Evaluation of effects caused by differentially spliced Ets-1 transcripts in fibroblasts

Int J Oncol. 2011 Nov;39(5):1073-82. doi: 10.3892/ijo.2011.1152. Epub 2011 Aug 9.

Abstract

The transcription factor Ets-1 is known to be involved in a broad variety of cellular functions such as cell proliferation, migration, invasion, apoptosis and angiogenesis. In nearly all these reports, the full-length Ets-1 (p51) is commonly considered to be the active form and the role of the Ets-1ΔVII splice variant (p42) has not been addressed. Therefore, we studied the functional effects of p42 Ets-1 in comparison to p51 Ets-1 expression in a well-characterized mouse fibroblast cell line. Furthermore, the specific role of Ets-1 was evaluated using mouse fibroblasts with a reduced Ets-1 expression caused by RNAi and compared to fibroblasts with a binding inhibition of the whole ETS transcription factor family by stably overexpressing the ETS DNA binding domain as transdominant-negative mutant. Our results demonstrate that p42 Ets-1 has quite different functions and target genes compared to p51 Ets-1 (e.g. TIMP-4, MMP-3, MMP-9, MMP-13). In some cases (e.g. in cytokine expression) p42 Ets-1 is a functional transcription factor which acts in the same manner as a transdominant-negative approach.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing / genetics*
  • Animals
  • Cell Movement / genetics
  • Cell Proliferation
  • Fibroblasts / metabolism*
  • Gene Expression
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Intracellular Space / metabolism
  • Mice
  • NIH 3T3 Cells
  • Protein Transport
  • Proto-Oncogene Protein c-ets-1 / genetics*
  • Transcription, Genetic

Substances

  • Proto-Oncogene Protein c-ets-1