.  The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus.

Authors:  C Wijmenga; S T Winokur; G W Padberg; M I Skraastad; M R Altherr; J J Wasmuth; J C Murray; M H Hofker; R R Frants
Journal:  Hum Genet       Date:  1993-09       Impact factor: 4.132

10.  Linkage, but not gene order, of homologous loci, including alpha-L-iduronidase (Idua), is conserved in the Huntington disease region of the mouse and human genomes.

Authors:  T Koizumi; M MacDonald; M Búcan; J J Hopwood; C P Morris; H S Scott; J F Gusella; J H Nadeau
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

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