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Comparison of DNA Replication Termination in Bacillus subtilis and Escherichia coli

Termination sites in B.subtilis and E. coli

Chromosome map of the 4.6 Mb E.Coli genome indicating the location and orientation of Ter sites. The two groups of Ter sites are depicted in red and black respectively. An origin of replication (OriC) is also shown.
Chromosome map of the 4.6 Mb E.Coli genome indicating the location and orientation of Ter sites. The two groups of Ter sites are depicted in red and black respectively. An origin of replication (OriC) is also shown.

Many bacteria that have a circular chromosome utilise a bidirectional mechanism of DNA replication [1]. Replication proceeds from the OriC site in two directions and terminate at some point ~180° away. DNA replication in Gram-negative Escherichia coli and Gram-positive Bacillus subtilis terminates at discrete Ter sites. Ter sites block the movement of the replication fork when the replication fork approaches from one direction (the non-permissive direction) but not the other (permissive direction). Ter sites stall replication forks only when bound by proteins Tus in E.Coli and Replication Termination Protein (RTP) in B.subtilis [2]. This molecular “trap” restricts the meeting of the replication forks to a small region of the chromosome and may be necessary for orderly segregation of the daughter strands [3].

Ter sites in E.Coli

There are 10 Ter sites present in E.Coli [4]. TerC, TerB, TerF, TerG and TerJ are oriented to block the clockwise movement of replication forks whilst TerA, TerD, TerE, TerI and TerH block the anticlockwise movement of replication forks. Most of the replication forks are trapped in the region between TerC and TerA [5]. If the clockwise replication fork is delayed during DNA replication, termination occurs at TerA site. If the anticlockwise replication fork is delayed during DNA replication, termination occurs at TerC site.

Ter sites in E.Coli are 23 bp in length and are asymmetric. A comparison of all Ter sites revealed a consensus sequence (shown below) consisting of a highly conserved 13-bp core region and a strictly conserved GC6 base pair [6]. In the orientation shown, replication forks are blocked when travelling from the left and are unimpeded from the right. The nucleotides that interact with the Tus protein are shown in bold [7].

Ter sites in B.subtilis

Chromosome map of the 4.2 Mb B. Subtilis genome indicating the location and orientation of Ter sites. The two groups of Ter sites are depicted in red and black respectively. An origin of replication (OriC) is also shown
Chromosome map of the 4.2 Mb B. Subtilis genome indicating the location and orientation of Ter sites. The two groups of Ter sites are depicted in red and black respectively. An origin of replication (OriC) is also shown

There are nine Ter sites present in B.subtilis [8]. TerIX, TerV, TerIII and TerI are oriented to block the clockwise movement of replication forks whilst TerII, TerVIII, TerIV, TerVII and TerVI block the anticlockwise movement of replication forks. In B.subtilis, replication termination occurs mostly at TerI site because the anticlockwise replication fork takes longer to reach the termination region.

The TerI site is ~30 bp in length and consists of two overlapping half-sites: the core and auxiliary sequences [9]. The core sequence binds to RTP and this sequence-specific protein-DNA interaction allows the binding of a second RTP monomer to the auxiliary sequence [10]. The auxiliary sequence cannot bind to RTP in the absence of the core site. The TerI site is shown below with nucleotides involved in protein interactions highlighted in bold. In the orientation shown, replication forks are blocked when travelling from the right and are unimpeded from the left.

Comparison of Ter sites in E.coli and B.subtilis

Both E.coli and B.subtilis have a similar number of Ter sites. However, the Ter sites do not show any sequence similarity [11]. The Ter sites in E.coli cover a large proportion of the genome with some sites closer to the origin of replication than the site of strand segregation. In contrast, the Ter sites in "B.subtilis" are clustered together in a small region of the chromosome close to the site of strand segregation.

Structures of the Replication Termination Proteins

Tus

The Tus protein consists of 308 amino acids with a mass of 35.7 kDa and pI of 7.5 [12]. Tus forms a unique structural motif and has three distinct structural regions: two α-helical regions and a central β-sheet structure which forms the central cleft [13]. The protein is composed of 35% α-helix and 28% β-sheet. The secondary structure of the RTP molecule and its functions are listed in a table below:



Tus exists as a monomer in solution as shown by gel filtration experiments [14].The tertiary structure of the protein can be seen in complex with DNA below (see section “Mechanisms of polar arrest”). A crystal structure on its own has not been isolated as yet. A number of important DNA-protein and protein-protein interactions are listed in a table below [15]:


RTP

Structure of RTP protein homodimer in solution

Drag the structure with the mouse to rotate

RTP is a homodimer of subunit molecular weight of 14.5 kDa. The protein belongs to the “winged helix” family of proteins. Each monomer consists of 122 amino acid residues making up four α-helices, three β-strands, an extended loop and an unstructured N-terminal arm [16]. The protein is made of approximately 56% α-helix and 12% β-sheet. The secondary structure of the RTP molecule and its functions are listed in a table below:



The tertiary structure of RTP protein in solution is shown to the right [17]. A number of important DNA-protein [18] and protein-protein interactions are listed in a table below:


Comparison of Tus and RTP Protein Structures

Both Tus and RTP bind to their respective Ter sites on the bacterial chromosome and induce a direction-dependent replication fork arrest. However, rather surprisingly, the proteins do not have a common structural domain [19]. The Tus protein is a large asymmetric monomer that utilises mainly the β-sheet conformation to make specific interactions with DNA. In contrast, RTP binds to DNA as a symmetric homodimer and utilises mainly the α-helix conformation to make specific interactions with DNA.

In summary, whilst the two replication termination systems appear to share a common biological function, they do not share any DNA-binding sequence or structural homology. This strongly suggests an independent evolution of these systems.

Mechanisms of Polar Arrest

RTP

Structure of RTP complexed with a native RTP B site

Drag the structure with the mouse to rotate

The ability of RTP to induce polar fork arrest in B. subtilis poses a problem, namely, how does a symmetrical dimer block the replication fork? Early analysis of the B. subtilis ter sites revealed two RTP binding sites; a high affinity core site (B site) and a low affinity auxiliary site (A site)[20] . Mutagenic studies noted that generally contrahelicase activity was inversely correlated with binding affinity. However, some mutant forms were also found that showed no loss in DNA binding affinity despite a partial or complete loss in contrahelicase activity [20] [21].

In contrast, initial studies of RTP suggested that polar fork arrest was more complex than just DNA binding affinity. Separate mutagenesis studies showed that contrahelicase activity was dependent on dimer-dimer interactions between RTP molecules bound to the ter site [22]. Early studies of the protein structure predicted an asymmetrical complex would aid in the contrahelicase activity of RTP [23].

The issue of RTP and polar fork arrest was further complicated by Duggin et al. (2001) [24]. Using X-ray crystallography and NMR spectroscopy, the group found RTP formed a symmetric complex with a synthetic symmetric RTP B site (sRB). It was found that in the symmetrical form, extensive dimer interactions caused an increase in DNA binding affinity. This led to the Differential Binding Affinity (DBA) model. In this model, polar fork arrest is generated from the different affinities of the B site and A sites within the ter sequence, caused by altered contact bases within the two sites.

However, a series of experiments displayed the DBA model to be inadequate in explaining polar fork arrest. Dixon et al. (2005) showed sRB to be a poor terminator sequence in vitro, and found no correlation between fork arrest activity and the affinity of the proximal binding site [25]. Furthermore, Duggin (2006) showed that fusing peptides to the C-terminus of RTP could eliminate fork arrest activity, independent of size of amino acid sequence. The fusion of the peptide did not affect any DNA binding sites, though modelling suggests it would be able to contact the oncoming helicase [26].

Such lines of evidence led to a revaluation of the RTP-ter structure. Porter et al. (2007) determined the crystal structure of RTP with a native RTP B binding site (nRB) [27]. The paper found that the RTP dimer formed an asymmetric complex with nRB due to differences in downstream base contacts with the α3 recognition helix of RTP, creating a “wing-up”/”wing-down” dimer. Modelling of the structure showed the asymmetric complex would allow for extensive protein interactions between the RTP dimers. This underlies the cooperative binding that is crucial for fork arrest.

Taken together, these lines of evidence suggest that the polar fork arrest activity of RTP is dependent upon asymmetric contacts between RTP and the oncoming helicase, as mediated by the C-terminus [28].

Tus

Structure of the Tus-Ter B complex

Drag the structure with the mouse to rotate

Despite the polar fork arrest activity of the Tus-ter complex in E. coli, fundamental differences exist between it and the RTP-ter system found in B. subtilis. A basic difference is that Tus binds to ter as a monomer, rather than a dimer as is the case with RTP. This intrinsic asymmetry was predicted to be the basis of Tus’ polar fork arrest activity [28]. Furthermore, the crystal structures of RTP and Tus show vastly different tertiary protein folds and DNA binding motifs [29].

Early studies of the Tus fork arrest mechanism led to the formation of two separate models; the “clamp model” and the “interactions model” [30]. Structural analysis appeared to support the “clamp model”, showing Tus would bind tightly to DNA and sterically impede the replication fork with the αIV and αV helices [29]. However, some biochemical data seemed to indicate that a strong interaction occurred between Tus and the helicase. For instance, Bastia et al. (2001) showed that protein-protein interactions existed between Tus and DnaB using GST affinity chromatography and the yeast two-hybrid system. Furthermore, a series of mutants were identified with reduced Tus-DnaB interactions. These mutants were found to have substitutions within the L1 loop, and were shown to be deficient in fork arrest activity despite having higher DNA binding affinities [31]. However, much of the biochemical data is inconsistent, and Tus has been known to block fork arrest of unrelated helicases in a polar manner, both supporting the clamp model [30].

Cross et al. (2006) presented evidence for a modified clamp model [32]. Using a series of forked Tus-ter complexes, the group was able to show that fork progression from the non-permissive face leads to an increase in the stability of the complex. Further analysis of the forked complexes identified the C (6) residue in ter to be responsible for the locking via a base flipping mechanism. X-ray crystallography found the cytosine residue flipped into a binding pocket where it could hydrogen bond to Gly 149, His 144 and Leu 150 as well as forming hydrophobic interactions with Ile 79 and Phe 140. This “molecular mousetrap” was proposed to be the basis of fork arrest on the non-permissive face of Tus. Doubly forked complexes showed Tus was removed from the complex as DNA contacts were removed as the fork progressed on the permissive side, thus accounting for polarity.

However, recent evidence suggests specific interactions between Tus and the oncoming helicase may be the basis of polar fork arrest. Using a sliding helicase lacking strand separation activity, Bastia et al. (2008) showed Tus was able to block the sliding helicase on the non-permissive side even when the bases preceding C(6) were cross linked, and when the cytosine had been substituted. Hence, Tus was able to induce fork arrest without the base flipping mechanism. Furthermore, the group showed mutations in the L1 loop of Tus diminished its ability to arrest the sliding helicase [33].

Such evidence led to the establishment of a polar fork arrest model as seen in Bastia and Kaplan (2009) [28]. In this mechanism, a helicase approaching from the non-permissive face of the Tus-ter complex specifically interacts with Tus, whilst also being sterically impeded. In this mechanism, the base-flipping lock is used a fail-safe to ensure fork arrest. At the same time, a helicase approaching from the permissive face would be able to dislodge Tus due to the lack of protein-protein interactions.

Comparison between the mechanism of RTP and Tus

It is important to note that there is a degree of similarity between the polar arrest mechanisms of RTP and Tus. Both RTP and Tus require specific interactions with an oncoming helicase to induce fork arrest. In both cases, the polarity is established by a structural asymmetry. The idea that the two proteins have some basic mechanistic similarity is supported by the fact that RTP can arrest fork progression in E. coli, as can Tus in B. subtilis, albeit with far less efficiency [28].

However, this asymmetry is accomplished in distinct ways; Tus is an inherently asymmetric monomer, whereas RTP takes on an asymmetric conformation once bound to DNA. RTP also lacks any specific base locking mechanism, as seen by the flipping of C (6) in the Tus-ter complex. The fact that such different proteins can have similar functions whilst sharing some basic similarities in mechanism supports the idea of independent, convergent evolution of the systems in E. coli and B. subtilis [29].

Evolution of Tus and RTP systems

Basic representations of the phylogenetic trees of E. coli and B. subtilis.
Basic representations of the phylogenetic trees of E. coli and B. subtilis.

The study of Tus and the RTP systems reveal two systems which are key in the termination of replication in their hosts. However, while both systems induce termination, considerable differences in their structure and mechanisms of action strongly indicate that the systems evolved independently [34].

Studies of the Tus-ter system have revealed the evolutionary development of the Tus protein in E. Coli [35]. Although it has not been conserved identically in other species, there are organisms in which Tus-like proteins with high sequence homology have been identified [36]. A study by Rocklein and Kuempel (1992) specifically identified S. enterica serovar Typhimurium as carrying a termination protein very similar to Tus with 78% sequence homology [37]. More recent work has identified Tus-ter systems in Y. pestis and K. pneumonia both with sequence homologies over 50% [38]. Furthermore, there have been studies showing Tus-like genes which have been found in plasmids. Specifically two proteins R394 and rts-1 have been found by Koch in two IncT plasmids [39].

Likewise, the RTP system of B. subtilius has many homologues in other species. Griffiths et al., (1998) found RTP homologs in B.atrophaeus, b. amyloliquefaciens, B mojavensis and B. vallismortis. The sequences of RTP across the species were similar, but had up to 17.2% (B. atrophaeus) different bases. Yet despite this, only five amino acids were changed [40]. This contrasts with Tus evolution, which has shown much greater sequence differences.

The research on the development of RTP in Bacillus utilized phylogenetic trees mapping the different species [41]. This allowed the study to conclude that the RTP gene arose only after they had diverged from a common ancestor known as B. licheniformis [42]. A more recent study, mapped the entire genome of B. licheniformis confirming that no RTP like gene existed. Furthermore, no RTP gene has been found on B. Halodurans, narrowing the window in which RTP likely arose [43].

The Dif site: The real termination point?

Chromosome map of the 4.2 Mb B. Subtilis genome indicating the location and orientation of Ter sites. The two groups of Ter sites are depicted in red and black respectively. An origin of replication (OriC) is also shown along with the dif site
Chromosome map of the 4.2 Mb B. Subtilis genome indicating the location and orientation of Ter sites. The two groups of Ter sites are depicted in red and black respectively. An origin of replication (OriC) is also shown along with the dif site

In bacteria, replication of DNA occurs by the way of two replication forks diverging away from the origin of replication, oriC, before fusing and terminating at the terminus region. This system of replication is utilized in both E. Coli and B. Subtilis [44]. These prokaryotes utilize two distinct termination systems, Tus and RTP respectively, to end replication. One interesting feature of replication in organisms with circular chromosomes, is the formation of chromosomal multimers. These multimers must be resolved through the use of Xer recombinases at a site called Dif. Without this, daughter cells cannot be segregated[45].

Discussion on the importance of the Dif site intensified after a study by Hendrickson and Lawrence (2007) suggested that it was the main site of replication termination [46]. Prior to this, work suggested that numerous sites called Ter sites were the key to termination. These sites were arranged in a fashion such that they would “trap” and “arrest” termination in the terminus region [47]. However, Hendrickson and Lawrences' (2007) study utilized bioinformatics to suggest an alternative site of termination – the dif site. This inference was made by analysing G-C skew along the replication terminus. GC skew occurs because the lagging strand is more prone to mutation. Their cumulative plot of GC skewing demonstrated a peak where fork arrest occurred. The work by Hendrickson and Lawrence discovered such a peak very close to the dif site but not near any Ter site [48]. Indeed, this finding held true in 8 different bacteria studied. While they did not directly suggest that the dif site was where termination occurred, they proposed a secondary mechanism whereby XerC/D recombinases binding to the dif site blocked the replication fork [49].

Duggin and Bell (2009) challenged the earlier findings and addressed these by utilizing 2D agarose gels to examine cells undergoing different stages of replication. Their findings showed clearly that there was fork arrest at ter sites and that these occurred at a reliable frequency that depended on their natural efficiency to induce fork arrest [50]. Furthermore when they studied dif sites using a set of fragments of the dif region they found that there was no significant fork arrest anywhere near the dif region. Using these results they conclusively showed that the fork trap model with Ter sites was the most likely model of replication termination.

While the work performed in previous studies had studied bacteria, Duggin and Bell (2011) most recently performed a study on the Archaeon Sulfolobus solfataricus. This Archea shares a degree of similiarity with the previously studied bacteria in possessing a circular chromosome with replication origins and also possessing dif sites. Importantly however, the paper showed that the dif site is not implicated in termination and furthermore exists outside fork fusion zones [51].

References

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  2. ↑ Hill TM. Arrest of bacterial DNA replication. Annu Rev Microbiol. 1992;46:603-33. PMID:1444268 doi:http://dx.doi.org/10.1146/annurev.mi.46.100192.003131
  3. ↑ Duggin IG, Wake RG, Bell SD, Hill TM. The replication fork trap and termination of chromosome replication. Mol Microbiol. 2008 Dec;70(6):1323-33. Epub 2008 Oct 17. PMID:19019156 doi:10.1111/j.1365-2958.2008.06500.x
  4. ↑ Griffiths AA, Andersen PA, Wake RG. Replication terminator protein-based replication fork-arrest systems in various Bacillus species. J Bacteriol. 1998 Jul;180(13):3360-7. PMID:9642188
  5. ↑ Breier AM, Weier HU, Cozzarelli NR. Independence of replisomes in Escherichia coli chromosomal replication. Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):3942-7. Epub 2005 Feb 28. PMID:15738384 doi:10.1073/pnas.0500812102
  6. ↑ Kaplan DL, Bastia D. Mechanisms of polar arrest of a replication fork. Mol Microbiol. 2009 Apr;72(2):279-85. Epub 2009 Mar 4. PMID:19298368 doi:10.1111/j.1365-2958.2009.06656.x
  7. ↑ Neylon C, Kralicek AV, Hill TM, Dixon NE. Replication termination in Escherichia coli: structure and antihelicase activity of the Tus-Ter complex. Microbiol Mol Biol Rev. 2005 Sep;69(3):501-26. PMID:16148308 doi:10.1128/MMBR.69.3.501-526.2005
  8. ↑ Coskun-Ari FF, Hill TM. Sequence-specific interactions in the Tus-Ter complex and the effect of base pair substitutions on arrest of DNA replication in Escherichia coli. J Biol Chem. 1997 Oct 17;272(42):26448-56. PMID:9334221
  9. ↑ Lewis PJ, Ralston GB, Christopherson RI, Wake RG. Identification of the replication terminator protein binding sites in the terminus region of the Bacillus subtilis chromosome and stoichiometry of the binding. J Mol Biol. 1990 Jul 5;214(1):73-84. PMID:2115089 doi:http://dx.doi.org/10.1016/0022-2836(90)90147-E
  10. ↑ Carrigan CM, Pack RA, Smith MT, Wake RG. Normal terC-region of the Bacillus subtilis chromosome acts in a polar manner to arrest the clockwise replication fork. J Mol Biol. 1991 Nov 20;222(2):197-207. PMID:1960722
  11. ↑ Hill TM. Arrest of bacterial DNA replication. Annu Rev Microbiol. 1992;46:603-33. PMID:1444268 doi:http://dx.doi.org/10.1146/annurev.mi.46.100192.003131
  12. ↑ Neylon C, Kralicek AV, Hill TM, Dixon NE. Replication termination in Escherichia coli: structure and antihelicase activity of the Tus-Ter complex. Microbiol Mol Biol Rev. 2005 Sep;69(3):501-26. PMID:16148308 doi:10.1128/MMBR.69.3.501-526.2005
  13. ↑ Kamada K, Horiuchi T, Ohsumi K, Shimamoto N, Morikawa K. Structure of a replication-terminator protein complexed with DNA. Nature. 1996 Oct 17;383(6601):598-603. PMID:8857533 doi:http://dx.doi.org/10.1038/383598a0
  14. ↑ Coskun-Ari FF, Hill TM. Sequence-specific interactions in the Tus-Ter complex and the effect of base pair substitutions on arrest of DNA replication in Escherichia coli. J Biol Chem. 1997 Oct 17;272(42):26448-56. PMID:9334221
  15. ↑ Kamada K, Horiuchi T, Ohsumi K, Shimamoto N, Morikawa K. Structure of a replication-terminator protein complexed with DNA. Nature. 1996 Oct 17;383(6601):598-603. PMID:8857533 doi:http://dx.doi.org/10.1038/383598a0
  16. ↑ Bussiere DE, Bastia D, White SW. Crystal structure of the replication terminator protein from B. subtilis at 2.6 A. Cell. 1995 Feb 24;80(4):651-60. PMID:7867072
  17. ↑ Bussiere DE, Bastia D, White SW. Crystal structure of the replication terminator protein from B. subtilis at 2.6 A. Cell. 1995 Feb 24;80(4):651-60. PMID:7867072
  18. ↑ Vivian JP, Porter CJ, Wilce JA, Wilce MC. An asymmetric structure of the Bacillus subtilis replication terminator protein in complex with DNA. J Mol Biol. 2007 Jul 13;370(3):481-91. Epub 2007 Mar 2. PMID:17521668 doi:S0022-2836(07)00259-8
  19. ↑ Wake R, King G. A tale of two terminators: crystal structures sharpen the debate on DNA replication fork arrest mechanisms. Structure. 1997 Jan 15;5(1):1-5. PMID:9016713
  20. ↑ 20.0 20.1 Bussiere DE, Bastia D. Termination of DNA replication of bacterial and plasmid chromosomes. Mol Microbiol. 1999 Mar;31(6):1611-8. PMID:10209736
  21. ↑ Pai KS, Bussiere DE, Wang F, Hutchison CA 3rd, White SW, Bastia D. The structure and function of the replication terminator protein of Bacillus subtilis: identification of the 'winged helix' DNA-binding domain. EMBO J. 1996 Jun 17;15(12):3164-73. PMID:8670817
  22. ↑ Manna AC, Pai KS, Bussiere DE, White SW, Bastia D. The dimer-dimer interaction surface of the replication terminator protein of Bacillus subtilis and termination of DNA replication. Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3253-8. PMID:8622923
  23. ↑ Bussiere DE, Bastia D, White SW. Crystal structure of the replication terminator protein from B. subtilis at 2.6 A. Cell. 1995 Feb 24;80(4):651-60. PMID:7867072
  24. ↑ Wilce JA, Vivian JP, Hastings AF, Otting G, Folmer RH, Duggin IG, Wake RG, Wilce MC. Structure of the RTP-DNA complex and the mechanism of polar replication fork arrest. Nat Struct Biol. 2001 Mar;8(3):206-10. PMID:11224562 doi:10.1038/84934
  25. ↑ Duggin IG, Matthews JM, Dixon NE, Wake RG, Mackay JP. A complex mechanism determines polarity of DNA replication fork arrest by the replication terminator complex of Bacillus subtilis. J Biol Chem. 2005 Apr 1;280(13):13105-13. Epub 2005 Jan 18. PMID:15657033 doi:10.1074/jbc.M414187200
  26. ↑ Duggin IG. DNA replication fork arrest by the Bacillus subtilis RTP-DNA complex involves a mechanism that is independent of the affinity of RTP-DNA binding. J Mol Biol. 2006 Aug 4;361(1):1-6. Epub 2006 Jun 21. PMID:16822523 doi:10.1016/j.jmb.2006.06.013
  27. ↑ Vivian JP, Porter CJ, Wilce JA, Wilce MC. An asymmetric structure of the Bacillus subtilis replication terminator protein in complex with DNA. J Mol Biol. 2007 Jul 13;370(3):481-91. Epub 2007 Mar 2. PMID:17521668 doi:S0022-2836(07)00259-8
  28. ↑ 28.0 28.1 28.2 28.3 Kaplan DL, Bastia D. Mechanisms of polar arrest of a replication fork. Mol Microbiol. 2009 Apr;72(2):279-85. Epub 2009 Mar 4. PMID:19298368 doi:10.1111/j.1365-2958.2009.06656.x
  29. ↑ 29.0 29.1 29.2 Kamada K, Horiuchi T, Ohsumi K, Shimamoto N, Morikawa K. Structure of a replication-terminator protein complexed with DNA. Nature. 1996 Oct 17;383(6601):598-603. PMID:8857533 doi:http://dx.doi.org/10.1038/383598a0
  30. ↑ 30.0 30.1 Neylon C, Kralicek AV, Hill TM, Dixon NE. Replication termination in Escherichia coli: structure and antihelicase activity of the Tus-Ter complex. Microbiol Mol Biol Rev. 2005 Sep;69(3):501-26. PMID:16148308 doi:10.1128/MMBR.69.3.501-526.2005
  31. ↑ Mulugu S, Potnis A, Shamsuzzaman, Taylor J, Alexander K, Bastia D. Mechanism of termination of DNA replication of Escherichia coli involves helicase-contrahelicase interaction. Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9569-74. Epub 2001 Aug 7. PMID:11493686 doi:10.1073/pnas.171065898
  32. ↑ Mulcair MD, Schaeffer PM, Oakley AJ, Cross HF, Neylon C, Hill TM, Dixon NE. A molecular mousetrap determines polarity of termination of DNA replication in E. coli. Cell. 2006 Jun 30;125(7):1309-19. PMID:16814717 doi:10.1016/j.cell.2006.04.040
  33. ↑ Bastia D, Zzaman S, Krings G, Saxena M, Peng X, Greenberg MM. Replication termination mechanism as revealed by Tus-mediated polar arrest of a sliding helicase. Proc Natl Acad Sci U S A. 2008 Sep 2;105(35):12831-6. Epub 2008 Aug 15. PMID:18708526 doi:10.1073/pnas.0805898105
  34. ↑ Kamada K, Horiuchi T, Ohsumi K, Shimamoto N, Morikawa K. Structure of a replication-terminator protein complexed with DNA. Nature. 1996 Oct 17;383(6601):598-603. PMID:8857533 doi:http://dx.doi.org/10.1038/383598a0
  35. ↑ Henderson TA, Nilles AF, Valjavec-Gratian M, Hill TM. Site-directed mutagenesis and phylogenetic comparisons of the Escherichia coli Tus protein: DNA-protein interactions alone can not account for Tus activity. Mol Genet Genomics. 2001 Aug;265(6):941-53. PMID:11523786
  36. ↑ Neylon C, Kralicek AV, Hill TM, Dixon NE. Replication termination in Escherichia coli: structure and antihelicase activity of the Tus-Ter complex. Microbiol Mol Biol Rev. 2005 Sep;69(3):501-26. PMID:16148308 doi:10.1128/MMBR.69.3.501-526.2005
  37. ↑ Roecklein BA, Kuempel PL. In vivo characterization of tus gene expression in Escherichia coli. Mol Microbiol. 1992 Jun;6(12):1655-61. PMID:1495392
  38. ↑ Henderson TA, Nilles AF, Valjavec-Gratian M, Hill TM. Site-directed mutagenesis and phylogenetic comparisons of the Escherichia coli Tus protein: DNA-protein interactions alone can not account for Tus activity. Mol Genet Genomics. 2001 Aug;265(6):941-53. PMID:11523786
  39. ↑ Koch WH, Fernandez de Henestrosa AR, Woodgate R. Identification of mucAB-like homologs on two IncT plasmids, R394 and Rts-1. Mutat Res. 2000 Dec 20;457(1-2):1-13. PMID:11106794
  40. ↑ Griffiths AA, Andersen PA, Wake RG. Replication terminator protein-based replication fork-arrest systems in various Bacillus species. J Bacteriol. 1998 Jul;180(13):3360-7. PMID:9642188
  41. ↑ Takami H, Nakasone K, Takaki Y, Maeno G, Sasaki R, Masui N, Fuji F, Hirama C, Nakamura Y, Ogasawara N, Kuhara S, Horikoshi K. Complete genome sequence of the alkaliphilic bacterium Bacillus halodurans and genomic sequence comparison with Bacillus subtilis. Nucleic Acids Res. 2000 Nov 1;28(21):4317-31. PMID:11058132
  42. ↑ Griffiths AA, Andersen PA, Wake RG. Replication terminator protein-based replication fork-arrest systems in various Bacillus species. J Bacteriol. 1998 Jul;180(13):3360-7. PMID:9642188
  43. ↑ Rey MW, Ramaiya P, Nelson BA, Brody-Karpin SD, Zaretsky EJ, Tang M, Lopez de Leon A, Xiang H, Gusti V, Clausen IG, Olsen PB, Rasmussen MD, Andersen JT, Jorgensen PL, Larsen TS, Sorokin A, Bolotin A, Lapidus A, Galleron N, Ehrlich SD, Berka RM. Complete genome sequence of the industrial bacterium Bacillus licheniformis and comparisons with closely related Bacillus species. Genome Biol. 2004;5(10):R77. Epub 2004 Sep 13. PMID:15461803 doi:gb-2004-5-10-r77
  44. ↑ Andersen PA, Griffiths AA, Duggin IG, Wake RG. Functional specificity of the replication fork-arrest complexes of Bacillus subtilis and Escherichia coli: significant specificity for Tus-Ter functioning in E. coli. Mol Microbiol. 2000 Jun;36(6):1327-35. PMID:10931283
  45. ↑ Kono N, Arakawa K, Tomita M. Comprehensive prediction of chromosome dimer resolution sites in bacterial genomes. BMC Genomics. 2011 Jan 11;12:19. PMID:21223577 doi:10.1186/1471-2164-12-19
  46. ↑ Hendrickson H, Lawrence JG. Mutational bias suggests that replication termination occurs near the dif site, not at Ter sites. Mol Microbiol. 2007 Apr;64(1):42-56. PMID:17376071 doi:10.1111/j.1365-2958.2007.05596.x
  47. ↑ Bussiere DE, Bastia D. Termination of DNA replication of bacterial and plasmid chromosomes. Mol Microbiol. 1999 Mar;31(6):1611-8. PMID:10209736
  48. ↑ Hendrickson H, Lawrence JG. Mutational bias suggests that replication termination occurs near the dif site, not at Ter sites. Mol Microbiol. 2007 Apr;64(1):42-56. PMID:17376071 doi:10.1111/j.1365-2958.2007.05596.x
  49. ↑ Hendrickson H, Lawrence JG. Mutational bias suggests that replication termination occurs near the dif site, not at Ter sites. Mol Microbiol. 2007 Apr;64(1):42-56. PMID:17376071 doi:10.1111/j.1365-2958.2007.05596.x
  50. ↑ Duggin IG, Bell SD. Termination structures in the Escherichia coli chromosome replication fork trap. J Mol Biol. 2009 Apr 3;387(3):532-9. Epub 2009 Feb 20. PMID:19233209 doi:10.1016/j.jmb.2009.02.027
  51. ↑ Duggin IG, Dubarry N, Bell SD. Replication termination and chromosome dimer resolution in the archaeon Sulfolobus solfataricus. EMBO J. 2011 Jan 5;30(1):145-53. Epub 2010 Nov 26. PMID:21113132 doi:10.1038/emboj.2010.301

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