A PROTEIN THAT BINDS TO THE P1 ORIGIN CORE AND THE ORIC 13MER REGION IN A METHYLATION-SPECIFIC FASHION IS THE PRODUCT OF THE HOST SEQA GENE

被引:91
作者
BRENDLER, T [1 ]
ABELES, A [1 ]
AUSTIN, S [1 ]
机构
[1] NCI,FREDERICK CANC RES & DEV CTR,ABL BASIC RES PROGRAM,CHROMOSOME BIOL LAB,FREDERICK,MD 21702
关键词
METHYLATION; ORIC; P; 1; ORIR; REPLICATION; SEQUESTRATION;
D O I
10.1002/j.1460-2075.1995.tb00080.x
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 P1 plasmid replication origin P1oriR is controlled by methylation of four GATC adenine methylation sites within heptamer repeats, A comparable (13mer) region is present in the host origin, oriC. The two origins show comparable responses to methylation; negative control by recognition of hemimethylated DNA (sequestration) and a positive requirement for methylation for efficient function, We have isolated a host protein that recognizes the P1 origin region only when it is isolated from a strain proficient for adenine methylation, The substantially purified 22 kDa protein also binds to the 13mer region of oriC in a methylation-specific fashion, It proved to be the product of the seqA gene that acts in the negative control of oriC by sequestration, We conclude that the role of the SeqA protein in sequestration is to recognize the methylation state of P1oriR and oriC by direct DNA binding, Using synthetic substrates we show that SeqA binds exclusively to the hemimethylated forms of these origins, forms that are the immediate products of replication in a methylation-proficient strain. We also show that the protein can recognize sequences with multiple GATC sites, irrespective of the surrounding sequence, The basis for origin specificity is primarily the persistence of hemimethylated forms that are over-represented in the natural DNA preparations relative to controls.
引用
收藏
页码:4083 / 4089
页数:7
相关论文
共 26 条
[1]   EVIDENCE FOR 2 LEVELS OF CONTROL OF P1 ORIR AND HOST ORIC REPLICATION ORIGINS BY DNA ADENINE METHYLATION [J].
ABELES, A ;
BRENDLER, T ;
AUSTIN, S .
JOURNAL OF BACTERIOLOGY, 1993, 175 (24) :7801-7807
[2]   P1 PLASMID REPLICATION REQUIRES METHYLATED DNA [J].
ABELES, AL ;
AUSTIN, SJ .
EMBO JOURNAL, 1987, 6 (10) :3185-3189
[3]   P1 PLASMID REPLICATION - REPLICON STRUCTURE [J].
ABELES, AL ;
SNYDER, KM ;
CHATTORAJ, DK .
JOURNAL OF MOLECULAR BIOLOGY, 1984, 173 (03) :307-324
[4]   METHYLATION OF GATC SITES IS REQUIRED FOR PRECISE TIMING BETWEEN ROUNDS OF DNA-REPLICATION IN ESCHERICHIA-COLI [J].
BAKKER, A ;
SMITH, DW .
JOURNAL OF BACTERIOLOGY, 1989, 171 (10) :5738-5742
[5]   THE ROLE OF DAM METHYLTRANSFERASE IN THE CONTROL OF DNA-REPLICATION IN ESCHERICHIA-COLI [J].
BOYE, E ;
LOBNEROLESEN, A .
CELL, 1990, 62 (05) :981-989
[6]   A MODEL FOR INITIATION AT ORIGINS OF DNA-REPLICATION [J].
BRAMHILL, D ;
KORNBERG, A .
CELL, 1988, 54 (07) :915-918
[7]   DUPLEX OPENING BY DNAA PROTEIN AT NOVEL SEQUENCES IN INITIATION OF REPLICATION AT THE ORIGIN OF THE ESCHERICHIA-COLI CHROMOSOME [J].
BRAMHILL, D ;
KORNBERG, A .
CELL, 1988, 52 (05) :743-755
[8]   CRITICAL SEQUENCES IN THE CORE OF THE P1 PLASMID REPLICATION ORIGIN [J].
BRENDLER, T ;
ABELES, A ;
AUSTIN, S .
JOURNAL OF BACTERIOLOGY, 1991, 173 (13) :3935-3942
[9]   ESCHERICHIA-COLI ORIC AND THE DNAA GENE PROMOTER ARE SEQUESTERED FROM DAM METHYLTRANSFERASE FOLLOWING THE PASSAGE OF THE CHROMOSOMAL REPLICATION FORK [J].
CAMPBELL, JL ;
KLECKNER, N .
CELL, 1990, 62 (05) :967-979