Two domains of the Borna disease virus p40 protein are required for interaction with the p23 protein

被引:26
作者
Berg, M
Ehrenborg, C
Blomberg, J
Pipkorn, R
Berg, AL
机构
[1] Swedish Univ Agr Sci, Dept Vet Microbiol, Immunol Sect, S-75123 Uppsala, Sweden
[2] Swedish Univ Agr Sci, Dept Pathol, S-75123 Uppsala, Sweden
[3] Uppsala Grad Sch Biomed Res, Uppsala, Sweden
[4] Uppsala Univ, Acad Hosp, Dept Clin Microbiol, Sect Virol, Uppsala, Sweden
[5] Deutsch Krebsforschungszentrum, D-6900 Heidelberg, Germany
关键词
D O I
10.1099/0022-1317-79-12-2957
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
Borna disease virus (BDV) has five major open reading frames, which encode the proteins p40, p23, gp18, p57 and p190, By analogy with other negative-strand RNA viruses, p40 is a putative nucleoprotein and p23 is a putative phosphoprotein. These proteins are known to form complexes with each other and with the polymerase protein in other viruses. In this paper, it is shown that BDV p40 and p23 can form complexes with each other in infected cells. Furthermore, the amino acids of p40 that are necessary for formation of this complex have been mapped.
引用
收藏
页码:2957 / 2963
页数:7
相关论文
共 19 条
[1]   BORNA DISEASE VIRUS-SPECIFIC ANTIGENS .2. THE SOLUBLE-ANTIGEN IS A PROTEIN COMPLEX [J].
BAUSENIEDRIG, I ;
JACKSON, M ;
SCHEIN, E ;
LUDWIG, H ;
PAULI, G .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1992, 31 (3-4) :361-369
[2]   THE P-GENE OF THE PORCINE PARAMYXOVIRUS LPMV ENCODES 3 POSSIBLE POLYPEPTIDES-P, POLYPEPTIDE-V AND POLYPEPTIDE-C - THE P-PROTEIN MESSENGER-RNA IS EDITED [J].
BERG, M ;
HJERTNER, B ;
MORENOLOPEZ, J ;
LINNE, T .
JOURNAL OF GENERAL VIROLOGY, 1992, 73 :1195-1200
[3]  
BODE L, 1995, CURR TOP MICROBIOL, V190, P103
[4]   GENOMIC ORGANIZATION OF BORNA-DISEASE VIRUS [J].
BRIESE, T ;
SCHNEEMANN, A ;
LEWIS, AJ ;
PARK, YS ;
KIM, S ;
LUDWIG, H ;
LIPKIN, WI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) :4362-4366
[5]   CHARACTERIZATION OF A GLIAL-CELL LINE PERSISTENTLY INFECTED WITH BORNA DISEASE VIRUS (BDV) - INFLUENCE OF NEUTROPHIC FACTORS ON BDV PROTEIN AND RNA EXPRESSION [J].
CARBONE, KM ;
RUBIN, SA ;
SIERRAHONIGMANN, AM ;
LEDERMAN, HM .
JOURNAL OF VIROLOGY, 1993, 67 (03) :1453-1460
[6]   SEQUENCE AND GENOME ORGANIZATION OF BORNA-DISEASE VIRUS [J].
CUBITT, B ;
OLDSTONE, C ;
DELATORRE, JC .
JOURNAL OF VIROLOGY, 1994, 68 (03) :1382-1396
[7]   COOPERATIVE BINDING OF MULTIMERIC PHOSPHOPROTEIN (P) OF VESICULAR STOMATITIS-VIRUS TO POLYMERASE (L) AND TEMPLATE - PATHWAYS OF ASSEMBLY [J].
GAO, Y ;
LENARD, J .
JOURNAL OF VIROLOGY, 1995, 69 (12) :7718-7723
[8]  
GAUSEPOHL H, 1992, PEPTIDE RES, V5, P315
[9]   PURIFICATION AND PROPERTIES OF AN INTRANUCLEAR VIRUS-SPECIFIC ANTIGEN FROM TISSUE INFECTED WITH BORNA DISEASE VIRUS [J].
HAAS, B ;
BECHT, H ;
ROTT, R .
JOURNAL OF GENERAL VIROLOGY, 1986, 67 :235-241
[10]   COMPLEXES OF SENDAI VIRUS NP-P AND P-L PROTEINS ARE REQUIRED FOR DEFECTIVE INTERFERING PARTICLE GENOME REPLICATION INVITRO [J].
HORIKAMI, SM ;
CURRAN, J ;
KOLAKOFSKY, D ;
MOYER, SA .
JOURNAL OF VIROLOGY, 1992, 66 (08) :4901-4908