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Phylogenomics Provides New Insights Into Gains and Losses of Selenoproteins Among Archaeplastida

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Phylogenomics Provides New Insights Into Gains and Losses of Selenoproteins Among Archaeplastida Phylogenomics Provides New Insights into Gains and Losses of Selenoproteins among Archaeplastida Liang, Hongping; Wei, Tong; Xu, Yan; Li, Linzhou; Sahu, Sunil Kumar; Wang, Hongli; Li, Haoyuan; Fu, Xian; Zhang, Gengyun; Melkonian, Michael; Liu, Xin; Wang, Sibo; Liu, Huan Published in: International Journal of Molecular Sciences (Online) DOI: 10.3390/ijms20123020 Publication date: 2019 Document version Publisher's PDF, also known as Version of record Document license: CC BY Citation for published version (APA): Liang, H., Wei, T., Xu, Y., Li, L., Sahu, S. K., Wang, H., Li, H., Fu, X., Zhang, G., Melkonian, M., Liu, X., Wang, S., & Liu, H. (2019). Phylogenomics Provides New Insights into Gains and Losses of Selenoproteins among Archaeplastida. International Journal of Molecular Sciences (Online), 20(12), [3020]. https://doi.org/10.3390/ijms20123020 Download date: 29. Sep. 2021 International Journal of Molecular Sciences Article Phylogenomics Provides New Insights into Gains and Losses of Selenoproteins among Archaeplastida 1,2,3, 2,3,4, 1,2,3, 2,3,5 2,3,4 Hongping Liang y , Tong Wei y, Yan Xu y, Linzhou Li , Sunil Kumar Sahu , Hongli Wang 1,2,3, Haoyuan Li 1,2, Xian Fu 2,3, Gengyun Zhang 2,4, Michael Melkonian 6, Xin Liu 2,3,4, Sibo Wang 2,4,7,* and Huan Liu 2,4,7,* 1 Beijing Genomics Institute (BGI) Education Center, University of Chinese Academy of Sciences, Beijing 100049, China; [email protected] (H.L.); [email protected] (Y.X.); [email protected] (H.W.); [email protected] (H.L.) 2 Beijing Genomics Institute (BGI) Shenzhen, Beishan Industrial Zone, Yantian District, Shenzhen 518083, China; [email protected] (T.W.); [email protected] (L.L.); [email protected] (S.K.S.); [email protected] (X.F.); [email protected] (G.Z.); [email protected] (X.L.) 3 China National Gene Bank, Institute of New Agricultural Resources, BGI-Shenzhen, Jinsha Road, Shenzhen 518120, China 4 State Key Laboratory of Agricultural Genomics, Beijing Genomics Institute (BGI) Shenzhen, Shenzhen 518083, China 5 School of Biology and Biological Engineering, South China University of Technology,Guangzhou 510006, China 6 Botanical Institute, Cologne Biocenter, University of Cologne, D-50674 Cologne, Germany; [email protected] 7 Department of Biology, University of Copenhagen, DK-1165 Copenhagen, Denmark * Correspondence: [email protected] (S.W.); [email protected] (H.L.) These authors contributed equally to this work. y Received: 5 May 2019; Accepted: 18 June 2019; Published: 20 June 2019 Abstract: Selenoproteins that contain selenocysteine (Sec) are found in all kingdoms of life. Although they constitute a small proportion of the proteome, selenoproteins play essential roles in many organisms. In photosynthetic eukaryotes, selenoproteins have been found in algae but are missing in land plants (embryophytes). In this study, we explored the evolutionary dynamics of Sec incorporation by conveying a genomic search for the Sec machinery and selenoproteins across Archaeplastida. We identified a complete Sec machinery and variable sizes of selenoproteomes in the main algal lineages. However, the entire Sec machinery was missing in the Bangiophyceae-Florideophyceae clade (BV) of Rhodoplantae (red algae) and only partial machinery was found in three species of Archaeplastida, indicating parallel loss of Sec incorporation in different groups of algae. Further analysis of genome and transcriptome data suggests that all major lineages of streptophyte algae display a complete Sec machinery, although the number of selenoproteins is low in this group, especially in subaerial taxa. We conclude that selenoproteins tend to be lost in Archaeplastida upon adaptation to a subaerial or acidic environment. The high number of redox-active selenoproteins found in some bloom-forming marine microalgae may be related to defense against viral infections. Some of the selenoproteins in these organisms may have been gained by horizontal gene transfer from bacteria. Keywords: evolution; horizontal gene transfer; phylogenomics; selenoproteins; selenocysteine; Sec machinery Int. J. Mol. Sci. 2019, 20, 3020; doi:10.3390/ijms20123020 www.mdpi.com/journal/ijms Int. J. Mol. Sci. 2019, 20, 3020 2 of 14 1. Introduction Selenium (Se) is an essential trace element for human health and its deficiency leads to various diseases, such as Keshan and Kashin-Beck diseases, and affects the immune system and promotes cancer development [1,2]. An essential Se metabolism is present in many organisms, including bacteria, archaea, and eukaryotes [1,3,4]. However, higher concentrations of Se are toxic by functioning as a pro-oxidant, which affects the intracellular glutathione (GSH) pool leading to an enhanced level of Reactive oxygen species (ROS) accumulation [5,6]. Se is essential for growth and development of numerous algal species but not for terrestrial plants (embryophytes), although it accumulates in certain plant species and can serve as dietary sources for Se uptake [3,7–9]. Se is incorporated into nascent polypeptides in the form of selenocysteine (Sec), the 21st amino acid [10]. Se incorporation requires a specialized machinery and Sec insertion sequence (SECIS) elements present in selenoprotein mRNAs [11,12]. In eukaryotes, it consists of Sec synthesis and Sec incorporation. Sec synthesis starts with tRNASec, aminoacylated with serine, which is phosphorylated by O-phosphoseryl-transfer tRNASec kinase (PSTK) and then catalyzed by Sec synthase (SecS) to produce selenocysteinyl-tRNASec from selenophosphate [10–13]. The Sec donor, selenophosphate, is generated from selenide by selenophosphate synthetase 2 (SPS2), which is often a selenoprotein itself [14,15]. During Sec incorporation, SECIS-binding protein 2 (SBP2) recognizes the SECIS elements in the 30-untranslated region (30-UTR) and recruits the Sec-specific elongation factor (eEFSec) that delivers selenocysteinyl-tRNASec to the ribosome at the in-frame Sec-coding UGA (amber codon) stop codon. Bacteria possess a similar machinery including selB (Sec-specific elongation factor), selC (tRNASec) and selD (selenophosphate synthase), except that Sec synthesis is catalyzed by a single bacterial Sec synthase, SelA [10]. Although selenoproteins constitute only a small fraction of the proteome in any living organism, they play important roles in redox regulation, antioxidation, and thyroid hormone activation in animals including humans [16]. Sec incorporation has been well documented in animals, bacteria, and archaea, while the largest selenoproteome was reported in algae. In the pelagophyte alga Aureococcus anophagefferens, 59 selenoproteins were identified in its genome, compared with 25 selenoproteins in humans [17,18]. The green alga Chlamydomonas reinhardtii has at least ten selenoproteins, whereas the picoplanktonic, marine green alga Ostreococcus lucimarinus harbors 20 selenoprotein genes in its genome [3,19]. Considering that Se is essential for growth in at least 33 algal species that belong to six phyla, Sec incorporation is thought to be universal in diverse algal lineages [20]. In a previous study, no selenoproteins were found in any land plants [7], suggesting a complete loss of Sec incorporation after streptophyte terrestrialization. Exploring the Sec machinery across the Archaeplastida, especially in algae, would provide insight into its evolutionary dynamics in this important lineage of photosynthetic eukaryotes. Here in this study, we searched 38 plant genomes, including 33 algal species that represent the major algal lineages, for the Sec machinery and selenoproteins. 2. Results 2.1. Sec Machinery in Algae To cover the plant tree of life, we selected 33 genomes of algal species and five embryophyte species with a focus on Archaeplastida, the major group of photosynthetic eukaryotes with primary plastids (Supplementary Figure S1). The 33 algal species include one glaucophyte, six rhodophytes, 16 chlorophytes, and seven streptophyte algae. Another three species, the pelagophyte A. anophagefferens, the diatom Thalassiosira pseudonana, and the coccolithophorid Emiliania huxleyi, were also included to represent other distinct algal lineages (Supplementary Table S1A). The Sec machinery was searched in 38 genome assemblies using Selenoprofiles [21] (See Methods). As shown in Figure1, embryophytes lack the entire Sec machinery as previously reported (Figure2a [7]). Interestingly, the Sec machinery is not intact in all tested algal species. Among 33 algae, Int. J. Mol. Sci. 2019, 20, 3020 3 of 14 three Rhodoplantae lack the entire Sec machinery as in embryophytes. The chlorophyte Monoraphidium neglectum, and the rhodophyte Cyanidioschyzon merolae lack PSTK, and the glaucophyte Cyanophora paradoxa SBP2. According to the species tree, it seems that the Sec machinery was lost completely in one rhodophyte clade that includes Porphyra umbilicalis, Pyropia yezoensis, and Chondrus crispus and partially in a few other algal species (Figure1). Figure 1. The number and distribution of selenoproteins, and enzymes involved in the Sec machinery. TheFigure phylogenetic 1. The number tree wasand distribution retrieved from of selenoproteins, the National Center and enzymes for Biotechnology involved in Information the Sec machinery. (NCBI) taxonomyThe phylogenetic database tree and was the retrieved 1000 Plants from (1KP)the Nation Projectal Center (http: //forwww.onekp.com Biotechnology ).Information Presence (NCBI) (green symbols)taxonomy or database absence and (empty the symbols)1,000 Plants of the (1KP) enzymes
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