Determination of Phytogenetic Relationships among Isoetes Species Using Random Primers

Isoetes L. is an ancient, primitive genus of lycopsids. The genus occupies a unique position in plant evolution as the closest relatives of tree lycopods. The morphological characters, namely leaf size, comb, and sporophyll size, are used diagnostically to help in the identification of the Isoetes species. Thus, species identification of Isoetes is always problematic and the knowledge on the genetic relationship of Isoetes species is also limited. Therefore, in order to find a suitable method for species identification and estimation of genetic relationship among different species of Isoetes, a Random Amplified Polymorphic DNA (RAPD) technique based on Polymerase Chain Reaction (PCR) was used for the described purpose. Out of 150 decamer primers tested, 58 produced good amplification products. A total of 4442 amplification products were scored and only 3479 bands (78.11%) were found to be polymorphic, with sizes ranging from 200 to 5500 bp. Unweighted pair group method using arithmetic average cluster analysis revealed a clear genetic difference among Isoetes species. The scientific data presented in this study suggest that RAPD-PCR could be a valuable tool for identification and estimation of genetic relationship among species of Isoetes L.

Determination of Phytogenetic Relationships among Isoetes Species Using Random Primers

Isoetes L. is an ancient, primitive genus of lycopsids. The genus occupies a unique position in plant evolution as the closest relatives of tree lycopods. The morphological characters, namely leaf size, comb, and sporophyll size, are used diagnostically to help in the identification of the Isoetes species. Thus, species identification of Isoetes is always problematic and the knowledge on the genetic relationship of Isoetes species is also limited. Therefore, in order to find a suitable method for species identification and estimation of genetic relationship among different species of Isoetes, a Random Amplified Polymorphic DNA (RAPD) technique based on Polymerase Chain Reaction (PCR) was used for the described purpose. Out of 150 decamer primers tested, 58 produced good amplification products. A total of 4442 amplification products were scored and only 3479 bands (78.11%) were found to be polymorphic, with sizes ranging from 200 to 5500 bp. Unweighted pair group method using arithmetic average cluster analysis revealed a clear genetic difference among Isoetes species. The scientific data presented in this study suggest that RAPD-PCR could be a valuable tool for identification and estimation of genetic relationship among species of Isoetes L.

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  • Bradshaw HD, Wilbert SM, Otto KG & Schemske DW (1995). Genetic mapping of floral traits associated with reproductive isolation in monkey flowers (Mimulus). Nature 376: 762-765.
  • Dellaporta SL, Wood J & Hicks JB (1983). A plant DNA preparation: Version II, Plant Molecular Biology Reporter 1: 19-21.
  • Goswami HK (1996). Three decades with Isoetes. Indian Fern 13: 51- 61.
  • Hoot SB, Napier NS & Taylor WC. (2004). Revealing unknown or extinct lineages within Isoetes (isoetaceae) using DNA sequences from hybrids. Am J Bot 91: 899-904
  • Jaccard P (1908). Bull. Societies Vaud Science. Nature 44: 223-270.
  • Ma R, Mattila, TY & Pulli S (2004). Phylogenetic relationships among genotypes of worldwide collection of spring and winter ryes (Secale cereale L.) determined by RAPD-PCR markers. Hereditas 140: 210-221.
  • Stuber CW (1989a). Isozyme as markers for studying and manipulating quantitative traits. In: D. Soltis & P. Soltis (Eds.), Isozymes in Plant Biology. Discorides Press, Portland. 206-220.
  • Stuber CW (1989b). Marker based selection for quantitative traits. In: G. Robbelen (ed.), Science for Plant Breeding, Proceedings of the XII congress of Eucarpia. Paul Parey Scientific Publishers, Berlin. 31-49.
  • Stuber CW (1989c). Molecular marker in the manipulation of quantitative characters. In: A. Brown, M Clegg, A Kankr & B Weir (Eds), Plant Population Genetics, Breeding and Genetic Resource. Sinauer Associate, Inc. Sonderland, MA. 334-350.
  • Swoboda I & Bhalla PL (1997). RAPD analysis of genetic variation in the Australian fan flower, Scaevala. Genome 40: 600-606.
  • Tripathi Yogendra K, Gurha P, Ghosh D, Kumar RV, Goswami HK, Goswami R, Yadav VP & Singh N (2005). Amplification based nucleic acid scanning of Isoetes pantii using random primer. Plant Archives 5: 465-468.
  • Tripathi Yogendra K & Ghosh D (2002). Isolation and RAPD PCR amplification of genomic DNA from white button mushroom Agaricus bisporus. Bionature 22: 99-103.
  • Williams JGK, Kubelik AR & Livak KJ (1990). DNA polymorphism amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Res 18: 6531-/6535.
Turkish Journal of Botany-Cover
  • ISSN: 1300-008X
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK