Literature DB >> 1729675

Construction of a map of chromosome 16 by using radiation hybrids.

I Ceccherini1, G Romeo, S Lawrence, M H Breuning, P C Harris, H Himmelbauer, A M Frischauf, G R Sutherland, G G Germino, S T Reeders.   

Abstract

A human-hamster cell hybrid carrying a single copy of chromosome 16 as the only human genetic material was irradiated with a single dose of gamma-rays (7000 rads; 1 rad = 0.01 Gy) and then fused with a thymidine kinase-deficient hamster cell line (RJKM) to generate radiation hybrids retaining unselected fragments of this human chromosome. In two experiments, 223 hybrids were isolated in hypoxanthine/aminopterine/thymidine (HAT) medium and screened with 38 DNA probes, corresponding to anonymous DNA or gene sequences localized on chromosome 16. The most likely order and location of the 38 DNA sequences were established by multiple pairwise analysis and scaled to estimate physical distance in megabases. The order and the distances thus obtained are mostly consistent with available data on genetic and physical mapping of these markers, illustrating the usefulness of radiation hybrids for mapping.

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Year:  1992        PMID: 1729675      PMCID: PMC48184          DOI: 10.1073/pnas.89.1.104

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  33 in total

1.  Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

Authors:  V J Hyland; K E Fernandez; D F Callen; R N MacKinnon; E Baker; K Friend; G R Sutherland
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

2.  A linkage group with FRA16B (the fragile site at 16q22.1).

Authors:  J C Mulley; V J Hyland; A Fratini; L J Bates; A K Gedeon; G R Sutherland
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

3.  Irradiation-reduced human chromosome 21 hybrids.

Authors:  S Graw; J Davidson; J Gusella; P Watkins; R Tanzi; R Neve; D Patterson
Journal:  Somat Cell Mol Genet       Date:  1988-05

4.  Anonymous DNA probes to human chromosome 16 derived from a flow-purified library.

Authors:  V J Hyland; S Grist; D F Callen; G R Sutherland
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

5.  Regional localization of the autosomal dominant polycystic kidney disease locus.

Authors:  S T Reeders; T Keith; P Green; G G Germino; N J Barton; O J Lehmann; V A Brown; P Phipps; J Morgan; J C Bear
Journal:  Genomics       Date:  1988-08       Impact factor: 5.736

6.  Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.

Authors:  P Harris; M Lalande; H Stroh; G Bruns; A Flint; S A Latt
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

7.  Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.

Authors:  L Roncuzzi; S Fadda; M Mochi; L Prosperi; S Sangiorgi; R Santamaria; D Sbarra; D Besana; L Morandi; M Rocchi
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

8.  The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II.

Authors:  E M Westphal; E Natt; T Grimm; M Odievre; G Scherer
Journal:  Hum Genet       Date:  1988-07       Impact factor: 4.132

9.  Improved early diagnosis of adult polycystic kidney disease with flanking DNA markers.

Authors:  M H Breuning; S T Reeders; H Brunner; J W Ijdo; J J Saris; A Verwest; G J van Ommen; P L Pearson
Journal:  Lancet       Date:  1987-12-12       Impact factor: 79.321

10.  Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid.

Authors:  D R Cox; C A Pritchard; E Uglum; D Casher; J Kobori; R M Myers
Journal:  Genomics       Date:  1989-04       Impact factor: 5.736

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  9 in total

1.  Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease.

Authors:  T Watnick; B Phakdeekitcharoen; A Johnson; M Gandolph; M Wang; G Briefel; K W Klinger; W Kimberling; P Gabow; G G Germino
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

2.  Interspersed repetitive sequence (IRS)-PCR for typing of whole genome radiation hybrid panels.

Authors:  H Himmelbauer; L C Schalkwyk; H Lehrach
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

3.  A radiation hybrid map spanning the entire human X chromosome integrating YACs, genes, and STS markers.

Authors:  J Kumlien; A Grigoriev; H Roest Crollius; M Ross; P N Goodfellow; H Lehrach
Journal:  Mamm Genome       Date:  1996-10       Impact factor: 2.957

Review 4.  Irradiation and fusion gene transfer.

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

5.  Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.

Authors:  M H Breuning; H G Dauwerse; G Fugazza; J J Saris; L Spruit; H Wijnen; N Tommerup; C B van der Hagen; K Imaizumi; Y Kuroki; M J van den Boogaard; J M de Pater; E C Mariman; B C Hamel; H Himmelbauer; A M Frischauf; R Stallings; G C Beverstock; G J van Ommen; R C Hennekam
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

6.  Construction of radiation-reduced hybrids and their use in mapping of microclones from chromosome 10p11.2-q11.2.

Authors:  S Fujita; E Shin; T Nakamura; H Kurahashi; Y Kaneda; K Tanaka; T Mori; S Takai; I Nishisho
Journal:  Jpn J Hum Genet       Date:  1993-12

7.  A radiation hybrid framework map of bovine chromosome 13.

Authors:  J Schläpfer; Y Yang; C Rexroad; J E Womack
Journal:  Chromosome Res       Date:  1997-12       Impact factor: 5.239

8.  Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies.

Authors:  I Aksentijevich; E Pras; L Gruberg; Y Shen; K Holman; S Helling; L Prosen; G R Sutherland; R I Richards; M Ramsburg
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

9.  Human-Specific Abnormal Alternative Splicing of Wild-Type PKD1 Induces Premature Termination of Polycystin-1.

Authors:  Wendy A Lea; Stephen C Parnell; Darren P Wallace; James P Calvet; Lesya V Zelenchuk; Nehemiah S Alvarez; Christopher J Ward
Journal:  J Am Soc Nephrol       Date:  2018-09-05       Impact factor: 10.121

  9 in total

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