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Pathogenic Bacteria Target NEDD8-Conjugated Cullins to Hijack Host-Cell Signaling Pathways


The cycle inhibiting factors (Cif), produced by pathogenic bacteria isolated from vertebrates and invertebrates, belong to a family of molecules called cyclomodulins that interfere with the eukaryotic cell cycle. Cif blocks the cell cycle at both the G1/S and G2/M transitions by inducing the stabilization of cyclin-dependent kinase inhibitors p21waf1 and p27kip1. Using yeast two-hybrid screens, we identified the ubiquitin-like protein NEDD8 as a target of Cif. Cif co-compartmentalized with NEDD8 in the host cell nucleus and induced accumulation of NEDD8-conjugated cullins. This accumulation occurred early after cell infection and correlated with that of p21 and p27. Co-immunoprecipitation revealed that Cif interacted with cullin-RING ubiquitin ligase complexes (CRLs) through binding with the neddylated forms of cullins 1, 2, 3, 4A and 4B subunits of CRL. Using an in vitro ubiquitylation assay, we demonstrate that Cif directly inhibits the neddylated CUL1-associated ubiquitin ligase activity. Consistent with this inhibition and the interaction of Cif with several neddylated cullins, we further observed that Cif modulates the cellular half-lives of various CRL targets, which might contribute to the pathogenic potential of diverse bacteria.


Vyšlo v časopise: Pathogenic Bacteria Target NEDD8-Conjugated Cullins to Hijack Host-Cell Signaling Pathways. PLoS Pathog 6(9): e32767. doi:10.1371/journal.ppat.1001128
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1001128

Souhrn

The cycle inhibiting factors (Cif), produced by pathogenic bacteria isolated from vertebrates and invertebrates, belong to a family of molecules called cyclomodulins that interfere with the eukaryotic cell cycle. Cif blocks the cell cycle at both the G1/S and G2/M transitions by inducing the stabilization of cyclin-dependent kinase inhibitors p21waf1 and p27kip1. Using yeast two-hybrid screens, we identified the ubiquitin-like protein NEDD8 as a target of Cif. Cif co-compartmentalized with NEDD8 in the host cell nucleus and induced accumulation of NEDD8-conjugated cullins. This accumulation occurred early after cell infection and correlated with that of p21 and p27. Co-immunoprecipitation revealed that Cif interacted with cullin-RING ubiquitin ligase complexes (CRLs) through binding with the neddylated forms of cullins 1, 2, 3, 4A and 4B subunits of CRL. Using an in vitro ubiquitylation assay, we demonstrate that Cif directly inhibits the neddylated CUL1-associated ubiquitin ligase activity. Consistent with this inhibition and the interaction of Cif with several neddylated cullins, we further observed that Cif modulates the cellular half-lives of various CRL targets, which might contribute to the pathogenic potential of diverse bacteria.


Zdroje

1. Samba-LouakaA

TaiebF

NougayredeJP

OswaldE

2009 Cif type III effector protein: a smart hijacker of the host cell cycle. Future Microbiol 4 867 877

2. NougayredeJP

TaiebF

De RyckeJ

OswaldE

2005 Cyclomodulins: bacterial effectors that modulate the eukaryotic cell cycle. Trends Microbiol 13 103 110

3. OswaldE

NougayredeJP

TaiebF

SugaiM

2005 Bacterial toxins that modulate host cell-cycle progression. Curr Opin Microbiol 8 83 91

4. MarchesO

LedgerTN

BouryM

OharaM

TuX

2003 Enteropathogenic and enterohaemorrhagic Escherichia coli deliver a novel effector called Cif, which blocks cell cycle G2/M transition. Mol Microbiol 50 1553 1567

5. YaoQ

CuiJ

ZhuY

WangG

HuL

2009 A bacterial type III effector family uses the papain-like hydrolytic activity to arrest the host cell cycle. Proc Natl Acad Sci U S A 106 3716 3721

6. JubelinG

ChavezCV

TaiebF

BanfieldMJ

Samba-LouakaA

2009 Cycle inhibiting factors (CIFs) are a growing family of functional cyclomodulins present in invertebrate and mammal bacterial pathogens. PLoS ONE 4 e4855

7. MillsE

BaruchK

CharpentierX

KobiS

RosenshineI

2008 Real-time analysis of effector translocation by the type III secretion system of enteropathogenic Escherichia coli. Cell Host Microbe 3 104 113

8. CharpentierX

OswaldE

2004 Identification of the secretion and translocation domain of the enteropathogenic and enterohemorrhagic Escherichia coli effector Cif, using TEM-1 beta-lactamase as a new fluorescence-based reporter. J Bacteriol 186 5486 5495

9. CrowA

RacePR

JubelinG

Varela ChavezC

EscoubasJM

2009 Crystal structures of Cif from bacterial pathogens Photorhabdus luminescens and Burkholderia pseudomallei. PLoS One 4 e5582

10. HsuY

JubelinG

TaiebF

NougayredeJP

OswaldE

2008 Structure of the cyclomodulin Cif from pathogenic Escherichia coli. J Mol Biol 384 465 477

11. NougayredeJP

BouryM

TascaC

MarchesO

MilonA

2001 Type III secretion-dependent cell cycle block caused in HeLa cells by enteropathogenic Escherichia coli O103. Infect Immun 69 6785 6795

12. De RyckeJ

ComtetE

ChalarengC

BouryM

TascaC

1997 Enteropathogenic Escherichia coli O103 from rabbit elicits actin stress fibers and focal adhesions in HeLa epithelial cells, cytopathic effects that are linked to an analog of the locus of enterocyte effacement. Infect Immun 65 2555 2563

13. Samba-LouakaA

NougayredeJP

WatrinC

OswaldE

TaiebF

2009 The EPEC effector Cif induces delayed apoptosis in epithelial cells. Infect Immun 77 5471 5477

14. TaiebF

NougayredeJP

WatrinC

Samba-LouakaA

OswaldE

2006 Escherichia coli cyclomodulin Cif induces G2 arrest of the host cell cycle without activation of the DNA-damage checkpoint-signalling pathway. Cell Microbiol 8 1910 1921

15. Samba-LouakaA

NougayredeJP

WatrinC

JubelinG

OswaldE

2008 Bacterial cyclomodulin Cif blocks the host cell cycle by stabilizing the cyclin-dependent kinase inhibitors p21 and p27. Cell Microbiol 10 2496 2508

16. CayrolC

KnibiehlerM

DucommunB

1998 p21 binding to PCNA causes G1 and G2 cell cycle arrest in p53-deficient cells. Oncogene 16 311 320

17. CiechanoverA

FinleyD

VarshavskyA

1984 The ubiquitin-mediated proteolytic pathway and mechanisms of energy-dependent intracellular protein degradation. J Cell Biochem 24 27 53

18. PickartCM

CohenRE

2004 Proteasomes and their kin: proteases in the machine age. Nat Rev Mol Cell Biol 5 177 187

19. DudaDM

BorgLA

ScottDC

HuntHW

HammelM

2008 Structural insights into NEDD8 activation of cullin-RING ligases: conformational control of conjugation. Cell 134 995 1006

20. SahaA

DeshaiesRJ

2008 Multimodal activation of the ubiquitin ligase SCF by Nedd8 conjugation. Mol Cell 32 21 31

21. RabutG

PeterM

2008 Function and regulation of protein neddylation. ‘Protein modifications: beyond the usual suspects’ review series. EMBO Rep 9 969 976

22. NakayamaKI

NakayamaK

2005 Regulation of the cell cycle by SCF-type ubiquitin ligases. Semin Cell Dev Biol 16 323 333

23. YuJ

FinleyRLJr

2009 Combining multiple positive training sets to generate confidence scores for protein-protein interactions. Bioinformatics 25 105 111

24. KamitaniT

KitoK

NguyenHP

YehET

1997 Characterization of NEDD8, a developmentally down-regulated ubiquitin-like protein. J Biol Chem 272 28557 28562

25. XirodimasDP

2008 Novel substrates and functions for the ubiquitin-like molecule NEDD8. Biochem Soc Trans 36 802 806

26. JonesJ

WuK

YangY

GuerreroC

NillegodaN

2008 A targeted proteomic analysis of the ubiquitin-like modifier nedd8 and associated proteins. J Proteome Res 7 1274 1287

27. BosuDR

KipreosET

2008 Cullin-RING ubiquitin ligases: global regulation and activation cycles. Cell Div 3 7

28. WelckerM

ClurmanBE

2008 FBW7 ubiquitin ligase: a tumour suppressor at the crossroads of cell division, growth and differentiation. Nat Rev Cancer 8 83 93

29. YeX

NalepaG

WelckerM

KesslerBM

SpoonerE

2004 Recognition of phosphodegron motifs in human cyclin E by the SCF(Fbw7) ubiquitin ligase. J Biol Chem 279 50110 50119

30. KleigerG

SahaA

LewisS

KuhlmanB

DeshaiesRJ

2009 Rapid E2-E3 assembly and disassembly enable processive ubiquitylation of cullin-RING ubiquitin ligase substrates. Cell 139 957 968

31. PierceNW

KleigerG

ShanSO

DeshaiesRJ

2009 Detection of sequential polyubiquitylation on a millisecond timescale. Nature 462 615 619

32. PetroskiMD

DeshaiesRJ

2005 Function and regulation of cullin-RING ubiquitin ligases. Nat Rev Mol Cell Biol 6 9 20

33. MerletJ

BurgerJ

GomesJE

PintardL

2009 Regulation of cullin-RING E3 ubiquitin-ligases by neddylation and dimerization. Cell Mol Life Sci 66 1924 1938

34. ChewEH

HagenT

2007 Substrate-mediated regulation of cullin neddylation. J Biol Chem 282 17032 17040

35. BornsteinG

GanothD

HershkoA

2006 Regulation of neddylation and deneddylation of cullin1 in SCFSkp2 ubiquitin ligase by F-box protein and substrate. Proc Natl Acad Sci U S A 103 11515 11520

36. ChenY

YangZ

MengM

ZhaoY

DongN

2009 Cullin mediates degradation of RhoA through evolutionarily conserved BTB adaptors to control actin cytoskeleton structure and cell movement. Mol Cell 35 841 855

37. JinJ

AriasEE

ChenJ

HarperJW

WalterJC

2006 A family of diverse Cul4-Ddb1-interacting proteins includes Cdt2, which is required for S phase destruction of the replication factor Cdt1. Mol Cell 23 709 721

38. NishitaniH

SugimotoN

RoukosV

NakanishiY

SaijoM

2006 Two E3 ubiquitin ligases, SCF-Skp2 and DDB1-Cul4, target human Cdt1 for proteolysis. EMBO J 25 1126 1136

39. SengaT

SivaprasadU

ZhuW

ParkJH

AriasEE

2006 PCNA is a cofactor for Cdt1 degradation by CUL4/DDB1-mediated N-terminal ubiquitination. J Biol Chem 281 6246 6252

40. XouriG

DimakiM

BastiaensPI

LygerouZ

2007 Cdt1 interactions in the licensing process: a model for dynamic spatiotemporal control of licensing. Cell Cycle 6 1549 1552

41. CleversH

2006 Wnt/beta-catenin signaling in development and disease. Cell 127 469 480

42. HicksSW

GalanJE

2010 Hijacking the host ubiquitin pathway: structural strategies of bacterial E3 ubiquitin ligases. Curr Opin Microbiol 13 41 46

43. SpallekT

RobatzekS

GohreV

2009 How microbes utilize host ubiquitination. Cell Microbiol 11 1425 1434

44. AngotA

VergunstA

GeninS

PeetersN

2007 Exploitation of eukaryotic ubiquitin signaling pathways by effectors translocated by bacterial type III and type IV secretion systems. PLoS Pathog 3 e3

45. RytkonenA

HoldenDW

2007 Bacterial interference of ubiquitination and deubiquitination. Cell Host Microbe 1 13 22

46. Collier-HyamsLS

SloaneV

BattenBC

NeishAS

2005 Cutting edge: bacterial modulation of epithelial signaling via changes in neddylation of cullin-1. J Immunol 175 4194 4198

47. KumarA

WuH

Collier-HyamsLS

HansenJM

LiT

2007 Commensal bacteria modulate cullin-dependent signaling via generation of reactive oxygen species. EMBO J 26 4457 4466

48. GastaldelloS

HildebrandS

FaridaniO

CallegariS

PalmkvistM

A deneddylase encoded by Epstein-Barr virus promotes viral DNA replication by regulating the activity of cullin-RING ligases. Nat Cell Biol 12 351 361

49. FormstecherE

ArestaS

ColluraV

HamburgerA

MeilA

2005 Protein interaction mapping: a Drosophila case study. Genome Res 15 376 384

50. PortalD

RosendorffA

KieffE

2006 Epstein-Barr nuclear antigen leader protein coactivates transcription through interaction with histone deacetylase 4. Proc Natl Acad Sci U S A 103 19278 19283

51. HuangDT

AyraultO

HuntHW

TaherbhoyAM

DudaDM

2009 E2-RING expansion of the NEDD8 cascade confers specificity to cullin modification. Mol Cell 33 483 495

52. NougayredeJP

MarchesO

BouryM

MainilJ

CharlierG

1999 The long-term cytoskeletal rearrangement induced by rabbit enteropathogenic Escherichia coli is Esp dependent but intimin independent. Mol Microbiol 31 19 30

53. MarchesO

NougayredeJP

BoullierS

MainilJ

CharlierG

2000 Role of tir and intimin in the virulence of rabbit enteropathogenic Escherichia coli serotype O103:H2. Infect Immun 68 2171 2182

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Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

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PLOS Pathogens


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