#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

RSR-2, the Ortholog of Human Spliceosomal Component SRm300/SRRM2, Regulates Development by Influencing the Transcriptional Machinery


Protein components of the spliceosome are highly conserved in eukaryotes and can influence several steps of the gene expression process. RSR-2, the Caenorhabditis elegans ortholog of the human spliceosomal protein SRm300/SRRM2, is essential for viability, in contrast to the yeast ortholog Cwc21p. We took advantage of mutants and RNA interference (RNAi) to study rsr-2 functions in C. elegans, and through genetic epistasis analysis found that rsr-2 is within the germline sex determination pathway. Intriguingly, transcriptome analyses of rsr-2(RNAi) animals did not reveal appreciable splicing defects but instead a slight global decrease in transcript levels. We further investigated this effect in transcription and observed that RSR-2 colocalizes with DNA in germline nuclei and coprecipitates with chromatin, displaying a ChIP-Seq profile similar to that obtained for the RNA Polymerase II (RNAPII). Consistent with a novel transcription function we demonstrate that the recruitment of RSR-2 to chromatin is splicing-independent and that RSR-2 interacts with RNAPII and affects RNAPII phosphorylation states. Proteomic analyses identified proteins associated with RSR-2 that are involved in different gene expression steps, including RNA metabolism and transcription with PRP-8 and PRP-19 being the strongest interacting partners. PRP-8 is a core component of the spliceosome and PRP-19 is the core component of the PRP19 complex, which interacts with RNAPII and is necessary for full transcriptional activity. Taken together, our study proposes that RSR-2 is a multifunctional protein whose role in transcription influences C. elegans development.


Vyšlo v časopise: RSR-2, the Ortholog of Human Spliceosomal Component SRm300/SRRM2, Regulates Development by Influencing the Transcriptional Machinery. PLoS Genet 9(6): e32767. doi:10.1371/journal.pgen.1003543
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1003543

Souhrn

Protein components of the spliceosome are highly conserved in eukaryotes and can influence several steps of the gene expression process. RSR-2, the Caenorhabditis elegans ortholog of the human spliceosomal protein SRm300/SRRM2, is essential for viability, in contrast to the yeast ortholog Cwc21p. We took advantage of mutants and RNA interference (RNAi) to study rsr-2 functions in C. elegans, and through genetic epistasis analysis found that rsr-2 is within the germline sex determination pathway. Intriguingly, transcriptome analyses of rsr-2(RNAi) animals did not reveal appreciable splicing defects but instead a slight global decrease in transcript levels. We further investigated this effect in transcription and observed that RSR-2 colocalizes with DNA in germline nuclei and coprecipitates with chromatin, displaying a ChIP-Seq profile similar to that obtained for the RNA Polymerase II (RNAPII). Consistent with a novel transcription function we demonstrate that the recruitment of RSR-2 to chromatin is splicing-independent and that RSR-2 interacts with RNAPII and affects RNAPII phosphorylation states. Proteomic analyses identified proteins associated with RSR-2 that are involved in different gene expression steps, including RNA metabolism and transcription with PRP-8 and PRP-19 being the strongest interacting partners. PRP-8 is a core component of the spliceosome and PRP-19 is the core component of the PRP19 complex, which interacts with RNAPII and is necessary for full transcriptional activity. Taken together, our study proposes that RSR-2 is a multifunctional protein whose role in transcription influences C. elegans development.


Zdroje

1. WahlMC, WillCL, LuhrmannR (2009) The spliceosome: design principles of a dynamic RNP machine. Cell 136: 701–718.

2. ZahlerAM (2012) Pre-mRNA splicing and its regulation in Caenorhabditis elegans. Worm Book 1–21.

3. JuricaMS, MooreMJ (2003) Pre-mRNA splicing: awash in a sea of proteins. Mol Cell 12: 5–14.

4. ShepardPJ, HertelKJ (2009) The SR protein family. Genome Biol 10: 242.

5. BoucherL, OuzounisCA, EnrightAJ, BlencoweBJ (2001) A genome-wide survey of RS domain proteins. Rna 7: 1693–1701.

6. LongJC, CaceresJF (2009) The SR protein family of splicing factors: master regulators of gene expression. Biochem J 417: 15–27.

7. ZhongXY, WangP, HanJ, RosenfeldMG, FuXD (2009) SR proteins in vertical integration of gene expression from transcription to RNA processing to translation. Mol Cell 35: 1–10.

8. WangGS, CooperTA (2007) Splicing in disease: disruption of the splicing code and the decoding machinery. Nat Rev Genet 8: 749–761.

9. GraingerRJ, BarrassJD, JacquierA, RainJC, BeggsJD (2009) Physical and genetic interactions of yeast Cwc21p, an ortholog of human SRm300/SRRM2, suggest a role at the catalytic center of the spliceosome. Rna 15: 2161–2173.

10. BlencoweBJ, IssnerR, NickersonJA, SharpPA (1998) A coactivator of pre-mRNA splicing. Genes Dev 12: 996–1009.

11. BlencoweBJ, BaurenG, EldridgeAG, IssnerR, NickersonJA, et al. (2000) The SRm160/300 splicing coactivator subunits. Rna 6: 111–120.

12. KhannaM, Van BakelH, TangX, CalarcoJA, BabakT, et al. (2009) A systematic characterization of Cwc21, the yeast ortholog of the human spliceosomal protein SRm300. Rna 15: 2174–2185.

13. ChanaratS, SeizlM, StrasserK (2011) The Prp19 complex is a novel transcription elongation factor required for TREX occupancy at transcribed genes. Genes Dev 25: 1147–1158.

14. LongmanD, McGarveyT, McCrackenS, JohnstoneIL, BlencoweBJ, et al. (2001) Multiple interactions between SRm160 and SR family proteins in enhancer-dependent splicing and development of C. elegans. Curr Biol 11: 1923–1933.

15. CeronJ, RualJF, ChandraA, DupuyD, VidalM, et al. (2007) Large-scale RNAi screens identify novel genes that interact with the C. elegans retinoblastoma pathway as well as splicing-related components with synMuv B activity. BMC Dev Biol 7: 30.

16. BrodyY, Shav-TalY (2011) Transcription and splicing: when the twain meet. Transcription 2: 216–220.

17. DasR, YuJ, ZhangZ, GygiMP, KrainerAR, et al. (2007) SR proteins function in coupling RNAP II transcription to pre-mRNA splicing. Mol Cell 26: 867–881.

18. DermodyJL, DreyfussJM, VillenJ, OgundipeB, GygiSP, et al. (2008) Unphosphorylated SR-like protein Npl3 stimulates RNA polymerase II elongation. PLoS One 3: e3273.

19. LinS, Coutinho-MansfieldG, WangD, PanditS, FuXD (2008) The splicing factor SC35 has an active role in transcriptional elongation. Nat Struct Mol Biol 15: 819–826.

20. FurgerA, O'SullivanJM, BinnieA, LeeBA, ProudfootNJ (2002) Promoter proximal splice sites enhance transcription. Genes Dev 16: 2792–2799.

21. DamgaardCK, KahnsS, Lykke-AndersenS, NielsenAL, JensenTH, et al. (2008) A 5′ splice site enhances the recruitment of basal transcription initiation factors in vivo. Mol Cell 29: 271–278.

22. SpiluttiniB, GuB, BelagalP, SmirnovaAS, NguyenVT, et al. (2010) Splicing-independent recruitment of U1 snRNP to a transcription unit in living cells. J Cell Sci 123: 2085–2093.

23. KornblihttAR, de la MataM, FededaJP, MunozMJ, NoguesG (2004) Multiple links between transcription and splicing. Rna 10: 1489–1498.

24. RualJF, CeronJ, KorethJ, HaoT, NicotAS, et al. (2004) Toward improving Caenorhabditis elegans phenome mapping with an ORFeome-based RNAi library. Genome Res 14: 2162–2168.

25. Porta-de-la-RivaM, FontrodonaL, VillanuevaA, CeronJ (2012) Basic Caenorhabditis elegans Methods: Synchronization and Observation. J Vis Exp (64)L e4019. doi:10.379/4019

26. MacMorrisM, BrockerC, BlumenthalT (2003) UAP56 levels affect viability and mRNA export in Caenorhabditis elegans. Rna 9: 847–857.

27. EllisR, SchedlT (2007) Sex determination in the germ line. Worm Book 1–13.

28. ZarkowerD (2006) Somatic sex determination. Worm Book 1–12.

29. GallegosM, AhringerJ, CrittendenS, KimbleJ (1998) Repression by the 3′ UTR of fem-3, a sex-determining gene, relies on a ubiquitous mog-dependent control in Caenorhabditis elegans. Embo J 17: 6337–6347.

30. ContrinoS, SmithRN, ButanoD, CarrA, HuF, et al. (2012) modMine: flexible access to modENCODE data. Nucleic Acids Res 40: D1082–1088.

31. ReinkeV, GilIS, WardS, KazmerK (2004) Genome-wide germline-enriched and sex-biased expression profiles in Caenorhabditis elegans. Development 131: 311–323.

32. LamontLB, KimbleJ (2007) Developmental expression of FOG-1/CPEB protein and its control in the Caenorhabditis elegans hermaphrodite germ line. Dev Dyn 236: 871–879.

33. RamaniAK, NelsonAC, KapranovP, BellI, GingerasTR, et al. (2009) High resolution transcriptome maps for wild-type and nonsense-mediated decay-defective Caenorhabditis elegans. Genome Biol 10: R101.

34. AndersKR, GrimsonA, AndersonP (2003) SMG-5, required for C.elegans nonsense-mediated mRNA decay, associates with SMG-2 and protein phosphatase 2A. Embo J 22: 641–650.

35. EvansTC (2006) Transformation and microinjection. Worm Book 1–15.

36. MerrittC, SeydouxG (2010) Transgenic solutions for the germline. Worm Book 1–21.

37. MerrittC, RasolosonD, KoD, SeydouxG (2008) 3′ UTRs are the primary regulators of gene expression in the C. elegans germline. Curr Biol 18: 1476–1482.

38. LamondAI, SpectorDL (2003) Nuclear speckles: a model for nuclear organelles. Nat Rev Mol Cell Biol 4: 605–612.

39. ZhangY, LiuT, MeyerCA, EeckhouteJ, JohnsonDS, et al. (2008) Model-based analysis of ChIP-Seq (MACS). Genome Biol 9: R137.

40. BuratowskiS (2009) Progression through the RNA polymerase II CTD cycle. Mol Cell 36: 541–546.

41. BaughLR, DemodenaJ, SternbergPW (2009) RNA Pol II accumulates at promoters of growth genes during developmental arrest. Science 324: 92–94.

42. ZhongM, NiuW, LuZJ, SarovM, MurrayJI, et al. (2010) Genome-wide identification of binding sites defines distinct functions for Caenorhabditis elegans PHA-4/FOXA in development and environmental response. PLoS Genet 6: e1000848.

43. KamathRS, FraserAG, DongY, PoulinG, DurbinR, et al. (2003) Systematic functional analysis of the Caenorhabditis elegans genome using RNAi. Nature 421: 231–237.

44. McCrackenS, LongmanD, MarconE, MoensP, DowneyM, et al. (2005) Proteomic analysis of SRm160-containing complexes reveals a conserved association with cohesin. J Biol Chem 280: 42227–42236.

45. BresV, GomesN, PickleL, JonesKA (2005) A human splicing factor, SKIP, associates with P-TEFb and enhances transcription elongation by HIV-1 Tat. Genes Dev 19: 1211–1226.

46. LehnertS, GotzC, KartariusS, SchaferB, MontenarhM (2008) Protein kinase CK2 interacts with the splicing factor hPrp3p. Oncogene 27: 2390–2400.

47. RamaniAK, CalarcoJA, PanQ, MavandadiS, WangY, et al. (2011) Genome-wide analysis of alternative splicing in Caenorhabditis elegans. Genome Res 21: 342–348.

48. BelfioreM, PugnaleP, SaudanZ, PuotiA (2004) Roles of the C. elegans cyclophilin-like protein MOG-6 in MEP-1 binding and germline fates. Development 131: 2935–2945.

49. GrahamPL, SchedlT, KimbleJ (1993) More mog genes that influence the switch from spermatogenesis to oogenesis in the hermaphrodite germ line of Caenorhabditis elegans. Dev Genet 14: 471–484.

50. KasturiP, ZanettiS, PassannanteM, SaudanZ, MullerF, et al. (2010) The C. elegans sex determination protein MOG-3 functions in meiosis and binds to the CSL co-repressor CIR-1. Dev Biol 344: 593–602.

51. KonishiT, UodomeN, SugimotoA (2008) The Caenorhabditis elegans DDX-23, a homolog of yeast splicing factor PRP28, is required for the sperm-oocyte switch and differentiation of various cell types. Dev Dyn 237: 2367–2377.

52. ZanettiS, MeolaM, BochudA, PuotiA (2011) Role of the C. elegans U2 snRNP protein MOG-2 in sex determination, meiosis, and splice site selection. Dev Biol 354: 232–241.

53. PuotiA, KimbleJ (1999) The Caenorhabditis elegans sex determination gene mog-1 encodes a member of the DEAH-Box protein family. Mol Cell Biol 19: 2189–2197.

54. PuotiA, KimbleJ (2000) The hermaphrodite sperm/oocyte switch requires the Caenorhabditis elegans homologs of PRP2 and PRP22. Proc Natl Acad Sci U S A 97: 3276–3281.

55. BelfioreM, MathiesLD, PugnaleP, MoulderG, BarsteadR, et al. (2002) The MEP-1 zinc-finger protein acts with MOG DEAH box proteins to control gene expression via the fem-3 3′ untranslated region in Caenorhabditis elegans. Rna 8: 725–739.

56. KerinsJA, HanazawaM, DorsettM, SchedlT (2010) PRP-17 and the pre-mRNA splicing pathway are preferentially required for the proliferation versus meiotic development decision and germline sex determination in Caenorhabditis elegans. Dev Dyn 239: 1555–1572.

57. de AlmeidaSF, Carmo-FonsecaM (2012) Design principles of interconnections between chromatin and pre-mRNA splicing. Trends Biochem Sci 37: 248–253.

58. PanditS, WangD, FuXD (2008) Functional integration of transcriptional and RNA processing machineries. Curr Opin Cell Biol 20: 260–265.

59. MieleA, MedinaR, van WijnenAJ, SteinGS, SteinJL (2007) The interactome of the histone gene regulatory factor HiNF-P suggests novel cell cycle related roles in transcriptional control and RNA processing. J Cell Biochem 102: 136–148.

60. RenL, McLeanJR, HazbunTR, FieldsS, Vander KooiC, et al. (2011) Systematic two-hybrid and comparative proteomic analyses reveal novel yeast pre-mRNA splicing factors connected to Prp19. PLoS One 6: e16719.

61. KroganNJ, KimM, AhnSH, ZhongG, KoborMS, et al. (2002) RNA polymerase II elongation factors of Saccharomyces cerevisiae: a targeted proteomics approach. Mol Cell Biol 22: 6979–6992.

62. de AlmeidaSF, Carmo-FonsecaM (2008) The CTD role in cotranscriptional RNA processing and surveillance. FEBS Lett 582: 1971–1976.

63. GilchristDA, FrommG, dos SantosG, PhamLN, McDanielIE, et al. (2012) Regulating the regulators: the pervasive effects of Pol II pausing on stimulus-responsive gene networks. Genes Dev 26: 933–944.

64. ZeitlingerJ, StarkA, KellisM, HongJW, NechaevS, et al. (2007) RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo. Nat Genet 39: 1512–1516.

65. MunozMJ, Perez SantangeloMS, ParonettoMP, de la MataM, PelischF, et al. (2009) DNA damage regulates alternative splicing through inhibition of RNA polymerase II elongation. Cell 137: 708–720.

66. LinCL, LeuS, LuMC, OuyangP (2004) Over-expression of SR-cyclophilin, an interaction partner of nuclear pinin, releases SR family splicing factors from nuclear speckles. Biochem Biophys Res Commun 321: 638–647.

67. ZimowskaG, ShiJ, MungubaG, JacksonMR, AlpatovR, et al. (2003) Pinin/DRS/memA interacts with SRp75, SRm300 and SRrp130 in corneal epithelial cells. Invest Ophthalmol Vis Sci 44: 4715–4723.

68. SpectorDL, LamondAI (2010) Nuclear Speckles. Cold Spring Harb Perspect Biol

69. DujardinG, LafailleC, PetrilloE, BuggianoV, Gomez AcunaLI, et al. (2013) Transcriptional elongation and alternative splicing. Biochim Biophys Acta 1829: 134–140.

70. Garrido-LeccaA, BlumenthalT (2010) RNA polymerase II C-terminal domain phosphorylation patterns in Caenorhabditis elegans operons, polycistronic gene clusters with only one promoter. Mol Cell Biol 30: 3887–3893.

71. GuangS, BochnerAF, BurkhartKB, BurtonN, PavelecDM, et al. (2010) Small regulatory RNAs inhibit RNA polymerase II during the elongation phase of transcription. Nature 465: 1097–1101.

72. AllemandE, BatscheE, MuchardtC (2008) Splicing, transcription, and chromatin: a menage a trois. Curr Opin Genet Dev 18: 145–151.

73. StiernagleT (2006) Maintenance of C. elegans. Worm Book 1–11.

74. LeeMH, SchedlT (2006) RNA in situ hybridization of dissected gonads. Worm Book 1–7.

75. DuerrJS (2006) Immunohistochemistry. Worm Book 1–61.

76. SempleJI, Garcia-VerdugoR, LehnerB (2010) Rapid selection of transgenic C. elegans using antibiotic resistance. Nat Methods 7: 725–727.

77. BlankenbergD, Von KusterG, CoraorN, AnandaG, LazarusR, et al. (2010) Galaxy: a web-based genome analysis tool for experimentalists. Curr Protoc Mol Biol Chapter 19: Unit 19 10 11–21.

78. GoecksJ, NekrutenkoA, TaylorJ (2010) Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences. Genome Biol 11: R86.

79. LefrancoisP, EuskirchenGM, AuerbachRK, RozowskyJ, GibsonT, et al. (2009) Efficient yeast ChIP-Seq using multiplex short-read DNA sequencing. BMC Genomics 10: 37.

80. TrapnellC, RobertsA, GoffL, PerteaG, KimD, et al. (2010) Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nat Protoc 7: 562–578.

81. RappsilberJ, MannM, IshihamaY (2007) Protocol for micro-purification, enrichment, pre-fractionation and storage of peptides for proteomics using StageTips. Nat Protoc 2: 1896–1906.

82. GersteinMB, LuZJ, Van NostrandEL, ChengC, ArshinoffBI, et al. (2010) Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project. Science 330: 1775–1787.

83. BaughLR, HillAA, SlonimDK, BrownEL, HunterCP (2003) Composition and dynamics of the Caenorhabditis elegans early embryonic transcriptome. Development 130: 889–900.

84. MeissnerB, WarnerA, WongK, DubeN, LorchA, et al. (2009) An integrated strategy to study muscle development and myofilament structure in Caenorhabditis elegans. PLoS Genet 5: e1000537.

85. WangX, ZhaoY, WongK, EhlersP, KoharaY, et al. (2009) Identification of genes expressed in the hermaphrodite germ line of C. elegans using SAGE. BMC Genomics 10: 213.

86. AllenMA, HillierLW, WaterstonRH, BlumenthalT (2011) A global analysis of C. elegans trans-splicing. Genome Res 21: 255–264.

Štítky
Genetika Reprodukčná medicína

Článok vyšiel v časopise

PLOS Genetics


2013 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#