Transcriptome sequencing of a toxic dinoflagellate, Karenia mikimotoi subjected to stress from solar ultraviolet radiation

•Using next-generation sequencing, 202600 unigenes (>300bp) were assembled, of which 60.55% were annotated in seven databases.•RNA-seq analysis revealed that 722 genes (only 0.36% of unigenes) responded to UVR (defined as being within a |log2 fold change| ≥ 2 and padj ≤ 0.05).•Only the ribosome,...

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Veröffentlicht in:Harmful algae 2019-09, Vol.88, p.101640-101640, Article 101640
Hauptverfasser: Wang, Xinjie, Niu, Xiaoqin, Chen, Yiji, Sun, Zhewei, Han, Axiang, Lou, Xiayuan, Ge, Jingke, Li, Xuanwen, Yang, Yuqian, Jian, Jianbo, Gonçalves, Rodrigo J., Guan, Wanchun
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Sprache:eng
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Zusammenfassung:•Using next-generation sequencing, 202600 unigenes (>300bp) were assembled, of which 60.55% were annotated in seven databases.•RNA-seq analysis revealed that 722 genes (only 0.36% of unigenes) responded to UVR (defined as being within a |log2 fold change| ≥ 2 and padj ≤ 0.05).•Only the ribosome, endocytosis and steroid biosynthesis pathways responded significantly to UVR.•Transcriptome data indicate that K. mikimotoi is a mixotrophic species, and the endocytosis is impaired by solar UVR.•K. mikimotoi has a limited transcriptomic regulation, but is relatively tolerant to exposure under natural ultraviolet radiation. Solar ultraviolet radiation (UVR) is a stress factor in aquatic environments and may act directly or indirectly on orgnisms in the upper layers of the water column. However, UVR effects are usually species-specific and difficult to extrapolate. Here we use the HAB-forming, toxic dinoflagellate Karenia mikimotoi (which was found to be relatively resistant in previous studies) to investigate its transcriptional responses to a one-week UVR exposure. For this, batch cultures of K. mikimotoi were grown with and without UVR, and their transcriptomes (generated via RNAseq technology) were compared. RNA-seq generated 45.31 million reads, which were further assembled to 202600 unigenes (>300bp). Among these, ca. 61% were annotated with NCBI, NR, GO, KOG, PFAM, Swiss-Prot, and KEGG database. Transcriptomic analysis revealed 722 differentially expressed unigenes (DEGs, defined as being within a |log2 fold change| ≥ 2 and padj < 0.05) responding to solar UVR, which were only 0.36% of all unigenes. 716 unigenes were down-regulated, and only 6 unigenes were up-regulated in the UVR compared to non-UVR treatment. KEGG pathway further analysis revealed DEGs were involved in the different pathway; genes involved in the ribosome, endocytosis and steroid biosynthesis pathways were highly down-regulated, but this was not the case for those involved in the energy metabolisms (including photosynthesis, oxidative phosphorylation) which may contribute to the sustainable growth observed in UVR treatment. The up-regulated expression of both zinc-finger proteins (ZFPs) and ribosomal protein L11 (RPL11) may be one of the acclimated mechanisms against UVR. In addition, this work identified down-regulated genes involved in fatty acid degradation and the hydrophobic branched chain amino acids (e.g., Valine, leucine, and isoleucine), which act as structural components of cell m
ISSN:1568-9883
1878-1470
DOI:10.1016/j.hal.2019.101640