A number of dinoflagellate species are known to produce potent neurotoxins. Their blooms are commonly referred to as ''red tides.''An understanding of the genetic regulatory mechanisms that affect bloom growth and, in particular, the development of biomarkers to assess bloom growth status is essential for the development of scientifically sound management and mitigation policies. The genetic organization and regulation of these organisms has been shown to be distinct from non-protist eukaryotes. Dinoflagellates are remarkable for their extremely large genomes that show little transcriptional regulation and with genes present as multiple tandem copies that are polycistronically processed through coupled trans-splicing and polyadenylation. A broad range of investigations has implicated mRNA recruitment as a major site of regulation of gene expression. However, relatively little is understood regarding translational initiation and its regulation in these organisms. The goal of this application is to unravel the roles of the likely key players in translational regulation, eIF2 and eIF4, along with the spliced leader cap structures in regulating gene expression. Using the icthyotoxic dinoflagellate, Karlodinium veneficum and the toxin producing Karenia brevis, the investigators will a) determine whether changes in eIF2-alpha phosphorylation underlie dial changes in gene expression or responses to different stressors;b) begin characterization of the eIF2-alpha-kinases from K. veneficum;c) characterize the ability of K.veneficum eIF4E family member to bind to cap structures and translational binding partners;d) assess the role of K.veneficum eIF4E members in mRNA recruitment. The investigators current understanding of translational regulation is derived mainly from studies in mouse, yeast and plants and does not allow for the diversity of eukaryotic life, the bulk of which is to be found in the Protista. The investigators'results are expected to define a new paradigm for translational regulation in dinoflagellates and represent an innovative approach to increase our understanding of the translational process itself as well as to bridge the gap between genomics and physiological complexity in dinoflagellates. Given the central role of translation in dinoflagellate gene expression, this will provide critical insight into mechanisms relevant to dinoflagellate growth, toxicity, and the regulation of harmful algal blooms. Public Health Relevance: A number of dinoflagellate species are known to produce potent neurotoxins. Their blooms are commonly referred to as ''red tides.''The investigators are studying the mechanisms by which these organisms can regulate their growth and respond to the environment. Because of their unique genome structure, dinoflagellates regulate themselves in unusual ways. The studies proposed here will provide critical insight into mechanisms relevant to dinoflagellate growth, toxicity, and the regulation of harmful algal blooms, with a lon term goal of providing avenues for intervention.

Public Health Relevance

(RELEVANCE) A number of dinoflagellate species are known to produce potent neurotoxins. Their blooms are commonly referred to as ''red tides.''We are studying the mechanisms by which these organisms can regulate their growth and respond to the environment. Because of their unique genome structure, dinoflagellates regulate themselves in unusual ways. The studies proposed here will provide critical insight into mechanisms relevant to dinoflagellate growth, toxicity, and the regulation of harmful algal blooms, with a long term goal of providing avenues for intervention.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
1R01ES021949-01
Application #
8388403
Study Section
Special Emphasis Panel (ZES1-LKB-J (R2))
Program Officer
Tyson, Frederick L
Project Start
2012-09-24
Project End
2017-07-31
Budget Start
2012-09-24
Budget End
2013-07-31
Support Year
1
Fiscal Year
2012
Total Cost
$128,823
Indirect Cost
$42,119
Name
Center for Environmental Science
Department
Type
DUNS #
021463831
City
Cambridge
State
MD
Country
United States
Zip Code
21613
Rasmussen, Silas Anselm; Binzer, Sofie Bjørnholt; Hoeck, Casper et al. (2017) Karmitoxin: An Amine-Containing Polyhydroxy-Polyene Toxin from the Marine Dinoflagellate Karlodinium armiger. J Nat Prod 80:1287-1293
Janouškovec, Jan; Gavelis, Gregory S; Burki, Fabien et al. (2017) Major transitions in dinoflagellate evolution unveiled by phylotranscriptomics. Proc Natl Acad Sci U S A 114:E171-E180
Haq, Saddef; Bachvaroff, Tsvetan R; Place, Allen R (2017) Characterization of Acetyl-CoA Carboxylases in the Basal Dinoflagellate Amphidinium carterae. Mar Drugs 15:
Liu, Chieh-Lun; Place, Allen R; Jagus, Rosemary (2017) Use of Antibiotics for Maintenance of Axenic Cultures of Amphidinium carterae for the Analysis of Translation. Mar Drugs 15:
Rodriguez, Juan D; Haq, Saddef; Bachvaroff, Tsvetan et al. (2017) Identification of a vacuolar proton channel that triggers the bioluminescent flash in dinoflagellates. PLoS One 12:e0171594
Williams, Ernest; Place, Allen; Bachvaroff, Tsvetan (2017) Transcriptome Analysis of Core Dinoflagellates Reveals a Universal Bias towards ""GC"" Rich Codons. Mar Drugs 15:
Cai, Pengjie; He, Shan; Zhou, Chengxu et al. (2016) Two new karlotoxins found in Karlodinium veneficum (strain GM2) from the East China Sea. Harmful Algae 58:66-73
Flowers, Emily M; Bachvaroff, Tsvetan R; Warg, Janet V et al. (2016) Genome Sequence Analysis of CsRV1: A Pathogenic Reovirus that Infects the Blue Crab Callinectes sapidus Across Its Trans-Hemispheric Range. Front Microbiol 7:126
Bentlage, Bastian; Rogers, Travis S; Bachvaroff, Tsvetan R et al. (2016) Complex Ancestries of Isoprenoid Synthesis in Dinoflagellates. J Eukaryot Microbiol 63:123-37
Waters, Amanda L; Oh, Joonseok; Place, Allen R et al. (2015) Stereochemical Studies of the Karlotoxin Class Using NMR Spectroscopy and DP4 Chemical-Shift Analysis: Insights into their Mechanism of Action. Angew Chem Int Ed Engl 54:15705-10

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