PHYLOGENETIC EVIDENCE FOR THE CRYPTOPHYTE ORIGIN OF THE PLASTID OF DINOPHYSIS (DINOPHYSIALES, DINOPHYCEAE) 1

By J. Hackett, Lucie Maranda, H. Yoon, Debashish Bhattacharya. 2003

113 citations recorded by the source corpus.

Subfields: Ecology, Molecular Biology, Oceanography

View Paper: https://www.semanticscholar.org/paper/7dd469b4f5719cc39138322bc174b199573b85ca

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Citations in the corpus

Acquired phototrophy in Mesodinium and Dinophysis – A review of cellular organization, prey selectivity, nutrient uptake and bioenergetics (2013, unknown): “; thence it has been suggested that the chloroplasts are sequestered continuously from ingested prey cells (Hackett et al., 2003; Janson, 2004; Minnhagen and Janson, 2006; Nagai et al., 2008; Minnhagen et al., 2011).”
First successful culture of the marine dinoflagellate Dinophysis acuminata (2006, background): “…that photosynthetic Dinophysis species contain plastids of cryptophyte origin (Schnepf & Elbrächter 1988, Lucas & Vesk 1990, Hewes et al. 1998, Takishita et al. 2002, Hackett et al. 2003, Janson & Granéli 2003, Janson 2004), the way in which they enter Dinophysis cells has not yet been confirmed.”
Harmful Dinophysis species: A review (2012, background): “amphioxeia support the kleptoplastid hypothesis as they all show a remarkable genetic similarity among the three organisms (Takishita et al., 2002; Hackett et al., 2003; Janson, 2004; Takahashi et al., 2005; Minnhagen and Janson, 2006; Nagai et al., 2008; Nishitani et al., 2008a,b; Park et al., 2008”
Analysis of photosynthetic picoeukaryote diversity at open ocean sites in the Arabian Sea using a PCR biased towards marine algal plastids (2006, background): “Certainly, since Dinophysis is known to harbour plastids of cryptophyte origin (Hackett et al. 2003) an endosymbiotic origin of this sequence is likely.”
Molecular data and the evolutionary history of dinoflagellates (2004, background): “, 2001): although most photosynthetic dinoflagellates harbour peridinin-containing plastids surrounded by two to three membranes (here called peridinin plastids), other forms probably arose from haptophyte, prasinophyte, cryptomonad or diatom endosymbionts (Watanabe and Sasa, 1991; Chesnick et al., ”
Mixotrophy, a major mode of nutrition for harmful algal species in eutrophic waters (2008, background): “Some dinoflagellates even have chloroplasts or pigments that clearly were derived from cryptophytes (e.g., Hu et al., 1980; Wilcox and Wedemayer, 1984; Schnepf et al., 1989; Skovgaard, 1998; Hackett et al., 2003).”
Acquired phototrophy in aquatic protists (2009, background): “Among the recent exciting results based on multi-gene phylogenies (Hackett et al. 2003, Burki et al. 2008) is the emergence of a super-group that contains all permanent phototrophic eukaryotes (with the exception of euglenoids) resulting from primary, secondary, and tertiary endosymbioses (Burki et…”
Pigment-based chloroplast types in dinoflagellates (2012, background): “…chloroplast Type 5 The genus Dinophysis includes both photosynthe - tic and non-photosynthetic (heterotrophic) species, and the former are known to possess cryptophytetype plastids that contain the phycobilin pigment phycoerythrin (Vesk et al. 1996, Hewes et al. 1998, Hackett et al. 2003).”
Successful cultivation of the toxic dinoflagellate Dinophysis caudata (Dinophyceae) (2008, background): “…sequences such as psbA, 16S-rDNA and rbcL genes, have shown that the plastid specifically originates from the cryptophytes T. amphioxeia or Geminigera cryophila Hill (Takishita et al. 2002, Hackett et al. 2003, Janson & Granéli 2003, Janson 2004, Takahashi et al. 2005, Minnhagen & Janson 2006).”