THE DIF RESOLVASE LOCUS OF THE ESCHERICHIA-COLI CHROMOSOME CAN BE REPLACED BY A 33-BP SEQUENCE, BUT FUNCTION DEPENDS ON LOCATION

被引:38
作者
TECKLENBURG, M [1 ]
NAUMER, A [1 ]
NAGAPPAN, O [1 ]
KUEMPEL, P [1 ]
机构
[1] UNIV COLORADO, DEPT MOLEC CELLULAR & DEV BIOL, BOULDER, CO 80309 USA
关键词
TERMINUS; DELETION; INVERSION;
D O I
10.1073/pnas.92.5.1352
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The dif locus (deletion-induced filamentation) of Escherichia coli is a resolvase site, located in the terminus region of the chromosome, that reduces chromosome multimers to monomers. In strains in which this site has been deleted, a fraction of the cells is filamentous, has abnormal nucleoid structure, and exhibits elevated levels of the SOS repair system. We have demonstrated that a 33-bp sequence, which is sufficient for RecA-independent recombination and which shows similarity to the cer site of pColE1, suppresses the Dif phenotype when inserted in the terminus region. Flanking sequences were not required, since suppression occurred in strains in which dif as well as 12 kb or 173 kb of DNA had been deleted. However, location was important, and insertions at a site 118 kb away from the normal site did not suppress the Dif phenotype. These sites mere otherwise still functional, and they exhibited wild-type levels of RecA-independent recombination with dif-containing plasmids and recombined with other chromosomal dif sites to cause deletions and inversions. It is proposed that the functions expressed by a dif site depend on chromosome location and structure, and analysis of these functions provides a way to examine the structure of the terminus region.
引用
收藏
页码:1352 / 1356
页数:5
相关论文
共 25 条
[1]   THE ROLE OF TOPOISOMERASE-IV IN PARTITIONING BACTERIAL REPLICONS AND THE STRUCTURE OF CATENATED INTERMEDIATES IN DNA-REPLICATION [J].
ADAMS, DE ;
SHEKHTMAN, EM ;
ZECHIEDRICH, EL ;
SCHMID, MB ;
COZZARELLI, NR .
CELL, 1992, 71 (02) :277-288
[2]  
BERG BL, 1990, GENETICS, V125, P691
[3]  
BLAKELY G, 1991, NEW BIOL, V3, P789
[4]   2 RELATED RECOMBINASES ARE REQUIRED FOR SITE-SPECIFIC RECOMBINATION AT DIF AND CER IN ESCHERICHIA-COLI K12 [J].
BLAKELY, G ;
MAY, G ;
MCCULLOCH, R ;
ARCISZEWSKA, LK ;
BURKE, M ;
LOVETT, ST ;
SHERRATT, DJ .
CELL, 1993, 75 (02) :351-361
[5]  
CLERGET M, 1991, NEW BIOL, V3, P780
[6]   RECOMBINATION AT COLE1 CER REQUIRES THE ESCHERICHIA-COLI XERC GENE-PRODUCT, A MEMBER OF THE LAMBDA-INTEGRASE FAMILY OF SITE-SPECIFIC RECOMBINASES [J].
COLLOMS, SD ;
SYKORA, P ;
SZATMARI, G ;
SHERRATT, DJ .
JOURNAL OF BACTERIOLOGY, 1990, 172 (12) :6973-6980
[7]   PLASMID PSC101 HARBORS A RECOMBINATION SITE, PSI, WHICH IS ABLE TO RESOLVE PLASMID MULTIMERS AND TO SUBSTITUTE FOR THE ANALOGOUS CHROMOSOMAL ESCHERICHIA-COLI SITE DIF [J].
CORNET, F ;
MORTIER, I ;
PATTE, J ;
LOUARN, JM .
JOURNAL OF BACTERIOLOGY, 1994, 176 (11) :3188-3195
[8]   CHROMOSOME PARTITION IN ESCHERICHIA-COLI REQUIRES POSTREPLICATION PROTEIN-SYNTHESIS [J].
DONACHIE, WD ;
BEGG, KJ .
JOURNAL OF BACTERIOLOGY, 1989, 171 (10) :5405-5409
[9]   NEW METHOD FOR GENERATING DELETIONS AND GENE REPLACEMENTS IN ESCHERICHIA-COLI [J].
HAMILTON, CM ;
ALDEA, M ;
WASHBURN, BK ;
BABITZKE, P ;
KUSHNER, SR .
JOURNAL OF BACTERIOLOGY, 1989, 171 (09) :4617-4622
[10]  
Helmstetter CE., 1987, ESCHERICHIA COLI SAL, P1594