#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

RNA∶DNA Hybrids Initiate Quasi-Palindrome-Associated Mutations in Highly Transcribed Yeast DNA


RNase H enzymes promote genetic stability by degrading aberrant RNA∶DNA hybrids and by removing ribonucleotide monophosphates (rNMPs) that are present in duplex DNA. Here, we report that loss of RNase H2 in yeast is associated with mutations that extend identity between the arms of imperfect inverted repeats (quasi-palindromes or QPs), a mutation type generally attributed to a template switch during DNA synthesis. QP events were detected using frameshift-reversion assays and were only observed under conditions of high transcription. In striking contrast to transcription-associated short deletions that also are detected by these assays, QP events do not require Top1 activity. QP mutation rates are strongly affected by the direction of DNA replication and, in contrast to their elevation in the absence of RNase H2, are reduced when RNase H1 is additionally eliminated. Finally, transcription-associated QP events are limited by components of the nucleotide excision repair pathway and are promoted by translesion synthesis DNA polymerases. We suggest that QP mutations reflect either a transcription-associated perturbation of Okazaki-fragment processing, or the use of a nascent transcript to resume replication following a transcription-replication conflict.


Vyšlo v časopise: RNA∶DNA Hybrids Initiate Quasi-Palindrome-Associated Mutations in Highly Transcribed Yeast DNA. PLoS Genet 9(11): e32767. doi:10.1371/journal.pgen.1003924
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003924

Souhrn

RNase H enzymes promote genetic stability by degrading aberrant RNA∶DNA hybrids and by removing ribonucleotide monophosphates (rNMPs) that are present in duplex DNA. Here, we report that loss of RNase H2 in yeast is associated with mutations that extend identity between the arms of imperfect inverted repeats (quasi-palindromes or QPs), a mutation type generally attributed to a template switch during DNA synthesis. QP events were detected using frameshift-reversion assays and were only observed under conditions of high transcription. In striking contrast to transcription-associated short deletions that also are detected by these assays, QP events do not require Top1 activity. QP mutation rates are strongly affected by the direction of DNA replication and, in contrast to their elevation in the absence of RNase H2, are reduced when RNase H1 is additionally eliminated. Finally, transcription-associated QP events are limited by components of the nucleotide excision repair pathway and are promoted by translesion synthesis DNA polymerases. We suggest that QP mutations reflect either a transcription-associated perturbation of Okazaki-fragment processing, or the use of a nascent transcript to resume replication following a transcription-replication conflict.


Zdroje

1. AguileraA, Garcia-MuseT (2012) R loops: from transcription byproducts to threats to genome stability. Mol Cell 46: 115–124.

2. LiX, ManleyJL (2006) Cotranscriptional processes and their influence on genome stability. Genes Dev 20: 1838–1847.

3. KimN, Jinks-RobertsonS (2012) Transcription as a source of genome instability. Nat Rev Genet 13: 204–214.

4. BurgersPM (2009) Polymerase dynamics at the eukaryotic DNA replication fork. J Biol Chem 284: 4041–4045.

5. ZhengL, ShenB (2011) Okazaki fragment maturation: nucleases take centre stage. J Mol Cell Biol 3: 23–30.

6. Nick McElhinnySA, WattsBE, KumarD, WattDL, LundstromEB, et al. (2010) Abundant ribonucleotide incorporation into DNA by yeast replicative polymerases. Proc Natl Acad Sci USA 107: 4949–4954.

7. ReijnsMA, RabeB, RigbyRE, MillP, AstellKR, et al. (2012) Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development. Cell 149: 1008–1022.

8. CerritelliSM, CrouchRJ (2009) Ribonuclease H: the enzymes in eukaryotes. FEBS J 276: 1494–1505.

9. OhtaniN, HarukiM, MorikawaM, CrouchRJ, ItayaM, et al. (1999) Identification of the genes encoding Mn2+-dependent RNase HII and Mg2+-dependent RNase HIII from Bacillus subtilis: classification of RNases H into three families. Biochemistry 38: 605–618.

10. ChonH, SparksJL, RychlikM, NowotnyM, BurgersPM, et al. (2013) RNase H2 roles in genome integrity revealed by unlinking its activities. Nucleic Acids Res 41 ((5)): 3130–43.

11. CerritelliSM, FrolovaEG, FengC, GrinbergA, LovePE, et al. (2003) Failure to produce mitochondrial DNA results in embryonic lethality in RNaseh1 null mice. Mol Cell 11: 807–815.

12. JeongHS, BacklundPS, ChenHC, KaravanovAA, CrouchRJ (2004) RNase H2 of Saccharomyces cerevisiae is a complex of three proteins. Nucleic Acids Res 32: 407–414.

13. SparksJL, ChonH, CerritelliSM, KunkelTA, JohanssonE, et al. (2012) RNase H2-initiated ribonucleotide excision repair. Mol Cell 47: 980–986.

14. ReaganMS, PittengerC, SiedeW, FriedbergEC (1995) Characterization of a mutant strain of Saccharomyces cerevisiae with a deletion of the RAD27 gene, a structural homolog of the RAD2 nucleotide excision repair gene. J Bacteriol 177: 364–371.

15. LazzaroF, NovarinaD, AmaraF, WattDL, StoneJE, et al. (2012) RNase H and postreplication repair protect cells from ribonucleotides incorporated in DNA. Mol Cell 45: 99–110.

16. CrowYJ, LeitchA, HaywardBE, GarnerA, ParmarR, et al. (2006) Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection. Nature Genet 38: 910–916.

17. Nick McElhinnySA, KumarD, ClarkAB, WattDL, WattsBE, et al. (2010) Genome instability due to ribonucleotide incorporation into DNA. Nat Chem Biol 6: 774–781.

18. KimN, HuangSY, WilliamsJS, LiYC, ClarkAB, et al. (2011) Mutagenic processing of ribonucleotides in DNA by yeast topoisomerase I. Science 332: 1561–1564.

19. ChoJE, KimN, LiYC, Jinks-RobertsonS (2013) Two distinct mechanisms of Topoisomerase 1-dependent mutagenesis in yeast. DNA Repair 12 ((3)): 205–11.

20. LippertMJ, KimN, ChoJE, LarsonRP, SchoenlyNE, et al. (2011) Role for topoisomerase 1 in transcription-associated mutagenesis in yeast. Proc Natl Acad Sci USA 108: 698–703.

21. PommierY, PourquierP, FanY, StrumbergD (1998) Mechanism of action of eukaryotic DNA topoisomerase I and drugs targeted to the enzyme. Biochim Biophys Acta 1400: 83–105.

22. SekiguchiJ, ShumanS (1997) Site-specific ribonuclease activity of eukaryotic DNA topoisomerase I. Mol Cell 1: 89–97.

23. GreeneCN, Jinks-RobertsonS (1997) Frameshift intermediates in homopolymer runs are removed efficiently by yeast mismatch repair proteins. Mol Cell Biol 17: 2844–2850.

24. HarfeBD, Jinks-RobertsonS (1999) Removal of frameshift intermediates by mismatch repair proteins in Saccharomyces cerevisiae. Mol Cell Biol 19: 4766–4773.

25. LehnerK, Jinks-RobertsonS (2009) The mismatch repair system promotes Polζ-dependent translesion synthesis in yeast. Proc Natl Acad Sci USA 106: 5749–5754.

26. ChenJZ, QiuJ, ShenB, HolmquistGP (2000) Mutational spectrum analysis of RNase H(35) deficient Saccharomyces cerevisiae using fluorescence-based directed termination PCR. Nucleic Acids Res 28: 3649–3656.

27. TurchiJJ, HuangL, MuranteRS, KimY, BambaraRA (1994) Enzymatic completion of mammalian lagging-strand DNA replication. Proc Natl Acad Sci USA 91: 9803–9807.

28. QiuJ, QianY, FrankP, WintersbergerU, ShenB (1999) Saccharomyces cerevisiae RNase H(35) functions in RNA primer removal during lagging-strand DNA synthesis, most efficiently in cooperation with Rad27 nuclease. Mol Cell Biol 19: 8361–8371.

29. RipleyLS (1990) Frameshift mutation: determinants of specificity. Annu Rev Genet 24: 189–213.

30. LovettST (2004) Encoded errors: mutations and rearrangements mediated by misalignment at repetitive DNA sequences. Molecular Microbio 52: 1243–1253.

31. TrinhTQ, SindenRR (1991) Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli. Nature 352: 544–547.

32. RoscheWA, RipleyLS, SindenRR (1998) Primer-template misalignments during leading strand DNA synthesis account for the most frequent spontaneous mutations in a quasipalindromic region in Escherichia coli. J Mol Biol 284: 633–646.

33. YoshiyamaK, HiguchiK, MatsumuraH, MakiH (2001) Directionality of DNA replication fork movement strongly affects the generation of spontaneous mutations in Escherichia coli. J Mol Biol 307: 1195–1206.

34. KimN, AbdulovicAL, GealyR, LippertMJ, Jinks-RobertsonS (2007) Transcription-associated mutagenesis in yeast is directly proportional to the level of gene expression and influenced by the direction of DNA replication. DNA Repair 6: 1285–1296.

35. ViswanathanM, LacirignolaJJ, HurleyRL, LovettST (2000) A novel mutational hotspot in a natural quasipalindrome in Escherichia coli. J Mol Biol 302: 553–564.

36. KimN, Jinks-RobertsonS (2009) dUTP incorporation into genomic DNA is linked to transcription in yeast. Nature 459: 1150–1153.

37. BoiteuxS, Jinks-RobertsonS (2013) DNA repair mechanisms and the bypass of DNA damage in Saccharomyces cerevisiae. Genetics 193: 1025–1064.

38. LyndakerAM, AlaniE (2009) A tale of tails: insights into the corrdination of 3′ end processing during homologous recombination. Bioessays 31: 315–321.

39. LinY, WilsonJH (2012) Nucleotide excision repair, mismatch repair, and R-loops modulate convergent transcription-induced cell death and repeat instability. PloS One 7: e46807.

40. KimN, Jinks-RobertsonS (2010) Abasic sites in the transcribed strand of yeast DNA are removed by transcription-coupled nucleotide excision repair. Mol Cell Biol 30: 3206–3215.

41. de BoerJG, RipleyLS (1984) Demonstration of the production of frameshift and base-substitution mutations by quasipalindromic DNA sequences. Proc Natl Acad Sci USA 81: 5528–5531.

42. GreenblattMS, GrollmanAP, HarrisCC (1996) Deletions and insertions in the p53 tumor suppressor gene in human cancers: confirmation of the DNA polymerase slippage/misalignment model. Cancer Res 56: 2130–2136.

43. RipleyLS (1982) Model for the participation of quasi-palindromic DNA sequences in frameshift mutation. Proc Natl Acad Sci USA 79: 4128–4132.

44. HicksWM, KimM, HaberJE (2010) Increased mutagenesis and unique mutation signature associated with mitotic gene conversion. Science 329: 82–85.

45. DeemA, KeszthelyiA, BlackgroveT, VaylA, CoffeyB, et al. (2011) Break-induced replication is highly inaccurate. PLoS Biol 9: e1000594.

46. SymingtonLS (2002) Role of RAD52 epistasis group genes in homologous recombination and double-strand break repair. Microbiol Mol Biol Rev 66: 630–670.

47. PapanicolaouC, RipleyLS (1991) An in vitro approach to identifying specificity determinants of mutagenesis mediated by DNA misalignments. J Mol Biol 221: 805–821.

48. SeierT, ZilberbergG, ZeigerDM, LovettST (2012) Azidothymidine and other chain terminators are mutagenic for template-switch-generated genetic mutations. Proc Natl Acad Sci USA 109: 6171–6174.

49. YoshiyamaK, MakiH (2003) Spontaneous hotspot mutations resistant to mismatch correction in Escherichia coli: transcription-dependent mutagenesis involving template-switching mechanisms. J Mol Biol 327: 7–18.

50. PrakashS, PrakashL (2002) Translesion DNA synthesis in eukaryotes: a one- or two-polymerase affair. Genes Dev 16: 1872–1883.

51. McDonaldJP, VaismanA, KubanW, GoodmanMF, WoodgateR (2012) Mechanisms employed by Escherichia coli to prevent ribonucleotide incorporation into genomic DNA by Pol V. PLoS Genet 8: e1003030.

52. WahlMC, SundaralingamM (2000) B-form to A-form conversion by a 3′-terminal ribose: crystal structure of the chimera d(CCACTAGTG)r(G). Nucleic Acids Res 28: 4356–4363.

53. PomerantzRT, O'DonnellM (2008) The replisome uses mRNA as a primer after colliding with RNA polymerase. Nature 456: 762–766.

54. DuttaD, ShatalinK, EpshteinV, GottesmanME, NudlerE (2011) Linking RNA polymerase backtracking to genome instability in E. coli. Cell 146: 533–543.

55. WattDL, JohanssonE, BurgersPM, KunkelTA (2011) Replication of ribonucleotide-containing DNA templates by yeast replicative polymerases. DNA Repair 10: 897–902.

56. WindM, ReinesD (2000) Transcription elongation factor SII. BioEssays 22: 327–336.

57. WilliamsJS, SmithDJ, MarjavaaraL, LujanSA, ChabesA, et al. (2013) Topoisomerase 1-mediated removal of ribonucleotides from nascent leading-strand DNA. Mol Cell 49 ((5)): 1010–5.

58. GueldenerU, HeinischJ, KoehlerGJ, VossD, HegemannJH (2002) A second set of loxP marker cassettes for Cre-mediated multiple gene knockouts in budding yeast. Nucleic Acids Res 30: e23.

59. LeaDE, CoulsonCA (1949) The distribution of the numbers of mutants in bacterial populations. J Genet 49: 264–285.

60. Spell RM, Jinks-Robertson S (2004) Determination of mitotic recombination rates by fluctuation analysis in Saccharomyces cerevisiae. In: Waldman AS, editor. Genetic Recombination: Reviews and Protocols. Totowa, NJ: Humana Press. pp. 3–12.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 11
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#