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. 1997 Jan;17(1):416–426. doi: 10.1128/mcb.17.1.416

Active mammalian replication origins are associated with a high-density cluster of mCpG dinucleotides.

T Rein 1, H Zorbas 1, M L DePamphilis 1
PMCID: PMC231766  PMID: 8972222

Abstract

ori-beta is a well-characterized origin of bidirectional replication (OBR) located approximately 17 kb downstream of the dihydrofolate reductase gene in hamster cell chromosomes. The approximately 2-kb region of ori-beta that exhibits greatest replication initiation activity also contains 12 potential methylation sites in the form of CpG dinucleotides. To ascertain whether DNA methylation might play a role at mammalian replication origins, the methylation status of these sites was examined with bisulfite to chemically distinguish cytosine (C) from 5-methylcytosine (mC). All of the CpGs were methylated, and nine of them were located within 356 bp flanking the minimal OBR, creating a high-density cluster of mCpGs that was approximately 10 times greater than average for human DNA. However, the previously reported densely methylated island in which all cytosines were methylated regardless of their dinucleotide composition was not detected and appeared to be an experimental artifact. A second OBR, located at the 5' end of the RPS14 gene, exhibited a strikingly similar methylation pattern, and the organization of CpG dinucleotides at other mammalian origins revealed the potential for high-density CpG methylation. Moreover, analysis of bromodeoxyuridine-labeled nascent DNA confirmed that active replication origins were methylated. These results suggest that a high-density cluster of mCpG dinucleotides may play a role in either the establishment or the regulation of mammalian replication origins.

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Selected References

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  1. Adams R. L. DNA methylation. The effect of minor bases on DNA-protein interactions. Biochem J. 1990 Jan 15;265(2):309–320. doi: 10.1042/bj2650309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Aladjem M. I., Groudine M., Brody L. L., Dieken E. S., Fournier R. E., Wahl G. M., Epner E. M. Participation of the human beta-globin locus control region in initiation of DNA replication. Science. 1995 Nov 3;270(5237):815–819. doi: 10.1126/science.270.5237.815. [DOI] [PubMed] [Google Scholar]
  3. Anachkova B., Hamlin J. L. Replication in the amplified dihydrofolate reductase domain in CHO cells may initiate at two distinct sites, one of which is a repetitive sequence element. Mol Cell Biol. 1989 Feb;9(2):532–540. doi: 10.1128/mcb.9.2.532. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Berberich S., Trivedi A., Daniel D. C., Johnson E. M., Leffak M. In vitro replication of plasmids containing human c-myc DNA. J Mol Biol. 1995 Jan 13;245(2):92–109. doi: 10.1006/jmbi.1994.0010. [DOI] [PubMed] [Google Scholar]
  5. Blow J. J., Sleeman A. M. Replication of purified DNA in Xenopus egg extract is dependent on nuclear assembly. J Cell Sci. 1990 Mar;95(Pt 3):383–391. doi: 10.1242/jcs.95.3.383. [DOI] [PubMed] [Google Scholar]
  6. Brendler T., Abeles A., Austin S. A protein that binds to the P1 origin core and the oriC 13mer region in a methylation-specific fashion is the product of the host seqA gene. EMBO J. 1995 Aug 15;14(16):4083–4089. doi: 10.1002/j.1460-2075.1995.tb00080.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Burhans W. C., Selegue J. E., Heintz N. H. Isolation of the origin of replication associated with the amplified Chinese hamster dihydrofolate reductase domain. Proc Natl Acad Sci U S A. 1986 Oct;83(20):7790–7794. doi: 10.1073/pnas.83.20.7790. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Burhans W. C., Selegue J. E., Heintz N. H. Replication intermediates formed during initiation of DNA synthesis in methotrexate-resistant CHOC 400 cells are enriched for sequences derived from a specific, amplified restriction fragment. Biochemistry. 1986 Jan 28;25(2):441–449. doi: 10.1021/bi00350a025. [DOI] [PubMed] [Google Scholar]
  9. Burhans W. C., Vassilev L. T., Caddle M. S., Heintz N. H., DePamphilis M. L. Identification of an origin of bidirectional DNA replication in mammalian chromosomes. Cell. 1990 Sep 7;62(5):955–965. doi: 10.1016/0092-8674(90)90270-o. [DOI] [PubMed] [Google Scholar]
  10. Burhans W. C., Vassilev L. T., Wu J., Sogo J. M., Nallaseth F. S., DePamphilis M. L. Emetine allows identification of origins of mammalian DNA replication by imbalanced DNA synthesis, not through conservative nucleosome segregation. EMBO J. 1991 Dec;10(13):4351–4360. doi: 10.1002/j.1460-2075.1991.tb05013.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Campbell J. L., Kleckner N. E. coli oriC and the dnaA gene promoter are sequestered from dam methyltransferase following the passage of the chromosomal replication fork. Cell. 1990 Sep 7;62(5):967–979. doi: 10.1016/0092-8674(90)90271-f. [DOI] [PubMed] [Google Scholar]
  12. Carroll S. M., DeRose M. L., Kolman J. L., Nonet G. H., Kelly R. E., Wahl G. M. Localization of a bidirectional DNA replication origin in the native locus and in episomally amplified murine adenosine deaminase loci. Mol Cell Biol. 1993 May;13(5):2971–2981. doi: 10.1128/mcb.13.5.2971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Cedar H. DNA methylation and gene activity. Cell. 1988 Apr 8;53(1):3–4. doi: 10.1016/0092-8674(88)90479-5. [DOI] [PubMed] [Google Scholar]
  14. Cheng X. Structure and function of DNA methyltransferases. Annu Rev Biophys Biomol Struct. 1995;24:293–318. doi: 10.1146/annurev.bb.24.060195.001453. [DOI] [PubMed] [Google Scholar]
  15. Clark S. J., Harrison J., Paul C. L., Frommer M. High sensitivity mapping of methylated cytosines. Nucleic Acids Res. 1994 Aug 11;22(15):2990–2997. doi: 10.1093/nar/22.15.2990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Cooney C. A., Eykholt R. L., Bradbury E. M. Methylation is co-ordinated on the putative replication origins of Physarum ribosomal DNA. J Mol Biol. 1988 Dec 20;204(4):889–901. doi: 10.1016/0022-2836(88)90049-6. [DOI] [PubMed] [Google Scholar]
  17. Cox L. S. DNA replication in cell-free extracts from Xenopus eggs is prevented by disrupting nuclear envelope function. J Cell Sci. 1992 Jan;101(Pt 1):43–53. doi: 10.1242/jcs.101.1.43. [DOI] [PubMed] [Google Scholar]
  18. Craig J. M., Bickmore W. A. The distribution of CpG islands in mammalian chromosomes. Nat Genet. 1994 Jul;7(3):376–382. doi: 10.1038/ng0794-376. [DOI] [PubMed] [Google Scholar]
  19. DePamphilis M. L. Eukaryotic DNA replication: anatomy of an origin. Annu Rev Biochem. 1993;62:29–63. doi: 10.1146/annurev.bi.62.070193.000333. [DOI] [PubMed] [Google Scholar]
  20. DePamphilis M. L. Origins of DNA replication in metazoan chromosomes. J Biol Chem. 1993 Jan 5;268(1):1–4. [PubMed] [Google Scholar]
  21. DePamphilis M. L. Origins of DNA replication that function in eukaryotic cells. Curr Opin Cell Biol. 1993 Jun;5(3):434–441. doi: 10.1016/0955-0674(93)90008-e. [DOI] [PubMed] [Google Scholar]
  22. Dijkwel P. A., Hamlin J. L. The Chinese hamster dihydrofolate reductase origin consists of multiple potential nascent-strand start sites. Mol Cell Biol. 1995 Jun;15(6):3023–3031. doi: 10.1128/mcb.15.6.3023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Dijkwel P. A., Vaughn J. P., Hamlin J. L. Replication initiation sites are distributed widely in the amplified CHO dihydrofolate reductase domain. Nucleic Acids Res. 1994 Nov 25;22(23):4989–4996. doi: 10.1093/nar/22.23.4989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Eden S., Cedar H. Role of DNA methylation in the regulation of transcription. Curr Opin Genet Dev. 1994 Apr;4(2):255–259. doi: 10.1016/s0959-437x(05)80052-8. [DOI] [PubMed] [Google Scholar]
  25. Feil R., Charlton J., Bird A. P., Walter J., Reik W. Methylation analysis on individual chromosomes: improved protocol for bisulphite genomic sequencing. Nucleic Acids Res. 1994 Feb 25;22(4):695–696. doi: 10.1093/nar/22.4.695. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Ferguson A. T., Lapidus R. G., Baylin S. B., Davidson N. E. Demethylation of the estrogen receptor gene in estrogen receptor-negative breast cancer cells can reactivate estrogen receptor gene expression. Cancer Res. 1995 Jun 1;55(11):2279–2283. [PubMed] [Google Scholar]
  27. Frommer M., McDonald L. E., Millar D. S., Collis C. M., Watt F., Grigg G. W., Molloy P. L., Paul C. L. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1827–1831. doi: 10.1073/pnas.89.5.1827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Gale J. M., Tobey R. A., D'Anna J. A. Localization and DNA sequence of a replication origin in the rhodopsin gene locus of Chinese hamster cells. J Mol Biol. 1992 Mar 20;224(2):343–358. doi: 10.1016/0022-2836(92)90999-z. [DOI] [PubMed] [Google Scholar]
  29. Giacca M., Zentilin L., Norio P., Diviacco S., Dimitrova D., Contreas G., Biamonti G., Perini G., Weighardt F., Riva S. Fine mapping of a replication origin of human DNA. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7119–7123. doi: 10.1073/pnas.91.15.7119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Gilbert D. M., Miyazawa H., DePamphilis M. L. Site-specific initiation of DNA replication in Xenopus egg extract requires nuclear structure. Mol Cell Biol. 1995 Jun;15(6):2942–2954. doi: 10.1128/mcb.15.6.2942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Gilbert D. M., Miyazawa H., Nallaseth F. S., Ortega J. M., Blow J. J., DePamphilis M. L. Site-specific initiation of DNA replication in metazoan chromosomes and the role of nuclear organization. Cold Spring Harb Symp Quant Biol. 1993;58:475–485. doi: 10.1101/sqb.1993.058.01.054. [DOI] [PubMed] [Google Scholar]
  32. Gögel E., Längst G., Grummt I., Kunkel E., Grummt F. Mapping of replication initiation sites in the mouse ribosomal gene cluster. Chromosoma. 1996 Apr;104(7):511–518. doi: 10.1007/BF00352115. [DOI] [PubMed] [Google Scholar]
  33. Handeli S., Klar A., Meuth M., Cedar H. Mapping replication units in animal cells. Cell. 1989 Jun 16;57(6):909–920. doi: 10.1016/0092-8674(89)90329-2. [DOI] [PubMed] [Google Scholar]
  34. Heintz N. H., Hamlin J. L. An amplified chromosomal sequence that includes the gene for dihydrofolate reductase initiates replication within specific restriction fragments. Proc Natl Acad Sci U S A. 1982 Jul;79(13):4083–4087. doi: 10.1073/pnas.79.13.4083. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Heintz N. H., Stillman B. W. Nuclear DNA synthesis in vitro is mediated via stable replication forks assembled in a temporally specific fashion in vivo. Mol Cell Biol. 1988 May;8(5):1923–1931. doi: 10.1128/mcb.8.5.1923. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Hsieh C. L., Lieber M. R. CpG methylated minichromosomes become inaccessible for V(D)J recombination after undergoing replication. EMBO J. 1992 Jan;11(1):315–325. doi: 10.1002/j.1460-2075.1992.tb05054.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Hyrien O., Maric C., Méchali M. Transition in specification of embryonic metazoan DNA replication origins. Science. 1995 Nov 10;270(5238):994–997. doi: 10.1126/science.270.5238.994. [DOI] [PubMed] [Google Scholar]
  38. Jenkins H., Hölman T., Lyon C., Lane B., Stick R., Hutchison C. Nuclei that lack a lamina accumulate karyophilic proteins and assemble a nuclear matrix. J Cell Sci. 1993 Sep;106(Pt 1):275–285. doi: 10.1242/jcs.106.1.275. [DOI] [PubMed] [Google Scholar]
  39. Kelly R. E., DeRose M. L., Draper B. W., Wahl G. M. Identification of an origin of bidirectional DNA replication in the ubiquitously expressed mammalian CAD gene. Mol Cell Biol. 1995 Aug;15(8):4136–4148. doi: 10.1128/mcb.15.8.4136. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Kimura T., Asai T., Imai M., Takanami M. Methylation strongly enhances DNA bending in the replication origin region of the Escherichia coli chromosome. Mol Gen Genet. 1989 Oct;219(1-2):69–74. doi: 10.1007/BF00261159. [DOI] [PubMed] [Google Scholar]
  41. Kitsberg D., Selig S., Keshet I., Cedar H. Replication structure of the human beta-globin gene domain. Nature. 1993 Dec 9;366(6455):588–590. doi: 10.1038/366588a0. [DOI] [PubMed] [Google Scholar]
  42. Krysan P. J., Smith J. G., Calos M. P. Autonomous replication in human cells of multimers of specific human and bacterial DNA sequences. Mol Cell Biol. 1993 May;13(5):2688–2696. doi: 10.1128/mcb.13.5.2688. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Leu T. H., Hamlin J. L. High-resolution mapping of replication fork movement through the amplified dihydrofolate reductase domain in CHO cells by in-gel renaturation analysis. Mol Cell Biol. 1989 Feb;9(2):523–531. doi: 10.1128/mcb.9.2.523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Lin M. S., Zhang A., Fujimoto A. Asynchronous DNA replication between 15q11.2q12 homologs: cytogenetic evidence for maternal imprinting and delayed replication. Hum Genet. 1995 Nov;96(5):572–576. doi: 10.1007/BF00197413. [DOI] [PubMed] [Google Scholar]
  45. Mah D. C., Dijkwel P. A., Todd A., Klein V., Price G. B., Zannis-Hadjopoulos M. ors12, a mammalian autonomously replicating DNA sequence, associates with the nuclear matrix in a cell cycle-dependent manner. J Cell Sci. 1993 Jul;105(Pt 3):807–818. doi: 10.1242/jcs.105.3.807. [DOI] [PubMed] [Google Scholar]
  46. Marians K. J. Prokaryotic DNA replication. Annu Rev Biochem. 1992;61:673–719. doi: 10.1146/annurev.bi.61.070192.003325. [DOI] [PubMed] [Google Scholar]
  47. McQueen H. A., Fantes J., Cross S. H., Clark V. H., Archibald A. L., Bird A. P. CpG islands of chicken are concentrated on microchromosomes. Nat Genet. 1996 Mar;12(3):321–324. doi: 10.1038/ng0396-321. [DOI] [PubMed] [Google Scholar]
  48. McWhinney C., Waltz S. E., Leffak M. Cis-acting effects of sequences within 2.4-kb upstream of the human c-myc gene on autonomous plasmid replication in HeLa cells. DNA Cell Biol. 1995 Jul;14(7):565–579. doi: 10.1089/dna.1995.14.565. [DOI] [PubMed] [Google Scholar]
  49. Meehan R. R., Lewis J. D., Bird A. P. Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA. Nucleic Acids Res. 1992 Oct 11;20(19):5085–5092. doi: 10.1093/nar/20.19.5085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Mitchell P. J., Carothers A. M., Han J. H., Harding J. D., Kas E., Venolia L., Chasin L. A. Multiple transcription start sites, DNase I-hypersensitive sites, and an opposite-strand exon in the 5' region of the CHO dhfr gene. Mol Cell Biol. 1986 Feb;6(2):425–440. doi: 10.1128/mcb.6.2.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Murchie A. I., Lilley D. M. Base methylation and local DNA helix stability. Effect on the kinetics of cruciform extrusion. J Mol Biol. 1989 Feb 5;205(3):593–602. doi: 10.1016/0022-2836(89)90228-3. [DOI] [PubMed] [Google Scholar]
  52. Nan X., Tate P., Li E., Bird A. DNA methylation specifies chromosomal localization of MeCP2. Mol Cell Biol. 1996 Jan;16(1):414–421. doi: 10.1128/mcb.16.1.414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Newport J. W., Wilson K. L., Dunphy W. G. A lamin-independent pathway for nuclear envelope assembly. J Cell Biol. 1990 Dec;111(6 Pt 1):2247–2259. doi: 10.1083/jcb.111.6.2247. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Ofverstedt L. G., Hammarström K., Balgobin N., Hjertén S., Pettersson U., Chattopadhyaya J. Rapid and quantitative recovery of DNA fragments from gels by displacement electrophoresis (isotachophoresis). Biochim Biophys Acta. 1984 Jun 16;782(2):120–126. doi: 10.1016/0167-4781(84)90014-9. [DOI] [PubMed] [Google Scholar]
  55. Orr-Weaver T. L. Drosophila chorion genes: cracking the eggshell's secrets. Bioessays. 1991 Mar;13(3):97–105. doi: 10.1002/bies.950130302. [DOI] [PubMed] [Google Scholar]
  56. Pelizon C., Diviacco S., Falaschi A., Giacca M. High-resolution mapping of the origin of DNA replication in the hamster dihydrofolate reductase gene domain by competitive PCR. Mol Cell Biol. 1996 Oct;16(10):5358–5364. doi: 10.1128/mcb.16.10.5358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Razin A., Kafri T. DNA methylation from embryo to adult. Prog Nucleic Acid Res Mol Biol. 1994;48:53–81. doi: 10.1016/s0079-6603(08)60853-3. [DOI] [PubMed] [Google Scholar]
  58. Reilly J. G., Thomas C. A., Jr, Lundell M. J. Methylation of mouse ribosomal RNA genes. DNA. 1982;1(3):259–266. doi: 10.1089/dna.1.1982.1.259. [DOI] [PubMed] [Google Scholar]
  59. Russell D. W., Zinder N. D. Hemimethylation prevents DNA replication in E. coli. Cell. 1987 Sep 25;50(7):1071–1079. doi: 10.1016/0092-8674(87)90173-5. [DOI] [PubMed] [Google Scholar]
  60. Selig S., Ariel M., Goitein R., Marcus M., Cedar H. Regulation of mouse satellite DNA replication time. EMBO J. 1988 Feb;7(2):419–426. doi: 10.1002/j.1460-2075.1988.tb02829.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Shimada T., Nienhuis A. W. Only the promoter region of the constitutively expressed normal and amplified human dihydrofolate reductase gene is DNase I hypersensitive and undermethylated. J Biol Chem. 1985 Feb 25;260(4):2468–2474. [PubMed] [Google Scholar]
  62. Slater S., Wold S., Lu M., Boye E., Skarstad K., Kleckner N. E. coli SeqA protein binds oriC in two different methyl-modulated reactions appropriate to its roles in DNA replication initiation and origin sequestration. Cell. 1995 Sep 22;82(6):927–936. doi: 10.1016/0092-8674(95)90272-4. [DOI] [PubMed] [Google Scholar]
  63. Stein R., Sciaky-Gallili N., Razin A., Cedar H. Pattern of methylation of two genes coding for housekeeping functions. Proc Natl Acad Sci U S A. 1983 May;80(9):2422–2426. doi: 10.1073/pnas.80.9.2422. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Swisshelm K., Disteche C. M., Thorvaldsen J., Nelson A., Salk D. Age-related increase in methylation of ribosomal genes and inactivation of chromosome-specific rRNA gene clusters in mouse. Mutat Res. 1990 May-Jul;237(3-4):131–146. doi: 10.1016/0921-8734(90)90019-n. [DOI] [PubMed] [Google Scholar]
  65. Szyf M., Bozovic V., Tanigawa G. Growth regulation of mouse DNA methyltransferase gene expression. J Biol Chem. 1991 Jun 5;266(16):10027–10030. [PubMed] [Google Scholar]
  66. Tasheva E. S., Roufa D. J. A densely methylated DNA island is associated with a chromosomal replication origin in the human RPS14 locus. Somat Cell Mol Genet. 1995 Nov;21(6):369–383. doi: 10.1007/BF02310205. [DOI] [PubMed] [Google Scholar]
  67. Tasheva E. S., Roufa D. J. A mammalian origin of bidirectional DNA replication within the Chinese hamster RPS14 locus. Mol Cell Biol. 1994 Sep;14(9):5628–5635. doi: 10.1128/mcb.14.9.5628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Tasheva E. S., Roufa D. J. Densely methylated DNA islands in mammalian chromosomal replication origins. Mol Cell Biol. 1994 Sep;14(9):5636–5644. doi: 10.1128/mcb.14.9.5636. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Vassilev L. T., Burhans W. C., DePamphilis M. L. Mapping an origin of DNA replication at a single-copy locus in exponentially proliferating mammalian cells. Mol Cell Biol. 1990 Sep;10(9):4685–4689. doi: 10.1128/mcb.10.9.4685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Virta-Pearlman V. J., Gunaratne P. H., Chinault A. C. Analysis of a replication initiation sequence from the adenosine deaminase region of the mouse genome. Mol Cell Biol. 1993 Oct;13(10):5931–5942. doi: 10.1128/mcb.13.10.5931. [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Vogel M. C., Papadopoulos T., Müller-Hermelink H. K., Drahovsky D., Pfeifer G. P. Intracellular distribution of DNA methyltransferase during the cell cycle. FEBS Lett. 1988 Aug 15;236(1):9–13. doi: 10.1016/0014-5793(88)80275-8. [DOI] [PubMed] [Google Scholar]
  72. Woodcock D. M., Crowther P. J., Diver W. P. The majority of methylated deoxycytidines in human DNA are not in the CpG dinucleotide. Biochem Biophys Res Commun. 1987 Jun 15;145(2):888–894. doi: 10.1016/0006-291x(87)91048-5. [DOI] [PubMed] [Google Scholar]
  73. Woodcock D. M., Simmons D. L., Crowther P. J., Cooper I. A., Trainor K. J., Morley A. A. Delayed DNA methylation is an integral feature of DNA replication in mammalian cells. Exp Cell Res. 1986 Sep;166(1):103–112. doi: 10.1016/0014-4827(86)90511-2. [DOI] [PubMed] [Google Scholar]
  74. Wu J. R., Gilbert D. M. A distinct G1 step required to specify the Chinese hamster DHFR replication origin. Science. 1996 Mar 1;271(5253):1270–1272. doi: 10.1126/science.271.5253.1270. [DOI] [PubMed] [Google Scholar]
  75. Yamaki H., Ohtsubo E., Nagai K., Maeda Y. The oriC unwinding by dam methylation in Escherichia coli. Nucleic Acids Res. 1988 Jun 10;16(11):5067–5073. doi: 10.1093/nar/16.11.5067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Yoon Y., Sanchez J. A., Brun C., Huberman J. A. Mapping of replication initiation sites in human ribosomal DNA by nascent-strand abundance analysis. Mol Cell Biol. 1995 May;15(5):2482–2489. doi: 10.1128/mcb.15.5.2482. [DOI] [PMC free article] [PubMed] [Google Scholar]
  77. Zacharias W., O'Connor T. R., Larson J. E. Methylation of cytosine in the 5-position alters the structural and energetic properties of the supercoil-induced Z-helix and of B-Z junctions. Biochemistry. 1988 Apr 19;27(8):2970–2978. doi: 10.1021/bi00408a046. [DOI] [PubMed] [Google Scholar]

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