Format

Send to

Choose Destination
Oncogene. 2014 Jul 17;33(29):3794-802. doi: 10.1038/onc.2013.360. Epub 2013 Sep 2.

The transcriptional co-activator SND1 is a novel regulator of alternative splicing in prostate cancer cells.

Author information

1
1] Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy [2] Laboratory of Neuroembryology, Fondazione Santa Lucia, Rome, Italy.
2
1] Laboratory of Cellular and Molecular Neurobiology, Fondazione Santa Lucia, Rome, Italy [2] Department of Health Sciences, University of Rome Foro Italico, Rome, Italy.
3
Department of Epidemiology and Preclinical Research, National Institute for Infectious Diseases 'Lazzaro Spallanzani', Rome, Italy.
4
Laboratory of Molecular Immunology, School of Medicine and Institute of Biomedical Technology, Biomeditech, University of Tampere, Tampere, Finland.
5
1] Laboratory of Molecular Immunology, School of Medicine and Institute of Biomedical Technology, Biomeditech, University of Tampere, Tampere, Finland [2] Department of Internal Medicine, Tampere University Hospital, Tampere, Finland.

Abstract

Splicing abnormalities have profound impact in human cancer. Several splicing factors, including SAM68, have pro-oncogenic functions, and their increased expression often correlates with human cancer development and progression. Herein, we have identified using mass spectrometry proteins that interact with endogenous SAM68 in prostate cancer (PCa) cells. Among other interesting proteins, we have characterized the interaction of SAM68 with SND1, a transcriptional co-activator that binds spliceosome components, thus coupling transcription and splicing. We found that both SAM68 and SND1 are upregulated in PCa cells with respect to benign prostate cells. Upregulation of SND1 exerts a synergic effect with SAM68 on exon v5 inclusion in the CD44 mRNA. The effect of SND1 on CD44 splicing required SAM68, as it was compromised after knockdown of this protein or mutation of the SAM68-binding sites in the CD44 pre-mRNA. More generally, we found that SND1 promotes the inclusion of CD44 variable exons by recruiting SAM68 and spliceosomal components on CD44 pre-mRNA. Inclusion of the variable exons in CD44 correlates with increased proliferation, motility and invasiveness of cancer cells. Strikingly, we found that knockdown of SND1, or SAM68, reduced proliferation and migration of PCa cells. Thus, our findings strongly suggest that SND1 is a novel regulator of alternative splicing that promotes PCa cell growth and survival.

PMID:
23995791
DOI:
10.1038/onc.2013.360
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Nature Publishing Group
Loading ...
Support Center