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Asynchronous Replication, Mono-Allelic Expression, and Long Range -Effects of
Mammalian chromosomes initiate DNA replication at multiple sites along their length during each S phase following a temporal replication program. The majority of genes on homologous chromosomes replicate synchronously. However, mono-allelically expressed genes such as imprinted genes, allelically excluded genes, and genes on female X chromosomes replicate asynchronously. We have identified a cis-acting locus on human chromosome 6 that controls this replication-timing program. This locus encodes a large intergenic non-coding RNA gene named Asynchronous replication and Autosomal RNA on chromosome 6, or ASAR6. Disruption of ASAR6 results in delayed replication, delayed mitotic chromosome condensation, and activation of the previously silent alleles of mono-allelic genes on chromosome 6. The ASAR6 gene resides within an ∼1.2 megabase domain of asynchronously replicating DNA that is coordinated with other random asynchronously replicating loci along chromosome 6. In contrast to other nearby mono-allelic genes, ASAR6 RNA is expressed from the later-replicating allele. ASAR6 RNA is synthesized by RNA Polymerase II, is not polyadenlyated, is restricted to the nucleus, and is subject to random mono-allelic expression. Disruption of ASAR6 leads to the formation of bridged chromosomes, micronuclei, and structural instability of chromosome 6. Finally, ectopic integration of cloned genomic DNA containing ASAR6 causes delayed replication of entire mouse chromosomes.
Vyšlo v časopise: Asynchronous Replication, Mono-Allelic Expression, and Long Range -Effects of. PLoS Genet 9(4): e32767. doi:10.1371/journal.pgen.1003423
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003423Souhrn
Mammalian chromosomes initiate DNA replication at multiple sites along their length during each S phase following a temporal replication program. The majority of genes on homologous chromosomes replicate synchronously. However, mono-allelically expressed genes such as imprinted genes, allelically excluded genes, and genes on female X chromosomes replicate asynchronously. We have identified a cis-acting locus on human chromosome 6 that controls this replication-timing program. This locus encodes a large intergenic non-coding RNA gene named Asynchronous replication and Autosomal RNA on chromosome 6, or ASAR6. Disruption of ASAR6 results in delayed replication, delayed mitotic chromosome condensation, and activation of the previously silent alleles of mono-allelic genes on chromosome 6. The ASAR6 gene resides within an ∼1.2 megabase domain of asynchronously replicating DNA that is coordinated with other random asynchronously replicating loci along chromosome 6. In contrast to other nearby mono-allelic genes, ASAR6 RNA is expressed from the later-replicating allele. ASAR6 RNA is synthesized by RNA Polymerase II, is not polyadenlyated, is restricted to the nucleus, and is subject to random mono-allelic expression. Disruption of ASAR6 leads to the formation of bridged chromosomes, micronuclei, and structural instability of chromosome 6. Finally, ectopic integration of cloned genomic DNA containing ASAR6 causes delayed replication of entire mouse chromosomes.
Zdroje
1. ThayerMJ (2012) Mammalian chromosomes contain cis-acting elements that control replication timing, mitotic condensation, and stability of entire chromosomes. Bioessays 2012.
2. zur HausenH (1967) Chromosomal changes of similar nature in seven established cell lines derived from the peripheral blood of patients with leukemia. J Natl Cancer Inst 38 : 683–696.
3. KatoH, SandbergAA (1968) Chromosome pulverization in human cells with micronuclei. J Natl Cancer Inst 40 : 165–179.
4. MilesCP, O'NeillF (1969) 3H labeling patterns of permanent cell line chromosomes showing pulverization or accentuated secondary constrictions. J Cell Biol 40 : 553–561.
5. SmithL, PlugA, ThayerM (2001) Delayed Replication Timing Leads to Delayed Mitotic Chromosome Condensation and Chromosomal Instability of Chromosome Translocations. Proc Natl Acad Sci U S A 98 : 13300–13305.
6. ChangBH, SmithL, HuangJ, ThayerM (2007) Chromosomes with delayed replication timing lead to checkpoint activation, delayed recruitment of Aurora B and chromosome instability. Oncogene 26 : 1852–1861.
7. BregerKS, SmithL, TurkerMS, ThayerMJ (2004) Ionizing radiation induces frequent translocations with delayed replication and condensation. Cancer Research 64 : 8231–8238.
8. BregerKS, SmithL, ThayerMJ (2005) Engineering translocations with delayed replication: evidence for cis control of chromosome replication timing. Hum Mol Genet 14 : 2813–2827.
9. StoffregenEP, DonleyN, StaufferD, SmithL, ThayerMJ (2011) An autosomal locus that controls chromosome-wide replication timing and mono-allelic expression. Hum Mol Genet 20 : 2366–2378.
10. PayerB, LeeJT (2008) X chromosome dosage compensation: how mammals keep the balance. Annu Rev Genet 42 : 733–772.
11. AuguiS, NoraEP, HeardE (2011) Regulation of X-chromosome inactivation by the X-inactivation centre. Nat Rev Genet 12 : 429–442.
12. Diaz-PerezS, OuyangY, PerezV, CisnerosR, RegelsonM, et al. (2005) The element(s) at the nontranscribed Xist locus of the active X chromosome controls chromosomal replication timing in the mouse. Genetics 171 : 663–672.
13. Diaz-PerezSV, FergusonDO, WangC, CsankovszkiG, TsaiSC, et al. (2006) A deletion at the mouse Xist gene exposes trans-effects that alter the heterochromatin of the inactive X chromosome and the replication time and DNA stability of both X chromosomes. Genetics 174 : 1115–1133.
14. GartlerSM, GoldsteinL, Tyler-FreerSE, HansenRS (1999) The timing of XIST replication: dominance of the domain. Hum Mol Genet 8 : 1085–1089.
15. ZwemerLM, ZakA, ThompsonBR, KirbyA, DalyMJ, et al. (2012) Autosomal monoallelic expression in the mouse. Genome Biol 13: R10.
16. GimelbrantA, HutchinsonJN, ThompsonBR, ChessA (2007) Widespread monoallelic expression on human autosomes. Science 318 : 1136–1140.
17. EnsmingerAW, ChessA (2004) Coordinated replication timing of monoallelically expressed genes along human autosomes. Hum Mol Genet 13 : 651–658.
18. GoldmitM, BergmanY (2004) Monoallelic gene expression: a repertoire of recurrent themes. Immunol Rev 200 : 197–214.
19. MostoslavskyR, SinghN, TenzenT, GoldmitM, GabayC, et al. (2001) Asynchronous replication and allelic exclusion in the immune system. Nature 414 : 221–225.
20. SinghN, EbrahimiFA, GimelbrantAA, EnsmingerAW, TackettMR, et al. (2003) Coordination of the random asynchronous replication of autosomal loci. Nat Genet 33 : 339–341.
21. SeligS, OkumuraK, WardDC, CedarH (1992) Delineation of DNA replication time zones by fluorescence in situ hybridization. EMBO J 11 : 1217–1225.
22. AzuaraV, BrownKE, WilliamsRR, WebbN, DillonN, et al. (2003) Heritable gene silencing in lymphocytes delays chromatid resolution without affecting the timing of DNA replication. Nat Cell Biol 5 : 668–674.
23. SchlesingerS, SeligS, BergmanY, CedarH (2009) Allelic inactivation of rDNA loci. Genes Dev 23 : 2437–2447.
24. GoodwinE, MeyneJ (1993) Strand-specific FISH reveals orientation of chromosome 18 alphoid DNA. Cytogenet Cell Genet 63 : 126–127.
25. ConsortiumEP (2011) A user's guide to the encyclopedia of DNA elements (ENCODE). PLoS Biol 9: e1001046 doi:10.1371/journal.pbio.1001046.
26. MeihlacM, KedingerC, ChambonP, FaulstichH, GovindanMV, et al. (1970) Amanitin binding to calf thymus RNA polymerase B. FEBS Lett 9 : 258–260.
27. WyersF, RougemailleM, BadisG, RousselleJC, DufourME, et al. (2005) Cryptic pol II transcripts are degraded by a nuclear quality control pathway involving a new poly(A) polymerase. Cell 121 : 725–737.
28. HirataR, ChamberlainJ, DongR, RussellDW (2002) Targeted transgene insertion into human chromosomes by adeno-associated virus vectors. Nat Biotechnol 20 : 735–738.
29. MinksJ, BrownCJ (2009) Getting to the center of X-chromosome inactivation: the role of transgenes. Biochem Cell Biol 87 : 759–766.
30. HallLL, ByronM, SakaiK, CarrelL, WillardHF, et al. (2002) An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells. Proc Natl Acad Sci U S A 99 : 8677–8682.
31. ChowJC, HallLL, LawrenceJB, BrownCJ (2002) Ectopic XIST transcripts in human somatic cells show variable expression and localization. Cytogenet Genome Res 99 : 92–98.
32. RasmussenTP, WutzAP, PehrsonJR, JaenischRR (2001) Expression of Xist RNA is sufficient to initiate macrochromatin body formation. Chromosoma 110 : 411–420.
33. LeeJT, JaenischR (1997) Long-range cis effects of ectopic X-inactivation centres on a mouse autosome. Nature 386 : 275–279.
34. MarinelliLJ, HatfullGF, PiuriM (2012) Recombineering: A powerful tool for modification of bacteriophage genomes. Bacteriophage 2 : 5–14.
35. HirataniI, TakebayashiS, LuJ, GilbertDM (2009) Replication timing and transcriptional control: beyond cause and effect–part II. Curr Opin Genet Dev 19 : 142–149.
36. SchwaigerM, SchubelerD (2006) A question of timing: emerging links between transcription and replication. Curr Opin Genet Dev 16 : 177–183.
37. RybaT, HirataniI, LuJ, ItohM, KulikM, et al. (2010) Evolutionarily conserved replication timing profiles predict long-range chromatin interactions and distinguish closely related cell types. Genome Res 20 : 761–770.
38. YaffeE, Farkash-AmarS, PoltenA, YakhiniZ, TanayA, et al. (2010) Comparative analysis of DNA replication timing reveals conserved large-scale chromosomal architecture. PLoS Genet 6: e1001011 doi:10.1371/journal.pgen.1001011.
39. DeS, MichorF (2011) DNA replication timing and long-range DNA interactions predict mutational landscapes of cancer genomes. Nat Biotechnol 29 : 1103–1108.
40. GilbertDM, TakebayashiSI, RybaT, LuJ, PopeBD, et al. (2011) Space and time in the nucleus: developmental control of replication timing and chromosome architecture. Cold Spring Harb Symp Quant Biol 75 : 143–153.
41. TorchiaBS, CallLM, MigeonBR (1994) DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late. Am J Hum Genet 55 : 96–104.
42. GomezM, BrockdorffN (2004) Heterochromatin on the inactive X chromosome delays replication timing without affecting origin usage. Proc Natl Acad Sci U S A 101 : 6923–6928.
43. HirataniI, RybaT, ItohM, RathjenJ, KulikM, et al. (2009) Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesis. Genome Res 20 : 155–169.
44. KruegerC, MorisonIM (2008) Random monoallelic expression: making a choice. Trends Genet 24 : 257–259.
45. ZakharovaIS, ShevchenkoAI, ZakianSM (2009) Monoallelic gene expression in mammals. Chromosoma 118 : 279–290.
46. LiSM, ValoZ, WangJ, GaoH, BowersCW, et al. (2012) Transcriptome-wide survey of mouse CNS-derived cells reveals monoallelic expression within novel gene families. PLoS ONE 7: e31751 doi:10.1371/journal.pone.0031751.
47. LeeJT, LuN, HanY (1999) Genetic analysis of the mouse X inactivation center defines an 80-kb multifunction domain. Proc Natl Acad Sci U S A 96 : 3836–3841.
48. HerzingLB, RomerJT, HornJM, AshworthA (1997) Xist has properties of the X-chromosome inactivation centre. Nature 386 : 272–275.
49. HeardE, MongelardF, ArnaudD, AvnerP (1999) Xist yeast artificial chromosome transgenes function as X-inactivation centers only in multicopy arrays and not as single copies. Mol Cell Biol 19 : 3156–3166.
50. BrockdorffN, AshworthA, KayGF, McCabeVM, NorrisDP, et al. (1992) The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus. Cell 71 : 515–526.
51. HasegawaY, BrockdorffN, KawanoS, TsutuiK, NakagawaS (2010) The matrix protein hnRNP U is required for chromosomal localization of Xist RNA. Dev Cell 19 : 469–476.
52. ZhaoJ, SunBK, ErwinJA, SongJJ, LeeJT (2008) Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome. Science 322 : 750–756.
53. GanesanS, SilverDP, DrapkinR, GreenbergR, FeunteunJ, et al. (2004) Association of BRCA1 with the inactive X chromosome and XIST RNA. Philos Trans R Soc Lond B Biol Sci 359 : 123–128.
54. StephensPJ, GreenmanCD, FuB, YangF, BignellGR, et al. (2011) Massive genomic rearrangement acquired in a single catastrophic event during cancer development. Cell 144 : 27–40.
55. CrastaK, GanemNJ, DagherR, LantermannAB, IvanovaEV, et al. (2012) DNA breaks and chromosome pulverization from errors in mitosis. Nature 2012.
56. LiuP, ErezA, NagamaniSC, DharSU, KolodziejskaKE, et al. (2011) Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. Cell 146 : 889–903.
57. KloostermanWP, GuryevV, van RoosmalenM, DuranKJ, de BruijnE, et al. (2011) Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline. Hum Mol Genet 20 : 1916–1924.
58. ZhuY, ByeS, StambrookPJ, TischfieldJA (1994) Single-base deletion induced by benzo[a]pyrene diol epoxide at the adenine phosphoribosyltransferase locus in human fibrosarcoma cell lines. Mutat Res 321 : 73–79.
59. Helm S (1995) Cancer Cytogenetics. New York: Wiley-Liss.
60. Trask B, Pinkel D (1990) Flow cytometry; Crissman HA, Darzynkiewica Z, editors. New York: Academic Press.
61. SmithL, ThayerM (2012) Chromosome replication timing combined with fluorescent in situ hybridization. JOVE in press.
62. WarmingS, CostantinoN, CourtDL, JenkinsNA, CopelandNG (2005) Simple and highly efficient BAC recombineering using galK selection. Nucleic Acids Res 33: e36.
63. ValenE, PascarellaG, ChalkA, MaedaN, KojimaM, et al. (2009) Genome-wide detection and analysis of hippocampus core promoters using DeepCAGE. Genome Res 19 : 255–265.
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