uu.seUppsala University Publications
Change search
ReferencesLink to record
Permanent link

Direct link
Phosphorylation of serine 11 and serine 92 as new positive regulators of human Snail1 function: potential involvement of casein kinase-2 and the cAMP-activated kinase protein kinase A
Departamento de Bioquímica, UAM, Instituto de Investigaciones Biome´dicas “Alberto Sols,” CSIC-UAM, 28029 Madrid, Spain.
Departamento de Bioquímica, UAM, Instituto de Investigaciones Biome´dicas “Alberto Sols,” CSIC-UAM, 28029 Madrid, Spain.
Karolinska Biomics Center, Department of Oncology-Pathology, Karolinska Institutet, SE-17176, Stockholm, Sweden.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm , Ludwig Institute for Cancer Research.
Show others and affiliations
2010 (English)In: Molecular Biology of the Cell, ISSN 1059-1524, E-ISSN 1939-4586, Vol. 21, no 2, 244-253 p.Article in journal (Refereed) Published
Abstract [en]

Snail1 is a major factor for epithelial-mesenchymal transition (EMT), an important event in tumor metastasis and in other pathologies. Snail1 is tightly regulated at transcriptional and posttranscriptional levels. Control of Snail1 protein stability and nuclear export by GSK3beta phosphorylation is important for Snail1 functionality. Stabilization mechanisms independent of GSK3beta have also been reported, including interaction with LOXL2 or regulation of the COP9 signalosome by inflammatory signals. To get further insights into the role of Snail1 phosphorylation, we have performed an in-depth analysis of in vivo human Snail1 phosphorylation combined with mutational studies. We identify new phosphorylation sites at serines 11, 82, and 92 and confirmed previously suggested phosphorylations at serine 104 and 107. Serines 11 and 92 participate in the control of Snail1 stability and positively regulate Snail1 repressive function and its interaction with mSin3A corepressor. Furthermore, serines 11 and 92 are required for Snail1-mediated EMT and cell viability, respectively. PKA and CK2 have been characterized as the main kinases responsible for in vitro Snail1 phosphorylation at serine 11 and 92, respectively. These results highlight serines 11 and 92 as new players in Snail1 regulation and suggest the participation of CK2 and PKA in the modulation of Snail1 functionality.

Place, publisher, year, edition, pages
2010. Vol. 21, no 2, 244-253 p.
National Category
Medical and Health Sciences
URN: urn:nbn:se:uu:diva-115540DOI: 10.1091/mbc.E09-06-0504ISI: 000273598900003PubMedID: 19923321OAI: oai:DiVA.org:uu-115540DiVA: diva2:295502
Available from: 2010-02-17 Created: 2010-02-17 Last updated: 2011-02-28Bibliographically approved

Open Access in DiVA

No full text

Other links

Publisher's full textPubMed
By organisation
Ludwig Institute for Cancer Research
In the same journal
Molecular Biology of the Cell
Medical and Health Sciences

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Altmetric score

Total: 189 hits
ReferencesLink to record
Permanent link

Direct link