Literature DB >> 2877932

A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locus.

H Scheffer, D van der Lelie, G H Aanstoot, N Goor, A J Nienhaus, A H van der Hout, P L Pearson, C H Buys.   

Abstract

From a human-Chinese hamster somatic cell hybrid a clone was derived containing chromosome 13 in duplicate as its only human material. This clone was used to construct a human chromosome 13-specific recombinant DNA-library. Overlapping Sau3AI DNA sequences (11.9-17.2 kb) from the cell hybrid were inserted into the lambda phage vector EMBL4. From eleven recombinants having a human insert thirteen putative unique DNA sequences were isolated and cloned into the plasmid vector pBR329. A human-mouse hybrid containing a human chromosome 13 with a deletion of 13q14 and lacking its undeleted homologue was constructed to be used in a selection procedure for DNA sequences belonging to band q14. Three probes originating from two different phages were assigned to 13q14 because they did not hybridise to DNA from this cell hybrid. One of these 13q14 probes detects a low frequency (2/44) MspI restriction fragment length polymorphism. The probes are now being used for screening a cosmid library to find adjacent polymorphic sequences with a RFLP information content suitable for application in the diagnosis of hereditary retinoblastoma.

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Year:  1986        PMID: 2877932     DOI: 10.1007/bf00282543

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  26 in total

1.  In vitro packaging of lambda and cosmid DNA.

Authors:  B Hohn
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

2.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

3.  Construction and characterization of new cloning vehicles. VI. Plasmid pBR329, a new derivative of pBR328 lacking the 482-base-pair inverted duplication.

Authors:  L Covarrubias; F Bolivar
Journal:  Gene       Date:  1982-01       Impact factor: 3.688

4.  A strategy to reveal high-frequency RFLPs along the human X chromosome.

Authors:  J Aldridge; L Kunkel; G Bruns; U Tantravahi; M Lalande; T Brewster; E Moreau; M Wilson; W Bromley; T Roderick
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

5.  Lambda replacement vectors carrying polylinker sequences.

Authors:  A M Frischauf; H Lehrach; A Poustka; N Murray
Journal:  J Mol Biol       Date:  1983-11-15       Impact factor: 5.469

6.  Banding of unfixed mitotic chromosomes in suspension after release from human lymphocytes and fibroblasts.

Authors:  C H Buys; T Koerts; A Y van der Veen
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Assignment of PGM3 to the long arm of human chromosome 6. Studies using Chinese hamster X human cell hybrids containing a human 6/15 translocation.

Authors:  T Mohandas; R S Sparkes; J D Shulkin; M C Sparkes; S Moedjono
Journal:  Cytogenet Cell Genet       Date:  1980

8.  A membrane-filter technique for the detection of complementary DNA.

Authors:  D T Denhardt
Journal:  Biochem Biophys Res Commun       Date:  1966-06-13       Impact factor: 3.575

9.  Y-encoded, species-specific DNA in mice: evidence that the Y chromosome exists in two polymorphic forms in inbred strains.

Authors:  E E Lamar; E Palmer
Journal:  Cell       Date:  1984-05       Impact factor: 41.582

10.  Retrieval of human DNA from rodent-human genomic libraries by a recombination process.

Authors:  R L Neve; G A Bruns; T P Dryja; D M Kurnit
Journal:  Gene       Date:  1983-09       Impact factor: 3.688

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  8 in total

1.  A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes.

Authors:  S Y Wang; M Cruts; J Del-Favero; Y Zhang; F Tissir; M C Potier; D Patterson; D Nizetic; A Bosch; H Chen; L Bennett; X Estivill; A Kessling; S E Antonarakis; C van Broeckhoven
Journal:  Genome Res       Date:  1999-11       Impact factor: 9.043

2.  Construction of the physical map for three loci in chromosome band 13q14: comparison to the genetic map.

Authors:  M J Higgins; C Turmel; J Noolandi; P E Neumann; M Lalande
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

3.  The anonymous probe pG50 identifying the locus D13S24 detects a two allele RFLP with SspI.

Authors:  A M Bowcock; J M Hebert; H Scheffer; D Penninga; C H Buys
Journal:  Nucleic Acids Res       Date:  1989-10-25       Impact factor: 16.971

4.  The single copy probe pG24E2.4 [D13S21] reveals a Bsp1286 RFLP at 13q14.1-q14.2.

Authors:  A M Bowcock; J M Hebert; H Scheffer; D Penninga; C H Buys
Journal:  Nucleic Acids Res       Date:  1989-10-25       Impact factor: 16.971

5.  Linkage analysis of families with hereditary retinoblastoma: nonpenetrance of mutation, revealed by combined use of markers within and flanking the RB1 gene.

Authors:  H Scheffer; G J te Meerman; Y C Kruize; A H van den Berg; D P Penninga; K E Tan; D J der Kinderen; C H Buys
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

6.  Eight closely linked loci place the Wilson disease locus within 13q14-q21.

Authors:  A M Bowcock; L A Farrer; J M Hebert; M Agger; I Sternlieb; I H Scheinberg; C H Buys; H Scheffer; M Frydman; T Chajek-Saul
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

7.  Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma.

Authors:  V Greger; S Kerst; E Messmer; W Höpping; E Passarge; B Horsthemke
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

8.  Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease.

Authors:  H Scheffer; I P Kema; I Kondo; A Y van der Veen; T Ikeuchi; C H Buys
Journal:  Hum Genet       Date:  1987-12       Impact factor: 4.132

  8 in total

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