Publication Date:
1998-12-04
Description:
Targeted disruption of the gene encoding MEK kinase 1 (MEKK1), a mitogen-activated protein kinase (MAPK) kinase kinase, defined its function in the regulation of MAPK pathways and cell survival. MEKK1(-/-) embryonic stem cells from mice had lost or altered responses of the c-Jun amino-terminal kinase (JNK) to microtubule disruption and cold stress but activated JNK normally in response to heat shock, anisomycin, and ultraviolet irradiation. Activation of JNK was lost and that of extracellular signal-regulated protein kinase (ERK) was diminished in response to hyperosmolarity and serum factors in MEKK1(-/-) cells. Loss of MEKK1 expression resulted in a greater apoptotic response of cells to hyperosmolarity and microtubule disruption. When activated by specific stresses that alter cell shape and the cytoskeleton, MEKK1 signals to protect cells from apoptosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yujiri, T -- Sather, S -- Fanger, G R -- Johnson, G L -- DK37871/DK/NIDDK NIH HHS/ -- GM30324/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1998 Dec 4;282(5395):1911-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Program in Molecular Signal Transduction, Division of Basic Sciences, National Jewish Medical and Research Center, Denver, CO 80206, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9836645" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
Anisomycin/pharmacology
;
Apoptosis
;
Calcium-Calmodulin-Dependent Protein Kinases/*metabolism
;
Cell Line
;
Cell Size
;
*Cell Survival
;
Enzyme Activation
;
Gene Targeting
;
JNK Mitogen-Activated Protein Kinases
;
Lysophospholipids/pharmacology
;
*MAP Kinase Kinase 4
;
*MAP Kinase Kinase Kinase 1
;
Mice
;
*Mitogen-Activated Protein Kinase Kinases
;
*Mitogen-Activated Protein Kinases
;
Nocodazole/pharmacology
;
Osmolar Concentration
;
Phosphorylation
;
Protein-Serine-Threonine Kinases/genetics/*metabolism
;
Protein-Tyrosine Kinases/metabolism
;
Recombinant Proteins/metabolism
;
Stem Cells
;
Temperature
;
Transfection
;
Ultraviolet Rays
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
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