Literature DB >> 19003279

Subtractive screening of genes involved in cellular senescence.

N Uehara1, Y Katakura, T Miura, S Shirahata.   

Abstract

We attempted to identify the genes involved in cellularsenescence, telomere maintenance and telomerase regulationthrough subtractive screening of cDNA libraries prepared froma human lung adenocarcinoma cell line A549 and its sublinesnamed A5DC7, CK and AST-9. Cell phenotypes of A5DC7, CK andAST-9 are normal cell-like, cancer cell-like and intermediate,respectively. These cell lines have different phenotypes interms of telomerase activity and telomere maintenance, andthus are thought to be useful for identifying the genesinvolved in cellular senescence and telomerase regulation. In this study, we identified 86 independent cDNA clones bysubtractive screening. Among these cDNA clones, subtractingA5DC7 cDNAs from A549 cDNAs and CK cDNAs gave 7 and 3 cDNAclones which highly and specifically expressed in tester celllines. Genes corresponding to these 10 cDNA clones mightparticipate in maintaining cancer-cell phenotypes. As aresult of database searching, each four of A549 specific cDNAclones are found to correspond to known cDNAs. Each two ofA549 specific and two of CK specific cDNA clones have highhomology to independent ESTs. Sequences having homology toeach one of A549 specific and one of CK specific cDNA cloneshave not been deposited in the Genbank database, indicatingthat these two cDNA clones are part of novel genes. Weanticipate that their involvement in telomerase regulationand/or senescence program can be clarified by functionalanalysis using each full-length cDNA.

Entities:  

Year:  2001        PMID: 19003279      PMCID: PMC3466619          DOI: 10.1023/A:1008103230335

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  29 in total

1.  Expression of p21 is not required for senescence of human fibroblasts.

Authors:  A S Medcalf; A J Klein-Szanto; V J Cristofalo
Journal:  Cancer Res       Date:  1996-10-15       Impact factor: 12.701

2.  Telomerase activity does not always imply telomere maintenance.

Authors:  M M Ouellette; D L Aisner; I Savre-Train; W E Wright; J W Shay
Journal:  Biochem Biophys Res Commun       Date:  1999-01-27       Impact factor: 3.575

3.  Extension of life-span by introduction of telomerase into normal human cells.

Authors:  A G Bodnar; M Ouellette; M Frolkis; S E Holt; C P Chiu; G B Morin; C B Harley; J W Shay; S Lichtsteiner; W E Wright
Journal:  Science       Date:  1998-01-16       Impact factor: 47.728

4.  Transforming growth factor beta triggers two independent-senescence programs in cancer cells.

Authors:  Y Katakura; E Nakata; T Miura; S Shirahata
Journal:  Biochem Biophys Res Commun       Date:  1999-02-05       Impact factor: 3.575

5.  Oncogenic ras provokes premature cell senescence associated with accumulation of p53 and p16INK4a.

Authors:  M Serrano; A W Lin; M E McCurrach; D Beach; S W Lowe
Journal:  Cell       Date:  1997-03-07       Impact factor: 41.582

6.  Expression of catalytically active telomerase does not prevent premature senescence caused by overexpression of oncogenic Ha-Ras in normal human fibroblasts.

Authors:  S Wei; S Wei; J M Sedivy
Journal:  Cancer Res       Date:  1999-04-01       Impact factor: 12.701

7.  Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics.

Authors:  C H Lai; C Y Chou; L Y Ch'ang; C S Liu; W Lin
Journal:  Genome Res       Date:  2000-05       Impact factor: 9.043

8.  A mammalian telomerase-associated protein.

Authors:  L Harrington; T McPhail; V Mar; W Zhou; R Oulton; M B Bass; I Arruda; M O Robinson
Journal:  Science       Date:  1997-02-14       Impact factor: 47.728

9.  Involvement of the cyclin-dependent kinase inhibitor p16 (INK4a) in replicative senescence of normal human fibroblasts.

Authors:  D A Alcorta; Y Xiong; D Phelps; G Hannon; D Beach; J C Barrett
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-26       Impact factor: 11.205

10.  Telomerase reverse transcriptase gene is a direct target of c-Myc but is not functionally equivalent in cellular transformation.

Authors:  R A Greenberg; R C O'Hagan; H Deng; Q Xiao; S R Hann; R R Adams; S Lichtsteiner; L Chin; G B Morin; R A DePinho
Journal:  Oncogene       Date:  1999-02-04       Impact factor: 9.867

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