Induction of apoptosis by SLK, a Ste20-related kinase

被引:72
作者
Sabourin, LA [1 ]
Rudnicki, MA [1 ]
机构
[1] McMaster Univ, MOBIX, Inst Mol Biol & Biotechnol, Hamilton, ON L8S 4K1, Canada
基金
英国医学研究理事会;
关键词
Ste20; kinase; apoptosis; JNK1;
D O I
10.1038/sj.onc.1203119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have cloned and characterized a novel murine Ste20-related kinase designated SLK, SLK displays high homology to the Ste20-related kinase LOK, and is more distantly related to MST1 and 2, both Ste20-like kinases, In addition, SLK displays high homology to microtubule and nuclear associated protein (M-NAP) and AT1-46, both of unknown function. SLK is ubiquitously expressed as multiple mRNAs in tissues and cell lines and is downregulated by mitogen depletion in differentiating myoblasts, Biochemical characterization showed that SLK overexpression activates c-Jun amino-terminal kinase 1 (JNK1), However, in vitro kinase assays indicated that SLK was not activated in response to various growth factors or stress-inducing agents. Immunofluorescence studies revealed that SLK colocalized to distinct cytosolic domains, preferentially at the periphery of the cells. In addition, prolonged overexpression of SLK in cultured fibroblasts resulted in apoptosis as demonstrated by annexin-V and TUNEL staining. Our results suggest that SLK belongs to a new family of protein kinases, mediating activation of the stress response pathway through a novel signaling cascade.
引用
收藏
页码:7566 / 7575
页数:10
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