Plant Biol (Stuttg) 2007; 9(4): 526-533
DOI: 10.1055/s-2007-964934
Research Paper

Georg Thieme Verlag Stuttgart KG · New York

Methylation-Sensitive Amplification Polymorphism in Date Palms (Phoenix dactylifera L.) and their Off-Shoots

J.-G. Fang1 , C. T. Chao2
  • 1Horticultural College, Nanjing Agricultural University, 1 Weigang, Nanjing 210095, China
  • 2Department of Botany and Plant Sciences, University of California-Riverside, 900 University Av., Riverside, CA 92521-0124, USA
Further Information

Publication History

Received: June 6, 2006

Accepted: December 5, 2006

Publication Date:
20 July 2007 (online)

Abstract

DNA methylation plays an important role in the regulation of gene expression in eukaryotes. In this study, the extent and patterns of DNA methylation were assessed in date palm mother-plants and their off-shoots using the methylation-sensitive amplified polymorphism (MSAP) technique. Three types of bands were generated using 12 pairs of primers. Type I were present in both EcoR I + Hpa II and EcoR I + Msp I lanes; type II were present in EcoR I + Hpa II lanes, but not in EcoR I + Msp I lanes; and type III bands were present in EcoR I + Msp I lanes, but not in EcoR I + Hpa II lanes. The total numbers of these three types of bands were 782, 55, and 34, respectively. Among these three types of bands, the polymorphic bands were, respectively, 37, 10, and 0. The distribution of polymorphic bands among mother-plants and off-shoots suggests the methylation variation was present in both the mother-plants and off-shoots. Forty- four out of these 47 polymorphic bands show clear difference between mother-plant and off-shoots: 38 were present only in off-shoots and 6 in both mother-plants and off-shoots. Compared to methylation status in mother-plants, the methylation variation during off-shoot growth of date palm can be characterized as a process involving primarily de-methylation. Hypomethylation of DNA in off-shoots, compared with mother-plants, reflects the marked expression of this molecular feature, which may be related to gene expression during off-shoot development. The methylation or de-methylation status of specific loci in the mother-plants and their off-shoots were probably random events.

References

  • 1 Azeqour M., Majourhat K., Baaziz M.. Morphological variations and isoenzyme polymorphism of date palm clones from in vitro culture acclimatized and established on soil in South Morocco.  Euphytica. (2002);  123 57-66
  • 2 Barrow S. C.. A monograph of Phoenix L. (Palmae: Coryphoideae).  Key Bulletin. (1998);  53 513-575
  • 3 Bassam B. J., Caetano-Anolles G., Gresshoff P. M.. Fast and sensitive silver staining of DNA in polyacrylamide gels.  Analytical Biochemistry. (1991);  196 80-83
  • 4 Baurens F. C., Bonnot F., Bienvenu D., Causse S., Legavre T.. Using SD-AFLP and MSAP to assess CCGG methylation in the banana genome.  Plant Molecular Biology Reporter. (2003);  21 339-348
  • 5 Cervera M. T., Ruiz-García L., Martínez-Zapater J. M.. Analysis of DNA methylation in Arabidopsis thaliana based on methylation-sensitive AFLP markers.  Molecular Genetics and Genomics. (2002);  268 543-552
  • 6 Cohen Y., Korchinsky R., Tripler E., Ziv G., Cohen R.. Fruit setting abnormalities in date palms of the cultivar Barhee originated from tissue culture.  Alon Hanotea. (2003);  57 275-279
  • 7 Corniquel B., Mercier L.. Date palm (Phoenix dactylifera L.) cultivar identification by RFLP and RAPD.  Plant Science Limerick. (1994);  101 163-172
  • 8 Corniquel B., Mercier L.. Identification of date palm (Phoenix dactylifera L.) cultivars by RFLP: partial characterization of a cDNA probe that contains a sequence encoding a zinc finger motif.  International Journal of Plant Sciences. (1997);  158 152-156
  • 9 Debasis C., Yu K. W., Paek K. Y.. Detection of DNA methylation changes during somatic embryogenesis of Siberian ginseng (Eleuterococcus senticosus).  Plant Science. (2003);  165 61-68
  • 10 Demeulemeester M. A. C., Van Stallen N., De Proft M. P.. Degree of DNA methylation in chicory (Cichorium intybus L.): influence of plant age and vernalization.  Plant Science. (1999);  142 101-108
  • 11 Devanand P. S., Chao C. T.. Genetic variation with “Medjool” and “Deglet Nur” date (Phoenix dactylifera L) cultivars in California detected by fluorescent-ALFP markers.  Journal of Horticultural Science and Biotechnology. (2003);  78 405-409
  • 12 Doerfler W.. DNA methylation and gene activity.  Annual Review of Biochemistry. (1983);  52 93-124
  • 13 El-Assar A. M., Krueger R. R., Devanand P. S., Chao C. T.. Genetic analysis of Egyptian date (Phoenix dactylifera L.) accessions using AFLP markers.  Genetic Resources and Crop Evolution. (2005);  52 601-607
  • 14 Fang J., Devanand P. S., Chao C. T.. Practical strategy of single-nucleotide-polymorphism discovery in fruiting-mei (Prunus mume Sieb. et Zucc.) from amplified-fragment-length-polymorphism fragments.  Plant Molecular Biology Reporter. (2005 a);  23 227-239
  • 15 Fang J., Qiao Y., Zhang Z., Chao C. T.. Genotyping fruiting-mei (Prunus mume Sieb. et Zucc.) cultivars using AFLP markers.  HortScience. (2005 b);  42 325-328
  • 16 Finnegan E. J., Peacock W. J., Dennis E. S.. DNA methylation, a key regulator of plant development and other processes.  Current Opinion of Genetics and Development. (2000);  10 217-223
  • 17 Fulnecek J., Matyàsek K., Kovarik A.. Distribution of 5-methylcytosine residues in 5S rRNA genes in Arabidopsis thaliana and Secale cereale.  Molecular Genetics and Genomics. (2002);  268 510-517
  • 18 Geuna F., Toschi M., Bassi D.. The use of AFLP markers for cultivar identification in apricot.  Plant Breeding. (2003);  122 526-531
  • 19 Gonzalgo M. L., Jones P. A.. Mutagenic and epigenetic effects of DNA methylation.  Mutation Research. (1997);  386 107-118
  • 20 Gurevich V., Lavi U., Cohen Y.. Genetic variation in date palms propagated from offshoots and tissue culture.  Journal of American Society for Horticultural Science. (2005);  130 46-53
  • 21 Hamama L., Cornee N., Leclerc V., Marionnet F., Javouhey M., Letouze R.. Date palm (Phoenix dactylifera) offshoot identification by PCR-ISSR markers.  Acta Horticulturae. (2003);  616 453-457
  • 22 Jaligot E., Beulé T., Baurens F. C., Billotte N., Rival A.. Search for methylation-sensitive amplification polymorphisms associated with the “mantled” variant phenotype in oil palm (Elaeis guineensis Jacq.).  Genome. (2004);  47 224-228
  • 23 Jacobsen S. E., Meyerowitz E. M.. Hypermethylated SU-PERMAN epigenetic alleles in Arabidopsis.  Science. (1997);  277 1100-1103
  • 24 Jacobsen S. E., Sakai H., Finnegan E. J., Cao X., Meyerowitz E. M.. Ectopic hypermethylation of flower-specific genes in Arabidopsis.  Current Biology. (2000);  10 179-186
  • 25 Kakutani T., Jeddeloh J. A., Richards E. J.. Characterization of an Arabidopsis thaliana DNA hypermethylation mutant.  Nucleic Acids Research. (1995);  23 130-137
  • 26 Kato M., Miura A., Bender J., Jacobsen S. E., Kakutani T.. Role of CG and non-CG methylation in immobilization of transposons in Arabidopsis.  Current Biology. (2003);  13 421-426
  • 27 Kishimoto N., Sakai H., Jackson J., Jacobsen S. E., Meyerowitz E. M., Dennis E. S., Finnegan E. J.. Site specificity of the Arabidopsis METI DNA methyltransferase demonstrated through hypermethylation of the superman locus.  Plant Molecular Biology. (2001);  46 171-183
  • 28 Lindroth A. M., Cao X., Jackson J. P., Ziberman D., McCallum C. M., Henikoff S., Jacobsen S. E.. Requirement of CHROMOMETHYLASE3 for maintenance of CpXpG methylation.  Science. (2001);  292 2077-2080
  • 29 Marianne F., Mcdonald L. E., Millar D. S., Collis C. M., Watt F., Grigg G. W., Molloy P. L., Paul C. L.. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands.  Proceedings of the National Academy of Sciences of the USA. (1992);  89 1827-1831
  • 30 McClelland M., Nelson M., Raschke E.. Effect of site-specific modification on restriction endonucleases and DNA modification methyltransferases.  Nucleic Acids Research. (1994);  22 3640-3659
  • 31 Montemurro C., Simeone R., Pasqualone A., Ferrar E., Blanco A.. Genetic relationships and cultivar identification among 112 olive accessions using AFLP and SSR markers.  Journal of Horticultural Science and Biotechnology. (2005);  80 105-110
  • 32 Nixon R. W., Carpenter J. B.. Growing dates in the United States. United States Department of Agriculture Bulletin. Washington D.C., USA; (1978)
  • 33 Palmgren G., Mattsson O., Okkels F. T.. Employment of hydrolytic enzymes in the study of the level of DNA methylation.  Biochimica Biophysica Acta. (1990);  1049 293-297
  • 34 Peraza-Echeverria S., Virginia A. H. V., Andrew J. K.. Detection of DNA methylation changes in micropropagated banana plants using methylation-sensitive amplification polymorphism (MSAP).  Plant Science. (2001);  161 359-367
  • 35 Rohlf F. J.. NTSYSpc, numerical taxonomy and multivariate analysis system, version 2.1 user guide. Exeter Software, Setauket, NY. (2000)
  • 36 Saker M. M., Moursi H. A.. Molecular characterization of Egyptian date palm cultivars: RAPD fingerprints.  Arab Journal of Biotechnology. (1999);  2 71-78
  • 37 Saker M. M., Bekheet S. A., Taha H. S., Fahmy A. S., Moursi H. A.. Detection of somclonal variations in tissue culture-derived date palm plants using isoenzyme analysis and RAPD fingerprints.  Biologia Plantarum. (2000);  43 347-351
  • 38 Sedra M. H., Lashermes P., Trouslot P., Combes M. C., Hamon S.. Identification and genetic diversity analysis of date palm (Phoenix dactylifera L.) varieties from Morocco using RAPD markers.  Euphytica. (1998);  103 75-82
  • 39 Sheldon C. C., Burn J. E., Perez P. P., Metzger J., Edwards J. A., Peacock W. J., Dennis E. S.. The FLF MADS box gene: a repressor of flowering in Arabidopsis regulated by vernalization and methylation.  Plant Cell. (1999);  11 445-458
  • 40 Sneath P. H. A., Sokal R. R.. Numerical Taxonomy: The Principles and Practice of Numerical Classification. San Francisco, CA, USA; W. H. Freeman and Co (1973)
  • 41 Steward N., Kusano T., Sano H.. Expression of ZmMET1, a gene encoding a DNA methyltransferase from maize, is associated not only with replication in actively proliferating cells, but also with altered DNA methylation status in cold-stressed quiescent cells.  Nucleic Acids Research. (2000);  28 3250-3259
  • 42 Vorster B. J., Kunert K. J., Cullis C. A.. Use of representational difference analysis for characterization of sequence between date palm varieties.  Plant Cell Reports. (2002);  21 271-275
  • 43 Vos P., Hogers R., Bleeker M., Reijans M., van de Lee T., Hornes M., Frijters A., Pot J., Peleman J., Kuiper M., Zabeau M.. AFLP: a new technique for DNA fingerprinting.  Nucleic Acids Research. (1995);  23 4407-4414
  • 44 Xiong L. Z., Xu C. G., Maroof S., Zhang Q.. Patterns of cytosine methylation in an elite rice hybrid and its parental lines, detected by a methylation-sensitive amplification polymorphism technique.  Molecular Genetics and Genomics. (1999);  261 439-466

J.-G. Fang

Horticultural College
Nanjing Agricultural University

1 Weigang

Nanjing 210095

China

Email: fanggg@njau.edu.cn

Editor: M. Koornneef