PUBLICATION
Lats2 kinase potentiates Snail1 activity by promoting nuclear retention upon phosphorylation
- Authors
- Zhang, K., Rodriguez-Aznar, E., Yabuta, N., Owen, R.J., Mingot, J.M., Nojima, H., Nieto, M.A., and Longmore, G.D.
- ID
- ZDB-PUB-111013-3
- Date
- 2012
- Source
- The EMBO journal 31(1): 29-43 (Journal)
- Registered Authors
- Mingot, Jose Manuel, Nieto, Angela
- Keywords
- breast cancer, Lats2, Snail1
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Cell Nucleus/metabolism*
- Cells, Cultured
- Dogs
- Embryo, Mammalian/metabolism
- Embryo, Nonmammalian/metabolism
- Epithelial-Mesenchymal Transition
- HCT116 Cells
- HEK293 Cells
- Humans
- Mice
- Molecular Sequence Data
- Phosphorylation
- Protein Serine-Threonine Kinases/genetics
- Protein Serine-Threonine Kinases/metabolism*
- RNA Interference
- Transcription Factors/genetics
- Transcription Factors/metabolism*
- Transfection
- Tumor Suppressor Proteins/genetics
- Tumor Suppressor Proteins/metabolism*
- Zebrafish
- PubMed
- 21952048 Full text @ EMBO J.
Citation
Zhang, K., Rodriguez-Aznar, E., Yabuta, N., Owen, R.J., Mingot, J.M., Nojima, H., Nieto, M.A., and Longmore, G.D. (2012) Lats2 kinase potentiates Snail1 activity by promoting nuclear retention upon phosphorylation. The EMBO journal. 31(1):29-43.
Abstract
Snail1 is a central regulator of epithelial cell adhesion and movement in epithelial-to-mesenchymal transitions (EMTs) during embryo development; a process reactivated during cancer metastasis. While induction of Snail1 transcription precedes EMT induction, post-translational regulation of Snail1 is also critical for determining Snail1's protein level, subcellular localization, and capacity to induce EMT. To identify novel post-translational regulators of Snail1, we developed a live cell, bioluminescence-based screen. From a human kinome RNAi screen, we have identified Lats2 kinase as a novel regulator of Snail1 protein level, subcellular localization, and thus, activity. We show that Lats2 interacts with Snail1 and directly phosphorylates Snail1 at residue T203. This occurs in the nucleus and serves to retain Snail1 in the nucleus thereby enhancing its stability. Lats2 was found to positively influence cellular EMT and tumour cell invasion, in a Snail1-dependent manner. Indeed during TGFβ-induced EMT Lats2 is activated and Snail1 phosphorylated at T203. Analysis in mouse and zebrafish embryo development confirms that Lats2 acts as a positive modulator of Snail1 protein level and potentiates its in vivo EMT activity.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping