Literature DB >> 3678822

Investigation of chromosome-mediated gene transfer using the HPRT region of the human X chromosome as a model.

C A Pritchard1, P N Goodfellow.   

Abstract

A panel of over 50 hybrid cells containing varying portions of the long arm of the human X chromosome have been obtained by chromosome-mediated gene transfer (CMGT) of human chromosomes to mouse cells deficient in HPRT. This panel is used to investigate the size and integrity of transfected human chromosome fragments and also to examine the effect of including a selectable DNA plasmid in the transfection mix. Chromosomal rearrangements are found to be generated in the chromosome transfer process, and the human X centromeric region is detected in the transfected cells at an unusually high frequency. Extensive lengths of X chromosome DNA are transferred intact, suggesting potential uses of CMGT in cloning large genes and loci for which only the chromosomal map position is known.

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Year:  1987        PMID: 3678822     DOI: 10.1101/gad.1.2.172

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  9 in total

1.  Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers.

Authors:  W Bickmore; S Christie; V van Heyningen; N D Hastie; D J Porteous
Journal:  Nucleic Acids Res       Date:  1988-01-11       Impact factor: 16.971

Review 2.  The molecular genetics of complex inherited diseases.

Authors:  R Williamson
Journal:  Br J Cancer Suppl       Date:  1988-12

3.  Chromosomes of older humans are more prone to aminopterine-induced breakage.

Authors:  D Esposito; G Fassina; P Szabo; P De Angelis; L Rodgers; M Weksler; M Siniscalco
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

4.  Isolation of a sequence which maps close to the human sex determining gene.

Authors:  C A Pritchard; P J Goodfellow; P N Goodfellow
Journal:  Nucleic Acids Res       Date:  1987-08-11       Impact factor: 16.971

Review 5.  Molecular approaches to dysmorphology.

Authors:  A Ivens; G Moore; R Williamson
Journal:  J Med Genet       Date:  1988-07       Impact factor: 6.318

6.  X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17.

Authors:  A Ivens; G E Moore; J Chambers; A Arnason; O Jensson; A Bjornsson; R Williamson
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

7.  Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.

Authors:  K Johnson; E Nimmo; P Jones; M Weiss; M L Savontaus; M Anvret; R Bartlett; A Roses; D Shaw; P S Harper
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

8.  Construction of a genetic map of human chromosome 17 by use of chromosome-mediated gene transfer.

Authors:  W M Xu; P A Gorman; S H Rider; P J Hedge; G Moore; C Prichard; D Sheer; E Solomon
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

9.  Molecular cloning of the human CTP synthetase gene by functional complementation with purified human metaphase chromosomes.

Authors:  M Yamauchi; N Yamauchi; M Meuth
Journal:  EMBO J       Date:  1990-07       Impact factor: 11.598

  9 in total

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