Cloning, mapping, and in vivo localization of a human member of the PKCI-1 protein family (PRKCNH1)

被引:22
作者
Brzoska, PM
Chen, HY
Levin, NA
Kuo, WL
Collins, C
Fu, KK
Gray, JW
Christman, MF
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT RADIAT ONCOL, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, DEPT LAB MED, DIV MOL CYTOMETRY, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1006/geno.1996.0435
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We report here the complete cDNA sequence, genomic mapping, and immunolocalization of the first human member of the protein kinase C inhibitor (PKCI-1) gene family. The predicted human protein (hPKCI-1) is 96% identical to bovine and 53% identical to maize members, indicating the great evolutionary conservation of this protein family. The hPKCI-1 gene (HGMV-approved symbol PRKCNH1) maps to human chromosome 5q31.2 by fluorescence in situ hybridization. Indirect immunofluorescence shows that hPKCI-1 localizes to cytoskeletal structures in the cytoplasm of a human fibroblast cell line and is largely excluded from the nucleus. The cytoplasmic localization of hPKCI-1 is consistent with a postulated role in mediating a membrane-derived signal in response to ionizing radiation. (C) 1996 Academic Press, Inc.
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收藏
页码:151 / 156
页数:6
相关论文
共 27 条
[1]   THE PRODUCT OF THE ATAXIA-TELANGIECTASIA GROUP-D COMPLEMENTING GENE, ATDC INTERACTS WITH A PROTEIN-KINASE-C SUBSTRATE AND INHIBITOR [J].
BRZOSKA, PM ;
CHEN, HY ;
ZHU, YF ;
LEVIN, NA ;
DISATNIK, MH ;
MOCHLYROSEN, D ;
MURNANE, JP ;
CHRISTMAN, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7824-7828
[2]   PURIFICATION OF A RAS-RESPONSIVE ADENYLYL CYCLASE COMPLEX FROM SACCHAROMYCES-CEREVISIAE BY USE OF AN EPITOPE ADDITION METHOD [J].
FIELD, J ;
NIKAWA, J ;
BROEK, D ;
MACDONALD, B ;
RODGERS, L ;
WILSON, IA ;
LERNER, RA ;
WIGLER, M .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2159-2165
[3]   THE MAJOR ENDOGENOUS BOVINE BRAIN PROTEIN-KINASE-C INHIBITOR IS A HEAT-LABILE PROTEIN [J].
FRASER, ED ;
WALSH, MP .
FEBS LETTERS, 1991, 294 (03) :285-289
[4]   TIGHT CONTROL OF GENE-EXPRESSION IN MAMMALIAN-CELLS BY TETRACYCLINE-RESPONSIVE PROMOTERS [J].
GOSSEN, M ;
BUJARD, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (12) :5547-5551
[5]   CDI1, A HUMAN G1-PHASE AND S-PHASE PROTEIN PHOSPHATASE THAT ASSOCIATES WITH CDK2 [J].
GYURIS, J ;
GOLEMIS, E ;
CHERTKOV, H ;
BRENT, R .
CELL, 1993, 75 (04) :791-803
[6]   MEMBRANE-DERIVED 2ND MESSENGER REGULATES X-RAY-MEDIATED TUMOR-NECROSIS-FACTOR-ALPHA GENE INDUCTION [J].
HALLAHAN, DE ;
VIRUDACHALAM, S ;
KUCHIBHOTLA, J ;
KUFE, DW ;
WEICHSELBAUM, RR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) :4897-4901
[7]   PROTEIN-KINASE-C ISOENZYMES - DIVERGENCE IN SIGNAL TRANSDUCTION [J].
HUG, H ;
SARRE, TF .
BIOCHEMICAL JOURNAL, 1993, 291 :329-343
[8]   STABLE RADIORESISTANCE IN ATAXIA-TELANGIECTASIA CELLS CONTAINING DNA FROM NORMAL HUMAN-CELLS [J].
KAPP, LN ;
PAINTER, RB .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1989, 56 (05) :667-675
[9]  
KAPP LN, 1992, AM J HUM GENET, V51, P45
[10]   A MAMMALIAN-CELL CYCLE CHECKPOINT PATHWAY UTILIZING P53 AND GADD45 IS DEFECTIVE IN ATAXIA-TELANGIECTASIA [J].
KASTAN, MB ;
ZHAN, QM ;
ELDEIRY, WS ;
CARRIER, F ;
JACKS, T ;
WALSH, WV ;
PLUNKETT, BS ;
VOGELSTEIN, B ;
FORNACE, AJ .
CELL, 1992, 71 (04) :587-597