1 Jari Valkonen RNA SILENCING as a tool in plant research and plant protection Jari Valkonen Department of Applied Biology University of Helsinki Faculty of Agriculture and Forestry Faculty of Agriculture and Forestry University of Helsinki University of Helsinki SBL SBL-KPAT KPAT Plant Pathology Group Plant Pathology Group Jari Valkonen Acknowledgements Department of Applied Biology, Helsinki - Wilmer Cuellar - Marjo Ala-Poikela - Tuuli Haikonen Genetics Center, SLU, Uppsala - Eugene Savenkov - Xiandong Li - Anna Germundsson - Elin Gammelgård - Andrey Zamyatnin International Potato Center, Peru - Jan Kreuze SBL SBL-KPAT KPAT Plant Pathology Group Plant Pathology Group Faculty of Agriculture and Forestry Faculty of Agriculture and Forestry University of Helsinki University of Helsinki
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1
Jari Valkonen
RNA SILENCINGas a tool in plant research
and plant protection
Jari Valkonen
Department of Applied BiologyUniversity of Helsinki
Faculty of Agriculture and ForestryFaculty of Agriculture and Forestry
University of HelsinkiUniversity of Helsinki
SBLSBL--KPATKPATPlant Pathology GroupPlant Pathology Group
The mechanism targets and destroys harmful, unnecessaryor inadvertently expressed RNA molecules in a sequence-specific manner, no matter if they are of cellular or viralorigin. It does not just “interfere” with gene expression or“silence genes”.
Jari Valkonen
1.RNA SILENCING
andTRANSGENIC PLANTS
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”Co-suppression”Beginning of a series of unexpected results on transgenic plants
Petunia plants were transformed with the chalcone synthase geneto enhance pigmentation of flowers.
However, transgenic plants lost expression of the endogenous, homologous geneand developed unpigmented flowers
• Napoli C, Lemieux C, Jorgensen R (1990) Plant Cell 2, 279• Van der Krol A, Mur L, Beld M, Mol J, Stuitje A (1990) Plant Cell, 2, 291
Jari Valkonen
Chalcone
Phenylalanine
Cinnamate
4-Coumarate
4-Coumaroyl-CoA
Naringenin
Dihydrokaempherol
Leucopelargonidin
Pelargonidin
Pelargonidin-3-O-glucoside
Pelargonidin-3-O-rutinoside
Dihydroquercetin
Leucocyanidin
Cyanidin
Cyanidin-O-glucoside
Cyanidin-O-rutinoside
PAL
C4H
4CL
CHS
CHI
F3HF3'H
DFRDFR
ANSANS
3GT 3GT
RT RT
Biosynthesis ofanthocyaninsin Gerbera
(c) Teemu Teeri
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Jari Valkonen
Anthocyanin biosynthesis is blocked in transgenicGerbera which harbors its own CHS gene is in an
antisense orientation
Phenylalanine
Cinnamate
4-Coumarate
4-Coumaroyl-CoA
PAL
C4H
4CL
CHS
(c) Teemu Teeri
35S
CHS
Jari Valkonen
Transformation of Gerbera with antisense forGGLO1 (a B class MADS box gene) converts thebrilliant red petals into greenish sepal like organs.
MADSMADS--box genes and organ identity in Gerberabox genes and organ identity in Gerbera
Yu et al.1999:Plant J. 17, 51-62.
control transformantB
A C
sepa
lpe
talan
ther
carp
el
A C
sepa
lse
pal
carp
elca
rpel
sepal
petal
anthercarpel
(c) Paula Elomaa
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Smith CJS, Watson CF, Morris PC, Bird CR, MorrisPC, Schuch W, Grierson D 1988,
Antisense RNA inhibition of polygalacturonasegene expression in transgenic tomatoes.
Nature 334: 724-726
The Flavr SavrTM tomato of Calgene wasintroduced to the market in USA in 1994.
Commercial applications of RNA silencing - 1
An antisense gene construct for the inhibition of fruit ripening and softening,by preventing production of polygalacturonase, one of the most abundant proteinsin ripe tomato fruit
Calgene was later bought by Monsanto.Flavr Savr tomatoes were withdrawn from the market in 1997.
Jari Valkonen
Commercial utilisation of RNA silencing – 2Transgenic resistance to viruses
Powell-Abel P, Nelson RS, De B, Hoffmann N, Rogers SG, Fraley RT, Beachy RN(1986). Delay of disease development in transgenic plants that express thetobacco mosaic virus coat protein gene. Science 232, 738-743
Sanford & Johnston (1985) The concept of parasite-derived resistance: derivingresistance genes from the parasite´s own genome. J Theor Biol 113: 395-405
”Interfere with the pathogenicity cycleby causing the host to express pathogen gene
at the wrong time, in the wrong amount, or in a counterfunctional form”
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Lawson C, Kaniewski W, Haley L, Rozman R, Newell C, SandersP & Tumer NE (1990) Engineering resistance to mixed virusinfection in a commercial potato cultivar: Resistance to potatovirus X and potato virus Y in transgenic Russet Burbank.Biotechnology 8:127-134
Kaniewski W, Lawson C, Sammons B, Haley L, Hart J, DealnnayX & Tumer NE (1990) Field resistance of transgenic RussetBurbank potato to effects of infection with potato virus X andpotato virus Y. Biotechnology 8: 750-754.
Commercial applications of RNA silencing in plant protection:virus-resistant transgenic potatoes
Reduced growth frominfected seed tuber
PVY-infected Healthy
Bintje
Significant virus disease problemsdue to vegetative propagation(cloning):
• potato• sweetpotato• cassava• garlic, onion• berry plants• fruit trees
Jari Valkonen
Milestones in discovery of RNA silencing
Transgenic plants that express viral sequences and are virus-resistant
Lindbo A, Silva-Rosales L, Proebsting WM, Dougherty WG (1993) Induction of a highly specificantiviral stage in transgenic plants: implications for regulation of gene expressionand virus resistance. Plant Cell 5, 1749-1759 (cited 325 times / Sept. 4, 2005)
Smith HA, Swaney SL, Parks TD, Wernsman EA, Dougherty WG (1994) Transgenic plant virusresistance mediated by untranslatable sense RNAs: expression, regulationand fate of nonessential RNAs. Plant Cell 6, 1441-1453
Goodwin J, Chapman K, Swaney S, Parks TD, Wernsman EA, Dougherty WG (1996)Genetic and biochemical dissection of transgenic RNA-mediated virus resistance.Plant Cell 8, 95-105
• Untranslatable and antisensetranscripts confer resistance
• Transgene is actively transcribed butonly low levels of mRNA accumulate
• Resistance specific to the virus fromwhich the transgene sequence wasderived
à Non protein-mediated
à Post-transcriptionaldegradation of mRNA
à Sequence-specific
Observation: Conclusion on the mechanism:
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Milestones in discovery of RNA silencing
The model by William Dougherty (1995)
“…many of these studies and their unexpected results may be telling us something newabout cellular gene expression. For the sake of argument, it is this latter explanationthat we develop in this article.
If one embraces this concept, then it may be possible to link many seemingly unrelatedbiological phenomena as manifestations of a common regulatory system.
If this turns out to be the case, then an 'underworld' of small RNA moleculeswill negatively regulate many aspects of gene expressionand transgenic organisms will provide a window to view this system.”
Dougherty WG & Parks TD (1995) Transgenes and gene suppression: telling us something new?Current Opinion in Cell Biology 7, 399-405
Jari Valkonen
Milestones in discovery of RNA silencing
Dougherty & Parks (1995) conceptualised the mechanism differently from others,taking the early examples of natural antisense-mediated regulation of endogenous gene expressionto an account (first example from 1984: Izant & Weintraub, Cell, 36, 1007-1015).
The model (1995) included: Experimental approval:
-dsRNA The sole inducer (Caenorhabditis elegans);Fire et al, 1998: Nature 391:806-810 (cited 2026 times)
- Endogenous RNase III ‘Dicer’ (Drosophila); Bernstein et al, 2001: Nature 409, 363-366
- Hairpin structures of Micro-RNA (miRNA) in plants; Llave et al, 2002: Science 297, 2053-2056endogenous RNA
- Small endogenous antisense A small temporal RNA, let-7, processed by ’Dicer’ and theRNAs (21 nt or 69 nt) RNA silencing machinery;(e.g., lin-4 of C. elegans; Hutvágner et al, 2001: Science 293, 834-838Lee et al, 1993: Cell, 75, 843-854)
-“Interfering small RNA” siRNA (in plants); Hamilton & Baulcombe 1999: Science 286, 950-952
Nuclease fraction from Drosophila contains siRNA specific tothe inducing dsRNA: RNA-induced silencing complex, RISC(Hammond et al, 2000: Nature 404, 293-296)
Jari Valkonen
RNA silencing
siRNA - small interferring dsRNA (effector), 21-25 nt.Contain 2-nt 3’ overhangs and a 3’ hydroxyl group.Prime sequence-specific RNA degradation.
dsRNA: inducer
RNase III DICER (DCL; multidomain protein):RNase III domains bind and cleave dsRNAto produce siRNA
Scans the cell for homologousRNA molecules for degradation
RISC RISC incorporates Dicer and the (-)strandof siRNA
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2.USING RNA SILENCING
WITHOUT TRANSGENIC PLANTS
Jari Valkonen
Instead of ”antisense RNA silencing”, endogenous genes could be silenced byadministrating homologous, short dsRNA to the nematode
Fire et al. 1998, Nature 391: 806-811“Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans”
Administration of dsRNA (or any RNA) to plants is difficult technically.However, endogenous production of dsRNA from a ”hairpin” construct results inefficient silencing of homologous transcripts.
Waterhouse et al. 2000, Nature 407: 319-320
Technical steps forward in using RNA silencing
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Jari ValkonenWaterhouse et al. 2000, Nature 407: 319-320
”Hairpin-RNA” for efficient induction of RNA silencing
endogenous gene (in this experimentalcase transgenic plant that expresses
green fluorescent protein, GFP)
GFP silencing
hpGFP
HairpinRNA,
inducer
hpGFPAgrobacterium
+GFP
Fluorescence disappears
Signaling for RNA silencing in plants
Agroinfiltration method:
Kapila et al. 1997, Plant Sci. 122:101-108.
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Jari ValkonenVoinnet 2005, Nature Rev. Genet 6:206-220
Agro-infiltration
Jari Valkonen
Local and systemic signaling for RNA silencingstudied in GFP-expressing transgenic plant by agroinfiltration
Himber et al. 2003, EMBO J. 22: 4523-4533 • Palaqui et al. 1997, EMBO J 16: 4738-4745(systemic signal exists)
• Yoo et al. 2004, Plant Cell 16: 1979-2000(transport of siRNA in phloem sap)
• Huang et al. 2005, Science 309: 1694-1696(mRNA is transported in phloem to actin other parts of the plant)
Kreuze et al. 2005, J. Virol. 79:7227-7238
Local spread of silencing signal(red ”borders”)
Anna Germundsson
Systemic GFP silencing
Infiltration
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VIRUS-INDUCED GENE SILENCING (VIGS)
Commonly used (in plant research) for silencing cellular genes
Potato virus X vector, (+)ssRNA virus or any host geneor fragment thereof
Kumagai et al. 1995, PNAS 92:1679-1683
Jari Valkonen
How to obtain silencing-inducing siRNA from thevector virus?
Cellular RNA-dependent RNA polymerase (RdRp)
•During (tombus)virus infection in plants, siRNA is generated from many but not all partsof the viral RNA genome; mostly from positions that form imperfect hairpinsSzittya et al. 2002, Plant Cell 14:369-372
•QDE-1 of Neurospora crassa synthesises template-long copies of the RNA moleculeor 9-21 nt long oligomers from any position of the templateMakeyev & Bamford 2002, Mol. Cell 10, 1417-1427
• Arabidopsis RDR2 is needed for synthesis of siRNA (Xie et al. 2004, PLoS Biol. 2, E104)
•Amplification of siRNA using the (-)strand as a primer à spread of silencing(plants and nematodes)
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VIRUS-INDUCED GENE SILENCING (VIGS) continues...
Potato virus X vector, (+)ssRNA virus or any host geneor fragment thereof
1. Post-transcriptional silencing:
• Virus replicates to high titres in cytoplasm• Virus-derived siRNAs accumulate (including the added sequences), which targets the virusand the homologous host mRNA to degradation in cytoplasm
• The encoding region of the gene may ultimately become methylated (in the nucleus)
2. Transcriptional silencing:
If the gene promoter sequence was expressed from the vector virus (in cytoplasm),promoter becomes methylated (in nucleus)
Tobacco rattle virus was usedas a vector to silence LeEILs,a gene of the ethylene synthesispathway (ethylene is involved infruit ripening)
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Park JA, Kim TW, Kim SK, et al.Silencing of NbECR encoding a putative enoyl-CoA reductase results indisorganized membrane structures and epidermal cell ablation in Nicotiana benthamianaFEBS LETTERS 579 (20): 4459-4464 AUG 15 2005
Hein I, Pacak MB, Hrubikova K, et al.Virus-induced gene silencing-based functional characterization of genesassociated with powdery mildew resistance in barley.PLANT PHYSIOLOGY 138 (4): 2155-2164 AUG 2005
Scofield SR, Huang L, Brandt AS, et al.Development of a virus-induced gene-silencing system for hexaploid wheatand its use in functional analysis of the Lr21-mediated leaf rust resistance pathwayPLANT PHYSIOLOGY 138 (4): 2165-2173 AUG 2005
Nasir KHB, Takahashi Y, Ito A, et al.High-throughput in planta expression screening identifies a class II ethylene-responsiveelement binding factor-like protein that regulates plant cell death and non-host resistancePLANT JOURNAL 43 (4): 491-505 AUG 2005
Park JA, Ahn JW, Kim YK, et al.Retinoblastoma protein regulates cell proliferation, differentiation, and endoreduplication in plantsPLANT JOURNAL 42 (2): 153-163 APR 2005
Valentine T, Shaw J, Blok VC, et al.Efficient virus-induced gene silencing in roots using a modified tobacco rattle virus vectorPLANT PHYSIOLOGY 136 (4): 3999-4009 DEC 2004
Jari Valkonen
OPEN QUESTIONS CONCERNING RNA SILENCING
How does RdRp recognise the ssRNA that should be degraded,so that it won’t synthesise dsRNA from RNAs that need tosurvive?
How is dsRNA recognised initially?
(After generation of siRNA, RISC finds new homologous RNA with help of thesiRNA (-)strand that incoporates in RISC)
What is the systemic signal?
How does siRNA mediate its effects on DNA methylation in thenucleus?
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3.VIRUSES AS TARGETS
OF RNA SILENCING
Jari Valkonen
Viruses as targetsof RNA silencing
Voinnet 2005 6: 206-220
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Recovery from virus infection
Ratcliff et al. 1997. Science 276:1558-1560.
Jari Valkonen
Resistance to poliovirus infection in human cellsGitlin, Karelsky &Andino 2002. Nature 418:430-434
• Poliovirus-derived dsRNA introducedà virus accumulation decreased, viruscleared from most cells
• Sequence-specific: a single nt-change within the target sequence enables the virusto escape the resistance mechanism
(Not attributable to “classical antisense mechanisms” or interferon-mediatedresponse)
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A cellular miRNA mediates antiviral defense in human cells
Lecellier et al. 2005, Science 308:557-560
Primate foamy virus type 1 (PFV-1), a HIV-like retrovirus
• Human miRNA-32 and PFV-1 have significant sequence identity
• Preventing miRNA pairing to PVF-1 (mutated) caused a 3-fold increasein PFV-1 accumulation
• PFV-1 encodes Tas protein that suppresses RNA silencingin mammalian and plant cells
Jari Valkonen
Ebstein-Barr virus (herpesvirus) and other herpesviruses encode miRNAsthat regulate viral gene expression
However, based on lack of sequence identity,the viral miRNA presumably do not regulate host gene expression
Pfeffer et al. 2005, Nature Methods 2: 269-276(opposite to the conclusion of Pfeffer et al. 2004, Science 304:734-736)
Virus-derived siRNA is rare in infected cells of vertebrates.
How important is RNA silencing as a virus defence system in vertebrates?
Masked by other defence systems (immuno-response and interferon-mediateddsRNA-induced defence)?
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4.VIRUSES SUPPRESS
RNA SILENCING
Jari Valkonen
SUPPRESSION OF TRANSGENIC RESISTANCE byINFECTION WITH A HETEROLOGOUS VIRUSA: N. benthamiana plants transformed with the PVA coat protein (CP) geneare resistant (immune) to PVA; no CP transgene mRNA is detected bynorthern analysis
B: Following infection with PVY, the CP transgene mRNA accumulates todetectable levels; plants are susceptible to PVA
A: healthy B: PVY-infected
Resistant Susceptible
PVA 5’-UTR+CP
1 2 3 4 5 6 1’ 2’ 3’ 4’ 5’ 6’c
Savenkov & Valkonen 2001,J. Gen. Virol. 82: 2275-2278
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P19, the best-characterisedviral RNA silencing suppressor
Tombusviruses, (+)ssRNA genome
Tomato bushy stunt virus (TBSV)Carnation Italian ringspot virus (CIRV)
Silhavy et al. 2002, EMBO J 21:3070-3080Vargason et al. 2003, Cell 115:799-811
Vargason et al. 2003, Cell 115:799-811
P19 sequesters siRNA:
(A) It binds siRNA duplexes (dsRNA) as a tail-to-tail dimer.Contacts are sequence-independent (via phosphate groups and end-capping)
(B) The N- and C-terminus interact in the homodimer(green, C-terminus; blue, N-terminus; violet, siRNA)
Jari Valkonen
P19, the best-characterisedviral RNA silencing suppressor (continues...)
Carnation Italian ringspot virus (CIRV)
Vargason et al. 2003, Cell 115:799-811
Trp39 and Trp42 (N-terminus)form stacking interactions with
the exposed basepairsat each end of the siRNA duplex
End-capping at each endof siRNA duplex,a ”pocket” fitting inthe dsRNA
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Revealing viral RNA silencing suppressors by AGRO-INFILTRATION
Co-infiltration
GFP silencing
hpGFP
A RSS?
Test protein,suppressor (?)
gene AAgrobacterium
GFP
Silencinginducer,hairpin
hpGFP
Reporter,GFP
Agrobacterium
Agrobacterium
GFP expression
+GFP
GFP Fluorescenceindicates suppression of silencing
Infiltration
Jari Valkonen
Agro-infiltration for co-expression ofGFP + hpGFP and one or two viral proteins
The leaf was photographed from undersideunder UV light at 10 days post-infiltration.
Green fluorescence observed in the spotsinfiltrated with p22 or HC-Pro indicated thatthese proteins suppressed RNA silencing.
Kreuze et al. 2005, J. Virol 79, 7227-7238
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RNA silencing suppressors affect different stepsof the silencing process
Kreuze et al. 2005, J. Virol. 79:7227-7238
Local spread of silencing signal(red ”borders”) inhibited
Himber et al. 2003, EMBO J. 22: 4523-4533
Potyvirus-encoded HCpro suppressorprevents:- initiation of silencing- maintenance of silencing- local movement of thesilencing signal
but not systemic signaling for silencing
Some suppressors inhibitonly the systemic signaling step
HCpro suppresses RNA silencingalso in animal cells