Mixed lineage kinase ZAK utilizing MKK7 and not MKK4 to activate the c-Jun N-terminal kinase and playing a role in the cell arrest

被引:37
作者
Yang, JJ [1 ]
机构
[1] Chung Shan Med Univ, Sch Dent, Taichung 402, Taiwan
关键词
leucine-zipper (LZ) and sterile-alpha motif (SAM) kinase (ZAK); mixed lineage kinase (MLK); JNK/SAPK; cell cycle;
D O I
10.1016/S0006-291X(02)02123-X
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
The leucine-zipper (LZ) and sterile-a motif (SAM) kinase (ZAK) belongs to the MAP kinase kinase kinase (MAP3K) when upon over-expression in mammalian cells activates the JNK/SAPK pathway. The mechanisms by which ZAK activity is regulated are not well understood. Co-expression of dominant-negative MKK7 but not MKK4 and ZAK significantly attenuates JNK/SAPK activation. This result suggests that ZAK activates JNK/SAPK mediated by downstream target, MKK7. Expression of ZAK but not kinase-dead ZAK in 10T1/2 cells results in the disruption of actin stress fibers and morphological changes. Therefore, ZAK activity may be involved in actin organization regulation. Expression of wild-type ZAK increases the cell population in the G(2)/M phase of the cell cycle, which may indicate G(2) arrest. Western blot analysis shows that the decreased cyclin E level correlated strongly with the low proliferative capacity of ZAK-expressed cells. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:105 / 110
页数:6
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