COWPOX VIRUS CONTAINS 2 COPIES OF AN EARLY GENE ENCODING A SOLUBLE SECRETED FORM OF THE TYPE-II TNF RECEPTOR

被引:163
作者
HU, FQ
SMITH, CA
PICKUP, DJ
机构
[1] DUKE UNIV, MED CTR, DEPT MICROBIOL, DURHAM, NC 27710 USA
[2] IMMUNEX RES & DEV CORP, SEATTLE, WA 98101 USA
关键词
D O I
10.1006/viro.1994.1539
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The inverted terminal repeats of the DNA of cowpox virus (Brighten Red strain) contain the crmB gene, an additional member of a family of viral genes that modify cytokine responses to infection. The crmB gene is transcribed from an early promoter. The primary product is a 355-amino-acid protein containing a signal peptide sequence and three potential N-linked glycosylation sites. The mature gene product is a secreted soluble protein that has an apparent molecular mass of 48 kDa. TNF alpha and TNF beta bind to this protein in a competitive manner, consistent with the sequence of its N-terminal 176 amino acids, which closely resembles the ligand-binding domains of the type II (75-kDa) human TNF receptor. The sequence of the C-terminal 161 amino acids or the CrmB protein is unlike that of human TNF receptors, but overall, the CrmB protein is similar to the T2 proteins of the leporipoxviruses (48% identity) and the predicted product of the G4R/G2R open reading frame of variola virus (85% identity), suggesting that not only the TNF-binding domains but also the C-terminal regions contribute to the functions of these viral proteins. These results show that orthopoxviruses such as cowpox virus encode secreted forms of TNF receptors that can contribute to the modification of TNF-mediated antiviral processes. (C) 1994 Academic Press, Inc.
引用
收藏
页码:343 / 356
页数:14
相关论文
共 67 条
[11]   ESCHERICHIA-COLI GPT GENE PROVIDES DOMINANT SELECTION FOR VACCINIA VIRUS OPEN READING FRAME EXPRESSION VECTORS [J].
FALKNER, FG ;
MOSS, B .
JOURNAL OF VIROLOGY, 1988, 62 (06) :1849-1854
[12]  
Fenner F., 1989, THE ORTHOPOXVIRUSES
[13]   ACUTE INFLAMMATORY RESPONSE TO COWPOX VIRUS-INFECTION OF THE CHORIOALLANTOIC MEMBRANE OF THE CHICK-EMBRYO [J].
FREDRICKSON, TN ;
SECHLER, JMG ;
PALUMBO, GJ ;
ALBERT, J ;
KHAIRALLAH, LH ;
BULLER, RML .
VIROLOGY, 1992, 187 (02) :693-704
[14]   PREVENTION OF VERTEBRATE NEURONAL DEATH BY THE CRMA GENE [J].
GAGLIARDINI, V ;
FERNANDEZ, PA ;
LEE, RKK ;
DREXLER, HCA ;
ROTELLO, RJ ;
FISHMAN, MC ;
YUAN, J .
SCIENCE, 1994, 263 (5148) :826-828
[15]   THE COMPLETE DNA-SEQUENCE OF VACCINIA VIRUS [J].
GOEBEL, SJ ;
JOHNSON, GP ;
PERKUS, ME ;
DAVIS, SW ;
WINSLOW, JP ;
PAOLETTI, E .
VIROLOGY, 1990, 179 (01) :247-266
[16]  
GOEBEL SJ, 1990, VIROLOGY, V179, P517
[17]   THE 10,400-DALTON AND 14,500-DALTON PROTEINS ENCODED BY REGION E3 OF ADENOVIRUS FUNCTION TOGETHER TO PROTECT MANY BUT NOT ALL MOUSE-CELL LINES AGAINST LYSIS BY TUMOR-NECROSIS-FACTOR [J].
GOODING, LR ;
RANHEIM, TS ;
TOLLEFSON, AE ;
AQUINO, L ;
DUERKSENHUGHES, P ;
HORTON, TM ;
WOLD, WSM .
JOURNAL OF VIROLOGY, 1991, 65 (08) :4114-4123
[18]   A 14,700 MW PROTEIN FROM THE E3 REGION OF ADENOVIRUS INHIBITS CYTOLYSIS BY TUMOR NECROSIS FACTOR [J].
GOODING, LR ;
ELMORE, LW ;
TOLLEFSON, AE ;
BRADY, HA ;
WOLD, WSM .
CELL, 1988, 53 (03) :341-346
[19]  
GOODING LR, 1992, CELL, V71, P5
[20]   MOLECULAR-CLONING AND EXPRESSION OF THE TYPE-1 AND TYPE-2 MURINE RECEPTORS FOR TUMOR-NECROSIS-FACTOR [J].
GOODWIN, RG ;
ANDERSON, D ;
JERZY, R ;
DAVIS, T ;
BRANNAN, CI ;
COPELAND, NG ;
JENKINS, NA ;
SMITH, CA .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (06) :3020-3026