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Molecular systematics in the genus Dictyota (Dictyotales, Phaeophyta): a first attempt based on restriction patterns of the Internal Transcribed Spacer 1 of the rDNA (ARDRA-ITS1)
De Clerck, O.; De Vos, P.; Gillis, M.; Coppejans, E. (2001). Molecular systematics in the genus Dictyota (Dictyotales, Phaeophyta): a first attempt based on restriction patterns of the Internal Transcribed Spacer 1 of the rDNA (ARDRA-ITS1) Syst. Geogr. Pl. 71: 25-35
In: Systematics and Geography of Plants. Nationale Plantentuin van Belgiƫ: Meise. ISSN 1374-7886, meer

Ook gepubliceerd als
  • De Clerck, O.; De Vos, P.; Gillis, M.; Coppejans, E. (2001). Molecular systematics in the genus Dictyota (Dictyotales, Phaeophyta): a first attempt based on restriction patterns of the Internal Transcribed Spacer 1 of the rDNA (ARDRA-ITS1), in: (2001). VLIZ Coll. Rep. 31(2001). VLIZ Collected Reprints: Marine and Coastal Research in Flanders, 31: pp. chapter 22 [Subsequent publication], meer

Beschikbaar in Auteurs 
    VLIZ: Open Repository 98632 [ OMA ]

Trefwoorden
    Chemotaxonomy; Moleculaire biologie; Dictyota [WoRMS]; Marien
Author keywords
    Dictyota; Phaeophyta; marine algae; molecular systematics; ARDRA; ITSI

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Abstract
    This study represents a first attempt to reconstruct the phylogenetic relationships in the genus Dictyota by means of an RFLP analysis of the amplified Internal Transcribed Spacer 1 of the ribosomal region (ARDRA-ITSI). To overcome DNA extraction problems, a new protocol based on a combination of a CTAB method and a Sephaglass Bandprep Kit is presented. Seven species, mostly including more than one specimen, were included. Padina boergesenii was used as an outgroup. The inferred phylogenetic picture was congruent with the morphological-anatomical data. Specimens belonging to the same species invariably group together and differences among geographically isolated populations are reflected in the tree. Parsimony-based bootstrap and jackknife supports for basal nodes are generally very low and phylogenetic relationships between species are poorly resolved. This poor resolution can probably be attributed to the considerable variation in length of the ITSI region among the species. This variation causes difficulties in sequence alignments and calls into question the use of this marker as a general tool in the genus.

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