#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

The NSL Complex Regulates Housekeeping Genes in


MOF is the major histone H4 lysine 16-specific (H4K16) acetyltransferase in mammals and Drosophila. In flies, it is involved in the regulation of X-chromosomal and autosomal genes as part of the MSL and the NSL complexes, respectively. While the function of the MSL complex as a dosage compensation regulator is fairly well understood, the role of the NSL complex in gene regulation is still poorly characterized. Here we report a comprehensive ChIP–seq analysis of four NSL complex members (NSL1, NSL3, MBD-R2, and MCRS2) throughout the Drosophila melanogaster genome. Strikingly, the majority (85.5%) of NSL-bound genes are constitutively expressed across different cell types. We find that an increased abundance of the histone modifications H4K16ac, H3K4me2, H3K4me3, and H3K9ac in gene promoter regions is characteristic of NSL-targeted genes. Furthermore, we show that these genes have a well-defined nucleosome free region and broad transcription initiation patterns. Finally, by performing ChIP–seq analyses of RNA polymerase II (Pol II) in NSL1- and NSL3-depleted cells, we demonstrate that both NSL proteins are required for efficient recruitment of Pol II to NSL target gene promoters. The observed Pol II reduction coincides with compromised binding of TBP and TFIIB to target promoters, indicating that the NSL complex is required for optimal recruitment of the pre-initiation complex on target genes. Moreover, genes that undergo the most dramatic loss of Pol II upon NSL knockdowns tend to be enriched in DNA Replication–related Element (DRE). Taken together, our findings show that the MOF-containing NSL complex acts as a major regulator of housekeeping genes in flies by modulating initiation of Pol II transcription.


Vyšlo v časopise: The NSL Complex Regulates Housekeeping Genes in. PLoS Genet 8(6): e32767. doi:10.1371/journal.pgen.1002736
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1002736

Souhrn

MOF is the major histone H4 lysine 16-specific (H4K16) acetyltransferase in mammals and Drosophila. In flies, it is involved in the regulation of X-chromosomal and autosomal genes as part of the MSL and the NSL complexes, respectively. While the function of the MSL complex as a dosage compensation regulator is fairly well understood, the role of the NSL complex in gene regulation is still poorly characterized. Here we report a comprehensive ChIP–seq analysis of four NSL complex members (NSL1, NSL3, MBD-R2, and MCRS2) throughout the Drosophila melanogaster genome. Strikingly, the majority (85.5%) of NSL-bound genes are constitutively expressed across different cell types. We find that an increased abundance of the histone modifications H4K16ac, H3K4me2, H3K4me3, and H3K9ac in gene promoter regions is characteristic of NSL-targeted genes. Furthermore, we show that these genes have a well-defined nucleosome free region and broad transcription initiation patterns. Finally, by performing ChIP–seq analyses of RNA polymerase II (Pol II) in NSL1- and NSL3-depleted cells, we demonstrate that both NSL proteins are required for efficient recruitment of Pol II to NSL target gene promoters. The observed Pol II reduction coincides with compromised binding of TBP and TFIIB to target promoters, indicating that the NSL complex is required for optimal recruitment of the pre-initiation complex on target genes. Moreover, genes that undergo the most dramatic loss of Pol II upon NSL knockdowns tend to be enriched in DNA Replication–related Element (DRE). Taken together, our findings show that the MOF-containing NSL complex acts as a major regulator of housekeeping genes in flies by modulating initiation of Pol II transcription.


Zdroje

1. Juven-GershonTKadonagaJT 2010 Regulation of gene expression via the core promoter and the basal transcriptional machinery. Dev Biol 339 225 229

2. KouzaridesT 2007 Chromatin modifications and their function. Cell 128 693 705

3. YangXJSetoE 2007 HATs and HDACs: from structure, function and regulation to novel strategies for therapy and prevention. Oncogene 26 5310 5318

4. JacobsonRHLadurnerAGKingDSTjianR 2000 Structure and function of a human TAFII250 double bromodomain module. Science 288 1422 1425

5. RuthenburgAJLiHMilneTADewellSMcGintyRK 2011 Recognition of a mononucleosomal histone modification pattern by BPTF via multivalent interactions. Cell 145 692 706

6. LugerKMaderAWRichmondRKSargentDFRichmondTJ 1997 Crystal structure of the nucleosome core particle at 2.8 A resolution. Nature 389 251 260

7. Shogren-KnaakMIshiiHSunJMPazinMJDavieJR 2006 Histone H4-K16 acetylation controls chromatin structure and protein interactions. Science 311 844 847

8. ShahbazianMDGrunsteinM 2007 Functions of site-specific histone acetylation and deacetylation. Annu Rev Biochem 76 75 100

9. VettingMWLPSdCYuMHegdeSSMagnetS 2005 Structure and functions of the GNAT superfamily of acetyltransferases. Arch Biochem Biophys 433 212 226

10. UtleyRTCoteJ 2003 The MYST family of histone acetyltransferases. Curr Top Microbiol Immunol 274 203 236

11. LeeKKWorkmanJL 2007 Histone acetyltransferase complexes: one size doesn't fit all. Nat Rev Mol Cell Biol 8 284 295

12. GrantPASchieltzDPray-GrantMGStegerDJReeseJC 1998 A subset of TAF(II)s are integral components of the SAGA complex required for nucleosome acetylation and transcriptional stimulation. Cell 94 45 53

13. SuganumaTGutierrezJLLiBFlorensLSwansonSK 2008 ATAC is a double histone acetyltransferase complex that stimulates nucleosome sliding. Nat Struct Mol Biol 15 364 372

14. HuisingaKLPughBF 2004 A genome-wide housekeeping role for TFIID and a highly regulated stress-related role for SAGA in Saccharomyces cerevisiae. Mol Cell 13 573 585

15. LebedevaLANabirochkinaENKurshakovaMMRobertFKrasnovAN 2005 Occupancy of the Drosophila hsp70 promoter by a subset of basal transcription factors diminishes upon transcriptional activation. Proc Natl Acad Sci U S A 102 18087 18092

16. KrebsARDemmersJKarmodiyaKChangNCChangAC 2010 ATAC and Mediator coactivators form a stable complex and regulate a set of non-coding RNA genes. EMBO Rep 11 541 547

17. NagyZRissAFujiyamaSKrebsAOrpinellM 2010 The metazoan ATAC and SAGA coactivator HAT complexes regulate different sets of inducible target genes. Cell Mol Life Sci 67 611 628

18. SuganumaTMushegianASwansonSKAbmayrSMFlorensL 2010 The ATAC acetyltransferase complex coordinates MAP kinases to regulate JNK target genes. Cell 142 726 736

19. CaiYJinJSwansonSKColeMDChoiSH 2010 Subunit composition and substrate specificity of a MOF-containing histone acetyltransferase distinct from the male-specific lethal (MSL) complex. J Biol Chem 285 4268 4272

20. MendjanSTaipaleMKindJHolzHGebhardtP 2006 Nuclear pore components are involved in the transcriptional regulation of dosage compensation in Drosophila. Mol Cell 21 811 823

21. RajaSJCharapitsaIConradTVaquerizasJMGebhardtP 2010 The nonspecific lethal complex is a transcriptional regulator in Drosophila. Mol Cell 38 827 841

22. StraubTBeckerPB 2007 Dosage compensation: the beginning and end of generalization. Nat Rev Genet 8 47 57

23. HallacliEAkhtarA 2009 X chromosomal regulation in flies: when less is more. Chromosome Res 17 603 619

24. ConradTAkhtarA 2011 Dosage compensation in Drosophila melanogaster: epigenetic fine-tuning of chromosome-wide transcription. Nat Rev Genet 13 123 134

25. AndersenDSRajaSJColombaniJShawRLLangtonPF 2010 Drosophila MCRS2 associates with RNA polymerase II complexes to regulate transcription. Mol Cell Biol 30 4744 4755

26. PrestelMFellerCStraubTMitlohnerHBeckerPB 2010 The activation potential of MOF is constrained for dosage compensation. Mol Cell 38 815 826

27. LiXWuLCorsaCAKunkelSDouY 2009 Two mammalian MOF complexes regulate transcription activation by distinct mechanisms. Mol Cell 36 290 301

28. CherbasLWillinghamAZhangDYangLZouY 2011 The transcriptional diversity of 25 Drosophila cell lines. Genome Res 21 301 314

29. FilionGJvan BemmelJGBraunschweigUTalhoutWKindJ 2010 Systematic protein location mapping reveals five principal chromatin types in Drosophila cells. Cell 143 212 224

30. KharchenkoPVAlekseyenkoAASchwartzYBMinodaARiddleNC 2011 Comprehensive analysis of the chromatin landscape in Drosophila melanogaster. Nature 471 480 485

31. GraveleyBRBrooksANCarlsonJWDuffMOLandolinJM 2011 The developmental transcriptome of Drosophila melanogaster. Nature 471 473 479

32. NechaevSFargoDCdos SantosGLiuLGaoY 2010 Global analysis of short RNAs reveals widespread promoter-proximal stalling and arrest of Pol II in Drosophila. Science 327 335 338

33. RachEAYuanHYMajorosWHTomancakPOhlerU 2009 Motif composition, conservation and condition-specificity of single and alternative transcription start sites in the Drosophila genome. Genome Biol 10 R73

34. HoskinsRALandolinJMBrownJBSandlerJETakahashiH 2011 Genome-wide analysis of promoter architecture in Drosophila melanogaster. Genome Res 21 182 192

35. NiTCorcoranDLRachEASongSSpanaEP 2010 A paired-end sequencing strategy to map the complex landscape of transcription initiation. Nat Methods 7 521 527

36. RachEAWinterDRBenjaminAMCorcoranDLNiT 2011 Transcription initiation patterns indicate divergent strategies for gene regulation at the chromatin level. PLoS Genet 7 doi:10.1371/journal.pgen.1001274 e1001274

37. MavrichTNJiangCIoshikhesIPLiXVentersBJ 2008 Nucleosome organization in the Drosophila genome. Nature 453 358 362

38. GilchristDADos SantosGFargoDCXieBGaoY 2010 Pausing of RNA polymerase II disrupts DNA-specified nucleosome organization to enable precise gene regulation. Cell 143 540 551

39. MuseGWGilchristDANechaevSShahRParkerJS 2007 RNA polymerase is poised for activation across the genome. Nat Genet 39 1507 1511

40. Juven-GershonTHsuJYTheisenJWKadonagaJT 2008 The RNA polymerase II core promoter - the gateway to transcription. Curr Opin Cell Biol 20 253 259

41. PughBF 1996 Mechanisms of transcription complex assembly. Curr Opin Cell Biol 8 303 311

42. FitzGeraldPCSturgillDShyakhtenkoAOliverBVinsonC 2006 Comparative genomics of Drosophila and human core promoters. Genome Biol 7 R53

43. OhlerULiaoGCNiemannHRubinGM 2002 Computational analysis of core promoters in the Drosophila genome. Genome Biol 3 RESEARCH0087

44. Thomas-ChollierMHuftonAHeinigMO'KeeffeSMasriNE 2011 Transcription factor binding predictions using TRAP for the analysis of ChIP-seq data and regulatory SNPs. Nat Protoc 6 1860 1869

45. FellerCPrestelMHartmannHStraubTSodingJ 2012 The MOF-containing NSL complex associates globally with housekeeping genes, but activates only a defined subset. Nucleic Acids Res 40 1509 1522

46. HochheimerAZhouSZhengSHolmesMCTjianR 2002 TRF2 associates with DREF and directs promoter-selective gene expression in Drosophila. Nature 420 439 445

47. van WervenFJvan TeeffelenHAHolstegeFCTimmersHT 2009 Distinct promoter dynamics of the basal transcription factor TBP across the yeast genome. Nat Struct Mol Biol 16 1043 1048

48. MizzenCAYangXJKokuboTBrownellJEBannisterAJ 1996 The TAF(II)250 subunit of TFIID has histone acetyltransferase activity. Cell 87 1261 1270

49. SermwittayawongDTanS 2006 SAGA binds TBP via its Spt8 subunit in competition with DNA: implications for TBP recruitment. EMBO J 25 3791 3800

50. WarfieldLRanishJAHahnS 2004 Positive and negative functions of the SAGA complex mediated through interaction of Spt8 with TBP and the N-terminal domain of TFIIA. Genes Dev 18 1022 1034

51. BlackJCChoiJELombardoSRCareyM 2006 A mechanism for coordinating chromatin modification and preinitiation complex assembly. Mol Cell 23 809 818

52. LangmeadBTrapnellCPopMSalzbergSL 2009 Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 10 R25

53. ZhangYLiuTMeyerCAEeckhouteJJohnsonDS 2008 Model-based analysis of ChIP-Seq (MACS). Genome Biol 9 R137

54. Salmon-DivonMDvingeHTammojaKBertoneP 2010 PeakAnalyzer: genome-wide annotation of chromatin binding and modification loci. BMC Bioinformatics 11 415

55. AndersSHuberW 2010 Differential expression analysis for sequence count data. Genome Biol 11 R106

56. ConradTCavalliFMHolzHHallacliEKindJ 2012 The MOF chromobarrel domain controls genome-wide H4K16 acetylation and spreading of the MSL complex. Dev Cell 22 610 624

57. GoecksJNekrutenkoATaylorJ 2010 Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences. Genome Biol 11 R86

58. QuinlanARHallIM 2010 BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 26 841 842

59. OliverosJC 2007 VENNY. An interactive tool for comparing lists with Venn Diagrams

60. VaquerizasJMKummerfeldSKTeichmannSALuscombeNM 2009 A census of human transcription factors: function, expression and evolution. Nat Rev Genet 10 252 263

61. KindJVaquerizasJMGebhardtPGentzelMLuscombeNM 2008 Genome-wide analysis reveals MOF as a key regulator of dosage compensation and gene expression in Drosophila. Cell 133 813 828

62. BaileyTLWilliamsNMislehCLiWW 2006 MEME: discovering and analyzing DNA and protein sequence motifs. Nucleic Acids Res 34 W369 373

63. RoiderHGMankeTO'KeeffeSVingronMHaasSA 2009 PASTAA: identifying transcription factors associated with sets of co-regulated genes. Bioinformatics 25 435 442

64. BaileyTLElkanC 1994 Fitting a mixture model by expectation maximization to discover motifs in biopolymers. Proc Int Conf Intell Syst Mol Biol 2 28 36

65. TomancakPBermanBPBeatonAWeiszmannRKwanE 2007 Global analysis of patterns of gene expression during Drosophila embryogenesis. Genome Biol 8 R145

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2012 Číslo 6
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#