Gertia stigmatica is a recently described member of the Kareniaceae with a peridinin-containing plastid rather than the aberrant, haptophyte-derived, tertiary plastid found in canonical Kareniaceae genera such as Karenia, Karlodinium, and Takayama. G. stigmatica provides a unique opportunity to compare biochemical traits, such as sterol composition, between these two fundamentally different types of Kareniaceae. To this point, canonical members of the Kareniaceae have been observed to typically produce a set of 4α-methyl-substituted, Δ-nuclear-unsaturated major sterols, such as (24R)-4α-methyl-5α-ergosta-8(14),22-dien-3β-ol (gymnodinosterol) and 27-nor-(24R)-4α-methyl-5α-ergosta-8(14),22-dien-3β-ol (brevesterol), which are very uncommon throughout other members of the class Dinophyceae. Our objective was to compare the sterols of G. stigmatica to canonical Kareniaceae to elucidate whether these same distinctive sterols are found, with our hypothesis being that they would because G. stigmatica is indeed a member of the Kareniaceae. Contrary to our hypothesis, G. stigmatica lacks gymnodinosterol and brevesterol, with its sterols instead dominated by 4-desmethyl sterols, such as cholesterol, 24-methylcholesta-5,22E-dien-3β-ol, and the unusual tri-unsaturated sterols ergosta-5,8(14),22E-trien-3β-ol and cholesta-5,8(14),22E-trien-3β-ol. No sterols were found to possess a 4α-methyl substituent or a single Δ nuclear unsaturation. Thus, G. stigmatica's sterol composition as a member of the Kareniaceae is atypical.
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http://dx.doi.org/10.1016/j.protis.2023.125939 | DOI Listing |
Protist
April 2023
Ecology and Evolution Group, Department of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Gertia stigmatica is a recently described member of the Kareniaceae with a peridinin-containing plastid rather than the aberrant, haptophyte-derived, tertiary plastid found in canonical Kareniaceae genera such as Karenia, Karlodinium, and Takayama. G. stigmatica provides a unique opportunity to compare biochemical traits, such as sterol composition, between these two fundamentally different types of Kareniaceae.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2019
Department of Botany, University of British Columbia, Vancouver, BC V6T 1Z4, Canada;
Plastid endosymbiosis has been a major force in the evolution of eukaryotic cellular complexity, but how endosymbionts are integrated is still poorly understood at a mechanistic level. Dinoflagellates, an ecologically important protist lineage, represent a unique model to study this process because dinoflagellate plastids have repeatedly been reduced, lost, and replaced by new plastids, leading to a spectrum of ages and integration levels. Here we describe deep-transcriptomic analyses of the Antarctic Ross Sea dinoflagellate (RSD), which harbors long-term but temporary kleptoplasts stolen from haptophyte prey, and is closely related to dinoflagellates with fully integrated plastids derived from different haptophytes.
View Article and Find Full Text PDFJ Phycol
April 2011
Department of Biology, Texas A&M University, College Station, Texas 77843, USADepartment of Biology, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543, USADepartment of Oceanography and Department of Biology, Texas A&M University, College Station, Texas 77843, USA.
Brachidinium capitatum F. J. R.
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