NUCLEAR FACTOR-I IS SPECIFICALLY TARGETED TO DISCRETE SUBNUCLEAR SITES IN ADENOVIRUS TYPE-2-INFECTED CELLS

被引:34
作者
BOSHER, J [1 ]
DAWSON, A [1 ]
HAY, RT [1 ]
机构
[1] UNIV ST ANDREWS,DEPT BIOCHEM & MICROBIOL,IRVINE BLDG,N ST,ST ANDREWS KY16 9AL,FIFE,SCOTLAND
关键词
D O I
10.1128/JVI.66.5.3140-3150.1992
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During the S phase of the eukaryotic cell cycle and in virus-infected cells, DNA replication takes place at discrete sites in the nucleus, although it is not clear how the proteins involved in the replicative process are directed to these sites. Nuclear factor I is a cellular, sequence-specific DNA-binding protein utilized by adenovirus type 2 to facilitate the assembly of a nucleoprotein complex at the viral origin of DNA replication. Immunofluorescence experiments reveal that in uninfected cells, nuclear factor I is distributed evenly throughout the nucleus. However, after a cell is infected with adenovirus type 2, the distribution of nuclear factor I is dramatically altered, being colocalized with the viral DNA-binding protein in a limited number of subnuclear sites which bromodeoxyuridine pulse-labeling experiments have identified as sites of viral DNA replication. Experiments with adenovirus type 4, which does not require nuclear factor I for viral DNA replication, indicate that although the adenovirus type 4 DNA-binding protein is localized to discrete nuclear sites, this does not result in the redistribution of nuclear factor I. Localization of nuclear factor I to discrete subnuclear sites is therefore likely to represent a specific targeting event that reflects the requirement for nuclear factor I in adenovirus type 2 DNA replication.
引用
收藏
页码:3140 / 3150
页数:11
相关论文
共 75 条
[1]  
ADHYA S, 1986, J BIOL CHEM, V261, P3339
[2]   NUCLEAR PROTEIN MATRIX - ASSOCIATION WITH NEWLY SYNTHESIZED DNA [J].
BEREZNEY, R ;
COFFEY, DS .
SCIENCE, 1975, 189 (4199) :291-293
[3]  
BOSHER J, 1990, New Biologist, V2, P1083
[4]   THE DNA-BINDING DOMAIN OF NUCLEAR FACTOR-I IS SUFFICIENT TO COOPERATE WITH THE ADENOVIRUS TYPE-2 DNA-BINDING PROTEIN IN VIRAL-DNA REPLICATION [J].
BOSHER, J ;
LEITH, IR ;
TEMPERLEY, SM ;
WELLS, M ;
HAY, RT .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :2975-2980
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   EXISTENCE OF 2 POPULATIONS OF CYCLIN PROLIFERATING CELL NUCLEAR ANTIGEN DURING THE CELL-CYCLE - ASSOCIATION WITH DNA-REPLICATION SITES [J].
BRAVO, R ;
MACDONALDBRAVO, H .
JOURNAL OF CELL BIOLOGY, 1987, 105 (04) :1549-1554
[7]   CYCLIN (PCNA, AUXILIARY PROTEIN OF DNA POLYMERASE-DELTA) IS A CENTRAL COMPONENT OF THE PATHWAY(S) LEADING TO DNA-REPLICATION AND CELL-DIVISION [J].
CELIS, JE ;
MADSEN, P ;
CELIS, A ;
NIELSEN, HV ;
GESSER, B .
FEBS LETTERS, 1987, 220 (01) :1-7
[8]  
CHALLBERG MD, 1989, ANNU REV BIOCHEM, V58, P671
[9]   TEMPLATE REQUIREMENTS FOR THE INITIATION OF ADENOVIRUS DNA-REPLICATION [J].
CHALLBERG, MD ;
RAWLINS, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (01) :100-104
[10]  
CHEN M, 1990, J BIOL CHEM, V265, P18634