Literature DB >> 8258294

Chromosomal location and expression of the genes coding for Ku p70 and p80 in human cell lines and normal tissues.

Q Q Cai1, A Plet, J Imbert, M Lafage-Pochitaloff, C Cerdan, J M Blanchard.   

Abstract

Ku protein is a relatively abundant DNA-binding nuclear protein complex composed of two polypeptide subunits, p70 and p80. Ku has been recently identified as the regulatory component of the DNA-dependent protein kinase that phosphorylates RNA polymerase II. To further characterize in vivo regulation of Ku protein, we studied the expression of the transcripts coding for the Ku p70 and p80 subunits in different human cell lines and normal tissues by Northern blot hybridization, using specific cDNA probes. The expression level of both genes was approximately 10-fold higher in established cell lines than in normal tissues. However, mRNA expression levels in permanent cell lines correlated more strongly with their proliferative state than with their level of malignant transformation. In purified T lymphocytes induced to proliferate by the combined action of monoclonal antibodies directed against the CD2 and CD28 adhesion molecules, Ku p70 and p80 mRNA steady-state levels increased as soon as 6 h after activation and lasted at least 72 h. The human genes coding for the Ku p70 and p80 subunits were localized by cytogenetic mapping, using fluorescence in situ hybridization, to 22q13 and 2q33-->q35, respectively.

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Year:  1994        PMID: 8258294     DOI: 10.1159/000133635

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  19 in total

1.  Construction of comparative cytogenetic maps of the Chinese hamster to mouse, rat and human.

Authors:  A Kuroiwa; K Tsuchiya; K Matsubara; T Namikawa; Y Matsuda
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

2.  Efficiency of nonhomologous DNA end joining varies among somatic tissues, despite similarity in mechanism.

Authors:  Sheetal Sharma; Bibha Choudhary; Sathees C Raghavan
Journal:  Cell Mol Life Sci       Date:  2010-08-03       Impact factor: 9.261

3.  Ku86 defines the genetic defect and restores X-ray resistance and V(D)J recombination to complementation group 5 hamster cell mutants.

Authors:  A Errami; V Smider; W K Rathmell; D M He; E A Hendrickson; M Z Zdzienicka; G Chu
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

4.  A DNA end-binding factor involved in double-strand break repair and V(D)J recombination.

Authors:  W K Rathmell; G Chu
Journal:  Mol Cell Biol       Date:  1994-07       Impact factor: 4.272

5.  The gene for severe combined immunodeficiency disease in Athabascan-speaking Native Americans is located on chromosome 10p.

Authors:  L Li; D Drayna; D Hu; A Hayward; S Gahagan; H Pabst; M J Cowan
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

6.  Telomere length deregulation and enhanced sensitivity to genotoxic stress in Arabidopsis mutants deficient in Ku70.

Authors:  Karel Riha; J Matthew Watson; Jeffrey Parkey; Dorothy E Shippen
Journal:  EMBO J       Date:  2002-06-03       Impact factor: 11.598

7.  DNA-dependent protein kinase activity is absent in xrs-6 cells: implications for site-specific recombination and DNA double-strand break repair.

Authors:  N J Finnie; T M Gottlieb; T Blunt; P A Jeggo; S P Jackson
Journal:  Proc Natl Acad Sci U S A       Date:  1995-01-03       Impact factor: 11.205

8.  Complementation of the ionizing radiation sensitivity, DNA end binding, and V(D)J recombination defects of double-strand break repair mutants by the p86 Ku autoantigen.

Authors:  N V Boubnov; K T Hall; Z Wills; S E Lee; D M He; D M Benjamin; C R Pulaski; H Band; W Reeves; E A Hendrickson
Journal:  Proc Natl Acad Sci U S A       Date:  1995-01-31       Impact factor: 11.205

9.  Involvement of the Ku autoantigen in the cellular response to DNA double-strand breaks.

Authors:  W K Rathmell; G Chu
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-02       Impact factor: 11.205

10.  10th International Conference on Methods in Protein Structure Analysis. September 8-13, 1994, Snowbird, Utah. Short communications and abstracts.

Authors: 
Journal:  J Protein Chem       Date:  1994-07
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