Rtt109 Prevents Hyper-Amplification of Ribosomal RNA Genes through Histone Modification in Budding Yeast
The genes encoding ribosomal RNA are the most abundant in the eukaryotic genome. They reside in tandem repetitive clusters, in some cases totaling hundreds of copies. Due to their repetitive structure, ribosomal RNA genes (rDNA) are easily lost by recombination events within the repeated cluster. We previously identified a unique gene amplification system driven by unequal sister-chromatid recombination during DNA replication. The system compensates for such copy number losses, thus maintaining proper copy number. Here, through a genome-wide screen for genes regulating rDNA copy number, we found that the rtt109 mutant exhibited a hyper-amplification phenotype (∼3 times greater than the wild-type level). RTT109 encodes an acetyl transferase that acetylates lysine 56 of histone H3 and which functions in replication-coupled nucleosome assembly. Relative to unequal sister-chromatid recombination-based amplification (∼1 copy/cell division), the rate of the hyper-amplification in the rtt109 mutant was extremely high (>100 copies/cell division). Cohesin dissociation that promotes unequal sister-chromatid recombination was not observed in this mutant. During hyper-amplification, production level of extra-chromosomal rDNA circles (ERC) by intra-chromosomal recombination in the rDNA was reduced. Interestingly, during amplification, a plasmid containing an rDNA unit integrated into the rDNA as a tandem array. These results support the idea that tandem DNA arrays are produced and incorporated through rolling-circle-type replication. We propose that, in the rtt109 mutant, rDNA hyper-amplification is caused by uncontrolled rolling-circle-type replication.
Vyšlo v časopise:
Rtt109 Prevents Hyper-Amplification of Ribosomal RNA Genes through Histone Modification in Budding Yeast. PLoS Genet 9(4): e32767. doi:10.1371/journal.pgen.1003410
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1003410
Souhrn
The genes encoding ribosomal RNA are the most abundant in the eukaryotic genome. They reside in tandem repetitive clusters, in some cases totaling hundreds of copies. Due to their repetitive structure, ribosomal RNA genes (rDNA) are easily lost by recombination events within the repeated cluster. We previously identified a unique gene amplification system driven by unequal sister-chromatid recombination during DNA replication. The system compensates for such copy number losses, thus maintaining proper copy number. Here, through a genome-wide screen for genes regulating rDNA copy number, we found that the rtt109 mutant exhibited a hyper-amplification phenotype (∼3 times greater than the wild-type level). RTT109 encodes an acetyl transferase that acetylates lysine 56 of histone H3 and which functions in replication-coupled nucleosome assembly. Relative to unequal sister-chromatid recombination-based amplification (∼1 copy/cell division), the rate of the hyper-amplification in the rtt109 mutant was extremely high (>100 copies/cell division). Cohesin dissociation that promotes unequal sister-chromatid recombination was not observed in this mutant. During hyper-amplification, production level of extra-chromosomal rDNA circles (ERC) by intra-chromosomal recombination in the rDNA was reduced. Interestingly, during amplification, a plasmid containing an rDNA unit integrated into the rDNA as a tandem array. These results support the idea that tandem DNA arrays are produced and incorporated through rolling-circle-type replication. We propose that, in the rtt109 mutant, rDNA hyper-amplification is caused by uncontrolled rolling-circle-type replication.
Zdroje
1. WarnerJR (1999) The economics of ribosome biosynthesis in yeast. Trends Biochem Sci 24: 437–40.
2. IdeS, MiyazakiT, MakiH, KobayashiT (2010) Abundance of ribosomal RNA gene copies maintains genome integrity. Science 327: 693–6.
3. KobayashiT, HeckDJ, NomuraM, HoriuchiT (1998) Expansion and contraction of ribosomal DNA repeats in Saccharomyces cerevisiae: requirement of replication fork blocking (Fob1) protein and the role of RNA polymerase I. Genes Dev 12: 3821–30.
4. KobayashiT (2006) Strategies to maintain the stability of the ribosomal RNA gene repeats–collaboration of recombination, cohesion, and condensation. Genes Genet Syst 81: 155–61.
5. KobayashiT (2003) The replication fork barrier site forms a unique structure with Fob1p and inhibits the replication fork. Mol Cell Biol 23: 9178–88.
6. KobayashiT, HoriuchiT, TongaonkarP, VuL, NomuraM (2004) SIR2 regulates recombination between different rDNA repeats, but not recombination within individual rRNA genes in yeast. Cell 117: 441–53.
7. KobayashiT, GanleyAR (2005) Recombination regulation by transcription-induced cohesin dissociation in rDNA repeats. Science 309: 1581–4.
8. DriscollR, HudsonA, JacksonSP (2007) Yeast Rtt109 promotes genome stability by acetylating histone H3 on lysine 56. Science 315: 649–52.
9. TsubotaT, BerndsenCE, ErkmannJA, SmithCL, YangL, FreitasMA, DenuJM, KaufmanPD (2007) Histone H3-K56 acetylation is catalyzed by histone chaperone-dependent complexes. Mol Cell 25: 703–12.
10. HanJ, ZhouH, HorazdovskyB, ZhangK, XuRM, ZhangZ (2007) Rtt109 acetylates histone H3 lysine 56 and functions in DNA replication. Science 315: 653–5.
11. HanJ, ZhouH, LiZ, XuRM, ZhangZ (2007) Acetylation of lysine 56 of histone H3 catalyzed by RTT109 and regulated by ASF1 is required for replisome integrity. J Biol Chem 282: 28587–96.
12. LiQ, ZhouH, WurteleH, DaviesB, HorazdovskyB, VerreaultA, ZhangZ (2008) Acetylation of histone H3 lysine 56 regulates replication-coupled nucleosome assembly. Cell 134: 244–55.
13. MasumotoH, HawkeD, KobayashiR, VerreaultA (2005) A role for cell-cycle-regulated histone H3 lysine 56 acetylation in the DNA damage response. Nature 436: 294–8.
14. PradoF, Cortes-LedesmaF, AguileraA (2004) The absence of the yeast chromatin assembly factor Asf1 increases genomic instability and sister chromatid exchange. EMBO Rep 5: 497–502.
15. DuroE, VaisicaJA, BrownGW, RouseJ (2008) Budding yeast Mms22 and Mms1 regulate homologous recombination induced by replisome blockage. DNA Repair (Amst) 7: 811–8.
16. EndoH, KawashimaS, SatoL, LaiMS, EnomotoT, SekiM, HorikoshiM (2010) Chromatin dynamics mediated by histone modifiers and histone chaperones in postreplicative recombination. Genes Cells 15: 945–58.
17. HouseleyJ, TollerveyD (2011) Repeat expansion in the budding yeast ribosomal DNA can occur independently of the canonical homologous recombination machinery. Nucleic Acids Res 39: 8778–91.
18. CelicI, VerreaultA, BoekeJD (2008) Histone H3 K56 hyperacetylation perturbs replisomes and causes DNA damage. Genetics 179: 1769–84.
19. RechtJ, TsubotaT, TannyJC, DiazRL, BergerJM, ZhangX, GarciaBA, ShabanowitzJ, BurlingameAL, HuntDF, KaufmanPD, AllisCD (2006) Histone chaperone Asf1 is required for histone H3 lysine 56 acetylation, a modification associated with S phase in mitosis and meiosis. Proc Nat Acad Sci USA 103: 6988–93.
20. SchneiderJ, BajwaP, JohnsonFC, BhaumikSR, ShilatifardA (2006) Rtt109 is required for proper H3K56 acetylation: a chromatin mark associated with the elongating RNA polymerase II. J Biol Chem 281: 37270–4.
21. BerndsenCE, TsubotaT, LindnerSE, LeeS, HoltonJM, KaufmanPD, KeckJL, DenuJM (2008) Molecular functions of the histone acetyltransferase chaperone complex Rtt109-Vps75. Nat Struct Mol Biol 15: 948–56.
22. ParkYJ, SudhoffKB, AndrewsAJ, StargellLA, LugerK (2008) Histone chaperone specificity in Rtt109 activation. Nat Struct Mol Biol 15: 957–64.
23. FillinghamJ, RechtJ, SilvaAC, SuterB, EmiliA, StagljarI, KroganNJ, AllisCD, KeoghMC, GreenblattJF (2008) Chaperone control of the activity and specificity of the histone H3 acetyltransferase Rtt109. Mol Cell Biol 28: 4342–53.
24. DefossezPA, PrustyR, KaeberleinM, LinSJ, FerrignoP, SilverPA, KeilRL, GuarenteL (1999) Elimination of replication block protein Fob1 extends the life span of yeast mother cells. Mol Cell 3: 447–55.
25. TakeuchiY, HoriuchiT, KobayashiT (2003) Transcription-dependent recombination and the role of fork collision in yeast rDNA. Genes Dev 17: 1497–506.
26. OakesM, SiddiqiI, VuL, ArisJ, NomuraM (1999) Transcription factor UAF, expansion and contraction of ribosomal DNA (rDNA) repeats, and RNA polymerase switch in transcription of yeast rDNA. Mol Cell Biol 19: 8559–69.
27. BernsteinKA, ReidRJ, SunjevaricI, DemuthK, BurgessRC, RothsteinR (2011) The Shu complex, which contains Rad51 paralogues, promotes DNA repair through inhibition of the Srs2 anti-recombinase. Mol Biol Cell 22: 1599–607.
28. DammannR, LucchiniR, KollerT, SogoJM (1993) Chromatin structures and transcription of rDNA in yeast Saccharomyces cerevisiae. Nucleic Acids Res 21: 2331–38.
29. GottliebS, EspositoRE (1989) A new role for a yeast transcriptional silencer gene, SIR2, in regulation of recombination in ribosomal DNA. Cell 56: 771–6.
30. FritzeCE, VerschuerenK, StrichR, Easton EspositoR (1997) Direct evidence for SIR2 modulation of chromatin structure in yeast rDNA. EMBO J 16: 6495–509.
31. ImaiS, JohnsonFB, MarciniakRA, McVeyM, ParkPU, GuarenteL (2000) Sir2: an NAD-dependent histone deacetylase that connects chromatin silencing, metabolism, and aging. Cold Spring Harb Symp Quant Biol 65: 297–302.
32. MichelAH, KornmannB, DubranaK, ShoreD (2005) Spontaneous rDNA copy number variation modulates Sir2 levels and epigenetic gene silencing. Genes Dev 19: 1199–210.
33. ZaidiIW, RabutG, PovedaA, ScheelH, MalmstromJ, UlrichH, HofmannK, PaseroP, PeterM, LukeB (2008) Rtt101 and Mms1 in budding yeast form a CUL4(DDB1)-like ubiquitin ligase that promotes replication through damaged DNA. EMBO Rep 9: 1034–40.
34. DuroE, LundinC, AskK, Sanchez-PulidoL, MacArtneyTJ, TothR, PontingCP, GrothA, HelledayT, RouseJ (2010) Identification of the MMS22L-TONSL complex that promotes homologous recombination. Mol Cell 40: 632–44.
35. KrausE, LeungW-Y, HaberJE (2001) Break-induced replication: a review and an example in budding yeast. Pro Natl Acad Sci 98: 8255–62.
36. WurteleH, et al. (2012) Histone H3 lysine 56 acetylation and the response to DNA replication fork damage. Mol Cell Biol 32: 154–72.
37. HourcadeD, DresslerD, WolfsonJ (1973) The amplification of ribosomal RNA genes involves a rolling circle intermediate. Proc Natl Acad Sci U S A 70: 2926–30.
38. BrownDD, DawidI (1968) Specific gene amplification in oocytes. Oocyte nuclei contain extrachromosomal replicas of the genes for ribosomal RNA. Science 160: 272–80.
39. GallJG (1968) Differential synthesis of the genes for ribosomal RNA during amphibian oögenesis. Proc Nat Acad Sci USA 60: 553–60.
40. AnderssonDI, HughesD (2009) Gene Amplification and Adaptive Evolution in Bacteria. Ann Rev Genet 43: 167–95.
41. AlbertsonDG (2006) Gene amplifiction and cancer. Trend Genet 22: 447–55.
42. ArcherSY, HodinRA (1999) Histon acetylation and cancer. Cur Opin Genet & Dev 9: 171–74.
43. IdeS, KobayashiT (2010) Analysis of DNA replication in Saccharomyces cerevisiae by two-dimensional and pulsed-field gel electrophoresis. Curr Protoc Cell Biol Chapter 22: Unit 22 14.
44. MillerA, YangB, FosterT, KirchmaierAL (2008) Proliferating cell nuclear antigen and ASF1 modulate silent chromatin in Saccharomyces cerevisiae via lysine 56 on histone H3. Genetics 179: 793–809.
45. NettikadanS, TokumasuF, TakeyasuK (1996) Quantitative analysis of the transcription factor AP2 binding to DNA by atomic force microscopy. Biochem Biophys Res Commun 1226: 645–9.
46. CherryJM, HongEL, AmundsenC, BalakrishnanR, BinkleyG, et al. (2012) Saccharomyces Genome Database: the genomics resource of budding yeast. Nucleic Acids Res 40(Database issue): D700–5.
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
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