The p542 gene encodes an autoantigen that cross-reacts with EBNA-1 of the Epstein Barr virus and which may be a heterogeneous nuclear ribonucleoprotein

被引:25
作者
Rhodes, GH
Valbracht, JR
Nguyen, MD
Vaughan, JH
机构
[1] UNIV CALIF SAN DIEGO,DEPT MED,LA JOLLA,CA 92093
[2] UNIV CALIF SAN DIEGO,SAM & ROSE STEIN INST RES AGING,LA JOLLA,CA 92093
[3] UNIV CALIF DAVIS,DEPT MED PATHOL,DAVIS,CA 95616
关键词
EBV; EBNA-1; autoantibodies; hnRNP; Raly; p542;
D O I
10.1006/jaut.1997.9996
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In infectious mononucleosis (IM), anti-EBNA-1 antibodies are produced which cross-react with multiple normal human proteins. The cross-reactions can be inhibited with synthetic peptides representing the glycine/alanine repeat in EBNA-1, which implies that the cross-reactivity is due to anti-gly/ala antibodies that cross-react with host proteins containing configurations like those in the EBNA-1 repeat. Here we report the isolation of five gene fragments from a Raji B lymphocyte cDNA library encoding peptides reactive with autoantibodies in an IM serum. One of these, p542, encodes a glycine rich 28-mer which constitutes its cross-reactive epitope, as shown elsewhere. By Northern blots, p542 was identifiable in three B lymphocyte lines, a T cell line, and an epithelial cell line. In a search of the GenBank for proteins with sequence similarity to p542, we found a high degree of identity with the mid-and 3' terminal regions of the recently published mouse gene, Raly, which encodes a protein with the structure of a heterogeneous nuclear ribonuclear protein (hnRNP). We confirmed by anchored RT-PCR our presumption that the 5' sequences of p542 also have a high degree of identity with Raly, including presence of RNA binding motifs characteristic of hnRNPs. There was also sequence homology with human hnRNP C2. From these observations and our previous studies, we conclude that the autoantigen for one of the crossreactive autoantibodies generated during immune responses to the Epstein Barr virus, anti-p542, is probably an hnRNP. (C) 1997 Academic Press Limited.
引用
收藏
页码:447 / 454
页数:8
相关论文
共 22 条
[1]   PRIMARY STRUCTURES OF THE HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN A2-PROTEIN, B1-PROTEIN, AND C2-PROTEIN - A DIVERSITY OF RNA-BINDING PROTEINS IS GENERATED BY SMALL PEPTIDE INSERTS [J].
BURD, CG ;
SWANSON, MS ;
GORLACH, M ;
DREYFUSS, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :9788-9792
[2]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[3]  
Fritzler Marvin J., 1993, Journal of Dermatology (Tokyo), V20, P257
[4]  
FRITZLER MJ, 1984, J IMMUNOL, V132, P1216
[5]  
HABETS WJ, 1983, CLIN EXP IMMUNOL, V54, P265
[6]   AUTOIMMUNE-RESPONSE TO THE SPLICEOSOME - AN IMMUNOLOGICAL LINK BETWEEN RHEUMATOID-ARTHRITIS, MIXED CONNECTIVE-TISSUE DISEASE, AND SYSTEMIC LUPUS-ERYTHEMATOSUS [J].
HASSFELD, W ;
STEINER, G ;
STUDNICKABENKE, A ;
SKRINER, K ;
GRANINGER, W ;
FISCHER, I ;
SMOLEN, JS .
ARTHRITIS AND RHEUMATISM, 1995, 38 (06) :777-785
[7]  
HASSFELD W, 1993, BRIT J RHEUMATOL, V32, P199
[8]   ONE OF 2 EPSTEIN-BARR VIRUS NUCLEAR ANTIGENS CONTAINS A GLYCINE-ALANINE CO-POLYMER DOMAIN [J].
HENNESSY, K ;
KIEFF, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (18) :5665-5669
[9]   THE EMBRYONIC LETHALITY OF HOMOZYGOUS LETHAL YELLOW MICE (A(Y)/A(Y)) IS ASSOCIATED WITH THE DISRUPTION OF A NOVEL RNA-BINDING PROTEIN [J].
MICHAUD, EJ ;
BULTMAN, SJ ;
STUBBS, LJ ;
WOYCHIK, RP .
GENES & DEVELOPMENT, 1993, 7 (7A) :1203-1213
[10]   MOLECULAR-CLONING OF THE CDNA-ENCODING THE EPSTEIN-BARR VIRUS/C3D RECEPTOR (COMPLEMENT RECEPTOR TYPE-2) OF HUMAN LYMPHOCYTES-B [J].
MOORE, MD ;
COOPER, NR ;
TACK, BF ;
NEMEROW, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9194-9198