Cell culture-induced gradual and frequent epigenetic reprogramming of invertedly repeated tobacco transgene epialleles
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19129419
PubMed Central
PMC2649402
DOI
10.1104/pp.108.133165
PII: pp.108.133165
Knihovny.cz E-zdroje
- MeSH
- alely * MeSH
- buněčné kultury MeSH
- epigeneze genetická * MeSH
- geneticky modifikované rostliny MeSH
- metylace DNA MeSH
- obrácené repetice genetika MeSH
- otevřené čtecí rámce genetika MeSH
- přeprogramování buněk genetika MeSH
- promotorové oblasti (genetika) genetika MeSH
- regenerace genetika MeSH
- regulace genové exprese u rostlin MeSH
- RNA rostlin metabolismus MeSH
- sekvenční analýza DNA MeSH
- siřičitany MeSH
- Southernův blotting MeSH
- tabák genetika fyziologie MeSH
- transgeny * MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- hydrogen sulfite MeSH Prohlížeč
- RNA rostlin MeSH
- siřičitany MeSH
Using a two-component transgene system involving two epiallelic variants of the invertedly repeated transgenes in locus 1 (Lo1) and a homologous single-copy transgene locus 2 (Lo2), we have studied the stability of the methylation patterns and trans-silencing interactions in cell culture and regenerated tobacco (Nicotiana tabacum) plants. The posttranscriptionally silenced (PTGS) epiallele of the Lo1 trans-silences and trans-methylates the target Lo2 in a hybrid (Lo1/Lo2 line), while its transcriptionally silenced variant (Lo1E) does not. This pattern was stable over several generations in plants. However, in early Lo1E/Lo2 callus, decreased transgene expression and partial loss of Lo1E promoter methylation compared with leaf tissue in the parental plant were observed. Analysis of small RNA species and coding region methylation suggested that the transgenes were silenced by a PTGS mechanism. The Lo1/Lo2 line remained silenced, but the nonmethylated Lo1 promoter acquired partial methylation in later callus stages. These data indicate that a cell culture process has brought both epialleles to a similar epigenetic ground. Bisulfite sequencing of the 35S promoter within the Lo1 silencer revealed molecules with no, intermediate, and high levels of methylation, demonstrating, to our knowledge for the first time, cell-to-cell methylation diversity of callus. Regenerated plants showed high interindividual but low intraindividual epigenetic variability, indicating that the callus-induced epiallelic variants were transmitted to plants and became fixed. We propose that epigenetic changes associated with dedifferentiation might influence regulatory pathways mediated by trans-PTGS processes.
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Aina R, Sgorbati S, Santagostino A, Labra M, Ghiani A, Citterio S (2004) Specific hypomethylation of DNA is induced by heavy metals in white clover and industrial hemp. Physiol Plant 121 472–480
Arnholdt-Schmitt B (2004) Stress-induced cell reprogramming: a role for global genome regulation? Plant Physiol 136 2579–2586 PubMed PMC
Berdasco M, Alcazar R, Garcia-Ortiz MV, Ballestar E, Fernandez AF, Roldán-Arjona T, Tiburcio AF, Altabella T, Buisine N, Quesneville H, et al (2008) Promoter DNA hypermethylation and gene repression in undifferentiated Arabidopsis cells. PLoS One 3 e3306. PubMed PMC
Correa WL, Gomes LL, Margis R, Vaslin MFS (2004) Suppression of post-transcriptional gene silencing by callus induction and virus infection reveals the existence of aberrant RNAs. Plant Sci 167 159–164
Dalmay T, Hamilton A, Rudd S, Angell S, Baulcombe DC (2000) An RNA-dependent RNA polymerase gene in Arabidopsis is required for posttranscriptional gene silencing mediated by a transgene but not by a virus. Cell 101 543–553 PubMed
De Neve M, De Buck S, De Wilde C, Van Houdt H, Strobbe I, Jacobs A, Van M, Depicker A (1999) Gene silencing results in instability of antibody production in transgenic plants. Mol Gen Genet 260 582–592 PubMed
Ebbs ML, Bartee L, Bender J (2005) H3 lysine 9 methylation is maintained on a transcribed inverted repeat by combined action of SUVH6 and SUVH4 methyltransferases. Mol Cell Biol 25 10507–10515 PubMed PMC
Finnegan EJ (2002) Epialleles: a source of random variation in times of stress. Curr Opin Plant Biol 5 101–106 PubMed
Fischer U, Kuhlmann M, Pecinka A, Schmidt R, Mette MF (2008) Local DNA features affect RNA-directed transcriptional gene silencing and DNA methylation. Plant J 53 1–10 PubMed
Fojtova M, Bleys A, Bedrichova J, Van Houdt H, Krizova K, Depicker A, Kovarik A (2006) The trans-silencing capacity of invertedly repeated transgenes depends on their epigenetic state in tobacco. Nucleic Acids Res 34 2280–2293 PubMed PMC
Fojtova M, Van Houdt H, Depicker A, Kovarik A (2003) Epigenetic switch from posttranscriptional to transcriptional silencing is correlated with promoter hypermethylation. Plant Physiol 133 1240–1250 PubMed PMC
Grandbastien MA (1998) Activation of plant retrotransposons under stress conditions. Trends Plant Sci 3 181–187
Hamilton AJ, Baulcombe DC (1999) A species of small antisense RNA in posttranscriptional gene silencing in plants. Science 286 950–952 PubMed
Hetzl J, Foerster AM, Raidl G, Mittelsten Scheid O (2007) CyMATE: a new tool for methylation analysis of plant genomic DNA after bisulfite sequencing. Plant J 51 526–536 PubMed
Hirochika H (1993) Activation of tobacco retrotransposons during tissue-culture. EMBO J 12 2521–2528 PubMed PMC
Ingelbrecht I, Van Houdt H, Van Montagu M, Depicker A (1994) Posttranscriptional silencing of reporter transgenes in tobacco correlates with DNA methylation. Proc Natl Acad Sci USA 91 10502–10506 PubMed PMC
Jaligot E, Rival A, Beule T, Dussert S, Verdeil JL (2000) Somaclonal variation in oil palm (Elaeis guineensis Jacg.): the DNA methylation hypothesis. Plant Cell Rep 19 684–690 PubMed
Kaeppler SM, Kaeppler HF, Rhee Y (2000) Epigenetic aspects of somaclonal variation in plants. Plant Mol Biol 43 179–188 PubMed
Kaeppler SM, Phillips RL (1993) Tissue culture-induced DNA methylation variation in maize. Proc Natl Acad Sci USA 90 8773–8776 PubMed PMC
Kakutani T (2002) Epi-alleles in plants: inheritance of epigenetic information over generations. Plant Cell Physiol 43 1106–1111 PubMed
Kanazawa A, O'Dell M, Hellens RP (2006) The binding of nuclear factors to the as-1 element in the CaMV 35S promoter is affected by cytosine methylation in vitro. Plant Biol 9 435–441 PubMed
Kanazawa A, O'Dell M, Hellens RP (2007) Epigenetic inactivation of chalcone synthase: a transgene transcription in petunia leads to a reversion of the post-transcriptional gene silencing phenotype. Plant Cell Physiol 48 638–647 PubMed
Karp A (1991) On the current understanding of somaclonal variation. Oxf Surv Plant Mol Cell Biol 7 1–58
Komarova NY, Grabe T, Huigen DJ, Hemleben V, Volkov RA (2004) Organization, differential expression and methylation of rDNA in artificial Solanum allopolyploids. Plant Mol Biol 56 439–463 PubMed
Koukalova B, Fojtova M, Lim KY, Fulnecek J, Leitch AR, Kovarik A (2005) Dedifferentiation of tobacco cells is associated with ribosomal RNA gene hypomethylation, increased transcription, and chromatin alterations. Plant Physiol 139 275–286 PubMed PMC
Kovarik A, Koukalova B, Bezdek M, Opatrny Z (1997) Hypermethylation of tobacco heterochromatic loci in response to osmotic stress. Theor Appl Genet 95 301–306
Kovarik A, Van Houdt H, Holy A, Depicker A (2000) Drug-induced hypomethylation of a posttranscriptionally silenced transgene locus of tobacco leads to partial release of silencing. FEBS Lett 467 47–51 PubMed
Kubis SE, Castilho AM, Vershinin A, Heslop-Harrison JS (2003) Retroelements, transposons and methylation status in the genome of oil palm (Elaeis guineensis) and the relationship to somaclonal variation. Plant Mol Biol 52 69–79 PubMed
Labra M, Ghiani A, Citterio S, Sgorbati S, Sala F, Vannini C, Ruffini-Castiglione M, Bracale M (2002) Analysis of cytosine methylation pattern in response to water deficit in pea root tips. Plant Biol 4 694–699
Lim KY, Kovarik A, Matyasek R, Bezdek M, Lichtenstein CP, Leitch AR (2000) Gene conversion of ribosomal DNA in Nicotiana tabacum is associated with undermethylated, decondensed and probably active gene units. Chromosoma 109 161–172 PubMed
LoSchiavo F, Pitto L, Giuliano G, Torti G, Nuti-Ronchi V, Maraziti D, Vergara R, Orselli S, Terzi M (1989) DNA methylation of embryogenic carrot cell cultures and its variations as caused by mutation, differentiation, hormones and hypomethylating drugs. Theor Appl Genet 77 325–331 PubMed
Mathieu O, Jasencakova Z, Vaillant I, Gendrel AV, Colot V, Schubert I, Tourmente S (2003) Changes in 5S rDNA chromatin organization and transcription during heterochromatin establishment in Arabidopsis. Plant Cell 15 2929–2939 PubMed PMC
Matzke MA, Matzke AJM (1990) Gene interactions and epigenetic variation in transgenic plants. Dev Genet 11 214–223
Meins F, Thomas M (2003) Meiotic transmission of epigenetic changes in the cell-division factor requirement of plant cells. Development 130 6201–6208 PubMed
Melquist S, Luff B, Bender J (1999) Arabidopsis PAI gene arrangements, cytosine methylation and expression. Genetics 153 401–413 PubMed PMC
Meng L, Ziv M, Lemaux PG (2006) Nature of stress and transgene locus influences transgene expression stability in barley. Plant Mol Biol 62 15–28 PubMed
Mette MF, Aufsatz W, van der Winden J, Matzke MA, Matzke AJ (2000) Transcriptional silencing and promoter methylation triggered by double-stranded RNA. EMBO J 19 5194–5201 PubMed PMC
Mitsuhara I, Shirasawa-Seo N, Iwai T, Nakamura S, Honkura R, Ohashi Y (2002) Release from post-transcriptional gene silencing by cell proliferation in transgenic tobacco plants: possible mechanism for noninheritance of the silencing. Genetics 160 343–352 PubMed PMC
Olhoft PM, Philips RL (1999) Genetic and epigenetic instability in tissue culture and regenerated progenies. In H Lerner, ed, Plant Responses to Environmental Stresses: From Phytohormones to Genome Reorganization. Marcel Dekker, New York, pp 111–148
Peredo EL, Revilla MA, Arroyo-Garcia R (2006) Assessment of genetic and epigenetic variation in hop plants regenerated from sequential subcultures of organogenic calli. J Plant Physiol 163 1071–1079 PubMed
Phillips RL, Kaeppler SM, Olhoft P (1994) Genetic instability of plant tissue cultures: breakdown of normal controls. Proc Natl Acad Sci USA 91 5222–5226 PubMed PMC
Richards E (2006) Inherited epigenetic variation: revisiting soft inheritance. Nat Rev Genet 7 395–401 PubMed
Schellenbaum P, Mohler V, Wenzel G, Walter B (2008) Variation in DNA methylation patterns of grapevine somaclones (Vitis vinifera L.). BMC Plant Biol 8 78. PubMed PMC
Smulders MJM, Rus-Kortekaas W, Vosman B (1995) Tissue culture-induced DNA methylation polymorphism in repetitive DNA of tomato calli and regenerated plants. Theor Appl Genet 91 1257–1264 PubMed
van Blokland R, ten Lohuis M, Meyer P (1997) Condensation of chromatin in transcriptional regions of an inactivated plant transgene: evidence for an active role of transcription in gene silencing. Mol Gen Genet 257 1–13 PubMed
Van Houdt H, Ingelbrech I, Van Montagu M, Depicker A (1997) 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 12 379–392
Van Houdt H, Kovarik A, Van Montagu M, Depicker A (2000. a) Cross-talk between posttranscriptionally silenced neomycin phosphotransferase II transgenes. FEBS Lett 467 41–46 PubMed
Van Houdt H, Van Montagu M, Depicker A (2000. b) Both sense and antisense RNAs are targets for the sense transgene-induced posttranscriptional silencing mechanism. Mol Gen Genet 263 995–1002 PubMed
Vaucheret H, Beclin C, Fagard M (2001) Post-transcriptional gene silencing in plants. J Cell Sci 114 3083–3091 PubMed
Vaucheret H, Fagard M (2001) Transcriptional gene silencing in plants: targets, inducers and regulators. Trends Genet 17 29–35 PubMed
Williams L, Zhao J, Morozova N, Li Y, Avivi Y, Grafi G (2003) Chromatin reorganization accompanying cellular dedifferentiation is associated with modifications of histone H3, redistribution of HP1, and activation of E2F-target genes. Dev Dyn 228 113–120 PubMed
Paramutation of tobacco transgenes by small RNA-mediated transcriptional gene silencing