Literature DB >> 438301

Characterization of cell lines showing growth control isolated from both the wild type and a leucyl-tRNA synthetase mutant of Chinese hamster ovary cells.

J W Pollard, C P Stanners.   

Abstract

The genetic approach to the problem of cellular growth control is limited by the availability of recessive mutations in cell lines which are capable of growth control in vitro. The CHO cell line has yielded many recessive mutations including, for example, tsH1, a temperature sensitive leucyl-tRNA synthetase mutant, which under non-permissive conditions rapidly shuts down protein synthesis and generates uncharged tRNA. Both CHO and tsH1 are transformed, however, and do not respond to environmental stimuli with the coordinated regulation of macromolecular processes observed in normal diploid fibroblasts. We describe here the isolation and characterization of growth control revertants obtained from both CHOwt and tsH1. The best of these GRC+L-73, isolated from tsH1, had 20 chromosomes, one less than tsH1, had normal fibroblastic morphology, would not grow in suspension, required high serum concentrations for growth, grew to relatively low cell densities at saturation in monolayer culture and showed a stationary phase characterized by arrest in a G1-like state with maintenance of high viability for several weeks. It is expected that this line as well as a ts revertant GRC+LR-73 will greatly facilitate the genetic investigation of growth control and, in particular, will help to elucidate the role of uncharged tRNA in the regulation of macromolecular synthesis in mammalian cells.

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Year:  1979        PMID: 438301     DOI: 10.1002/jcp.1040980315

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  23 in total

1.  Elements which stimulate gene amplification in mammalian cells: role of recombinogenic sequences/structures and transcriptional activation.

Authors:  J G McArthur; L K Beitel; J W Chamberlain; C P Stanners
Journal:  Nucleic Acids Res       Date:  1991-05-11       Impact factor: 16.971

2.  Functional analysis of chimeric genes obtained by exchanging homologous domains of the mouse mdr1 and mdr2 genes.

Authors:  E Buschman; P Gros
Journal:  Mol Cell Biol       Date:  1991-02       Impact factor: 4.272

3.  Gene inactivation as a mechanism for the expression of recessive phenotypes.

Authors:  S G Grant; C E Campbell; C Duff; S L Toth; R G Worton
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

4.  Identification of tyrosine residues on ELMO1 that are phosphorylated by the Src-family kinase Hck.

Authors:  Noriko Yokoyama; Colin D deBakker; Francesca Zappacosta; Michael J Huddleston; Roland S Annan; Kodi S Ravichandran; W Todd Miller
Journal:  Biochemistry       Date:  2005-06-21       Impact factor: 3.162

5.  Re-evaluating the roles of proposed modulators of mammalian target of rapamycin complex 1 (mTORC1) signaling.

Authors:  Xuemin Wang; Bruno D Fonseca; Hua Tang; Rui Liu; Androulla Elia; Michael J Clemens; Ulrich-Axel Bommer; Christopher G Proud
Journal:  J Biol Chem       Date:  2008-08-01       Impact factor: 5.157

6.  Evolution of a tumorigenic property conferred by glycophosphatidyl-inositol membrane anchors of carcinoembryonic antigen gene family members during the primate radiation.

Authors:  Fakhraddin Naghibalhossaini; Anne D Yoder; Martin Tobi; Clifford P Stanners
Journal:  Mol Biol Cell       Date:  2007-02-07       Impact factor: 4.138

7.  Isolation and characterization of full-length functional cDNA clones for human carcinoembryonic antigen.

Authors:  N Beauchemin; S Benchimol; D Cournoyer; A Fuks; C P Stanners
Journal:  Mol Cell Biol       Date:  1987-09       Impact factor: 4.272

8.  Neurotrimin mediates bifunctional effects on neurite outgrowth via homophilic and heterophilic interactions.

Authors:  O D Gil; G Zanazzi; A F Struyk; J L Salzer
Journal:  J Neurosci       Date:  1998-11-15       Impact factor: 6.167

9.  Use of the Escherichia coli gene for asparagine synthetase as a selective marker in a shuttle vector capable of dominant transfection and amplification in animal cells.

Authors:  M Cartier; M W Chang; C P Stanners
Journal:  Mol Cell Biol       Date:  1987-05       Impact factor: 4.272

10.  Cholera toxin treatment stimulates tumorigenicity of Rous sarcoma virus-transformed cells.

Authors:  M M Gottesman; C Roth; G Vlahakis; I Pastan
Journal:  Mol Cell Biol       Date:  1984-12       Impact factor: 4.272

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