Telomerase redefined: Integrated regulation of hTR and hTERT for telomere maintenance and telomerase activity

被引:97
作者
Cairney, C. J. [1 ]
Keith, W. N. [1 ]
机构
[1] Univ Glasgow, Ctr Oncol & Appl Pharmacol, Canc Res UK Beatson Labs, Glasgow G61 1BD, Lanark, Scotland
关键词
hTR; hTERT; telomerase; telomere; gene regulation;
D O I
10.1016/j.biochi.2007.07.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Telomerase activity is dependent on the expression of 2 main core component genes, hTERT, which encodes the catalytic component and hTR (also called TERC), which encodes the RNA component. The correlation between telomerase activity and carcinogenesis has made this molecule of great interest in cancer research, however in order to fully understand the regulation of telomerase the mechanisms controlling both telomerase genes need to be studied. Some of these mechanisms of regulation have begun to emerge, however many more remain to be deciphered. For many years hTERT has been regarded as the limiting component of telomerase and much of the research in this field has focussed on its regulation, however it was clear from an early stage that hTR expression was also tightly regulated in normal cells and disease. More recently evidence from biochemistry, promoter studies and mouse models has been steadily increasing for a role for hTR as a limiting and essential component for telomerase activity and telomere maintenance. Perhaps the time has come to redefine our view of telomerase regulation. Knowledge of the mechanisms controlling both telomerase genes in normal systems and cancer may aid our understanding of the role of telomerase in carcinogenesis or highlight potential areas for therapeutic intervention. Here we review the essential requirement of hTR for telomere maintenance and telomerase activity in normal tissues and disease and focus on recent advances in our understanding of hTR regulation in relation to hTERT. (c) 2007 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:13 / 23
页数:11
相关论文
共 81 条
[1]   Telomerase regulation: not just flipping the switch [J].
Aisner, DL ;
Wright, WE ;
Shay, JW .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2002, 12 (01) :80-85
[2]   Hypoxic regulation of telomerase gene expression by transcriptional and post-transcriptional mechanisms [J].
Anderson, CJ ;
Hoare, SF ;
Ashcroft, M ;
Bilsland, AE ;
Keith, WN .
ONCOGENE, 2006, 25 (01) :61-69
[3]   Frequent gain of the human telomerase gene TERC at 3q26 in cervical adenocarcinomas [J].
Andersson, S. ;
Wallin, K-L ;
Hellstroem, A-C ;
Morrison, L. E. ;
Hjerpe, A. ;
Auer, G. ;
Ried, T. ;
Larsson, C. ;
Heselmeyer-Haddad, K. .
BRITISH JOURNAL OF CANCER, 2006, 95 (03) :331-338
[4]   Lack of telomerase gene expression in alternative lengthening of telomere cells is associated with chromatin remodeling of the hTR and hTERT gene promoters [J].
Atkinson, SP ;
Hoare, SF ;
Glasspool, RM ;
Keith, WN .
CANCER RESEARCH, 2005, 65 (17) :7585-7590
[5]  
Avilion AA, 1996, CANCER RES, V56, P645
[6]   Reconstitution of human telomerase activity in vitro [J].
Beattie, TL ;
Zhou, W ;
Robinson, MO ;
Harrington, L .
CURRENT BIOLOGY, 1998, 8 (03) :177-180
[7]   Transcriptional repression of telomerase RNA gene expression by c-Jun-NH2-kinase and Sp1/Sp3 [J].
Bilsland, AE ;
Stevenson, K ;
Atkinson, S ;
Kolch, W ;
Keith, WN .
CANCER RESEARCH, 2006, 66 (03) :1363-1370
[8]   Selective ablation of human cancer cells by telomerase-specific adenoviral suicide gene therapy vectors expressing bacterial nitroreductase [J].
Bilsland, AE ;
Anderson, CJ ;
Fletcher-Monaghan, AJ ;
McGregor, F ;
Evans, TRJ ;
Ganly, I ;
Knox, RJ ;
Plumb, JA ;
Keith, WN .
ONCOGENE, 2003, 22 (03) :370-380
[9]   Telomere shortening and tumor formation by mouse cells lacking telomerase RNA [J].
Blasco, MA ;
Lee, HW ;
Hande, MP ;
Samper, E ;
Lansdorp, PM ;
DePinho, RA ;
Greider, CW .
CELL, 1997, 91 (01) :25-34
[10]   Extension of life-span by introduction of telomerase into normal human cells [J].
Bodnar, AG ;
Ouellette, M ;
Frolkis, M ;
Holt, SE ;
Chiu, CP ;
Morin, GB ;
Harley, CB ;
Shay, JW ;
Lichtsteiner, S ;
Wright, WE .
SCIENCE, 1998, 279 (5349) :349-352