Literature DB >> 9732752

Linkage of the leuS, emtB, and chr genes on chromosome 5 in humans and expression of human genes encoding protein synthetic components in human--Chinese hamster hybrids.

S Dana1, J J Wasmuth.   

Abstract

We isolated interspecific hybrids between normal human leukocytes and a Chinese hamster ovary cell line that has mutations in three genes, leuS, emtB, and chr, all of which are linked to chromosome 2. The conditionally lethal mutation in the leuS gene in this cell line affects leucyl-tRNA synthetase and renders the cell line nonviable at 39 degrees C. The mutation in the emtB locus alters ribosomal protein S14 and results in the cell line being resistant to the protein synthesis inhibitor, emetine, while the mutation in the chr locus renders the cells resistant to sodium chromate. The interspecific hybrids were selected at 39 degrees C so that they were required to retain and express the human leuS gene. Ten out of ten such heat-resistant hybrids also expressed the human emtB and chr genes. Segregants selected as having lost the human emtB gene simultaneously lost the human chr and leuS genes as well. The linkage relationship between these three genes has thus been conserved during the evolution of the human and Chinese hamster genomes. All three genes were localized to human chromosome 5. Furthermore, our results indicate that the ribosomal protein product of the human emtB gene is incorporated into functional ribosomes in place of the human corresponding Chinese hamster protein, raising several interesting questions concerning the coordinate regulation of genes encoding ribosomal proteins in mammalian cells.

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Year:  1982        PMID: 9732752     DOI: 10.1007/bf01538680

Source DB:  PubMed          Journal:  Somatic Cell Genet        ISSN: 0098-0366


  27 in total

1.  Primary structure, chromosomal localization, and functional expression of a voltage-gated sodium channel from human brain.

Authors:  C M Ahmed; D H Ware; S C Lee; C D Patten; A V Ferrer-Montiel; A F Schinder; J D McPherson; C B Wagner-McPherson; J J Wasmuth; G A Evans
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-01       Impact factor: 11.205

2.  Molecular cloning, chromosomal mapping, and functional expression of human brain glutamate receptors.

Authors:  W Sun; A V Ferrer-Montiel; A F Schinder; J P McPherson; G A Evans; M Montal
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

3.  The 5q- syndrome: biology and treatment.

Authors:  Eric Padron; Rami Komrokji; Alan F List
Journal:  Curr Treat Options Oncol       Date:  2011-12

4.  Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3.

Authors:  L Boghosian-Sell; D E Comings; J Overhauser
Journal:  Am J Hum Genet       Date:  1996-11       Impact factor: 11.025

5.  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

6.  Molecular analysis of an unbalanced deletion of the short arm of chromosome 5 that produces no phenotype.

Authors:  J Overhauser; M S Golbus; S A Schonberg; J J Wasmuth
Journal:  Am J Hum Genet       Date:  1986-07       Impact factor: 11.025

7.  Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5.

Authors:  J Overhauser; J McMahan; J J Wasmuth
Journal:  Nucleic Acids Res       Date:  1987-06-11       Impact factor: 16.971

8.  Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci.

Authors:  J C Murray; R Shiang; L R Carlock; M Smith; K H Buetow
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

9.  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

10.  Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage.

Authors:  S T Warren; S J Knight; J F Peters; C L Stayton; G G Consalez; F P Zhang
Journal:  Proc Natl Acad Sci U S A       Date:  1990-05       Impact factor: 11.205

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