Paramutation of tobacco transgenes by small RNA-mediated transcriptional gene silencing
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21521939
PubMed Central
PMC3121974
DOI
10.4161/epi.6.5.15764
PII: 15764
Knihovny.cz E-zdroje
- MeSH
- alely MeSH
- epigeneze genetická MeSH
- genetická transkripce MeSH
- geneticky modifikované rostliny genetika MeSH
- genomový imprinting MeSH
- malá interferující RNA genetika MeSH
- metylace DNA * MeSH
- promotorové oblasti (genetika) MeSH
- regulace genové exprese u rostlin * MeSH
- RNA interference MeSH
- tabák genetika MeSH
- transgeny genetika MeSH
- umlčovací elementy transkripční genetika MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- malá interferující RNA MeSH
It has been well established that trans-acting small RNAs guide promoter methylation leading to its inactivation and gene silencing at the transcriptional level (TGS). Here we addressed the question of the influence of the locus structure and epigenetic modifications of the target locus on its susceptibility for being paramutated by trans-acting small RNA molecules. Silencing was induced by crossing a 35S promoter silencer locus 271 with two different 35S-driven transgene loci, locus 2 containing a highly expressed single copy gene and locus 1 containing an inverted posttranscriptionally silenced (PTGS) repeat of this gene. Three generations of exposure to RNA signals from the 271 locus were required to complete silencing and methylation of the 35S promoter within locus 2. Segregating methylated locus 2 epialleles were obtained only from the third generation of hybrids, and this methylation was not correlated with silencing. Strikingly, only one generation was required for the PTGS locus 1 to acquire complete TGS and 35S promoter methylation. In this case, paramutated locus 1 epialleles bearing methylated and inactive 35S promoters segregated already from the first generation of hybrids. The results support the hypothesis that PTGS loci containing a palindrome structure and methylation in the coding region are more sensitive to paramutation by small RNAs and exhibit a strong tendency to formation of meiotically transmissible TGS epialleles. These features contrast with a non-methylated single copy transgenic locus that required several generations of contact with RNA silencing molecules to become imprinted in a stable epiallele.
Zobrazit více v PubMed
Chandler VL. Paramutation's properties and puzzles. Science. 2010;330:628–629. PubMed
Arteaga-Vazquez M, Sidorenko L, Rabanal FA, Shrivistava R, Nobuta K, Green PJ, et al. RNA-mediated trans-communication can establish paramutation at the b1 locus in maize. Proc Natl Acad Sci USA. 2010;107:12986–12991. PubMed PMC
Haring M, Bader R, Louwers M, Schwabe A, van Driel R, Stam M. The role of DNA methylation, nucleosome occupancy and histone modifications in paramutation. Plant J. 2010;63:366–378. PubMed
Vaucheret H, Beclin C, Fagard M. Post-transcriptional gene silencing in plants. J Cell Sci. 2001;114:3083–3091. PubMed
Vaucheret H, Fagard M. Transcriptional gene silencing in plants: targets, inducers and regulators. Trends Genet. 2001;17:29–35. PubMed
Kooter JM, Matzke MA, Meyer P. Listening to the silent genes: transgene silencing, gene regulation and pathogen control. Trends Plant Sci. 1999;4:340–347. PubMed
Jones L, Hamilton AJ, Voinnet O, Thomas CL, Maule AJ, Baulcombe DC. RNA-DNA interactions and DNA methylation in post-transcriptional gene silencing. Plant Cell. 1999;11:2291–2301. PubMed PMC
Wassenegger M. The role of the RNAi machinery in heterochromatin formation. Cell. 2005;122:13–16. PubMed
Matzke M, Aufsatz W, Kanno T, Daxinger L, Papp I, Mette MF, Matzke AJ. Genetic analysis of RNA-mediated transcriptional gene silencing. Biochim Biophys Acta. 2004;1677:129–141. PubMed
Meyer P. DNA methylation systems and targets in plants. Febs Lett. 2010;1 doi: 10.1016/j.febslet.2010.08.017. In press. PubMed DOI
Meyer P, Niedenhof I, ten Lohuis M. Evidence for cytosine methylation of non-symmetrical sequences in transgenic Petunia hybrida. EMBO J. 1994;13:2084–2088. PubMed PMC
Dieguez MJ, Vaucheret H, Paszkowski J, Mittelsten Scheid O. Cytosine methylation at CG and CNG sites is not a prerequisite for the initiation of transcriptional gene silencing in plants, but it is required for its maintenance. Mol Gen Genet. 1998;259:207–215. PubMed
Mishiba K, Nishihara M, Nakatsuka T, Abe Y, Hirano H, Yokoi T, Kikuchi A, et al. Consistent transcriptional silencing of 35S-driven transgenes in gentian. Plant J. 2005;44:541–556. PubMed
Pecinka A, Dinh HQ, Baubec T, Rosa M, Lettner N, Mittelsten Scheid O. Epigenetic regulation of repetitive elements is attenuated by prolonged heat stress in Arabidopsis. Plant Cell. 2010;22:3118–3129. PubMed PMC
Kumpatla SP, Hall TC. Longevity of 5-azacytidine-mediated gene expression and re-establishment of silencing in transgenic rice. Plant Mol Biol. 1998;38:1113–1122. PubMed
Nocarova E, Opatrny Z, Fischer L. Successive silencing of tandem reporter genes in potato (Solanum tuberosum) over 5 years of vegetative propagation. Ann Bot. 2010;106:565–572. PubMed PMC
Meyer P, Linn F, Heidmann I, Meyer H, Niedenhof I, Saedler H. Endogenous and environmental factors influence 35S promoter methylation of a maize A1 gene construct in transgenic petunia and its colour phenotype. Mol Gen Genet. 1992;231:345–352. PubMed
Kanazawa A, O'Dell M, Hellens RP. The binding of nuclear factors to the as-1 element in the CaMV 35S promoter is affected by cytosine methylation in vitro. Plant Biol. 2007;9:435–441. PubMed
De Buck S, Windels P, De Loose M, Depicker A. Single-copy T-DNAs integrated at different positions in the Arabidopsis genome display uniform and comparable beta-glucuronidase accumulation levels. Cell Mol Life Sci. 2004;61:2632–2645. PubMed
Fischer U, Kuhlmann M, Pecinka A, Schmidt R, Mette MF. Local DNA features affect RNA-directed transcriptional gene silencing and DNA methylation. Plant J. 2008;53:1–10. PubMed
Schubert D, Lechtenberg B, Forsbach A, Gils M, Bahadur S, Schmidt R. Silencing in Arabidopsis T-DNA transformants: The predominant role of a gene-specific RNA sensing mechanism versus position effects. Plant Cell. 2004;16:2561–2572. PubMed PMC
Mittelsten Scheid O, Afsar K, Paszkowski J. Formation of stable epialleles and their paramutation-like interaction in tetraploid Arabidopsis thaliana. Nat Genet. 2003;34:450–454. PubMed
Jakowitsch J, Papp I, Moscone EA, van der Winden J, Matzke M, Matzke AJM. Molecular and cytogenetic characterization of a transgene locus that induces silencing and methylation of homologous promoters in trans. Plant J. 1999;17:131–140. PubMed
Haring M, Bader R, Louwers M, Schwabe A, van Driel R, Stam M. The role of DNA methylation, nucleosome occupancy and histone modifications in paramutation. Plant J. 2010;63:366–378. PubMed
Kunz C, Narangajavana J, Jakowitsch J, Park YD, Delon TR, Kovarik A, et al. Studies on the effects of a flanking repetitive sequence on the expression of single-copy transgenes in Nicotiana sylvestris and in N-sylvestris-N-tomentosiformis hybrids. Plant Mol Biol. 2003;52:203–215. PubMed
De Bolle MFC, Butaye KMJ, Goderis IJWM, Wouters PFJ, Jacobs A, Delaure SL, et al. The influence of matrix attachment regions on transgene expression in Arabidopsis thaliana wild type and gene silencing mutants. Plant Mol Biol. 2007;63:533–543. PubMed
Mlynarova L, Hricova A, Loonen A, Nap JP. The presence of a chromatin boundary appears to shield a transgene in tobacco from RNA silencing. Plant Cell. 2003;15:2203–2217. PubMed PMC
Dalakouras A, Moser M, Krczal G, Wassenegger M. A chimeric satellite transgene sequence is inefficiently targeted by viroid-induced DNA methylation in tobacco. Plant Mol Biol. 2010;73:439–447. PubMed
Van Houdt H, Kovarik A, Van Montagu M, Depicker A. Cross-talk between posttranscriptionally silenced neomycin phosphotransferase II transgenes. Febs Lett. 2000;467:41–46. PubMed
Fojtova M, Bleys A, Bedrichova J, Van Houdt H, Krizova K, Depicker A, Kovarik A. The trans-silencing capacity of invertedly repeated transgenes depends on their epigenetic state in tobacco. Nucl Acids Res. 2006;34:2280–2293. PubMed PMC
Kovarik A, Van Houdt H, Holy A, Depicker A. Drug-induced hypomethylation of a posttranscriptionally silenced transgene locus of tobacco leads to partial release of silencing. Febs Lett. 2000;467:47–51. PubMed
Park YD, Papp I, Moscone EA, Iglesias VA, Vaucheret H, Matzke AJ, Matzke MA. Gene silencing mediated by promoter homology occurs at the level of transcription and results in meiotically heritable alterations in methylation and gene activity. Plant J. 1996;9:183–194. PubMed
Vaucheret H. Promoter-Dependent Trans-Inactivation in Transgenic Tobacco Plants—Kinetic Aspects of Gene Silencing and Gene Reactivation. Cr Acad Sci Iii-Vie. 1994;317:310–323.
Mourrain P, van Blokland R, Kooter JM, Vaucheret H. A single transgene locus triggers both transcriptional and post-transcriptional silencing through double-stranded RNA production. Planta. 2007;225:365–379. PubMed
Krizova K, Fojtova M, Depicker A, Kovarik A. Cell culture-induced gradual and frequent epigenetic reprogramming of invertedly repeated tobacco transgene epialleles. Plant Physiol. 2009;149:1493–1504. PubMed PMC
Van Houdt H, Ingelbrecht I, Van Montagu M, Depicker A. Post-transcriptional silencing of a neomycin phosphotransferase II transgene correlates with the accumulation of unproductive RNAs and with increased cytosine methylation of 3′ flanking regions. Plant J. 1997;12:379–392.
Dieguez MJ, Bellotto M, Afsar K, Mittelsten Scheid O, Paszkowski J. Methylation of cytosines in nonconventional methylation acceptor sites can contribute to reduced gene expression. Mol Gen Genet. 1997;253:581–588. PubMed
Fu X, Kohli A, Twyman RM, Christou P. Alternative silencing effects involve distinct types of non-spreading cytosine methylation at a three-gene, single-copy transgenic locus in rice. Mol Gen Genet. 2000;263:106–118. PubMed
Fojtova M, Van Houdt H, Depicker A, Kovarik A. Epigenetic switch from posttranscriptional to transcriptional silencing is correlated with promoter hypermethylation. Plant Physiol. 2003;133:1240–1250. PubMed PMC
Lunerova-Bedrichova J, Bleys A, Fojtova M, Khaitova L, Depicker A, Kovarik A. Trans-generation inheritance of methylation patterns in a tobacco transgene following a post-transcriptional silencing event. Plant J. 2008;54:1049–1062. PubMed
Kanazawa A, O'Dell M, Hellens RP. Epigenetic inactivation of chalcone synthase-A transgene transcription in petunia leads to a reversion of the post-transcriptional gene silencing phenotype. Plant Cell Physiol. 2007;48:638–647. PubMed
Gambino G, Perrone I, Carra A, Chitarra W, Boccacci P, Torello Marinoni D, et al. Transgene silencing in grapevines transformed with GFLV resistance genes: analysis of variable expression of transgene, siRNAs production and cytosine methylation. Transgenic Res. 2010;19:17–27. PubMed
Stam M, Mittelsten Scheid O. Paramutation: an encounter leaving a lasting impression. Trends Plant Sci. 2005;10:283–290. PubMed
Cubas P, Vincent C, Coen E. An epigenetic mutation responsible for natural variation in floral symmetry. Nature. 1999;401:157–161. PubMed
Ingelbrecht I, Van Houdt H, Van Montagu M, Depicker A. Posttranscriptional silencing of reporter transgenes in tobacco correlates with DNA methylation. Proc Natl Acad Sci USA. 1994;91:10502–10516. PubMed PMC
Fojtova M, Kovarik A, Matyasek R. Cytosine methylation of plastid genome in higher plants. Fact or artefact? Plant Sci. 2001;160:585–593. PubMed
Hetzl J, Foerster AM, Raidl G, Mittelsten Scheid O. CyMATE: a new tool for methylation analysis of plant genomic DNA after bisulphite sequencing. Plant J. 2007;51:526–536. PubMed
Hamilton AJ, Baulcombe DC. A species of small antisense RNA in posttranscriptional gene silencing in plants. Science. 1999;286:950–952. PubMed
Pall GS, Codony-Servat C, Byrne J, Ritchie L, Hamilton A. Carbodiimide-mediated cross-linking of RNA to nylon membranes improves the detection of siRNA, miRNA and piRNA by northern blot. Nucleic Acids Res. 2007;35:60. PubMed PMC
Matzke MA, Aufsatz W, Kanno T, Mette MF, Matzke AJM. Homology-dependent gene silencing and host defense in plants. In: Wu C, Dunlap J, editors. Homology Effects. 2002. pp. 243–275. PubMed
Odell JT, Nagy F, Chua NH. Identification of DNA-sequences required for activity of the cauliflower mosaic virus-35s promoter. Nature. 1985;313:810–812. PubMed