TY - JOUR
T1 - A Diatom Gene Regulating Nitric-Oxide Signaling and Susceptibility to Diatom-Derived Aldehydes
AU - Vardi, Assaf
AU - Bidle, Kay D.
AU - Kwityn, Clifford
AU - Hirsh, Donald J.
AU - Thompson, Stephanie M.
AU - Callow, James A.
AU - Falkowski, Paul
AU - Bowler, Chris
N1 - Funding Information:
We thank Valentin Starovoytov for transmission electron microscopy (TEM) analysis, Faye Rosin for her assistance with the Deltavision microscope, Felisa Wolfe-Simon, Christiane Lichtlé, Agnès Meichenin, Marc Heijde, Liti Haramaty, and Hui Lui for technical assistance. We thank Nigel Crawford for providing valuable advice during the course of this work and Kim Thamatrakoln for valuable feedback. This work was supported by a Marie Curie Intra-European fellowship to A.V. (EIF-515066), the EU-funded DIATOMICS project to J.A.C. and C.B. (LSHG-CT-2004-512035), the Agence Nationale de la Recherche (ANR) to C.B., and grants from the National Science Foundation IOB-0414536 to K.D.B. and P.G.F. and IOS-0717494 to K.D.B. and A.V.
PY - 2008/6/25
Y1 - 2008/6/25
N2 - Diatoms are unicellular phytoplankton accounting for ∼40% of global marine primary productivity [1], yet the molecular mechanisms underlying their ecological success are largely unexplored. We use a functional-genomics approach in the marine diatom Phaeodactylum tricornutum to characterize a novel protein belonging to the widely conserved YqeH subfamily [2] of GTP-binding proteins thought to play a role in ribosome biogenesis [3], sporulation [4], and nitric oxide (NO) generation [5]. Transgenic diatoms overexpressing this gene, designated PtNOA, displayed higher NO production, reduced growth, impaired photosynthetic efficiency, and a reduced ability to adhere to surfaces. A fused YFP-PtNOA protein was plastid localized, distinguishing it from a mitochondria-localized plant ortholog. PtNOA was upregulated in response to the diatom-derived unsaturated aldehyde 2E,4E/Z-decadienal (DD), a molecule previously shown to regulate intercellular signaling, stress surveillance [6], and defense against grazers [7]. Overexpressing cell lines were hypersensitive to sublethal levels of this aldehyde, manifested by altered expression of superoxide dismutase and metacaspases, key components of stress and death pathways [8, 9]. NOA-like sequences were found in diverse oceanic regions, suggesting that a novel NO-based system operates in diatoms and may be widespread in phytoplankton, providing a biological context for NO in the upper ocean [10].
AB - Diatoms are unicellular phytoplankton accounting for ∼40% of global marine primary productivity [1], yet the molecular mechanisms underlying their ecological success are largely unexplored. We use a functional-genomics approach in the marine diatom Phaeodactylum tricornutum to characterize a novel protein belonging to the widely conserved YqeH subfamily [2] of GTP-binding proteins thought to play a role in ribosome biogenesis [3], sporulation [4], and nitric oxide (NO) generation [5]. Transgenic diatoms overexpressing this gene, designated PtNOA, displayed higher NO production, reduced growth, impaired photosynthetic efficiency, and a reduced ability to adhere to surfaces. A fused YFP-PtNOA protein was plastid localized, distinguishing it from a mitochondria-localized plant ortholog. PtNOA was upregulated in response to the diatom-derived unsaturated aldehyde 2E,4E/Z-decadienal (DD), a molecule previously shown to regulate intercellular signaling, stress surveillance [6], and defense against grazers [7]. Overexpressing cell lines were hypersensitive to sublethal levels of this aldehyde, manifested by altered expression of superoxide dismutase and metacaspases, key components of stress and death pathways [8, 9]. NOA-like sequences were found in diverse oceanic regions, suggesting that a novel NO-based system operates in diatoms and may be widespread in phytoplankton, providing a biological context for NO in the upper ocean [10].
KW - EVO_ECOL
KW - SIGNALING
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U2 - 10.1016/j.cub.2008.05.037
DO - 10.1016/j.cub.2008.05.037
M3 - Article
C2 - 18538570
AN - SCOPUS:45249121298
SN - 0960-9822
VL - 18
SP - 895
EP - 899
JO - Current Biology
JF - Current Biology
IS - 12
ER -