#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

A Role for CF1A 3′ End Processing Complex in Promoter-Associated Transcription


The Cleavage Factor 1A (CF1A) complex, which is required for the termination of transcription in budding yeast, occupies the 3′ end of transcriptionally active genes. We recently demonstrated that CF1A subunits also crosslink to the 5′ end of genes during transcription. The presence of CF1A complex at the promoter suggested its possible involvement in the initiation/reinitiation of transcription. To check this possibility, we performed transcription run-on assay, RNAP II-density ChIP and strand-specific RT-PCR analysis in a mutant of CF1A subunit Clp1. As expected, RNAP II read through the termination signal in the temperature-sensitive mutant of clp1 at elevated temperature. The transcription readthrough phenotype was accompanied by a decrease in the density of RNAP II in the vicinity of the promoter region. With the exception of TFIIB and TFIIF, the recruitment of the general transcription factors onto the promoter, however, remained unaffected in the clp1 mutant. These results suggest that the CF1A complex affects the recruitment of RNAP II onto the promoter for reinitiation of transcription. Simultaneously, an increase in synthesis of promoter-initiated divergent antisense transcript was observed in the clp1 mutant, thereby implicating CF1A complex in providing directionality to the promoter-bound polymerase. Chromosome Conformation Capture (3C) analysis revealed a physical interaction of the promoter and terminator regions of a gene in the presence of a functional CF1A complex. Gene looping was completely abolished in the clp1 mutant. On the basis of these results, we propose that the CF1A-dependent recruitment of RNAP II onto the promoter for reinitiation and the regulation of directionality of promoter-associated transcription are accomplished through gene looping.


Vyšlo v časopise: A Role for CF1A 3′ End Processing Complex in Promoter-Associated Transcription. PLoS Genet 9(8): e32767. doi:10.1371/journal.pgen.1003722
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003722

Souhrn

The Cleavage Factor 1A (CF1A) complex, which is required for the termination of transcription in budding yeast, occupies the 3′ end of transcriptionally active genes. We recently demonstrated that CF1A subunits also crosslink to the 5′ end of genes during transcription. The presence of CF1A complex at the promoter suggested its possible involvement in the initiation/reinitiation of transcription. To check this possibility, we performed transcription run-on assay, RNAP II-density ChIP and strand-specific RT-PCR analysis in a mutant of CF1A subunit Clp1. As expected, RNAP II read through the termination signal in the temperature-sensitive mutant of clp1 at elevated temperature. The transcription readthrough phenotype was accompanied by a decrease in the density of RNAP II in the vicinity of the promoter region. With the exception of TFIIB and TFIIF, the recruitment of the general transcription factors onto the promoter, however, remained unaffected in the clp1 mutant. These results suggest that the CF1A complex affects the recruitment of RNAP II onto the promoter for reinitiation of transcription. Simultaneously, an increase in synthesis of promoter-initiated divergent antisense transcript was observed in the clp1 mutant, thereby implicating CF1A complex in providing directionality to the promoter-bound polymerase. Chromosome Conformation Capture (3C) analysis revealed a physical interaction of the promoter and terminator regions of a gene in the presence of a functional CF1A complex. Gene looping was completely abolished in the clp1 mutant. On the basis of these results, we propose that the CF1A-dependent recruitment of RNAP II onto the promoter for reinitiation and the regulation of directionality of promoter-associated transcription are accomplished through gene looping.


Zdroje

1. SvejstrupJQ (2004) The RNA polymerase II transcription cycle: cycling through chromatin. Biochim Biophys Acta 1677: 64–73.

2. WoychikNA, HampseyM (2002) The RNA polymerase II machinery: structure illuminates function. Cell 108: 453–463.

3. HahnS (2004) Structure and mechanism of the RNA polymerase II transcription machinery. Nat Struct Mol Biol 11: 394–403.

4. HahnS, YoungET (2011) Transcriptional regulation in Saccharomyces cerevisiae: transcription factor regulation and function, mechanisms of initiation, and roles of activators and coactivators. Genetics 189: 705–736.

5. SpitzF, FurlongEE (2012) Transcription factors: from enhancer binding to developmental control. Nat Rev Genet 13: 613–626.

6. MandelCR, BaiY, TongL (2008) Protein factors in pre-mRNA 3′-end processing. Cell Mol Life Sci 65: 1099–1122.

7. MillevoiS, VagnerS (2010) Molecular mechanisms of eukaryotic pre-mRNA 3′ end processing regulation. Nucleic Acids Res 38: 2757–2774.

8. RichardP, ManleyJL (2009) Transcription termination by nuclear RNA polymerases. Genes Dev 23: 1247–1269.

9. MischoHE, ProudfootNJ (2012) Disengaging polymerase: Terminating RNA polymerase II transcription in budding yeast. Biochim Biophys Acta 1829: 174–85.

10. KuehnerJN, PearsonEL, MooreC (2011) Unravelling the means to an end: RNA polymerase II transcription termination. Nat Rev Mol Cell Biol 12: 283–294.

11. CalvoO, ManleyJL (2003) Strange bedfellows: polyadenylation factors at the promoter. Genes Dev 17: 1321–1327.

12. WangY, RobertsSG (2010) New insights into the role of TFIIB in transcription initiation. Transcription 1: 126–129.

13. Lykke-AndersenS, MapendanoCK, JensenTH (2011) An ending is a new beginning: transcription termination supports re-initiation. Cell Cycle 10: 863–865.

14. ShandilyaJ, WangY, RobertsSG (2012) TFIIB dephosphorylation links transcription inhibition with the p53-dependent DNA damage response. Proc Natl Acad Sci U S A 109: 18797–18802.

15. SunZW, HampseyM (1996) Synthetic enhancement of a TFIIB defect by a mutation in SSU72, an essential yeast gene encoding a novel protein that affects transcription start site selection in vivo. Mol Cell Biol 16: 1557–1566.

16. El KaderiB, MedlerS, RaghunayakulaS, AnsariA (2009) Gene looping is conferred by activator-dependent interaction of transcription initiation and termination machineries. J Biol Chem 284: 25015–25025.

17. WangY, FairleyJA, RobertsSG (2010) Phosphorylation of TFIIB links transcription initiation and termination. Curr Biol 20: 548–553.

18. MedlerS, Al HusiniN, RaghunayakulaS, MukundanB, AldeaA, et al. (2011) Evidence for a complex of transcription factor IIB with poly(A) polymerase and cleavage factor 1 subunits required for gene looping. J Biol Chem 286: 33709–33718.

19. HenriquesT, JiZ, Tan-WongSM, CarmoAM, TianB, et al. (2012) Transcription termination between polo and snap, two closely spaced tandem genes of D. melanogaster. Transcription 3: 198–212.

20. MukundanB, AnsariA (2011) Novel role for mediator complex subunit Srb5/Med18 in termination of transcription. J Biol Chem 286: 37053–37057.

21. DantonelJC, MurthyKG, ManleyJL, ToraL (1997) Transcription factor TFIID recruits factor CPSF for formation of 3′ end of mRNA. Nature 389: 399–402.

22. SandersSL, JenningsJ, CanutescuA, LinkAJ, WeilPA (2002) Proteomics of the eukaryotic transcription machinery: identification of proteins associated with components of yeast TFIID by multidimensional mass spectrometry. Mol Cell Biol 22: 4723–4738.

23. LeeKK, SardiuME, SwansonSK, GilmoreJM, TorokM, et al. (2011) Combinatorial depletion analysis to assemble the network architecture of the SAGA and ADA chromatin remodeling complexes. Mol Syst Biol 7: 503.

24. MilgromE, WestRWJr, GaoC, ShenWC (2005) TFIID and Spt-Ada-Gcn5-acetyltransferase functions probed by genome-wide synthetic genetic array analysis using a Saccharomyces cerevisiae taf9-ts allele. Genetics 171: 959–973.

25. GavinAC, AloyP, GrandiP, KrauseR, BoescheM, et al. (2006) Proteome survey reveals modularity of the yeast cell machinery. Nature 440: 631–636.

26. HeX, KhanAU, ChengH, PappasDLJr, HampseyM, et al. (2003) Functional interactions between the transcription and mRNA 3′ end processing machineries mediated by Ssu72 and Sub1. Genes Dev 17: 1030–1042.

27. DichtlB, BlankD, OhnackerM, FriedleinA, RoederD, et al. (2002) A role for SSU72 in balancing RNA polymerase II transcription elongation and termination. Mol Cell 10: 1139–1150.

28. WuWH, PintoI, ChenBS, HampseyM (1999) Mutational analysis of yeast TFIIB. A functional relationship between Ssu72 and Sub1/Tsp1 defined by allele-specific interactions with TFIIB. Genetics 153: 643–652.

29. GanemC, DevauxF, TorchetC, JacqC, Quevillon-CheruelS, et al. (2003) Ssu72 is a phosphatase essential for transcription termination of snoRNAs and specific mRNAs in yeast. EMBO J 22: 1588–1598.

30. AnsariA, HampseyM (2005) A role for the CPF 3′-end processing machinery in RNAP II-dependent gene looping. Genes Dev 19: 2969–2978.

31. CollinsSR, MillerKM, MaasNL, RoguevA, FillinghamJ, et al. (2007) Functional dissection of protein complexes involved in yeast chromosome biology using a genetic interaction map. Nature 446: 806–810.

32. FiedlerD, BrabergH, MehtaM, ChechikG, CagneyG, et al. (2009) Functional organization of the S. cerevisiae phosphorylation network. Cell 136: 952–963.

33. CostanzoM, BaryshnikovaA, BellayJ, KimY, SpearED, et al. (2010) The genetic landscape of a cell. Science 327: 425–431.

34. NedeaE, HeX, KimM, PootoolalJ, ZhongG, et al. (2003) Organization and function of APT, a subcomplex of the yeast cleavage and polyadenylation factor involved in the formation of mRNA and small nucleolar RNA 3′-ends. J Biol Chem 278: 33000–33010.

35. KimM, KroganNJ, VasiljevaL, RandoOJ, NedeaE, et al. (2004) The yeast Rat1 exonuclease promotes transcription termination by RNA polymerase II. Nature 432: 517–522.

36. CalvoO, ManleyJL (2005) The transcriptional coactivator PC4/Sub1 has multiple functions in RNA polymerase II transcription. EMBO J 24: 1009–1020.

37. UetzP, GiotL, CagneyG, MansfieldTA, JudsonRS, et al. (2000) A comprehensive analysis of protein-protein interactions in Saccharomyces cerevisiae. Nature 403: 623–627.

38. CalvoO, ManleyJL (2001) Evolutionarily conserved interaction between CstF-64 and PC4 links transcription, polyadenylation, and termination. Mol Cell 7: 1013–1023.

39. GavinAC, BoscheM, KrauseR, GrandiP, MarziochM, et al. (2002) Functional organization of the yeast proteome by systematic analysis of protein complexes. Nature 415: 141–147.

40. JensenTH, BoulayJ, OlesenJR, ColinJ, WeylerM, et al. (2004) Modulation of transcription affects mRNP quality. Mol Cell 16: 235–244.

41. HolbeinS, WengiA, DecourtyL, FreimoserFM, JacquierA, et al. (2009) Cordycepin interferes with 3′ end formation in yeast independently of its potential to terminate RNA chain elongation. RNA 15: 837–849.

42. MapendanoCK, Lykke-AndersenS, KjemsJ, BertrandE, JensenTH (2010) Crosstalk between mRNA 3′ end processing and transcription initiation. Mol Cell 40: 410–422.

43. ZhangY, ZhangM, ZhangY (2011) Crystal structure of Ssu72, an essential eukaryotic phosphatase specific for the C-terminal domain of RNA polymerase II, in complex with a transition state analogue. Biochem J 434: 435–444.

44. DieciG, SentenacA (1996) Facilitated recycling pathway for RNA polymerase III. Cell 84: 245–252.

45. CoreLJ, WaterfallJJ, LisJT (2008) Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters. Science 322: 1845–1848.

46. NeilH, MalabatC, d'Aubenton-CarafaY, XuZ, SteinmetzLM, et al. (2009) Widespread bidirectional promoters are the major source of cryptic transcripts in yeast. Nature 457: 1038–1042.

47. XuZ, WeiW, GagneurJ, PerocchiF, Clauder-MunsterS, et al. (2009) Bidirectional promoters generate pervasive transcription in yeast. Nature 457: 1033–1037.

48. SeilaAC, CoreLJ, LisJT, SharpPA (2009) Divergent transcription: a new feature of active promoters. Cell Cycle 8: 2557–2564.

49. Tan-WongSM, ZauggJB, CamblongJ, XuZ, ZhangDW, et al. (2012) Gene loops enhance transcriptional directionality. Science 338: 671–675.

50. GordonJM, ShikovS, KuehnerJN, LirianoM, LeeE, et al. (2011) Reconstitution of CF IA from overexpressed subunits reveals stoichiometry and provides insights into molecular topology. Biochemistry 50: 10203–10214.

51. HaddadR, MauriceF, ViphakoneN, Voisinet-HakilF, FribourgS, et al. (2012) An essential role for Clp1 in assembly of polyadenylation complex CF IA and Pol II transcription termination. Nucleic Acids Res 40: 1226–1239.

52. GhazyMA, GordonJM, LeeSD, SinghBN, BohmA, et al. (2012) The interaction of Pcf11 and Clp1 is needed for mRNA 3′-end formation and is modulated by amino acids in the ATP-binding site. Nucleic Acids Res 40: 1214–1225.

53. HolbeinS, ScolaS, LollB, DichtlBS, HubnerW, et al. (2011) The P-loop domain of yeast Clp1 mediates interactions between CF IA and CPF factors in pre-mRNA 3′ end formation. PLoS One 6: e29139.

54. Ben-AroyaS, CoombesC, KwokT, O'DonnellKA, BoekeJD, et al. (2008) Toward a comprehensive temperature-sensitive mutant repository of the essential genes of Saccharomyces cerevisiae. Mol Cell 30: 248–258.

55. PetersenJG, Kielland-BrandtMC, Nilsson-TillgrenT, BornaesC, HolmbergS (1988) Molecular genetics of serine and threonine catabolism in Saccharomyces cerevisiae. Genetics 119: 527–534.

56. ZawelL, KumarKP, ReinbergD (1995) Recycling of the general transcription factors during RNA polymerase II transcription. Genes Dev 9: 1479–1490.

57. RanishJA, YudkovskyN, HahnS (1999) Intermediates in formation and activity of the RNA polymerase II preinitiation complex: holoenzyme recruitment and a postrecruitment role for the TATA box and TFIIB. Genes Dev 13: 49–63.

58. YudkovskyN, RanishJA, HahnS (2000) A transcription reinitiation intermediate that is stabilized by activator. Nature 408: 225–229.

59. JacquierA (2009) The complex eukaryotic transcriptome: unexpected pervasive transcription and novel small RNAs. Nat Rev Genet 10: 833–844.

60. CostaFF (2010) Non-coding RNAs: Meet thy masters. Bioessays 32: 599–608.

61. FlynnRA, AlmadaAE, ZamudioJR, SharpPA (2011) Antisense RNA polymerase II divergent transcripts are P-TEFb dependent and substrates for the RNA exosome. Proc Natl Acad Sci U S A 108: 10460–10465.

62. El KaderiB, MedlerS, AnsariA (2012) Analysis of interactions between genomic loci through Chromosome Conformation Capture (3C). Curr Protoc Cell Biol Chapter 22: Unit22 15.

63. ArigoJT, EylerDE, CarrollKL, CordenJL (2006) Termination of cryptic unstable transcripts is directed by yeast RNA-binding proteins Nrd1 and Nab3. Mol Cell 23: 841–851.

64. BrannanK, KimH, EricksonB, Glover-CutterK, KimS, et al. (2012) mRNA decapping factors and the exonuclease Xrn2 function in widespread premature termination of RNA polymerase II transcription. Mol Cell 46: 311–324.

65. BirseCE, LeeBA, HansenK, ProudfootNJ (1997) Transcriptional termination signals for RNA polymerase II in fission yeast. EMBO J 16: 3633–3643.

66. HirayoshiK, LisJT (1999) Nuclear run-on assays: assessing transcription by measuring density of engaged RNA polymerases. Methods Enzymol 304: 351–362.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 Číslo 8
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#