Document Detail

Telomere length dynamics in telomerase-positive immortal human cell populations.
MedLine Citation:
PMID:  9521855     Owner:  NLM     Status:  MEDLINE    
It has been proposed that the progressive shortening of telomeres in somatic cells eventually results in senescence. Previous experiments have demonstrated that many immortal cell lines have acquired telomerase activity leading to stabilization of telomere length. Telomere dynamics and telomerase activity were examined in the telomerase-positive immortal cell lines HeLa and 293 and subclones derived from them. A mass culture of HeLa cells had a stable mean telomere length over 60 population doublings (PD) in vitro. Subclones of this culture, however, had a range of mean telomere lengths indicating that telomeric heterogeneity exists within a population with a stable mean telomere length. Some of the subclones lacked detectable telomerase activity soon after isolation but regained it by PD 18, suggesting that at least some of the variation in telomere length can be attributed to variations in telomerase activity levels. 293 subclones also varied in telomere length and telomerase activity. Some telomerase-positive 293 subclones contained long telomeres that gradually shortened, demonstrating that factors other than telomerase also act to modulate telomere length. Fluctuations in telomere length in telomerase-positive immortalized cells may contribute to chromosomal instability and clonal evolution.
T M Bryan; A Englezou; M A Dunham; R R Reddel
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Experimental cell research     Volume:  239     ISSN:  0014-4827     ISO Abbreviation:  Exp. Cell Res.     Publication Date:  1998 Mar 
Date Detail:
Created Date:  1998-04-16     Completed Date:  1998-04-16     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0373226     Medline TA:  Exp Cell Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  370-8     Citation Subset:  IM    
Cancer Research Unit, Children's Medical Research Institute, Westmead, Sydney, NSW, Australia.
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MeSH Terms
Cell Aging
Cell Transformation, Neoplastic / genetics*
Chromosomes, Human / ultrastructure
Clone Cells
DNA, Neoplasm / analysis
Hela Cells
Neoplasm Proteins / metabolism*
Polymorphism, Restriction Fragment Length
Telomerase / metabolism*
Telomere / metabolism,  ultrastructure*
Reg. No./Substance:
0/DNA, Neoplasm; 0/Neoplasm Proteins; EC

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

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