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Detection of Very Long Antisense Transcripts by Whole Transcriptome RNA-Seq Analysis of Listeria monocytogenes by Semiconductor Sequencing Technology

机译:半导体测序技术通过单核细胞增生李斯特菌全转录组RNA-Seq分析检测非常长的反义转录物

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摘要

The Gram-positive bacterium Listeria monocytogenes is the causative agent of listeriosis, a severe food-borne infection characterised by abortion, septicaemia, or meningoencephalitis. L. monocytogenes causes outbreaks of febrile gastroenteritis and accounts for community-acquired bacterial meningitis in humans. Listeriosis has one of the highest mortality rates (up to 30%) of all food-borne infections. This human pathogenic bacterium is an important model organism for biomedical research to investigate cell-mediated immunity. L. monocytogenes is also one of the best characterised bacterial systems for the molecular analysis of intracellular parasitism. Recently several transcriptomic studies have also made the ubiquitous distributed bacterium as a model to understand mechanisms of gene regulation from the environment to the infected host on the level of mRNA and non-coding RNAs (ncRNAs). We have used semiconductor sequencing technology for RNA-seq to investigate the repertoire of listerial ncRNAs under extra- and intracellular growth conditions. Furthermore, we applied a new bioinformatic analysis pipeline for detection, comparative genomics and structural conservation to identify ncRNAs. With this work, in total, 741 ncRNA locations of potential ncRNA candidates are now known for L. monocytogenes, of which 611 ncRNA candidates were identified by RNA-seq. 441 transcribed ncRNAs have never been described before. Among these, we identified novel long non-coding antisense RNAs with a length of up to 5,400 nt e.g. opposite to genes coding for internalins, methylases or a high-affinity potassium uptake system, namely the kdpABC operon, which were confirmed by qRT-PCR analysis. RNA-seq, comparative genomics and structural conservation of L. monocytogenes ncRNAs illustrate that this human pathogen uses a large number and repertoire of ncRNA including novel long antisense RNAs, which could be important for intracellular survival within the infected eukaryotic host.
机译:革兰氏阳性单核细胞增生性李斯特菌是李斯特菌病的病原体,李斯特菌病是一种严重的食源性感染,特征在于流产,败血病或脑膜脑炎。单核细胞增生李斯特氏菌引起高热性胃肠炎的暴发,并导致人类在社区获得性细菌性脑膜炎。李斯特氏菌病是所有食源性感染中最高的死亡率之一(高达30%)。这种人类致病细菌是用于生物医学研究以研究细胞介导的免疫力的重要模型生物。单核细胞增生李斯特菌也是细胞内寄生虫分子分析中最有特色的细菌系统之一。最近,一些转录组学研究也使普遍分布的细菌成为模型,以了解从环境到受感染宿主的基因调控机制,涉及mRNA和非编码RNA(ncRNA)的水平。我们已使用半导体测序技术的RNA序列研究在细胞外和细胞内生长条件下利斯特氏菌ncRNA的组成。此外,我们将新的生物信息学分析流程应用于检测,比较基因组学和结构保守性鉴定ncRNA。通过这项工作,目前已知单核细胞增生李斯特氏菌潜在ncRNA候选基因的741个ncRNA位置,其中611个ncRNA候选物通过RNA-seq鉴定。以前从未描述过441种转录的ncRNA。在这些当中,我们鉴定出了新颖的长的非编码反义RNA,其长度高达5,400 nt,例如5,400nt。与通过qRT-PCR分析证实的编码Internalins,甲基化酶或高亲和力钾吸收系统的基因,即kdpABC操纵子相反。单核细胞增生李斯特氏菌ncRNA的RNA-seq,比较基因组学和结构保守性表明,这种人类病原体使用了大量ncRNA,包括新颖的长反义RNA,这对于感染的真核宿主内的细胞内存活可能很重要。

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