A cell-permeable peptide inhibits activation of PKR and enhances cell proliferation

被引:22
作者
Nekhai, S
Bottaro, DP
Woldehawariat, G
Spellerberg, A
Petryshyn, R
机构
[1] NCI, Cellular & Mol Biol Lab, NIH, Bethesda, MD 20892 USA
[2] Childrens Natl Med Ctr, Ctr Canc & Transplantat Biol, Washington, DC 20010 USA
[3] George Washington Univ, Sch Med, Dept Biochem & Mol Biol, Washington, DC 20010 USA
关键词
PKR; cell-permeable peptide; eIF-2 alpha phosphorylation; regulation of cell proliferation;
D O I
10.1016/S0196-9781(00)00297-7
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 double-stranded RNA dependent protein kinase (PKR) is a negative regulator of cell proliferation and thus itself a target for modulation. We show that a cell-permeable peptide (PRI), containing a conserved double-stranded RNA binding motif found in PKR, inhibits activation of the kinase and activity to phosphorylate its substrate. Further, the PRI-peptide localizes to the cytoplasm of murine embryonic fibroblasts and ablates: cellular. PKR activation. The PRI-peptide enhances cell proliferation compared to treatment with a variant control peptide, resulting in cultures with increased cell density. We conclude that peptides that interfere with PKR may be useful tools for regulating cell proliferation. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1449 / 1456
页数:8
相关论文
共 35 条
[11]   MAMMALIAN EUKARYOTIC INITIATION FACTOR-2-ALPHA KINASES FUNCTIONALLY SUBSTITUTE FOR GCN2 PROTEIN-KINASE IN THE GCN4 TRANSLATIONAL CONTROL MECHANISM OF YEAST [J].
DEVER, TE ;
CHEN, JJ ;
BARBER, GN ;
CIGAN, AM ;
FENG, L ;
DONAHUE, TF ;
LONDON, IM ;
KATZE, MG ;
HINNEBUSCH, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (10) :4616-4620
[12]   ACTIVATION OF DOUBLE-STRANDED RNA-DEPENDENT KINASE (DSL) BY THE TAR REGION OF HIV-1 MESSENGER-RNA - A NOVEL TRANSLATIONAL CONTROL MECHANISM [J].
EDERY, I ;
PETRYSHYN, R ;
SONENBERG, N .
CELL, 1989, 56 (02) :303-312
[13]   PHOSPHORYLATION OF INITIATION-FACTOR ELF-2 AND CONTROL OF RETICULOCYTE PROTEIN-SYNTHESIS [J].
FARRELL, PJ ;
BALKOW, K ;
HUNT, T ;
JACKSON, RJ ;
TRACHSEL, H .
CELL, 1977, 11 (01) :187-200
[14]   RAX, a cellular activator for double-stranded RNA-dependent protein kinase during stress signaling [J].
Ito, T ;
Yang, ML ;
May, WS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (22) :15427-15432
[15]  
KING DS, 1990, INT J PEPT PROT RES, V36, P255
[16]  
Kumar KU, 1999, MOL CELL BIOL, V19, P1116
[17]   INTERFERON, DOUBLE-STRANDED-RNA, AND PROTEIN-PHOSPHORYLATION [J].
LEBLEU, B ;
SEN, GC ;
SHAILA, S ;
CABRER, B ;
LENGYEL, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (09) :3107-3111
[18]   Role of the nuclear localization sequence in fibroblast growth factor-1-stimulated mitogenic pathways [J].
Lin, YZ ;
Yao, SY ;
Hawiger, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (10) :5305-5308
[19]   INHIBITION OF NUCLEAR TRANSLOCATION OF TRANSCRIPTION FACTOR NF-KAPPA-B BY A SYNTHETIC PEPTIDE-CONTAINING A CELL MEMBRANE-PERMEABLE MOTIF AND NUCLEAR-LOCALIZATION SEQUENCE [J].
LIN, YZ ;
YAO, SY ;
VEACH, RA ;
TORGERSON, TR ;
HAWIGER, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14255-14258
[20]   Structure of the double-stranded RNA-binding domain of the protein kinase PKR reveals the molecular basis of its dsRNA-mediated activation [J].
Nanduri, S ;
Carpick, BW ;
Yang, YW ;
Williams, BRG ;
Qin, J .
EMBO JOURNAL, 1998, 17 (18) :5458-5465