MICAL-1 is a negative regulator of MST-NDR kinase signaling and apoptosis.

Abstract

MICALs (molecules interacting with CasL) are atypical multidomain flavoenzymes with diverse cellular functions. The molecular pathways employed by MICAL proteins to exert their cellular effects remain largely uncharacterized. Via an unbiased proteomics approach, we identify MICAL-1 as a binding partner of NDR (nuclear Dbf2-related) kinases. NDR1/2 kinases are known to mediate apoptosis downstream of the mammalian Ste-20-like kinase MST1, and ablation of NDR1 in mice predisposes the mice to cancer as a result of compromised apoptosis. MST1 phosphorylates NDR1/2 kinases at their hydrophobic motif, thereby facilitating full NDR kinase activity and function. However, if and how this key phosphorylation event is regulated are unknown. Here we show that MICAL-1 interacts with the hydrophobic motif of NDR1/2 and that overexpression or knockdown of MICAL-1 reduces or augments NDR kinase activation or activity, respectively. Surprisingly, MICAL-1 is a phosphoprotein but not an NDR or MST1 substrate. Rather, MICAL-1 competes with MST1 for NDR binding and thereby antagonizes MST1-induced NDR activation. In line with this inhibitory effect, overexpression or knockdown of MICAL-1 inhibits or enhances, respectively, NDR-dependent proapoptotic signaling induced by extrinsic stimuli. Our findings unveil a previously unknown biological role for MICAL-1 in apoptosis and define a novel negative regulatory mechanism of MST-NDR signaling.

DOI: 10.1128/MCB.01389-10

Extracted Key Phrases

9 Figures and Tables

01002003002011201220132014201520162017
Citations per Year

611 Citations

Semantic Scholar estimates that this publication has 611 citations based on the available data.

See our FAQ for additional information.

Cite this paper

@article{Zhou2011MICAL1IA, title={MICAL-1 is a negative regulator of MST-NDR kinase signaling and apoptosis.}, author={Yeping Zhou and Youri Adolfs and W W M Pim Pijnappel and Stephen Fuller and Roel C. van der Schors and Ka Wan Li and Peter H. Sugden and August B. Smit and Alexander Hergovich and R Jeroen Pasterkamp}, journal={Molecular and cellular biology}, year={2011}, volume={31 17}, pages={3603-15} }