Literature DB >> 7177110

Selective linkage disruption in human-Chinese hamster cell hybrids: deletion mapping of the leuS, hexB, emtB, and chr genes on human chromosome 5.

S Dana, J J Wasmuth.   

Abstract

Chinese hamster-human interspecific hybrid cells, which contain human chromosome 5 and express four genes linked on that chromosome, were subjected to selective conditions requiring them to retain one of the four linked genes, leuS (encoding leucyl-tRNA synthetase), but lose another, either emtB (encoding ribosomal protein S14) or chr. Cytogenetic and biochemical analyses of spontaneous segregants isolated by using these unique selective pressures have enabled us to determine the order and regional location of the leuS, hexB, emtB, and chr genes on human chromosome 5. These segregants arise primarily by terminal deletions of various portions of the long arm of chromosome 5. Our results indicate that the order of at least three of these genes is the same on human chromosome 5 and Chinese hamster chromosome 2. Thus, there appears to be extensive homology between Chinese hamster chromosome 2 and human chromosome 5, which represents an extreme example of the conservation of gene organization between very divergent mammalian species. In addition, these hybrids and selective conditions provide a very simple and quantitative means to assess the potency of various agents suspected of inducing gross chromosomal damage.

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Year:  1982        PMID: 7177110      PMCID: PMC369921          DOI: 10.1128/mcb.2.10.1220-1228.1982

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  22 in total

1.  New method for mapping genes in human chromosomes.

Authors:  S J Goss; H Harris
Journal:  Nature       Date:  1975-06-26       Impact factor: 49.962

2.  Differential staining of interspecific chromosomes in somatic cell hybrids by alkaline Giemsa stain.

Authors:  K K Friend; S Chen; F H Ruddle
Journal:  Somatic Cell Genet       Date:  1976-03

3.  A mammalian cell mutant with a temperature-sensitive leucyl-transfer RNA synthetase.

Authors:  L H Thompson; J L Harkins; C P Stanners
Journal:  Proc Natl Acad Sci U S A       Date:  1973-11       Impact factor: 11.205

4.  Cytological mapping of the genes assigned to the human A 1 chromosome by use of radiation-induced chromosome breakage in a human-Chinese hamster hybrid cell line.

Authors:  W Burgerhout; H van Someren; D Bootsma
Journal:  Humangenetik       Date:  1973

5.  Karyotyping.

Authors:  R G Worton; C Duff
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

6.  Regional mapping of human genes for hexosaminidase B and diphtheria toxin sensitivity on chromosome 5 using mouse X human hybrid cells.

Authors:  D L George; U Francke
Journal:  Somatic Cell Genet       Date:  1977-11

7.  Induced segregation of human syntenic genes by 5-bromodeozyuridine + near-visible light.

Authors:  M L Law; F T Kao
Journal:  Somatic Cell Genet       Date:  1978-07

8.  The status of the gene map of the human chromosomes.

Authors:  V A McKusick; F H Ruddle
Journal:  Science       Date:  1977-04-22       Impact factor: 47.728

9.  Gene transfer by means of cell fusion I. Statistical mapping of the human X-chromosome by analysis of radiation-induced gene segregation.

Authors:  S J Goss; H Harris
Journal:  J Cell Sci       Date:  1977-06       Impact factor: 5.285

10.  Gene transfer by means of cell fusion. II. The mapping of 8 loci on human chromosome 1 by statistical analysis of gene assortment in somatic cell hybrids.

Authors:  S J Goss; H Harris
Journal:  J Cell Sci       Date:  1977-06       Impact factor: 5.285

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  23 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Mouse chromosome 13.

Authors:  M J Justice; D A Stephenson
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5.

Authors:  J Overhauser; U Bengtsson; J McMahon; J Ulm; M G Butler; L Santiago; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

Review 4.  Mouse chromosome 13.

Authors:  M J Justice; D A Stephenson
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

Review 5.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

6.  Familial 5q11.2----q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia.

Authors:  B C McGillivray; A S Bassett; S Langlois; T Pantzar; S Wood
Journal:  Am J Med Genet       Date:  1990-01

7.  A rare TaqI RFLP immediately 3' of the HEXB gene on chromosome 5.

Authors:  S Wood; M Schertzer; K Neote
Journal:  Nucleic Acids Res       Date:  1989-03-25       Impact factor: 16.971

8.  Deletion mapping of human chromosome 5 using chromosome-specific DNA probes.

Authors:  L R Carlock; D Skarecky; S L Dana; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1985-09       Impact factor: 11.025

9.  Overabundance of rare-cutting restriction endonuclease sites in the human genome.

Authors:  D I Smith; W Golembieski; J D Gilbert; L Kizyma; O J Miller
Journal:  Nucleic Acids Res       Date:  1987-02-11       Impact factor: 16.971

10.  Primary structure of human ribosomal protein S14 and the gene that encodes it.

Authors:  D D Rhoads; A Dixit; D J Roufa
Journal:  Mol Cell Biol       Date:  1986-08       Impact factor: 4.272

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