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拼接接头基元的宏转录组分析可识别甲藻中的隐藏基因组特征。

Spliced leader-based metatranscriptomic analyses lead to recognition of hidden genomic features in dinoflagellates.

机构信息

Department of Marine Sciences, University of Connecticut, Groton, CT 06340, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Nov 16;107(46):20033-8. doi: 10.1073/pnas.1007246107. Epub 2010 Nov 1.

Abstract

Environmental transcriptomics (metatranscriptomics) for a specific lineage of eukaryotic microbes (e.g., Dinoflagellata) would be instrumental for unraveling the genetic mechanisms by which these microbes respond to the natural environment, but it has not been exploited because of technical difficulties. Using the recently discovered dinoflagellate mRNA-specific spliced leader as a selective primer, we constructed cDNA libraries (e-cDNAs) from one marine and two freshwater plankton assemblages. Small-scale sequencing of the e-cDNAs revealed functionally diverse transcriptomes proven to be of dinoflagellate origin. A set of dinoflagellate common genes and transcripts of dominant dinoflagellate species were identified. Further analyses of the dataset prompted us to delve into the existing, largely unannotated dinoflagellate EST datasets (DinoEST). Consequently, all four nucleosome core histones, two histone modification proteins, and a nucleosome assembly protein were detected, clearly indicating the presence of nucleosome-like machinery long thought not to exist in dinoflagellates. The isolation of rhodopsin from taxonomically and ecotypically diverse dinoflagellates and its structural similarity and phylogenetic affinity to xanthorhodopsin suggest a common genetic potential in dinoflagellates to use solar energy nonphotosynthetically. Furthermore, we found 55 cytoplasmic ribosomal proteins (RPs) from the e-cDNAs and 24 more from DinoEST, showing that the dinoflagellate phylum possesses all 79 eukaryotic RPs. Our results suggest that a sophisticated eukaryotic molecular machine operates in dinoflagellates that likely encodes many more unsuspected physiological capabilities and, meanwhile, demonstrate that unique spliced leaders are useful for profiling lineage-specific microbial transcriptomes in situ.

摘要

针对真核微生物(例如,甲藻)的特定谱系进行环境转录组学(宏转录组学)对于揭示这些微生物对自然环境响应的遗传机制非常重要,但由于技术困难尚未得到利用。我们使用最近发现的甲藻 mRNA 特异性剪接先导作为选择性引物,从一个海洋和两个淡水浮游生物组合中构建了 cDNA 文库(e-cDNAs)。e-cDNAs 的小规模测序揭示了功能多样的转录组,这些转录组被证明来自甲藻。确定了一组甲藻共有基因和优势甲藻物种的转录本。对数据集的进一步分析促使我们深入研究现有的、基本上未注释的甲藻 EST 数据集(DinoEST)。结果,检测到所有四个核小体核心组蛋白、两种组蛋白修饰蛋白和一个核小体组装蛋白,这清楚地表明长期以来被认为不存在于甲藻中的核小体样机制的存在。从分类学和生态型上多样化的甲藻中分离出视蛋白,以及其与黄视蛋白的结构相似性和系统发育亲和力表明,甲藻具有非光合作用利用太阳能的共同遗传潜力。此外,我们从 e-cDNAs 中发现了 55 种细胞质核糖体蛋白(RPs),从 DinoEST 中发现了 24 种更多的 RPs,表明甲藻门拥有所有 79 种真核 RPs。我们的结果表明,一种复杂的真核分子机器在甲藻中运行,可能编码了更多未被察觉的生理功能,同时也证明了独特的剪接先导可用于原位分析谱系特异性微生物转录组。

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