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Regulation of DNA replication by homopurine/homopyrimidine sequences

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Abstract

The simple repeating homopurine/homopyrimidine sequences dispersed throughout many eukaryotic genomes are known to form triple helical structures comprising three-stranded and single-stranded DNA. Several lines of evidence suggest that these structures influence DNA replication in cells. Homopurine/homopyrimidine sequences cloned into simian virus 40 (SV40) or SV40 origin-containing plasmids caused a reduced rate of DNA synthesis due to the pausing of replication forks. More prominent arrests were observed in in vitro experiments using single-stranded and double-stranded DNA with triplex-forming sequences. Nucleotides unable to form triplexes when present in the template DNA or when incorporated into the nascent strand prevented termination. Similarly, mutations destroying the triplex potential did not cause arrest while compensatory mutations restoring triplex potential restored it. These and other observations from a number of laboratories indicating that homopurine/homopyrimidine sequences act as arrest signals in vitro and as pause sites in vivo during replication fork movement suggest that these naturally occurring sequences play a regulatory role in DNA replication and gene amplification.

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References

  1. Dayn A, Samadashwily GM, Mirkin, SM: Intramolecular DNA triplexes: unusual sequence requirements and influence on DNA polymerization. Proc Natl Acad Sci USA 89: 11406–11410, 1992

    Google Scholar 

  2. Frank-Kamenetskii MD: DNA supercoiling and unusual structures. In: N.R. Cozzarelli and J. Wang (eds). DNA Topology and Its Biological Effects. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1990, pp 185–215

    Google Scholar 

  3. Frank-Kamenetskii MD, Mirkin, SM: Triplex DNA structures. Ann Rev Biochem 64: 65–95, 1995

    Google Scholar 

  4. Hanvey JC, Shimizu M, Wells RD: Intramolecular DNA triplexes in supercoiled plasmids. Proc Natl Acad Sci USA 85: 6292–6296, 1988

    Google Scholar 

  5. Htun H, Dahlberg JE: Single strands, triple strands and kinks in HDNA. Science 241: 1791–1796, 1988

    Google Scholar 

  6. Johnston BH: The S1-sensitive form of d(C-T)n.d(A-G)n: chemical evidence for a three-stranded structure in plasmids. Science 241: 1800–1804, 1988

    Google Scholar 

  7. Lyamichev VI, Mirkin SM, Frank-Kamenetskii MD: Structures of homopurine-homopyrimidine tract in superhelical DNA. J Biomol Struct Dyn 3: 667–669, 1986

    Google Scholar 

  8. Kohwi Y, Kohwi-Shigematsu T: Magnesium ion-dependent triple-helix structure formed by homopurine-homopyrimidine sequences in supercoiled plasmid DNA. Proc Natl Acad Sci USA 85: 3781–3785, 1988

    Google Scholar 

  9. Vojtísková M, Mirkin S, Lyamichev V, Voloshin O, Frank-Kamenetskii MD, Palecek E: Chemical probing of the homopurine.homopyrimidine tract in supercoiled DNA at single nucleotide resolution. FEBS Lett 234: 295–299, 1988

    Google Scholar 

  10. Voloshin ON, Mirkin SM, Lyamichev VI, Belotserkovskii BP, Frank Kamenetskii MD: Chemical probing of homopurine.homopyrimidine mirror repeats in supercoiled DNA. Nature 333: 475–476, 1988

    Google Scholar 

  11. Wells RD, Collier DA, Hanvey JC, Shimizu M, Wohlrab F: The chemistry and biology of unusual DNA structures adopted by oligopurine.oligopyrimidine sequences. FASEB J 2: 2939–2949, 1988

    Google Scholar 

  12. Kubinsky H, Opara-Kubinsky Z, Szybalski W: Patterns of interaction between polyribonucleotides and individual DNA strands derived from several vertebrates, bacteria and bacteriophages. J Mol Biol 20: 313–329, 1966

    Google Scholar 

  13. Birnboim HC, Sederoff RR, Paterson MC: Distribution of polypyrimidine:polypurine segments in DNA from diverse organisms. Eur J Biochem 98: 301–307, 1979

    Google Scholar 

  14. Behe MJ:The DNA sequence of the human β-globin region is strongly biased in favor of long strings of contiguous purine or pyrimidine residues. Biochemistry 26: 7870–7875, 1987

    Google Scholar 

  15. Cheng HL, Blattner FR, Fitzmaurice L, Mushinski JF, Tucker PW: Structure of genes for membrane and secreted murine IgD heavy chains. Nature 296: 410–415, 1982

    Google Scholar 

  16. Crabtree GR, Kant JA: Organization of the rat γ-fibrinogen gene: alternative mRNA splice patterns produce the γA and γB (γ′) chains of fibrinogen. Cell 31: 159–166, 1982

    Google Scholar 

  17. Hentschel CC: Homocopolymer sequences in the spacer of a sea urchin histone gene repeat are sensitive to S1 nuclease. Nature 295: 714–716, 1982

    Google Scholar 

  18. Htun H, Lund E, Dahlberg JE: Human U1 RNA genes contain an unusually sensitive nuclease S1 cleavage site within the conserved 3′ flanking region. Proc Natl Acad Sci USA 81: 7288–7292, 1984

    Google Scholar 

  19. Richards JE, Gilliam AC, Shen A, Tucker PW, Blattner FR: Unusual sequences in the murine immunoglobulin μ-δ heavy-chain region. Nature 306: 483–487, 1983

    Google Scholar 

  20. Sures I, Lowry J, Kedes LH: The DNA sequence of a sea urchin (S. purpuratus) H2A, H2B and H3 histone coding and spacer regions. Cell 15: 1033–1044, 1978

    Google Scholar 

  21. Manor H, Rao BS, Martin RG: Abundance and degree of dispersion of genomic d(GA)n.d(TC)n sequences. J Mol Evo 127: 96–101, 1988

    Google Scholar 

  22. Wong AK, Lee HA, van de Sande JH, Rattner JB: Distribution of CT-rich tracts is conserved in vertebrate chromosomes. Chromosoma 99: 344–351, 1990

    Google Scholar 

  23. Hanvey JC, Williams EM, Besterman JM: DNA triple helix formation at physiological pH and temperature. Antisense Res Dev 1: 307–317, 1991

    Google Scholar 

  24. Lapidot A, Baran N, Manor H: (dT-dC)n and (dG-dA)n tracts arrest single stranded DNA replication in vitro. Nucleic Acids Res 17: 883–900, 1989

    Google Scholar 

  25. Michel D, Chatelain G, Herault Y, Brun G: The long repetitive polypurine/polypyrimidine sequence (TTCCC)48 forms DNA triplex with Pu-Pu-Py base triplets in vivo. Nucleic Acids Res 20: 439–443, 1992

    Google Scholar 

  26. Agazie YM, Lee JS, Burkholder GD: Characterization of a new monoclonal antibody to triplex DNA and immunofluorescent staining of mammalian chromosomes. J Biol Chem. 269: 7019–7023, 1994

    Google Scholar 

  27. Burkholder GD, Latimer LJ, Lee JS: Immunofluorescent staining of mammalian nuclei and chromosomes with a monoclonal antibody to triplex DNA. Chromosoma 97: 185–192, 1988

    Google Scholar 

  28. Burkholder GD, Latimer LJ, Lee JS: Immunofluorescent location of triplex DNA in polytene chromosomes of Chironomus and Drosophila. Chromosoma, 101: 11–18, 1991

    Google Scholar 

  29. Kiyama R, Camerini-Otero RD: A triplex DNA-binding protein from human cells: Purification and characterization. Proc Natl Acad Sci USA 88: 10450–10454, 1991

    Google Scholar 

  30. Aharoni A, Baran N, Manor H: Characterization of a multisubunit human protein which selectively binds single stranded d(GA)n and d(GT)n sequence repeats in DNA. Nucleic Acids Res 21: 5221–5228, 1993

    Google Scholar 

  31. Baran N, Lapidot A, Manor H: Unusual sequence element found at the end of an amplicon. Mol Cell Biol 7: 2636–2640, 1987

    Google Scholar 

  32. Rao BS, Manor H, Martin RG: Pausing in simian virus 40 DNA replication by a sequence containing (dG-dA)27.(dT-dC)27. Nucleic Acids Res 16: 8077–8094, 1988

    Google Scholar 

  33. Brinton BT, Caddle MS, Heintz NH: Position and orientation-dependent effects of a eukaryotic Z-triplex DNA motif on episomal DNA replication in cos-7 cells. J Biol Chem 266: 5153–5161, 1991

    Google Scholar 

  34. Danna KJ, Nathans D: Bidirectional replication of simian virus 40 DNA. Proc Natl Acad Sci USA 69: 3097–3100, 1972

    Google Scholar 

  35. Rao BS, Martin RG: Structural state of newly replicated closed circular simian virus 40 DNA. J Virol 62: 3879–3882, 1988

    Google Scholar 

  36. Rao BS: Pausing of simian virus 40 DNA replication fork movement in vivo by (dG-dA)n.(dT- dC)n tracts. Gene 140: 233–237, 1994

    Google Scholar 

  37. Brewer BJ, Fangman WL: The localization of replication origins on ARS plasmids in S. cerevisiae. Cell 51: 463–471, 1987

    Google Scholar 

  38. Bianchi A, Wells RD, Heintz NH, Caddle MS: Sequences near the origin of replication of the DHFR locus of Chinese hamster ovary cells adopt left-handed Z-DNA and triplex structures. J Biol Chem 265: 21789–21796, 1990

    Google Scholar 

  39. Baran N, Lapidot A, Manor H: Formation of DNA triplexes accounts for arrests of DNA synthesis at d(TC)n and d(GA)n tracts. Proc Natl Acad Sci USA 88: 507–511, 1991

    Google Scholar 

  40. Samadashwily GM, Dayn A, Mirkin SM: Suicidal nucleotide sequences for DNA polymerization. EMBO J 12: 4975–4983, 1993

    Google Scholar 

  41. Lyamichev VI, Brow MAD, Dahlberg JE: Structure-specific endonucleolytic cleavage of nucleic acids by eubacterial DNA polymerases. Science 260: 778–783, 1993

    Google Scholar 

  42. Samadashwily GM, Mirkin SM: Trapping DNA polymerases using triplex-forming oligodeoxyribonucleotides. Gene 149: 127–136, 1994

    Google Scholar 

  43. Duval-Valentin G, Bizemont TD, Takasugi M, Mergny JL, Bisagni E, Helene C: Triple-helix specific ligands stabilize H-DNA conformation. J Mol Biol 247: 847–858, 1995

    Google Scholar 

  44. Peleg M, Kopel V, Borowiec JA, Manor H: Formation of DNA triple helices inhibits DNA unwinding by the SV40 large T-antigen helicase. Nucl Acids Res 23: 1292–1299, 1995

    Google Scholar 

  45. Maine IP, Kodadek T: Efficient unwinding of triplex DNA by a DNA helicase. Biochem Biophys Res Comm 204: 1119–1124, 1994

    Google Scholar 

  46. Bergemann AD, Johnson EM: The HeLa Pur factor binds singlestranded DNA at a specific element conserved in gene flanking regions and origins of DNA replication. Mol Cell Biol 12: 1257–1265, 1992

    Google Scholar 

  47. Brunel F, Alzari PM, Ferrara P, Zakin MM: Cloning and sequencing of PYBP, a pyrimidine-rich specific single strand DNA-binding protein. Nucl Acids Res 19: 5237–5245, 1991

    Google Scholar 

  48. Bossone SA, Asselin C, Patel AJ, Marcu KB: MAZ, a zinc-finger protein, binds to c-MYC and C2 gene sequences regulating transcriptional initiation and termination. Proc Natl Acad Sci USA 89: 7452–7456, 1992

    Google Scholar 

  49. Gilmour DS, Thomas GH, Elgin SCR: Drosophila nuclear proteins bind to regions of alternating C and T residues in gene promoters. Science 245: 1487–1490, 1989

    Google Scholar 

  50. Kolluri R, Torrey TA, Kinniburgh AJ: A CT promoter element binding protein: definition of a double strand and a novel single-strand DNA binding motif. Nucleic Acids Res 20: 111–116, 1992

    Google Scholar 

  51. Kennedy GC, Butter WJ: Pur-1, a zinc-finger protein that binds to purine-rich sequences, transactivates an insulin promoter in heterologous cells. Proc Natl Acad Sci USA 89: 11498–11502, 1992

    Google Scholar 

  52. Bacolla A, Ulrich MJ, Larson JE, Ley TJ, Wells RD: An intramolecular triplex in the human 7-globin 5′-flanking region is altered by point mutations associated with hereditary persistence of fetal hemoglobin. J Biol Chem 270: 24556–24563, 1995

    Google Scholar 

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Sridhara Rao, B. Regulation of DNA replication by homopurine/homopyrimidine sequences. Mol Cell Biochem 156, 163–168 (1996). https://doi.org/10.1007/BF00426339

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  • DOI: https://doi.org/10.1007/BF00426339

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