Format

Send to

Choose Destination
FEBS Lett. 2007 Mar 20;581(6):1209-16. Epub 2007 Feb 28.

Dissecting yeast Hog1 MAP kinase pathway using a chemical genetic approach.

Author information

1
Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907, USA.

Abstract

Using a chemical genetic approach, we identified four novel physiological substrates of Hog1 kinase (Krs1, Tdh3, Hsp26, and Shm2). These substrates suggest plausible mechanisms for actin reorganization, cell cycle arrest and regulation of protein synthesis observed upon osmotic stress. We further show that the human homolog of Shm2 (SHMT1) is a novel physiological substrate of p38 MAP kinase in vitro and in vivo. Down-regulation of its enzymatic activity was observed following p38-mediated phosphorylation revealing a potential cancer-modulating property of p38 MAP kinase. This screen has uncovered several novel Hog1 substrates that provide new avenues for investigation into the mechanism of osmoadaptation by this kinase.

PMID:
17346711
DOI:
10.1016/j.febslet.2007.02.032
[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center