Replication of a unit-copy plasmid F in the bacterial cell cycle: a replication rate function analysis

被引:8
作者
Morrison, PF
Chattoraj, DK [1 ]
机构
[1] NCI, Biochem Lab, NIH, Bethesda, MD 20892 USA
[2] NIH, Div Bioengn & Phys Sci, ORS, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.plasmid.2004.04.001
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
For stability.. the replication of unit-copy plasmids ought to occur by a highly controlled process. We have characterized the replication dynamics of a unit-copy plasmid F by a replication rate function defined as the probability per unit age interval of the cell cycle that a plasmid will initiate replication. Analysis of baby-machine data [J. Bacteriol. 170 (1988) 1380 - J. Bacteriol. 179 (1997) 1393] by stochastics that make no detailed reference to underlying mechanism revealed that this rate function increased monotonically over the cell cycle with rapid increase near cell division. This feature is highly suggestive of a replication control mechanism that is designed to force most plasmids to replicate before cells undergo division. The replication rate function is developed anew from a mechanistic model incorporating the hypotheses that initiators are limiting and that steric hindrance of origins by handcuffing control initiation of replication. The model is based on correctly folded initiator protein monomers arising from an inactive dimer pool via chaperones in limiting amounts, their random distribution to high affinity sites (iterons) at the origin (ori) and an outside focus (incC), the statistical mechanics of bound monomer participation in pairing the two loci (cis-handcuffing), and initiation probability as proportional to the number of non-handcuffed ori-saturated plasmids. Provided cis-handcuffing is present, this model closely accounts for the shape of the replication rate function derived from experiment, and reproduces the observation that replication occurs throughout the cell cycle. Present concepts of iteron-based molecular mechanisms thus appear capable of yielding a quantitative description of unit-copy-number plasmid replication dynamics. Published by Elsevier Inc.
引用
收藏
页码:13 / 30
页数:18
相关论文
共 26 条
[1]   Control of P1 plasmid replication by iterons [J].
Abeles, AL ;
Reaves, LD ;
YoungrenGrimes, B ;
Austin, SJ .
MOLECULAR MICROBIOLOGY, 1995, 18 (05) :903-912
[2]   RANDOM DIFFUSION CAN ACCOUNT FOR TOPA-DEPENDENT SUPPRESSION OF PARTITION DEFECTS IN LOW-COPY-NUMBER PLASMIDS [J].
AUSTIN, SJ ;
EICHORN, BG .
JOURNAL OF BACTERIOLOGY, 1992, 174 (16) :5190-5195
[3]   Control of plasmid DNA replication by iterons: no longer paradoxical [J].
Chattoraj, DK .
MOLECULAR MICROBIOLOGY, 2000, 37 (03) :467-476
[4]   MINI-P1 PLASMID REPLICATION - THE AUTOREGULATION-SEQUESTRATION PARADOX [J].
CHATTORAJ, DK ;
MASON, RJ ;
WICKNER, SH .
CELL, 1988, 52 (04) :551-557
[5]   Structural changes in RepA, a plasmid replication initiator, upon binding to origin DNA [J].
Díaz-López, T ;
Lages-Gonzalo, M ;
Serrano-López, A ;
Alfonso, C ;
Rivas, G ;
Díaz-Orejas, R ;
Giraldo, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (20) :18606-18616
[6]   REPLICATION OF THE BROAD-HOST-RANGE PLASMID RK2 - DIRECT MEASUREMENT OF INTRACELLULAR CONCENTRATIONS OF THE ESSENTIAL TRFA REPLICATION PROTEINS AND THEIR EFFECT ON PLASMID COPY NUMBER [J].
DURLAND, RH ;
HELINSKI, DR .
JOURNAL OF BACTERIOLOGY, 1990, 172 (07) :3849-3858
[7]   A conformational switch between transcriptional repression and replication initiation in the RepA dimerization domain [J].
Giraldo, R ;
Fernández-Tornero, C ;
Evans, PR ;
Díaz-Orejas, R ;
Romero, A .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (07) :565-571
[8]   Replication and segregation of a miniF plasmid during the division cycle of Escherichia coli [J].
Helmstetter, CE ;
Thornton, M ;
Zhou, P ;
Bogan, JA ;
Leonard, AC ;
Grimwade, JE .
JOURNAL OF BACTERIOLOGY, 1997, 179 (04) :1393-1399
[9]   The RepA protein of plasmid pSC101 controls Escherichia coli cell division through the SOS response [J].
Ingmer, H ;
Miller, C ;
Cohen, SN .
MOLECULAR MICROBIOLOGY, 2001, 42 (02) :519-526
[10]   The localized melting of mini-F origin by the combined action of the mini-F initiator protein (RepE) and HU and DnaA of Escherichia coli [J].
Kawasaki, Y ;
Matsunaga, F ;
Kano, Y ;
Yura, T ;
Wada, C .
MOLECULAR & GENERAL GENETICS, 1996, 253 (1-2) :42-49