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首页> 外文期刊>BMC Genomics >The transcriptome of Leishmania major in the axenic promastigote stage: transcript annotation and relative expression levels by RNA-seq
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The transcriptome of Leishmania major in the axenic promastigote stage: transcript annotation and relative expression levels by RNA-seq

机译:利什曼原虫在轴突前鞭毛体阶段的转录组:RNA-seq的转录本注释和相对表达水平

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Background Although the genome sequence of the protozoan parasite Leishmania major was determined several years ago, the knowledge of its transcriptome was incomplete, both regarding the real number of genes and their primary structure. Results Here, we describe the first comprehensive transcriptome analysis of a parasite from the genus Leishmania. Using high-throughput RNA sequencing (RNA-seq), a total of 10285 transcripts were identified, of which 1884 were considered novel, as they did not match previously annotated genes. In addition, our data indicate that current annotations should be modified for many of the genes. The detailed analysis of the transcript processing sites revealed extensive heterogeneity in the spliced leader (SL) and polyadenylation addition sites. As a result, around 50% of the genes presented multiple transcripts differing in the length of the UTRs, sometimes in the order of hundreds of nucleotides. This transcript heterogeneity could provide an additional source for regulation as the different sizes of UTRs could modify RNA stability and/or influence the efficiency of RNA translation. In addition, for the first time for the Leishmania major promastigote stage, we are providing relative expression transcript levels. Conclusions This study provides a concise view of the global transcriptome of the L. major promastigote stage, providing the basis for future comparative analysis with other development stages or other Leishmania species.
机译:背景技术尽管原生动物寄生虫利什曼原虫的基因组序列是在几年前确定的,但就基因的真实数目及其一级结构而言,其转录组的知识尚不完整。结果在这里,我们描述了来自利什曼原虫属的一个寄生虫的第一个综合转录组分析。使用高通量RNA测序(RNA-seq),共鉴定出10285个转录本,其中1884个被认为是新的,因为它们与先前注释的基因不匹配。此外,我们的数据表明,目前对许多基因的注释都应进行修改。转录物加工位点的详细分析显示,在剪接的前导序列(SL)和聚腺苷酸加成位点中存在广泛的异质性。结果,大约50%的基因呈现出多个转录本,转录本的UTR长度不同,有时约为数百个核苷酸。该转录本的异质性可以为调控提供额外的来源,因为不同大小的UTR可以修​​饰RNA稳定性和/或影响RNA翻译的效率。此外,这是利什曼原虫主要前鞭毛体阶段的首次,我们提供了相对表达转录水平。结论本研究为L.major promastigote阶段的全球转录组提供了简明视图,为将来与其他发育阶段或其他利什曼原虫种类的比较分析提供了基础。

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