Measuring chromosome dynamics on different time scales using resolvases with varying half-lives

被引:47
作者
Stein, RA [1 ]
Deng, S [1 ]
Higgins, NP [1 ]
机构
[1] Univ Alabama Birmingham, Dept Biochem & Mol Genet, Birmingham, AL 35294 USA
关键词
D O I
10.1111/j.1365-2958.2005.04588.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 bacterial chromosome is organized into multiple independent domains, each capable of constraining the plectonemic negative supercoil energy introduced by DNA gyrase. Different experimental approaches have estimated the number of domains to be between 40 and 150. The site-specific resolution systems of closely related transposons Tn3 and y delta are valuable tools for measuring supercoil diffusion and analysing bacterial chromosome dynamics in vivo. Once made, the wild-type resolvase persists in cells for time periods greater than the cell doubling time. To examine chromosome dynamics over shorter time frames that are more closely tuned to processes like inducible transcription, we constructed a set of resolvases with cellular half-lives ranging from less than 5 min to 30 min. Analysing chromosomes on different time scales shows domain structure to be dynamic. Rather than the 150 domains detected with the Tn3 resolvase, wild-type cells measured over a 10 min time span have more than 400 domains per genome equivalent, and some gyrase mutants exceed 1000.
引用
收藏
页码:1049 / 1061
页数:13
相关论文
共 73 条
[41]   SUPERHELICAL TORSION IN CELLULAR DNA RESPONDS DIRECTLY TO ENVIRONMENTAL AND GENETIC-FACTORS [J].
MCCLELLAN, JA ;
BOUBLIKOVA, P ;
PALECEK, E ;
LILLEY, DMJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (21) :8373-8377
[42]   Multiple pathways process stalled replication forks [J].
Michel, B ;
Grompone, G ;
Florès, MJ ;
Bidnenko, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :12783-12788
[43]   CHROMOSOMAL SUPERCOILING IN ESCHERICHIA-COLI [J].
MILLER, WG ;
SIMONS, RW .
MOLECULAR MICROBIOLOGY, 1993, 10 (03) :675-684
[44]   THE ENERGETICS OF THE B-Z TRANSITION IN DNA [J].
MIRKIN, SM ;
LYAMICHEV, VI ;
KUMAREV, VP ;
KOBZEV, VF ;
NOSIKOV, VV ;
VOLOGODSKII, AV .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 1987, 5 (01) :79-88
[45]   In vivo supercoiling of plasmid and chromosomal DNA in an Escherichia coli hns mutant [J].
Mojica, FJM ;
Higgins, CF .
JOURNAL OF BACTERIOLOGY, 1997, 179 (11) :3528-3533
[46]   THE MECHANISM OF CRUCIFORM FORMATION IN SUPERCOILED DNA - INITIAL OPENING OF CENTRAL BASEPAIRS IN SALT-DEPENDENT EXTRUSION [J].
MURCHIE, AIH ;
LILLEY, DMJ .
NUCLEIC ACIDS RESEARCH, 1987, 15 (23) :9641-9654
[47]  
Niki H, 2000, GENE DEV, V14, P212
[48]   Path of DNA within the Mu transpososome: Transposase interactions bridging two Mu ends and the enhancer trap five DNA supercoils [J].
Pathania, S ;
Jayaram, M ;
Harshey, RM .
CELL, 2002, 109 (04) :425-436
[49]   A DNA GYRASE-BINDING SITE AT THE CENTER OF THE BACTERIOPHAGE MU GENOME IS REQUIRED FOR EFFICIENT REPLICATIVE TRANSPOSITION [J].
PATO, ML ;
HOWE, MM ;
HIGGINS, NP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :8716-8720
[50]   The Mu strong gyrase-binding site promotes efficient synapsis of the prophage termini [J].
Pato, ML ;
Banerjee, M .
MOLECULAR MICROBIOLOGY, 1996, 22 (02) :283-292