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本课件为《分子生物学》第12章复制子（The replicon），依据 Gene VII 教材编排，沿Origins can be、The bacterial等小节推进，讲解本章核心概念与分子机制，配逐页图示与文字版。
Chapter 12 The replicon
Replicon is a unit of the genome in which DNA is replicated; contains an origin for initiation of replication.
Replicon is a unit of the genome in which DNA is replicated; contains an origin for initiation of replication.
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Figure 11.2 Several types of independent genetic units exist in bacteria.
Replication fork is the point at which strands of parental duplex DNA are separated so that replication can proceed.
Figure 12.1 Replicated DNA is seen as a replication eye flanked by nonreplicated DNA.
Figure 12.2 Replicons may be unidirectional or bidirectional, depending on whether one or two replication forks are formed at the origin.
Figure 12.3 A replication eye forms a theta structure in circular DNA.
Figure 12.4 The replication eye becomes larger as the replication forks proceed along the replicon. Note that the "eye" becomes larger than the nonreplicated segment. The two sides of the eye can be defined because they are both the same length. Photograph kindly provided by Bernard Hirt.
Figure 12.5 Different densities of radioactive labeling can be used to distinguish unidirectional and bidirectional replication.
Figure 12.6 The position of the origin and the number of replicating forks determine the shape of a replicating restriction fragment, which can be followed by its electrophoretic path (solid line). The dashed line shows the path for a linear DNA.
Figure 12.7 Replication termini in E. coli are located beyond the point at which the replication forks actually meet.
Figure 12.7 Replication termini in E. coli are located beyond the point at which the replication forks actually meet.
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S phase is the restricted part of the eukaryotic cell cycle during which synthesis of DNA occurs.
Figure 12.5 Different densities of radioactive labeling can be used to distinguish unidirectional and bidirectional replication.
Figure 12.6 The position of the origin and the number of replicating forks determine the shape of a replicating restriction fragment, which can be followed by its electrophoretic path (solid line). The dashed line shows the path for a linear DNA.
Figure 12.8 Measuring the size of the replicon requires a stretch of DNA in which adjacent replicons are active.
Figure 12.9 Replication forks are organized into foci in the nucleus. Cells were labeled with BrdU. The left most panel was stained with propidium iodide to identify bulk DNA. The right panel was stained using an antibody to BrdU to identify replicating DNA.
12.4 Each eukaryotic chromosome contains many replicons
Figure 12.10 An ARS extends for ~50 bp and includes a consensus sequence (A) and additional elements (B1-B3).
D loop is a region within mitochondrial DNA in which a short stretch of RNA is paired with one strand of DNA, displacing the original partner DNA strand in this region. The same term is used also to describe the displacement of a region of one strand of duplex DNA by a single-stranded invader in the reaction catalyzed by RecA protein.
Figure 12.11 The D loop maintains an opening in mammalian mitochondrial DNA, which has separate origins for the replication of each strand.
Strand displacement is a mode of replication of some viruses in which a new DNA strand grows by displacing the previous (homologous) strand of the duplex.
Figure 12.12 Replication could run off the 3end of a newly synthesized linear strand, but could it initiate at a 5end?.
Figure 12.13 Adenovirus DNA replication is initiated separately at the two ends of the molecule and proceeds by strand displacement.
Figure 12.14 The 5terminal phosphate at each end of adenovirus DNA is covalently linked to serine in the 55 kD Ad-binding protein.
Figure 12.15 Adenovirus terminal protein binds to the 5end of DNA and provides a C-OH end to prime synthesis of a new DNA strand.
Rolling circle is a mode of replication in which a replication fork proceeds around a circular template for an indefinite number of revolutions; the DNA strand newly synthesized in each revolution displaces the strand synthesized in the previous revolution, giving a tail containing a linear series of sequences complementary to the circular template strand.
Figure 12.16 The rolling circle generates a multimeric single-stranded tail.
Figure 12.17 A rolling circle appears as a circular molecule with a linear tail by electron microscopy.
Figure 12.18 Rolling circles can be used for varying purposes, depending on the fate of the displaced tail. Cleavage at unit length generates monomers, which can be converted to duplex and circular forms. Cleavage of multimers generates a series of tandemly repeated copies of the original unit. Note that the conversion to double-stranded form could occur earlier, before the tail is cleaved from the rolling circle.
Figure 12.19 fX174 RF DNA is a template for synthesizing single-stranded viral circles. The A protein remains attached to the same genome through indefinite revolutions, each time nicking the origin on the viral (+) strand and transfer ring to the new 5end. At the same time, the released viral strand is circularized.
Figure 12.20 The tra region of the F plasmid contains the genes needed for bacterial conjugation.
Figure 12.21 Mating bacteria are initially connected when donor F pili contact the recipient bacterium.
Figure 12.22 Transfer of DNA occurs when the F factor is nicked at oriT and a single strand is led by the 5end into the recipient. Only one unit length is transferred. Complementary strands are synthesized to the single strand remaining in the donor and to the strand transferred into the recipient.
Figure 12.16 The rolling circle generates a multimeric single-stranded tail.
Figure 12.23 Transfer of chromosomal DNA occurs when an integrated F factor is nicked at oriT. Transfer of DNA starts with a short sequence of F DNA and continues until prevented by loss of contact between the bacteria.
Multiforked chromosome(in bacterium) has more than one replication fork, because a second initiation has occurred before the first cycle of replication has been completed.
Figure 12.24 The fixed interval of 60 minutes between initiation of replication and cell division produces multiforked chromosomes in rapidly growing cells. Note that only the replication forks moving in one direction are shown; actually the chromosome is replicated symmetrically by two sets of forks moving in opposite directions on circular chromosomes.
Figure 12.24 The fixed interval of 60 minutes between initiation of replication and cell division produces multiforked chromosomes in rapidly growing cells. Note that only the replication forks moving in one direction are shown; actually the chromosome is replicated symmetrically by two sets of forks moving in opposite directions on circular chromosomes.
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Septum constitutes the material that forms in the center of a bacterium to divide it into two daughter cells at the end of a division cycle.
Figure 12.25 Duplication and displacement of the periseptal annulus give rise to the formation of a septum that divides the cell.
Figure 12.26 Attachment of bacterial DNA to the membrane could provide a mechanism for segregation.
Minicell is an anucleate bacterial (E. coli) cell produced by a division that generates a cytoplasm without a nucleus.
Figure 12.27 Failure of cell division generates multinucleated filaments. Photograph kindly provided by Sota Hiraga.
Figure 12.28 E. coli generate anucleate cells when chromosome segregation fails. Cells with chromosomes stain blue; daughter cells lacking chromosomes have no blue stain. This field shows cells of the mukB mutant; both normal and abnormal div is ions can be seen.
Figure 12.25 Duplication and displacement of the periseptal annulus give rise to the formation of a septum that divides the cell.
Figure 12.29 MinC/D is a division inhibitor, whose action is confined to the polar sites by MinE.
Figure 12.26 Attachment of bacterial DNA to the membrane could provide a mechanism for segregation.
Figure 12.30 A common segregation system consists of genes parA and parB and the target site parS.
Figure 9.23 Sporul at ion involves successive changes in the sigma factors that control the initiation specificity of RNA polymerase. The cascades in the forespore (left) and the mother cell (right) are related by signals passed across the septum (indicated by horizontal arrows).
12.14 Multiple systems ensure plasmid survival in bacterial popul at ions Figure 12.31 Intermolecular recombination merges monomers into dimers, and intr a molecular recombination releases individual units from oligomers.
12.14 Multiple systems ensure plasmid survival in bacterial popul at ions Figure 12.32 Plasmids may ensure that bacteria cannot live without them by synthesizing a long-lived killer and a short-lived antidote.
12.14 Multiple systems ensure plasmid survival in bacterial popul at ions Figure 12.30 A common segregation system consists of genes parA and parB and the target site parS.
12.14 Multiple systems ensure plasmid survival in bacterial popul at ions Figure 12.26 Attachment of bacterial DNA to the membrane could provide a mechanism for segregation.
Compatibility groupof plasmids contains members unable to coexist in the same bacterial cell.
12.15 Plasmid incompatibility is connected with copy number Figure 12.33 Two plasmids are incompatible (they belong to the same compatibility group) if their origins cannot be distinguished at the stage of initiation. The same model could apply to segregation.
12.15 Plasmid incompatibility is connected with copy number Figure 12.34 Replication of ColE1 DNA is initiated by cleaving the primer RNA to generate a 3-OH end. The primer forms a persistent hybrid in the origin region.
12.15 Plasmid incompatibility is connected with copy number Figure 12.35 The sequence of RNA I is complementary to the 5region of primer RNA.
12.15 Plasmid incompatibility is connected with copy number Figure 12.36 Base pairing with RNA I may change the secondary structure of the primer RNA sequence and thus prevent cleavage from generating a 3-OH end.
12.15 Plasmid incompatibility is connected with copy number Figure 12.37 Mutations in the region coding for RNA I and the primer precursor need not affect their ability to pair; but they may prevent pairing with the complementary RNA coded by a different plasmid.
1.The entire chromosome is replicated once for every cell division cycle. 2.Eukaryotic replication is (at least) an order of magnitude slower than bacterial replication. 3.The minimal E. coli origin consists of ~245 bp and initiates bidirectional replication. 4.The rolling circle is an alternative form of replication for circular DNA molecules in which an origin is nicked to provide a priming end. 5.Rolling circles are used to replicate some phages.
Summary
6.Rolling circles also are involved in bacterial conjugation, when an F plasmid is transferred from a donor to a recipient cell, following the initiation of contact between the cells by means of the F-pili. 7.A fixed time of 40 minutes is required to replicate the E. coli chromosome and a further 20 minutes is required before the cell can divide. 8.Segregation involves additional sequences that have not yet been characterized. 9.Plasmids have a variety of systems that ensure or assist partiti on, and an individual plasmid may carry systems of several types.
Summary
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