Variant forms of upstream stimulatory factors (USFs) control the promoter activity of hTERT, the human gene encoding the catalytic subunit of telomerase

FEBS Lett. 2002 Jun 5;520(1-3):40-6. doi: 10.1016/s0014-5793(02)02757-6.

Abstract

It is known that Myc regulates the expression of TERT, the telomerase catalytic subunit gene, by binding to E box. Here we show that another E box-binding protein, upstream stimulatory factor (USF), also regulates TERT expression. Specifically, the N-terminally truncated form of USF2 is present in telomerase-negative/resting human lymphocytes, but not in telomerase-positive/phytohemagglutinin-activated lymphocytes. In electrophoretic mobility shift assay, both full-length and truncated USF2s bound to the TERT E box. In a transient expression assay, the truncated USF had a dominant-negative effect on both exogenous full-length USF and endogenous positive regulators for activating TERT expression. These results suggest that the differential abundance of truncated USF2 may regulate telomerase activity during lymphocyte activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Blotting, Western
  • Cells, Cultured
  • DNA / genetics
  • DNA / metabolism
  • DNA-Binding Proteins*
  • Electrophoretic Mobility Shift Assay
  • Gene Expression Regulation, Enzymologic
  • Humans
  • Lymphocytes / metabolism
  • Molecular Sequence Data
  • Mutation
  • Plasmids / genetics
  • Promoter Regions, Genetic / genetics*
  • Protein Binding
  • Telomerase / genetics*
  • Telomerase / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*
  • Upstream Stimulatory Factors

Substances

  • DNA-Binding Proteins
  • Transcription Factors
  • USF1 protein, human
  • USF2 protein, human
  • Upstream Stimulatory Factors
  • DNA
  • TERT protein, human
  • Telomerase