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Experimental annotation of the human pathogen Histoplasma capsulatum transcribed regions using high-resolution tiling arrays

机译:使用高分辨率切片阵列对人类病原体荚膜组织胞浆菌转录区进行实验注释

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Background The fungal pathogen Histoplasma capsulatum is thought to be the most common cause of fungal respiratory infections in immunocompetent humans, yet little is known about its biology. Here we provide the first genome-wide studies to experimentally validate its genome annotation. A functional interrogation of the Histoplasma genome provides critical support for continued investigation into the biology and pathogenesis of H. capsulatum and related fungi. Results We employed a three-pronged approach to provide a functional annotation for the H. capsulatum G217B strain. First, we probed high-density tiling arrays with labeled cDNAs from cells grown under diverse conditions. These data defined 6,172 transcriptionally active regions (TARs), providing validation of 6,008 gene predictions. Interestingly, 22% of these predictions showed evidence of anti-sense transcription. Additionally, we detected transcription of 264 novel genes not present in the original gene predictions. To further enrich our analysis, we incorporated expression data from whole-genome oligonucleotide microarrays. These expression data included profiling under growth conditions that were not represented in the tiling experiment, and validated an additional 2,249 gene predictions. Finally, we compared the G217B gene predictions to other available fungal genomes, and observed that an additional 254 gene predictions had an ortholog in a different fungal species, suggesting that they represent genuine coding sequences. Conclusions These analyses yielded a high confidence set of validated gene predictions for H. capsulatum. The transcript sets resulting from this study are a valuable resource for further experimental characterization of this ubiquitous fungal pathogen. The data is available for interactive exploration at http://histo.ucsf.edu webcite .
机译:背景技术真菌病原体荚膜组织胞浆被认为是具有免疫能力的人中真菌呼吸道感染的最常见原因,但对其生物学知之甚少。在这里,我们提供了第一个全基因组研究,以通过实验验证其基因组注释。组织胞浆基因组的功能性询问为继续调查荚膜嗜血杆菌和相关真菌的生物学和发病机理提供了重要的支持。结果我们采用三管齐下的方法为荚膜荚膜梭菌G217B菌株提供功能注释。首先,我们用来自在​​不同条件下生长的细胞的标记的cDNA探测了高密度的切片阵列。这些数据定义了6,172个转录活性区(TAR),从而验证了6,008个基因预测。有趣的是,这些预测中有22%显示出反义转录的证据。此外,我们检测到原始基因预测中不存在的264个新基因的转录。为了进一步丰富我们的分析,我们纳入了全基因组寡核苷酸微阵列的表达数据。这些表达数据包括在平铺实验中未显示的生长条件下进行谱分析,并验证了另外的2249个基因预测。最后,我们将G217B基因预测与其他可用的真菌基因组进行了比较,并观察到另外254个基因预测在不同的真菌物种中具有直系同源物,表明它们代表了真正的编码序列。结论这些分析为荚膜荚膜梭菌的验证基因预测提供了高可信度。这项研究产生的转录本是进一步研究这种无处不在的真菌病原体的宝贵资源。可以在http://histo.ucsf.edu webcite上进行交互式探索。

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