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Publication : SRF Co-factors Control the Balance between Cell Proliferation and Contractility.

First Author  Gualdrini F Year  2016
Journal  Mol Cell Volume  64
Issue  6 Pages  1048-1061
PubMed ID  27867007 Mgi Jnum  J:252206
Mgi Id  MGI:6094689 Doi  10.1016/j.molcel.2016.10.016
Citation  Gualdrini F, et al. (2016) SRF Co-factors Control the Balance between Cell Proliferation and Contractility. Mol Cell 64(6):1048-1061
abstractText  The ERK-regulated ternary complex factors (TCFs) act with the transcription factor serum response factor (SRF) to activate mitogen-induced transcription. However, the extent of their involvement in the immediate-early transcriptional response, and their wider functional significance, has remained unclear. We show that, in MEFs, TCF inactivation significantly inhibits over 60% of TPA-inducible gene transcription and impairs cell proliferation. Using integrated SRF ChIP-seq and Hi-C data, we identified over 700 TCF-dependent SRF direct target genes involved in signaling, transcription, and proliferation. These also include a significant number of cytoskeletal gene targets for the Rho-regulated myocardin-related transcription factor (MRTF) SRF cofactor family. The TCFs act as general antagonists of MRTF-dependent SRF target gene expression, competing directly with the MRTFs for access to SRF. As a result, TCF-deficient MEFs exhibit hypercontractile and pro-invasive behavior. Thus, competition between TCFs and MRTFs for SRF determines the balance between antagonistic proliferative and contractile programs of gene expression.
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