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PMID: 14707138 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The death effector domain protein PEA-15 prevents nuclear entry of ERK2 by inhibiting required interactions.

The Journal of biological chemistry ·Vol. 279 ·No. 13 ·2004-03-26 ·Pages 12840-7

Whitehurst AW, Robinson FL, Moore MS, Cobb MH

Abstract

ERK2 nuclear-cytoplasmic distribution is regulated in response to hormones and cellular state without the requirement for karyopherin-mediated nuclear import. One proposed mechanism for the movement of ERK2 into the nucleus is through a direct interaction between ERK2 and nucleoporins present in the nuclear pore complex. Previous reports have attributed regulation of ERK2 localization to proteins that activate or deactivate ERK2, such as the mitogen-activated protein (MAP) kinase kinase MEK1 and MAP kinase phosphatases. Recently, a small non-catalytic protein, PEA-15, has also been demonstrated to promote a cytoplasmic ERK2 localization. We found that the MAP kinase insert in ERK2 is required for its interaction with PEA-15. Consistent with its recognition of the MAP kinase insert, PEA-15 blocked activation of ERK2 by MEK1, which also requires the MAP kinase insert to interact productively with ERK2. To determine how PEA-15 influences the localization of ERK2, we used a permeabilized cell system to examine the effect of PEA-15 on the localization of ERK2 and mutants that have lost the ability to bind PEA-15. Wild type ERK2 was unable to enter the nucleus in the presence of an excess of PEA-15; however, ERK2 lacking the MAP kinase insert largely retained the ability to enter the nucleus. Binding assays demonstrated that PEA-15 interfered with the ability of ERK2 to bind to nucleoporins. These results suggest that PEA-15 sequesters ERK2 in the cytoplasm at least in part by interfering with its ability to interact with nucleoporins, presenting a potential paradigm for regulation of ERK2 localization.

MeSH Terms
Active Transport, Cell Nucleus Animals Apoptosis Regulatory Proteins Cell Nucleus/metabolism Cytoplasm/metabolism Dose-Response Relationship, Drug Fungal Proteins/metabolism Green Fluorescent Proteins Luminescent Proteins/metabolism MAP Kinase Kinase 1 MAP Kinase Signaling System Mitogen-Activated Protein Kinase 1/metabolism Mitogen-Activated Protein Kinase Kinases/metabolism Models, Molecular Mutation Nuclear Pore Complex Proteins/chemistry,metabolism Phosphoproteins/chemistry Protein Binding Protein Structure, Tertiary Rats Recombinant Proteins/chemistry Two-Hybrid System Techniques
Chemicals
Apoptosis Regulatory Proteins Fungal Proteins Luminescent Proteins Nuclear Pore Complex Proteins Nup153 protein, rat Pea15 protein, rat Phosphoproteins Recombinant Proteins Green Fluorescent Proteins Mitogen-Activated Protein Kinase 1 MAP Kinase Kinase 1 MAP2K1 protein, human Mitogen-Activated Protein Kinase Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Whitehurst Angelique W
Department of Pharmacology, the University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9041, USA.
Robinson Fred L
Moore Mary Shannon
Cobb Melanie H
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2004-03-26
Epub
2004-00-05
Pages
12840-7
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK 34128 · United States
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