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引用次数: 0
摘要
鞭毛藻是一种多样的微型浮游生物,包括自由生活、共生和寄生物种。变形虫是寄生鞭毛虫的一种基础谱系,感染多种海洋微生物,包括有害的形成水华的藻类。虽然目前有三个已发表的变形虫基因组,但该属具有相当大的基因组多样性。我们添加到变形虫不断增长的基因组数据与注释基因组组装变形虫sp. ex Karlodinium veneficum。这个物种似乎翻译所有三个规范的停止密码子上下文。停止密码子存在于大约一半的预测基因模型的开放阅读框中,包括对细胞功能至关重要的基因。帧内停止密码子可能是由在组装中识别的抑制trna翻译的。我们还组装了线粒体基因组,这在以前的变形虫基因组组装中仍然难以捉摸。线粒体基因组由许多片段组成,这些片段在基因内具有高序列同一性,而在基因间具有低序列同一性。核和线粒体编码的蛋白质表明,变形虫不像以前分析的变形虫物种那样具有两部分电子传递链。这项研究强调了分析来自高度多样化属(如变形虫属)的多个基因组的重要性。
The nuclear and mitochondrial genomes of amoebophrya sp. ex Karlodinium veneficum.
Dinoflagellates are a diverse group of microplankton that include free-living, symbiotic, and parasitic species. Amoebophrya, a basal lineage of parasitic dinoflagellates, infects a variety of marine microorganisms, including harmful-bloom-forming algae. Although there are currently 3 published Amoebophrya genomes, this genus has considerable genomic diversity. We add to the growing genomic data for Amoebophrya with an annotated genome assembly for Amoebophrya sp. ex Karlodinium veneficum. This species appears to translate all 3 canonical stop codons contextually. Stop codons are present in the open reading frames of about half of the predicted gene models, including genes essential for cellular function. The in-frame stop codons are likely translated by suppressor tRNAs that were identified in the assembly. We also assembled the mitochondrial genome, which has remained elusive in the previous Amoebophrya genome assemblies. The mitochondrial genome assembly consists of many fragments with high sequence identity in the genes but low sequence identity in intergenic regions. Nuclear and mitochondrially-encoded proteins indicate that Amoebophrya sp. ex K. veneficum does not have a bipartite electron transport chain, unlike previously analyzed Amoebophrya species. This study highlights the importance of analyzing multiple genomes from highly diverse genera such as Amoebophrya.
期刊介绍:
G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights.
G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.