ENHANCEMENT OF DNA-REPLICATION BY TRANSCRIPTION FACTORS NFI AND NFIII/OCT-1 DEPENDS CRITICALLY ON THE POSITIONS OF THEIR BINDING-SITES IN THE ADENOVIRUS ORIGIN OF REPLICATION

被引:18
作者
COENJAERTS, FEJ [1 ]
DEVRIES, E [1 ]
PRUIJN, GJM [1 ]
VANDRIEL, W [1 ]
BLOEMERS, SM [1 ]
VANDERLUGT, NMT [1 ]
VANDERVLIET, PC [1 ]
机构
[1] STATE UNIV UTRECHT,PHYSIOL CHEM LAB,VONDELLAAN 24A,3521 GG UTRECHT,NETHERLANDS
关键词
NFI; NFIII; OCT-1; ADENOVIRUS; DNA REPLICATION;
D O I
10.1016/0167-4781(91)90037-M
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
The origin of DNA replication of many human adenoviruses is composed of a highly conserved core origin and an auxiliary region, containing the binding sites for NFI and NFIII/Oct-1. We examined enhancement of DNA replication in vitro by the purified functional DNA-binding domains of NFI (NFI-BD) and NFIII/Oct-1 (the POU domain), using origins in which the positions of the binding sites for these proteins were transposed. Insertion or deletion of two or three base pairs between the core origin and the NFI binding site resulted in a 3-5-fold decrease of stimulation, whereas larger insertions gradually reduced the stimulation further. Mutants in which the NFI binding site was separated approximately one or two helical turns from the core origin by AT-rich sequences could still be stimulated by NFI. In contrast, insertion of two or more base pairs between the NFI and NFIII/Oct-1 binding sites abolished stimulation by NFIII/Oct-1 almost completely. Furthermore, stimulation by this protein was lost when the Ad2 NFIII/Oct-1 binding site was transposed to a position closer to the core origin, destroying the NFI binding site. This shows that the position of the NFIII/Oct-1 binding site is essential for stimulation. Models to explain these position-dependent effects on stimulation are discussed.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 40 条
[1]  
ADHYA S, 1986, J BIOL CHEM, V261, P3339
[2]   OBP100 BINDS REMARKABLY DEGENERATE OCTAMER MOTIFS THROUGH SPECIFIC INTERACTIONS WITH FLANKING SEQUENCES [J].
BAUMRUKER, T ;
STURM, R ;
HERR, W .
GENES & DEVELOPMENT, 1988, 2 (11) :1400-1413
[3]  
BOSHER H, 1990, NEW BIOL, V2, P1083
[4]   SYNTHETIC CURVED DNA-SEQUENCES CAN ACT AS TRANSCRIPTIONAL ACTIVATORS IN ESCHERICHIA-COLI [J].
BRACCO, L ;
KOTLARZ, D ;
KOLB, A ;
DIEKMANN, S ;
BUC, H .
EMBO JOURNAL, 1989, 8 (13) :4289-4296
[5]  
CHALLBERG MD, 1989, ANNU REV BIOCHEM, V58, P671
[6]  
CHEN M, 1990, J BIOL CHEM, V265, P18634
[7]   TRANSCRIPTIONAL ELEMENTS AS COMPONENTS OF EUKARYOTIC ORIGINS OF DNA-REPLICATION [J].
DEPAMPHILIS, ML .
CELL, 1988, 52 (05) :635-638
[8]   CONTACTPOINT ANALYSIS OF THE HELA NUCLEAR FACTOR-I RECOGNITION SITE REVEALS SYMMETRICAL BINDING AT ONE SIDE OF THE DNA HELIX [J].
DEVRIES, E ;
VANDRIEL, W ;
VANDENHEUVEL, SJL ;
VANDERVLIET, PC .
EMBO JOURNAL, 1987, 6 (01) :161-168
[9]   ADENOVIRUS DNA-REPLICATION INVITRO - SITE-DIRECTED MUTAGENESIS OF THE NUCLEAR FACTOR-I BINDING-SITE OF THE AD2 ORIGIN [J].
DEVRIES, E ;
VANDRIEL, W ;
TROMP, M ;
VANBOOM, J ;
VANDERVLIET, PC .
NUCLEIC ACIDS RESEARCH, 1985, 13 (13) :4935-4952
[10]   STRINGENT SPACING REQUIREMENTS FOR TRANSCRIPTION ACTIVATION BY CRP [J].
GASTON, K ;
BELL, A ;
KOLB, A ;
BUC, H ;
BUSBY, S .
CELL, 1990, 62 (04) :733-743