荆晓丽, 米铁柱, 甄毓, 付保忠, 李成峰, 于志刚. 基于玛氏骨条藻(Skeletonema marinoi)转录组的氮代谢途径解析[J]. 海洋环境科学, 2016, 35(5): 703-711. DOI: 10.13634/j.cnki.mes20160511
引用本文: 荆晓丽, 米铁柱, 甄毓, 付保忠, 李成峰, 于志刚. 基于玛氏骨条藻(Skeletonema marinoi)转录组的氮代谢途径解析[J]. 海洋环境科学, 2016, 35(5): 703-711. DOI: 10.13634/j.cnki.mes20160511
JING Xiao-li, MI Tie-zhu, ZHEN Yu, FU Bao-zhong, LI Cheng-feng, YU Zhi-gang. Description of nitrogen metabolism pathway based on Skeletonema marinoi transcriptome[J]. Chinese Journal of MARINE ENVIRONMENTAL SCIENCE, 2016, 35(5): 703-711. DOI: 10.13634/j.cnki.mes20160511
Citation: JING Xiao-li, MI Tie-zhu, ZHEN Yu, FU Bao-zhong, LI Cheng-feng, YU Zhi-gang. Description of nitrogen metabolism pathway based on Skeletonema marinoi transcriptome[J]. Chinese Journal of MARINE ENVIRONMENTAL SCIENCE, 2016, 35(5): 703-711. DOI: 10.13634/j.cnki.mes20160511

基于玛氏骨条藻(Skeletonema marinoi)转录组的氮代谢途径解析

Description of nitrogen metabolism pathway based on Skeletonema marinoi transcriptome

  • 摘要: 本研究分别选取了不同生长时期、不同温度培养以及低硅条件培养的玛氏骨条藻(Skeletonema marinoi),以Illumina Hiseq 2000平台进行转录组高通量测序分析,共获得39,098个转录本。通过NR注释、GO注释和KEGG通路注释等一系列生物信息学手段对该转录组进行了基因注释和代谢途径分析。在此基础上重点分析了玛氏骨条藻的氮代谢途径,发现共存在20种酶和蛋白及6条相关代谢途径。对38个编码这些酶的基因序列比对结果表明,其与假微型海链藻同源基因具有较高的一致性。同时对这些样品进行数字基因表达谱分析,获得不同生长时期氮代谢途径中酶和蛋白的编码基因的差异表达情况:与对数期相比,在稳定期参与硝酸盐同化过程的两种酶(硝酸盐还原酶、亚硝酸还原酶)的基因和参与氨氮代谢的两种酶(氨甲酰磷酸合成酶和氨基甲酸激酶)的基因均有明显的上调表达,这是玛氏骨条藻对所处的不同生长状态下氮元素存在形态的变化所做出的分子响应。由转录组测序构建的代谢途径及相关基因的差异表达信息有助于对玛氏骨条藻氮代谢关键酶基因调控过程的解析,为进一步研究赤潮藻氮素营养限制过程中相关基因的表达调控模式奠定了基础,可为深入了解赤潮藻对营养元素的利用提供依据。

     

    Abstract: The transcriptomeof Skeletonema marinoi at different growth stages,different temperatures and low silicon concentration was analyzed with Illumina Hiseq 2000 platform sequencing technology,producing and identifying 39,098 transcripts totally.Assembled sequences were subjected to NR BLAST similarity searches and annotated with Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes orthology (KO) identifiers.These analyses identified the important metabolic pathways and genes of S.marinoi,especially the nitrogen metabolism pathway involving 20 enzymes and proteins.Comparative analysis of enzyme-coding genes among S.marinoi,Thalassiosira pseudonana and Phaeodactylum tricornutum using BLASTx revealed relatively high homologous genes between S.marinoi and T.pseudonana.Using the Digital Gene Expression Profiling,we also found different gene expression in the pathway.Compared to exponential growth phase (EP),three genes coding nitrate reductase or nitrite reductase which were involved in nitrate assimilation process showed significantly increasing expression in stationary phase (SP),as well as carbamoyl-phosphate synthase-coding and carbamate kinase-coding genes.The results indicated the molecular responses of S.marinoi on the nitrogen changes in different growth phases.Our study will contribute to analyze gene regulation of key enzymes involved in nitrogen metabolism of S.marinoi,providing a basis to enhance our knowledge about gene expression and regulation patterns in nitrogen limitation,which will be beneficial to in-depth understand the nutrients utilization in harmful algae bloom species.

     

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