Both transcriptional and posttranscriptional mechanisms regulate human telomerase template RNA levels

Xiaoming Yi, Valerie M. Tesmer, Isabelle Savre-Train, Jerry W. Shay, Woodring E. Wright

Research output: Contribution to journalArticlepeer-review

121 Scopus citations

Abstract

The human telomerase RNA component (hTR) is present in normal somatic cells at lower levels than in cancer-derived cell lines. To understand the mechanisms regulating hTR levels in different cell types, we have compared the steady-state hTR levels in three groups of cells: (i) normal telomerase- negative human diploid cells; (ii) normal cells transfected with the human telomerase catalytic subunit, hTERT; and (iii) cells immortalized in vitro and cancer cells expressing their own endogenous hTERT. To account for the differences in steady-state hTR levels observed in these cell types, we compared the transcription rate and half-life of hTR in a subset of these cells. The half-life of hTR in telomerase-negative cells is about 5 days and is increased 1.6-fold in the presence of hTERT. The transcription rate of hTR is essentially unchanged in cells expressing exogenous hTERT, and the increased steady-state hTR level appears to be due to the increased half- life. However, the transcription rate of hTR is greatly increased in cells expressing endogenous hTERT, suggesting some overlap in transcriptional regulatory control. We conclude that the higher hTR level in cells expressing an endogenous telomerase can be a result of both increased transcription and a longer half-life and that the longer half-life might be partially a result of protection or stabilization by the telomerase catalytic subunit. The 4- week half-life of hTR in H1299 tumor cells is the longest half-life yet reported for any RNA.

Original languageEnglish (US)
Pages (from-to)3989-3997
Number of pages9
JournalMolecular and cellular biology
Volume19
Issue number6
DOIs
StatePublished - Jun 1999

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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