Literature DB >> 2828023

Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several 'HTF islands'.

C Nguyen1, P Pontarotti, D Birnbaum, G Chimini, J A Rey, J F Mattei, B R Jordan.   

Abstract

In spite of the large amount of genetic data obtained on the X chromosome and of the availability of many cloned sequences little is known about the physical map of this chromosome. The construction of large-scale restriction maps is now possible with pulsed field gel methods and data has recently been obtained in the region of band Xq28. We present here results of physical mapping in the Xq27 region, i.e. proximal to the fragile site at Xq27.3 associated with mental retardation, and show physical linkage between the coagulation factor IX gene and the mcf.2 transforming sequence recently localized to Xq27. Our data also indicate partial methylation of some sites in this region, and locate several 'HTF islands', i.e. CpG-rich, unmethylated sequences, containing several sites for 'rare cutter' enzymes, which are believed to be associated with expressed 'housekeeping' genes.

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Year:  1987        PMID: 2828023      PMCID: PMC553781          DOI: 10.1002/j.1460-2075.1987.tb02647.x

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  16 in total

1.  Report of the Committee on the Genetic Constitution of the X and Y Chromosomes.

Authors:  P N Goodfellow; K E Davies; H H Ropers
Journal:  Cytogenet Cell Genet       Date:  1985

2.  Linkage analysis of X-linked mental retardation with and without fragile-X using factor IX gene probe.

Authors:  K H Choo; D George; G Filby; J L Halliday; M Leversha; G Webb; D M Danks
Journal:  Lancet       Date:  1984-08-11       Impact factor: 79.321

3.  Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresis.

Authors:  G F Carle; M V Olson
Journal:  Nucleic Acids Res       Date:  1984-07-25       Impact factor: 16.971

Review 4.  The fragile X chromosome.

Authors:  G R Sutherland
Journal:  Int Rev Cytol       Date:  1983

5.  Genomic sequencing.

Authors:  G M Church; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

6.  The genetic linkage map of the human X chromosome.

Authors:  D Drayna; R White
Journal:  Science       Date:  1985-11-15       Impact factor: 47.728

7.  Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis.

Authors:  D C Schwartz; C R Cantor
Journal:  Cell       Date:  1984-05       Impact factor: 41.582

8.  Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.

Authors:  G Camerino; M G Mattei; J F Mattei; M Jaye; J L Mandel
Journal:  Nature       Date:  1983 Dec 15-21       Impact factor: 49.962

9.  An electrophoretic karyotype for yeast.

Authors:  G F Carle; M V Olson
Journal:  Proc Natl Acad Sci U S A       Date:  1985-06       Impact factor: 11.205

10.  Localization of the mcf.2 transforming sequence to the X chromosome.

Authors:  T Noguchi; M G Mattei; I Oberlè; J Planche; J Imbert; C Pelassy; F Birg; D Birnbaum
Journal:  EMBO J       Date:  1987-05       Impact factor: 11.598

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  10 in total

1.  A simple method for the direct use of total cosmid clones as hybridization probes.

Authors:  M Djabali; C Nguyen; D Roux; J Demengeot; H M Yang; B R Jordan
Journal:  Nucleic Acids Res       Date:  1990-10-25       Impact factor: 16.971

2.  Very high molecular weight DNA for pulsed field gel studies can be obtained routinely from conventional frozen blood aliquots.

Authors:  C Nguyen; M Djabali; D Roux; B R Jordan
Journal:  Nucleic Acids Res       Date:  1991-01-25       Impact factor: 16.971

3.  Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.

Authors:  M A Voelckel; M G Mattei; C N'Guyen; N Philip; F Birg; J F Mattei
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.

Authors:  M A Voelckel; N Philip; C Piquet; M C Pellissier; I Oberlé; F Birg; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

5.  Molecular studies of haemophilia B in Sweden. Identification of patients with total deletion of the factor IX gene and without inhibitory antibodies.

Authors:  C Wadelius; M Blombäck; U Pettersson
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

6.  Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters.

Authors:  A H Beggs; B R Migeon
Journal:  Mol Cell Biol       Date:  1989-06       Impact factor: 4.272

Review 7.  Recombination within a subclass of restriction fragment length polymorphisms may help link classical and molecular genetics.

Authors:  R B Meagher; M D McLean; J Arnold
Journal:  Genetics       Date:  1988-11       Impact factor: 4.562

8.  Proximity of the CTLA-1 serine esterase and Tcr alpha loci in mouse and man.

Authors:  K Harper; M G Mattéi; D Simon; M Suzan; J L Guénet; P Haddad; M Sasportes; P Golstein
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

9.  Identification of CpG islands around the DXS178 locus in the region of the X-linked agammaglobulinaemia gene locus in Xq22.

Authors:  M A O'Reilly; L A Alterman; S Malcolm; R J Levinsky; C Kinnon
Journal:  Hum Genet       Date:  1992-11       Impact factor: 4.132

10.  Nullisomic deletion of the mcf.2 transforming gene in two haemophilia B patients.

Authors:  D S Anson; D J Blake; P R Winship; D Birnbaum; G G Brownlee
Journal:  EMBO J       Date:  1988-09       Impact factor: 11.598

  10 in total

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