Genome-Wide Control of RNA Polymerase II Activity by Cohesin
Cohesin is a well-known mediator of sister chromatid cohesion, but it also influences gene expression and development. These non-canonical roles of cohesin are not well understood, but are vital: gene expression and development are altered by modest changes in cohesin function that do not disrupt chromatid cohesion. To clarify cohesin's roles in transcription, we measured how cohesin controls RNA polymerase II (Pol II) activity by genome-wide chromatin immunoprecipitation and precision global run-on sequencing. On average, cohesin-binding genes have more transcriptionally active Pol II and promoter-proximal Pol II pausing than non-binding genes, and are more efficient, producing higher steady state levels of mRNA per transcribing Pol II complex. Cohesin depletion frequently decreases gene body transcription but increases pausing at cohesin-binding genes, indicating that cohesin often facilitates transition of paused Pol II to elongation. In many cases, this likely reflects a role for cohesin in transcriptional enhancer function. Strikingly, more than 95% of predicted extragenic enhancers bind cohesin, and cohesin depletion can reduce their association with Pol II, indicating that cohesin facilitates enhancer-promoter contact. Cohesin depletion decreases the levels of transcriptionally engaged Pol II at the promoters of most genes that don't bind cohesin, suggesting that cohesin controls expression of one or more broadly acting general transcription factors. The multiple transcriptional roles of cohesin revealed by these studies likely underlie the growth and developmental deficits caused by minor changes in cohesin activity.
Vyšlo v časopise:
Genome-Wide Control of RNA Polymerase II Activity by Cohesin. PLoS Genet 9(3): e32767. doi:10.1371/journal.pgen.1003382
Kategorie:
Research Article
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pgen.1003382
Souhrn
Cohesin is a well-known mediator of sister chromatid cohesion, but it also influences gene expression and development. These non-canonical roles of cohesin are not well understood, but are vital: gene expression and development are altered by modest changes in cohesin function that do not disrupt chromatid cohesion. To clarify cohesin's roles in transcription, we measured how cohesin controls RNA polymerase II (Pol II) activity by genome-wide chromatin immunoprecipitation and precision global run-on sequencing. On average, cohesin-binding genes have more transcriptionally active Pol II and promoter-proximal Pol II pausing than non-binding genes, and are more efficient, producing higher steady state levels of mRNA per transcribing Pol II complex. Cohesin depletion frequently decreases gene body transcription but increases pausing at cohesin-binding genes, indicating that cohesin often facilitates transition of paused Pol II to elongation. In many cases, this likely reflects a role for cohesin in transcriptional enhancer function. Strikingly, more than 95% of predicted extragenic enhancers bind cohesin, and cohesin depletion can reduce their association with Pol II, indicating that cohesin facilitates enhancer-promoter contact. Cohesin depletion decreases the levels of transcriptionally engaged Pol II at the promoters of most genes that don't bind cohesin, suggesting that cohesin controls expression of one or more broadly acting general transcription factors. The multiple transcriptional roles of cohesin revealed by these studies likely underlie the growth and developmental deficits caused by minor changes in cohesin activity.
Zdroje
1. DorsettD (2011) Cohesin: genomic insights into controlling gene transcription and development. Curr Opin Genet Dev 21: 199–206.
2. DorsettD, StrömL (2012) The ancient and evolving roles of cohesin in gene expression and DNA repair. Curr Biol 22: R240–250.
3. NasmythK, HaeringCH (2009) Cohesin: its roles and mechanisms. Annu Rev Genet 43: 525–558.
4. DorsettD, KrantzID (2009) On the molecular etiology of Cornelia de Lange syndrome. Ann N Y Acad Sci 1151: 22–37.
5. PauliA, van BemmelJG, OliveiraRA, ItohT, ShirahigeK, et al. (2010) A direct role for cohesin in gene regulation and ecdysone response in Drosophila salivary glands. Curr Biol 20: 1787–1798.
6. SeitanVC, HaoB, Tachibana-KonwalskiK, LavagnolliT, Mira-BontenbalH, et al. (2011) A role for cohesin in T-cell-receptor rearrangement and thymocyte differentiation. Nature 476: 467–467.
7. KageyMH, NewmanJJ, BilodeauS, ZhanY, OrlandoDA, et al. (2010) Mediator and cohesin connect gene expression and chromatin architecture. Nature 467: 430–435.
8. LiuJ, ZhangZ, BandoM, ItohT, DeardorffMA, et al. (2009) Transcriptional dysregulation in NIPBL and cohesin mutant human cells. PLoS Biol 7: e1000119 doi:10.1371/journal.pbio.1000119.
9. MisulovinZ, SchwartzYB, LiXY, KahnTG, GauseM, et al. (2008) Association of cohesin and Nipped-B with transcriptionally active regions of the Drosophila melanogaster genome. Chromosoma 117: 89–102.
10. ParelhoV, HadjurS, SpivakovM, LeleuM, SauerS, et al. (2008) Cohesins functionally associate with CTCF on mammalian chromosome arms. Cell 132: 422–433.
11. WendtKS, YoshidaK, ItohT, BandoM, KochB, et al. (2008) Nature 451: 796–801.
12. FayA, MisulovinZ, LiJ, SchaafCA, GauseM, et al. (2011) Cohesin selectively binds and regulates genes with paused RNA polymerase. Curr Biol 21: 1624–1634.
13. SchaafCA, MisulovinZ, SahotaG, SiddiquiAM, SchwartzYB, et al. (2009) Regulation of the Drosophila Enhancer of split and invected-engrailed gene complexes by sister chromatid cohesion proteins. PLoS ONE 4: e6202 doi:10.1371/journal.pone.0006202.
14. MuseGW, GilchristDA, NechaevS, ShahR, ParkerJS, et al. (2007) RNA polymerase is poised for activation across the genome. Nat Genet 39: 1507–1511.
15. KwakH, FudaNJ, CoreLJ, LisJT (2013) Precise maps of RNA polymerase reveal how promoters direct initiation and pausing. Science in press.
16. CoreLJ, LisJT (2008) Transcription regulation through promoter-proximal pausing of RNA polymerase II. Science 319: 1791–1792.
17. CoreLJ, WaterfallJJ, GilchristDA, FargoDC, KwakH, et al. (2012) Defining the status of RNA polymerase at promoters,. Cell Rep 2: 1025–1035.
18. GilchristDA, FargoDC, AdelmanK (2009) Using ChIP-chip and ChIP-seq to study the regulation of gene expression: genome-wide localization studies reveal widespread regulation of transcription elongation. Methods 48: 398–408.
19. RollinsRA, MorcilloP, DorsettD (1999) Nipped-B, a Drosophila homologue of chromosomal adherins, participates in activation by remote enhancers in the cut and Ultrabithorax genes. Genetics 152: 577–593.
20. ChienR, ZengW, KawauchiS, BenderMA, SantosR, et al. (2011) Cohesin mediates chromatin interactions that regulate mammalian β-globin expression. J Biol Chem 286: 17870–17878.
21. MastonGA, LandtSG, SnyderM, GreenMR (2012) Characterization of enhancer function from genome-wide analyses. Annu Rev Genomics Hum Genet 13: 29–57.
22. KharchenkoPV, AlekseyenkoAA, SchwartzYB, MinodaA, RiddleNC, et al. (2011) Comprehensive analysis of the chromatin landscape in Drosophila melanogaster. Nature 471: 480–485.
23. GalloSM, GerrardDT, MinerD, SimichM, Des SoyeB, et al. (2011) REDfly v3.0: toward a comprehensive database of transcriptional regulatory elements in Drosophila. Nucleic Acids Res 39 (Database issue) D118–123.
24. JackJ, DeLottoY (1995) Structure and regulation of a complex locus: the cut gene of Drosophila. Genetics 139: 1689–1700.
25. JackJ, DorsettD, DelottoY, LiuS (1991) Expression of the cut locus in the Drosophila wing margin is required for cell type specification and is regulated by a distant enhancer. Development 113: 735–747.
26. JackJW (1985) Molecular organization of the cut locus of Drosophila melanogaster. Cell 42: 869–876.
27. RhodesJM, BentleyFK, PrintCG, DorsettD, MisulovinZ, et al. (2010) Positive regulation of c-Myc by cohesin is direct, and evolutionarily conserved. Dev Biol 344: 637–649.
28. PierceSB, YostC, AndersonSA, FlynnEM, DelrowJ, et al. (2008) Drosophila growth and development in the absence of dMyc and dMnt. Dev Biol 315: 303–316.
29. LinCY, LovénJ, RahlPB, ParanalRM, BurgeCB, et al. (2012) Transcriptional amplification in tumor cells with elevated c-Myc. Cell 151: 56–67.
30. NieZ, HuG, WeiG, CuiK, YamaneA, et al. (2012) c-Myc is a universal amplifier of expressed genes in lymphocytes and embryonic stem cells. Cell 151: 68–79.
31. PeterlinBM, PriceDH (2006) Controlling the elongation phase of transcription with P-TEFb. Mol Cell 23: 297–305.
32. BartkowiakB, LiuP, PhatnaniHP, FudaNJ, CooperJJ, et al. (2010) CDK12 is a transcription elongation-associated CTD kinase, the metazoan ortholog of yeast Ctk1. Genes Dev 24: 2303–2316.
33. BurattiE, BaralleFE (2010) The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation. RNA Biol 7: 420–429.
34. KimS, KimH, FongN, EricksonB, BentleyDL (2011) Pre-mRNA splicing is a determinant of histone H3K36 methylation. Proc Natl Acad Sci U S A 108: 13564–13569.
35. LucoRF, PanQ, TominagaK, BlencoweBJ, Pereira-SmithOM, et al. (2010) Regulation of alternative splicing by histone modifications. Science 327: 996–1000.
36. PolymenidouM, Lagier-TourenneC, HuttKR, HuelgaSC, MoranJ, et al. (2011) Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nat Neurosci 14: 459–468.
37. FaureAJ, SchmidtD, WattS, SchwaliePC, WilsonMD, et al. (2012) Cohesin regulates tissue-specific expression by stabilizing highly occupied cis-regulatory modules. Genome Res 22: 2163–2175.
38. KremerSB, KimS, JeonJO, MoustafaYW, ChenA, et al. (2012) Role of Mediator in regulating Pol II elongation and nucleosome displacement in Saccharomyces cerevisiae. Genetics 191: 95–106.
39. MalikS, BarreroMJ, JonesT (2007) Identification of a regulator of transcription elongation as an accessory factor for the human Mediator coactivator. Proc Natl Acad Sci U S A 104: 6182–6187.
40. TakahashiH, ParmelyTJ, SatoS, Tomomori-SatoC, BanksCA, et al. (2011) Human mediator subunit MED26 functions as a docking site for transcription elongation factors. Cell 146: 92–104.
41. RahlPB, LinCY, SeilaAC, FlynnRA, McCuineS, et al. (2010) c-Myc regulates transcriptional pause release. Cell 141: 432–445.
42. KawauchiS, CalofAL, SantosR, Lopez-BurksME, YoungCM, et al. (2009) Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/−) mouse, a model of Cornelia de Lange Syndrome. PLoS Genet 5: e1000650 doi:10.1371/journal.pgen.1000650.
43. KlineAD, BarrM, JacksonLG (1993) Growth manifestations in the Brachmann-de Lange syndrome. Am J Med Genet 47: 1042–1049.
44. LarschanE, AlekseyenkoAA, GortchakovAA, PengS, LiB, et al. (2007) MSL complex is attracted to genes marked by H3K36 trimethylation using a sequence-independent mechanism. Mol Cell 28: 121–133.
45. Hanyu-NakamuraK, Sonobe-NojimaH, TanigawaA, LaskoP, NakamuraA (2008) Drosophila Pgc protein inhibits P-TEFb recruitment to chromatin in primordial germ cells. Nature 451: 730–733.
46. JohnsonWE, LiW, MeyerCA, GottardoR, CarrollJS, et al. (2006) Model-based analysis of tiling-arrays for ChIP-chip. Proc Natl Acad Sci U S A 103: 12457–12462.
47. JohnsonDS, LiW, GordonDB, BhattacharjeeA, CurryB, et al. (2008) Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets. Genome Res 18: 393–403.
48. ChenY, NegreN, LiQ, MieczkowskaJO, SlatteryM, et al. (2012) Systematic evaluation of factors influencing ChIP-seq fidelity. Nat Methods 9: 609–614.
49. R Development Core Team. 2008. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07- Available: http://www.R-project.org.
50. QuinlanAR, HallIM (2010) BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 26: 841–842 Available: http://code.google.com/p/bedtools/
51. CherbasL, WillinghamA, ZhangD, YangL, ZouY, et al. (2011) The transcriptional diversity of 25 Drosophila cell lines. Genome Res 21: 301–314.
Štítky
Genetika Reprodukčná medicínaČlánok vyšiel v časopise
PLOS Genetics
2013 Číslo 3
- Je „freeze-all“ pro všechny? Odborníci na fertilitu diskutovali na virtuálním summitu
- Gynekologové a odborníci na reprodukční medicínu se sejdou na prvním virtuálním summitu
Najčítanejšie v tomto čísle
- Fine Characterisation of a Recombination Hotspot at the Locus and Resolution of the Paradoxical Excess of Duplications over Deletions in the General Population
- Molecular Networks of Human Muscle Adaptation to Exercise and Age
- Recurrent Rearrangement during Adaptive Evolution in an Interspecific Yeast Hybrid Suggests a Model for Rapid Introgression
- Genome-Wide Association Study and Gene Expression Analysis Identifies as a Predictor of Response to Etanercept Therapy in Rheumatoid Arthritis