Stability and nuclear distribution of mammalian replication protein A heterotrimeric complex

被引:56
作者
Dimitrova, DS [1 ]
Gilbert, DM [1 ]
机构
[1] SUNY Hlth Sci Ctr, Dept Biochem & Mol Biol, Syracuse, NY 13210 USA
关键词
RPA complex; detergent extraction; replication foci; cell nucleus; cell cycle;
D O I
10.1006/excr.1999.4770
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Replication protein A (RPA), a stable complex of three polypeptides, is the single-stranded DNA-binding protein essential for DNA replication in eukaryotic cells, Previous studies of the subcellular distribution and stability of the RPA heterotrimer during the mammalian cell cycle have produced conflicting results, Here, we present evidence that these inconsistencies can be accounted for by the presence of an extractable pool of soluble RPA within the nucleus. Indirect immunofluorescence experiments in both CHO and HeLa cells showed that all three RPA subunits associated specifically with sites of ongoing DNA synthesis, similar to the replication fork protein proliferating cell nuclear antigen. Furthermore, we found no evidence for disassembly of the chromatin-bound heterotrimeric RPA complex in vivo. Our results are consistent with a role for RPA in the initiation and elongation steps of replication, as previously defined in the viral in vitro replication systems. (C) 2000 Academic Press.
引用
收藏
页码:321 / 327
页数:7
相关论文
共 27 条
[1]   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
[2]  
BRENOTBOSC F, 1995, CHROMOSOMA, V103, P517, DOI 10.1007/BF00355316
[3]   REPLICATION FACTOR-A FROM SACCHAROMYCES-CEREVISIAE IS ENCODED BY 3 ESSENTIAL GENES COORDINATELY EXPRESSED AT S-PHASE [J].
BRILL, SJ ;
STILLMAN, B .
GENES & DEVELOPMENT, 1991, 5 (09) :1589-1600
[4]   REVERSAL OF TERMINAL DIFFERENTIATION AND CONTROL OF DNA-REPLICATION - CYCLIN-A AND CDK2 SPECIFICALLY LOCALIZE AT SUBNUCLEAR SITES OF DNA-REPLICATION [J].
CARDOSO, MC ;
LEONHARDT, H ;
NADALGINARD, B .
CELL, 1993, 74 (06) :979-992
[5]   The spatial position and replication timing of chromosomal domains are both established in early G1 phase [J].
Dimitrova, DS ;
Gilbert, DM .
MOLECULAR CELL, 1999, 4 (06) :983-993
[6]   Mcm2, but not RPA, is a component of the mammalian early G1-phase prereplication complex [J].
Dimitrova, DS ;
Todorov, IT ;
Melendy, T ;
Gilbert, DM .
JOURNAL OF CELL BIOLOGY, 1999, 146 (04) :709-722
[7]   IDENTIFICATION OF CELLULAR-COMPONENTS REQUIRED FOR SV40-DNA REPLICATION INVITRO [J].
FAIRMAN, M ;
PRELICH, G ;
TSURIMOTO, T ;
STILLMAN, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 951 (2-3) :382-387
[8]   CELLULAR FACTORS REQUIRED FOR MULTIPLE STAGES OF SV40 DNA-REPLICATION INVITRO [J].
FAIRMAN, MP ;
STILLMAN, B .
EMBO JOURNAL, 1988, 7 (04) :1211-1218
[9]   DEFINING ORIGINS OF REPLICATION IN MAMMALIAN-CELLS [J].
HAMLIN, JL ;
MOSCA, PJ ;
LEVENSON, VV .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1994, 1198 (2-3) :85-111
[10]  
KENNY MK, 1990, J BIOL CHEM, V265, P769