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2007 | 48 | 4 |

Tytuł artykułu

Somaclonal variation at the nucleotide sequence level in rice [Oryza sativa L.] as revealed by RAPD and ISSR markers, and by pairwise sequence analysis

Autorzy

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The nature of somaclonal variation at the nucleotide sequence level was studied in rice cv. Nipponbare. First, we investigated genomic variations by using 2 molecular marker systems: RAPD (random amplified polymorphic DNA) and ISSR (inter-simple sequence repeat). This was followed by sequencing of selected bands that represented genomic variations, and pairwise sequence analysis taking advantage of the whole genome sequence of rice. In addition, transpositional activity of the active MITE, mPing, was analysed by locus-specific PCR amplifications. The 2-year-old calli and their regenerated plants, analysed with 24 RAPD and 20 ISSR primers, showed moderate levels of genomic variation (20.83% and 17.04%, respectively). To test whether DNA methylation plays a role in somaclonal variation, the calli were treated with 5-azacytidine, a chemical agent that reduces cytosine methylation by blocking the activity of DNA methyltransferase. Though dwarfism occurred in regenerants from treated calli (a hallmark of the drug treatment), there was only a slight increase in the frequency of somaclonal variation detected in the treated calli and their regenerated plants relative to untreated controls. The transposon mPing also remained immobile in both treated and untreated calli. Nevertheless, dendrograms constructed according to the Jaccard coefficient calculated by UPGMA of the ISSR bands revealed that the 5-azacytidine-treated and untreated somaclones were grouped into 2 distinct clusters, suggesting a possible indirect effect of the treatment on the genomic changes, depending on the marker used. Sequence analysis indicated a low level of variation (0.31%), with single-base-pair substitutions predominating.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

48

Numer

4

Opis fizyczny

p.329-336,fig.,ref.

Twórcy

autor
  • Laboratory of Molecular Epigenetics of MOE, Institute of Genetics and Cytology, Northwest Normal University, Changchun 130024, China
  • Ecole Normale Supérieure, Bujumbura, Burundi
autor
  • The National Centre of Transgenic Plant Research & Commercialization, Gongzuling, China
autor
  • Laboratory of Molecular Epigenetics of MOE, Institute of Genetics and Cytology, Northwest Normal University, Changchun 130024, China

Bibliografia

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  • Feng Q, Zhang YJ, Hao P, et al. 2002. Sequence and analysis of rice chromosome-4. Nature 420: 316-320.
  • Guo WL, Gong L, Ding ZF, Li YD, Li FX, Zhao YP, Liu B, 2006. Genomie instability in phenotypically normal regenerants of medicinal plant Codonopsis lanceolata Benth. et Hook, f., as revealed by ISSR and RAPD markers. Plant Cell Rep 25: 896-906.
  • Jaccard P, 1908. Nouvelles recherches sur la distribution florale. Bull Soc Vaud Sci Nat 44: 223-270.
  • Janousek B, Zluvova J, Vyskot B, 2000. Histone H4 acetylation and DNA methylation dynamics during pollen development. Protoplasma 211: 116-122.
  • Jiang N, Bao Z, Zhang X, Hirochika H, Eddy SR, McCouch SR, Wessler SR, 2003. An active DNA transposon family in rice. Nature 421: 163-167.
  • Kidwell KK, Osborn TC, 1992. Simple plant DNA isolation procedures. In: Beckman JS, Osborn TC, eds. Plant genomes, methods for genetic and physical mapping. Kluwer Academic Publishers, Amsterdam, the Netherlands: 1-13.
  • Kikuchi K, Terauchi K, Wada M, Hirano, H-Y, 2003. The plant MITE mPing is mobilized in anther culture. Nature 421: 163-167.
  • Kim DS, Lee IS, Hyun DY, Jang CS, Song HS, Seo YW, Lee YE, 2003. Detection of DNA instability induced from tissue culture and irradiation in Oryza sativa L. by RAPD analysis. J Plant Biotech 5: 25-31.
  • Kuznetsova OL, Ash OA, Hartina GA Gostimskii SA, 2005. RAPD and ISSR analyses of regenerated pea Pisum sativum L. plants. Rus J Genet 41: 60-65.
  • Larkin P, Scowcroft N, 1981. Somaclonal variation: a novel source of variability from cell for plant improvement. Theor Appl Genet 60: 197-214.
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  • Muller E, Brown PTH, Hartke S, Lorz HTI, 1990. DNA variation in tissue-culture-derived rice plants. Theor Appl Genet 80: 673-679.
  • Osipova ES, Koveza OV, Troitskii AV, Dolgikh YI, Shamina ZB, Gostimskii SA, 2003. Analysis of specific RAPD and ISSR fragments in maize (Zea mays L.) somaclones and development of SCAR markers on their basis. Rus J Genet 39: 1412-1419.
  • Polanco C, Ruiz ML, 2002. AFLP analysis of somaclonal variation in Arabidopsis thaliana regenerated plants. Plant Sci 162: 817-824.
  • Rohlf FJ, 1993. NTSYS-pc. Numerical taxonomy and multivariate analysis system, version 2.02. Setauket (New York): Exeter Publishing.
  • Rohlf FJ, 1997. NTSYSpc: numerical taxonomy and multivariate analysis system, version 2.02. Setauket (New York): Exeter Publishing.
  • Roy B, Mandal AB, 2005. Anther culture response in indica rice and variations in major agronomic characters among the androclones of a scented cultivar, Karnal local. African J Biotech 4: 235-240.
  • Sano H, Kamada I, Youssefian S, Katsumi M, Wabiko H, 1990. A single treatment of rice seedlings with 5-azacytidine induces heritable dwarfism and undermethylation of genomic DNA. Molec. Genet Gen 220: 441-447.
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Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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