Interaction of EBV latent origin of replication with the nuclear matrix: identification of S/MAR sequences and protein components

被引:6
作者
Mearini, G
Chichiarelli, S
Zampieri, M
Masciarelli, S
D'Erme, M
Ferraro, A
Mattia, E
机构
[1] Univ Roma La Sapienza, Dept Publ Hlth Sci, Rome, Italy
[2] Univ Roma La Sapienza, Dept Biochem Sci, Rome, Italy
来源
FEBS LETTERS | 2003年 / 547卷 / 1-3期
关键词
Epstein Barr virus; nuclear matrix; S/MAR; cross-linking;
D O I
10.1016/S0014-5793(03)00690-2
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
During latency, Epstein Barr virus (EBV) genome, as an episome, is attached to the nuclear matrix (NM) via the latent origin of replication ori P. Within this element, we have found that a region, 580 bp long, encompassing the replicator DS element, shows the strongest affinity for the NM. In addition, by cross-linking with cis-diamminedichloroplatinum, we have identified two NM proteins with an apparent molecular weight of 85 and 60 kDa that, with high affinity and specificity, bind ori P. These proteins are not induced by EBV infection, but their interaction with ori P is lost upon induction of EBV lytic cycle. These data strongly suggest that the binding of ori P to specific components of the NM is required for EBV latent replication. (C) 2003 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:119 / 124
页数:6
相关论文
共 45 条
[1]   PREFERENTIAL, COOPERATIVE BINDING OF DNA TOPOISOMERASE-II TO SCAFFOLD-ASSOCIATED REGIONS [J].
ADACHI, Y ;
KAS, E ;
LAEMMLI, UK .
EMBO JOURNAL, 1989, 8 (13) :3997-4006
[2]   REPLICATION OF LATENT EPSTEIN-BARR-VIRUS GENOMES IN RAJI CELLS [J].
ADAMS, A .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1743-1746
[3]   DROSOPHILA SCAFFOLD-ATTACHED REGIONS BIND NUCLEAR SCAFFOLDS AND CAN FUNCTION AS ARS ELEMENTS IN BOTH BUDDING AND FISSION YEASTS [J].
AMATI, B ;
GASSER, SM .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) :5442-5454
[4]   DNA-SEQUENCE AND EXPRESSION OF THE B95-8 EPSTEIN-BARR VIRUS GENOME [J].
BAER, R ;
BANKIER, AT ;
BIGGIN, MD ;
DEININGER, PL ;
FARRELL, PJ ;
GIBSON, TJ ;
HATFULL, G ;
HUDSON, GS ;
SATCHWELL, SC ;
SEGUIN, C ;
TUFFNELL, PS ;
BARRELL, BG .
NATURE, 1984, 310 (5974) :207-211
[5]   IDENTIFICATION OF A NUCLEAR PROTEIN MATRIX [J].
BEREZNEY, R ;
COFFEY, DS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1974, 60 (04) :1410-1417
[6]  
Berezney R, 1995, INT REV CYTOL, V162A, P1
[7]   CHROMATIN DOMAIN SURROUNDING THE HUMAN INTERFERON-BETA GENE AS DEFINED BY SCAFFOLD-ATTACHED REGIONS [J].
BODE, J ;
MAASS, K .
BIOCHEMISTRY, 1988, 27 (13) :4706-4711
[8]   BIOLOGICAL SIGNIFICANCE OF UNWINDING CAPABILITY OF NUCLEAR MATRIX ASSOCIATING DNAS [J].
BODE, J ;
KOHWI, Y ;
DICKINSON, L ;
JOH, T ;
KLEHR, D ;
MIELKE, C ;
KOHWISHIGEMATSU, T .
SCIENCE, 1992, 255 (5041) :195-197
[9]   CHROMATIN STRUCTURE AND INDUCTION-DEPENDENT CONFORMATIONAL-CHANGES OF HUMAN INTERFERON-BETA GENES IN A MOUSE HOST-CELL [J].
BODE, J ;
PUCHER, HJ ;
MAASS, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 158 (02) :393-401
[10]   Human DNA replication initiation factors, ORC and MCM, associate with oriP of Epstein-Barr virus [J].
Chaudhuri, B ;
Xu, HZ ;
Todorov, I ;
Dutta, A ;
Yates, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10085-10089