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A Quantitative Systems Approach Reveals Dynamic Control of tRNA Modifications during Cellular Stress


Decades of study have revealed more than 100 ribonucleoside structures incorporated as post-transcriptional modifications mainly in tRNA and rRNA, yet the larger functional dynamics of this conserved system are unclear. To this end, we developed a highly precise mass spectrometric method to quantify tRNA modifications in Saccharomyces cerevisiae. Our approach revealed several novel biosynthetic pathways for RNA modifications and led to the discovery of signature changes in the spectrum of tRNA modifications in the damage response to mechanistically different toxicants. This is illustrated with the RNA modifications Cm, m5C, and m22G, which increase following hydrogen peroxide exposure but decrease or are unaffected by exposure to methylmethane sulfonate, arsenite, and hypochlorite. Cytotoxic hypersensitivity to hydrogen peroxide is conferred by loss of enzymes catalyzing the formation of Cm, m5C, and m22G, which demonstrates that tRNA modifications are critical features of the cellular stress response. The results of our study support a general model of dynamic control of tRNA modifications in cellular response pathways and add to the growing repertoire of mechanisms controlling translational responses in cells.


Vyšlo v časopise: A Quantitative Systems Approach Reveals Dynamic Control of tRNA Modifications during Cellular Stress. PLoS Genet 6(12): e32767. doi:10.1371/journal.pgen.1001247
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1001247

Souhrn

Decades of study have revealed more than 100 ribonucleoside structures incorporated as post-transcriptional modifications mainly in tRNA and rRNA, yet the larger functional dynamics of this conserved system are unclear. To this end, we developed a highly precise mass spectrometric method to quantify tRNA modifications in Saccharomyces cerevisiae. Our approach revealed several novel biosynthetic pathways for RNA modifications and led to the discovery of signature changes in the spectrum of tRNA modifications in the damage response to mechanistically different toxicants. This is illustrated with the RNA modifications Cm, m5C, and m22G, which increase following hydrogen peroxide exposure but decrease or are unaffected by exposure to methylmethane sulfonate, arsenite, and hypochlorite. Cytotoxic hypersensitivity to hydrogen peroxide is conferred by loss of enzymes catalyzing the formation of Cm, m5C, and m22G, which demonstrates that tRNA modifications are critical features of the cellular stress response. The results of our study support a general model of dynamic control of tRNA modifications in cellular response pathways and add to the growing repertoire of mechanisms controlling translational responses in cells.


Zdroje

1. AlbertsB

2008 Molecular biology of the cell, 5th edition. Extended version New York Garland Science

2. CrainPF

RozenskiJ

McCloskeyJA

1999 The RNA modification database.

3. CzerwoniecA

Dunin-HorkawiczS

PurtaE

KaminskaKH

KasprzakJM

2009 MODOMICS: a database of RNA modification pathways. 2008 update. Nucleic Acids Res 37 D118 121

4. AgrisPF

VendeixFA

GrahamWD

2007 tRNA's wobble decoding of the genome: 40 years of modification. J Mol Biol 366 1 13

5. YarianC

TownsendH

CzestkowskiW

SochackaE

MalkiewiczAJ

2002 Accurate translation of the genetic code depends on tRNA modified nucleosides. J Biol Chem 277 16391 16395

6. UrbonaviciusJ

QianQ

DurandJM

HagervallTG

BjorkGR

2001 Improvement of reading frame maintenance is a common function for several tRNA modifications. EMBO J 20 4863 4873

7. BjorkGR

DurandJM

HagervallTG

LeipuvieneR

LundgrenHK

1999 Transfer RNA modification: influence on translational frameshifting and metabolism. FEBS Lett 452 47 51

8. MotorinY

HelmM

2010 tRNA stabilization by modified nucleotides. Biochemistry 49 4934 4944

9. AlexandrovA

ChernyakovI

GuW

HileySL

HughesTR

2006 Rapid tRNA decay can result from lack of nonessential modifications. Mol Cell 21 87 96

10. ThompsonDM

ParkerR

2009 Stressing out over tRNA cleavage. Cell 138 215 219

11. BegleyU

DyavaiahM

PatilA

RooneyJP

DirenzoD

2007 Trm9-catalyzed tRNA modifications link translation to the DNA damage response. Mol Cell 28 860 870

12. NetzerN

GoodenbourJM

DavidA

DittmarKA

JonesRB

2009 Innate immune and chemically triggered oxidative stress modifies translational fidelity. Nature 462 522 526

13. EmilssonV

NaslundAK

KurlandCG

1992 Thiolation of transfer RNA in Escherichia coli varies with growth rate. Nucleic Acids Res 20 4499 4505

14. BegleyTJ

RosenbachAS

IdekerT

SamsonLD

2004 Hot spots for modulating toxicity identified by genomic phenotyping and localization mapping. Mol Cell 16 117 125

15. BennettCB

LewisLK

KarthikeyanG

LobachevKS

JinYH

2001 Genes required for ionizing radiation resistance in yeast. Nat Genet 29 426 434

16. RooneyJP

GeorgeAD

PatilA

BegleyU

BessetteE

2008 Systems based mapping demonstrates that recovery from alkylation damage requires DNA repair, RNA processing, and translation associated networks. Genomics 10 524

17. KalhorHR

ClarkeS

2003 Novel methyltransferase for modified uridine residues at the wobble position of tRNA. Mol Cell Biol 23 9283 9292

18. WeissenbachJ

DirheimerG

1978 Pairing properties of the methylester of 5-carboxymethyl uridine in the wobble position of yeast tRNA3Arg. Biochim Biophys Acta 518 530 534

19. SuzukiT

IkeuchiY

NomaA

SakaguchiY

2007 Mass spectrometric identification and characterization of RNA-modifying enzymes. Methods Enzymol 425 211 229

20. MengZ

LimbachPA

2006 Mass spectrometry of RNA: linking the genome to the proteome. Brief Funct Genomic Proteomic 5 87 95

21. MorrisJC

1966 The acid ionization constant of HOCl. J Phys Chem 70 3798 3805

22. ZhouX

AritaA

EllenTP

LiuX

BaiJ

2009 A genome-wide screen in Saccharomyces cerevisiae reveals pathways affected by arsenic toxicity. Genomics 94 294 307

23. FryRC

BegleyTJ

SamsonLD

2005 Genome-wide responses to DNA-damaging agents. Annu Rev Microbiol 59 357 377

24. SingerB

GrunbergerD

1983 Molecular Biology of Mutagens and Carcinogens. New York Plenum

25. LoechlerEL

1994 A violation of the Swain-Scott principle, and not SN1 versus SN2 reaction mechanisms, explains why carcinogenic alkylating agents can form different proportions of adducts at oxygen versus nitrogen in DNA. Chem Res Toxicol 7 277 280

26. HamptonMB

KettleAJ

WinterbournCC

1998 Inside the neutrophil phagosome: oxidants, myeloperoxidase, and bacterial killing. Blood 92 3007 3017

27. WinterbournCC

KettleAJ

2000 Biomarkers of myeloperoxidase-derived hypochlorous acid. Free Radic Biol Med 29 403 409

28. OhshimaH

TatemichiM

SawaT

2003 Chemical basis of inflammation-induced carcinogenesis. Arch Biochem Biophys 417 3 11

29. SuzukiT

MasudaM

FriesenMD

FenetB

OhshimaH

2002 Novel products generated from 2′-deoxyguanosine by hypochlorous acid or a myeloperoxidase-H2O2-Cl−-system: identification of diimino-imidazole and amino-imidazole nucleosides. Nucleic Acids Res 30 2555 2564

30. HigashikawaY

KazuiY

SuzukiS

OhtsuruO

2008 Arsenic speciation of arsine-exposed blood samples by high-performance liquid chromatography-inductively coupled plasma mass spectrometry and As-adduct, a possible indicator of AsH3 exposure. J Anal Toxicol 32 344 348

31. KitchinKT

2001 Recent advances in arsenic carcinogenesis: modes of action, animal model systems, and methylated arsenic metabolites. Toxicol Appl Pharmacol 172 249 261

32. HeiTK

FilipicM

2004 Role of oxidative damage in the genotoxicity of arsenic. Free Radic Biol Med 37 574 581

33. MotorinY

GrosjeanH

1999 Multisite-specific tRNA:m5C-methyltransferase (Trm4) in yeast Saccharomyces cerevisiae: identification of the gene and substrate specificity of the enzyme. RNA 5 1105 1118

34. PintardL

LecointeF

BujnickiJM

BonnerotC

GrosjeanH

2002 Trm7p catalyses the formation of two 2′-O-methylriboses in yeast tRNA anticodon loop. EMBO J 21 1811 1820

35. El YacoubiB

LyonsB

CruzY

ReddyR

NordinB

2009 The universal YrdC/Sua5 family is required for the formation of threonylcarbamoyladenosine in tRNA. Nucleic Acids Res 37 2894 2909

36. EllisSR

MoralesMJ

LiJM

HopperAK

MartinNC

1986 Isolation and characterization of the TRM1 locus, a gene essential for the N2,N2-dimethylguanosine modification of both mitochondrial and cytoplasmic tRNA in Saccharomyces cerevisiae. J Biol Chem 261 9703 9709

37. BegleyTJ

RosenbachAS

IdekerT

SamsonLD

2002 Damage recovery pathways in Saccharomyces cerevisiae revealed by genomic phenotyping and interactome mapping. Mol Cancer Res 1 103 112

38. BirrellGW

BrownJA

WuHI

GiaeverG

ChuAM

2002 Transcriptional response of Saccharomyces cerevisiae to DNA-damaging agents does not identify the genes that protect against these agents. Proc Natl Acad Sci USA 99 8778 8783

39. Wohlgamuth-BenedumJM

RubioMA

ParisZ

LongS

PoliakP

2009 Thiolation controls cytoplasmic tRNA stability and acts as a negative determinant for tRNA editing in mitochondria. J Biol Chem 284 23947 23953

40. AgrisPF

1996 The importance of being modified: roles of modified nucleosides and Mg2+ in RNA structure and function. Prog Nucleic Acid Res Mol Biol 53 79 129

41. SprinzlM

VassilenkoKS

2005 Compilation of tRNA sequences and sequences of tRNA genes. Nucleic Acids Res 33 D139 140

42. KotelawalaL

GrayhackEJ

PhizickyEM

2008 Identification of yeast tRNA Um44 2′-O-methyltransferase (Trm44) and demonstration of a Trm44 role in sustaining levels of specific tRNASer species. RNA 14 158 169

43. JohanssonMJO

BystromAS

2005 Transfer RNA modification and modifying enzymes in Saccharomyces cerevisae.

GrosjeanH

Topics in current genetics: Fine-tuning of RNA functions by modification and editing Berlin; New York Springer 87 120

44. EllisSR

MoralesMJ

LiJM

HopperAK

MartinNC

1986 Isolation and characterization of the TRM1 locus, a gene essential for the N2,N2-dimethylguanosine modification of both mitochondrial and cytoplasmic tRNA in Saccharomyces cerevisiae. J Biol Chem 261 9703 9709

45. NguyenVC

ClellandBW

HockmanDJ

Kujat-ChoySL

MewhortHE

2010 Replication stress checkpoint signaling controls tRNA gene transcription. Nat Struct Mol Biol 17 976 981

46. GerberA

GrosjeanH

MelcherT

KellerW

1998 Tad1p, a yeast tRNA-specific adenosine deaminase, is related to the mammalian pre-mRNA editing enzymes ADAR1 and ADAR2. Embo J 17 4780 4789

47. BjörkGR

JacobssonK

NilssonK

JohanssonMJO

ByströmAS

2001 A primordial tRNA modification required for the evolution of life? EMBO J 20 231–239

48. PomerantzSC

McCloskeyJA

1990 Analysis of RNA hydrolyzates by liquid chromatography-mass spectrometry. Methods Enzymol 193 796 824

49. DudleyE

TuyttenR

BondA

LemiereF

BrentonAG

2005 Study of the mass spectrometric fragmentation of pseudouridine: comparison of fragmentation data obtained by matrix-assisted laser desorption/ionisation post-source decay, electrospray ion trap multistage mass spectrometry, and by a method utilising electrospray quadrupole time-of-flight tandem mass spectrometry and in-source fragmentation. Rapid Commun Mass Spectrom 19 3075 3085

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Genetika Reprodukčná medicína

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PLOS Genetics


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