UMMS Affiliation

Department of Biochemistry and Molecular Biology; Program in Molecular Medicine

Publication Date


Document Type



3T3 Cells; Animals; CHO Cells; Calcium-Calmodulin-Dependent Protein Kinases; inhibitors; Cricetinae; DNA-Binding Proteins; Enzyme Activation; Enzyme Inhibitors; GTP-Binding Proteins; *GTPase-Activating Proteins; Gene Expression Regulation, Enzymologic; Genes, fos; Interleukin-1; JNK Mitogen-Activated Protein Kinases; Macromolecular Substances; Mice; *Mitogen-Activated Protein Kinases; Proto-Oncogene Proteins; Receptor Protein-Tyrosine Kinases; Signal Transduction; Transcription Factors; Transcription, Genetic; ets-Domain Protein Elk-1; p38 Mitogen-Activated Protein Kinases


Life Sciences | Medicine and Health Sciences


The transcription factors Elk-1 and SAP-1 bind together with serum response factor to the serum response element present in the c-fos promoter and mediate increased gene expression. The ERK, JNK, and p38 groups of mitogen-activated protein (MAP) kinases phosphorylate and activate Elk-1 in response to a variety of extracellular stimuli. In contrast, SAP-1 is activated by ERK and p38 MAP kinases but not by JNK. The proinflammatory cytokine interleukin-1 (IL-1) activates JNK and p38 MAP kinases and induces the transcriptional activity of Elk-1 and SAP-1. These effects of IL-1 appear to be mediated by Rho family GTPases. To examine the relative roles of the JNK and p38 MAP kinase pathways, we examined the effects of IL-1 on CHO and NIH 3T3 cells. Studies of NIH 3T3 cells demonstrated that both the JNK and p38 MAP kinases are required for IL-1-stimulated Elk-1 transcriptional activity, while only p38 MAP kinase contributes to IL-1-induced activation of SAP-1. In contrast, studies of CHO cells demonstrated that JNK (but not the p38 MAP kinase) is required for IL-1-stimulated Elk-1-dependent gene expression and that neither JNK nor p38 MAP kinase is required for IL-1 signaling to SAP-1. We conclude that (i) distinct MAP kinase signal transduction pathways mediate IL-1 signaling to ternary complex transcription factors (TCFs) in different cell types and (ii) individual TCFs show different responses to the JNK and p38 signaling pathways. The differential utilization of TCF proteins and MAP kinase signaling pathways represents a potential mechanism for the determination of cell-type-specific responses to extracellular stimuli.


Mol Cell Biol. 1997 May;17(5):2360-71.

Journal/Book/Conference Title

Molecular and cellular biology

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PubMed ID