Abstract
REST/NRSF is a transcriptional repressor of neuronal genes that has been implicated in development and cancer. In epithelial tissues, REST acts as a tumor suppressor and in breast cancer, loss of REST is associated with disease recurrence and poor prognosis. Here, we identify TSPYL2 (also known as CDA1 and DENTT) as a novel component of the REST protein complex. We show that REST and TSPYL2 are regulators of TGFβ signaling and that cell-cycle arrest induced by TGFβ requires both REST and TSPYL2. Importantly, knockdown of REST or TSPYL2 resulted in transformation of human mammary epithelial cells. Mechanistically, we demonstrate that the TSPYL2/REST complex promotes TGFβ signaling by repressing the expression of genes, such as the proto-oncogene neurotrophic tyrosine kinase receptor C (TrkC). These data provide insight into the role of RESTas a tumor suppressor in epithelial tissues through the regulation of the TGFβ pathway.
| Original language | English |
|---|---|
| Pages (from-to) | 1353-1362 |
| Number of pages | 10 |
| Journal | Cell Death and Differentiation |
| Volume | 22 |
| Issue number | 8 |
| DOIs | |
| State | Published - 7 Aug 2015 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Cell Biology
Fingerprint
Dive into the research topics of 'TSPYL2 is an essential component of the REST/NRSF transcriptional complex for TGFβ signaling activation'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver