4.7 Article

Temperature-dependent sRNA transcriptome of the Lyme disease spirochete

期刊

BMC GENOMICS
卷 18, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12864-016-3398-3

关键词

Borrelia burgdorferi; sRNA transcriptome; Regulatory RNA; Antisense RNA (asRNA); Intragenic RNA (intraRNA); Riboswitch

资金

  1. Austrian Science Fund (FWF) [FWF F4301, F4308]
  2. University of Vienna
  3. University of Colorado Colorado Springs
  4. RNA-DK Biology [W1207-B09]

向作者/读者索取更多资源

Background: Transmission of Borrelia burgdorferi from its tick vector to a vertebrate host requires extensive reprogramming of gene expression. Small regulatory RNAs (sRNA) have emerged in the last decade as important regulators of bacterial gene expression. Despite the widespread observation of sRNA-mediated gene regulation, only one sRNA has been characterized in the Lyme disease spirochete B. burgdorferi. We employed an sRNAspecific deep-sequencing approach to identify the small RNA transcriptome of B. burgdorferi at both 23 degrees C and 37 degrees C, which mimics in vitro the transmission from the tick vector to the mammalian host. Results: We identified over 1000 sRNAs in B. burgdorferi revealing large amounts of antisense and intragenic sRNAs, as well as characteristic intergenic and 5' UTR-associated sRNAs. A large fraction of the novel sRNAs (43%) are temperature-dependent and differentially expressed at the two temperatures, suggesting a role in gene regulation for adaptation during transmission. In addition, many genes important for maintenance of Borrelia during its enzootic cycle are associated with antisense RNAs or 5' UTR sRNAs. RNA-seq data were validated for twenty-two of the sRNAs via Northern blot analyses. Conclusions: Our study demonstrates that sRNAs are abundant and differentially expressed by environmental conditions suggesting that gene regulation via sRNAs is a common mechanism utilized in B. burgdorferi. In addition, the identification of antisense and intragenic sRNAs impacts the broadly used loss-of-function genetic approach used to study gene function and increases the coding potential of a small genome. To facilitate access to the analyzed RNA-seq data we have set-up a website at http://www.cibiv.at/similar to niko/bbdb/ that includes a UCSC browser track hub. By clicking on the respective link, researchers can interactively inspect the data in the UCSC genome browser

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据