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基于转录组学从蜡样芽孢杆菌ATCC14579中鉴定银胁迫响应小RNA

Transcriptome based Identification of silver stress responsive sRNAs from Bacillus cereus ATCC14579.

作者信息

Sridhar Jayavel, Gayathri Manickam

机构信息

Department of Biotechnology (DDE), Madurai Kamaraj University, Madurai-625021, Tamil Nadu, India.

出版信息

Bioinformation. 2019 Jul 31;15(7):474-479. doi: 10.6026/97320630015474. eCollection 2019.

Abstract

Microbes modulate their metabolic and physiological mechanisms in response to changing environmental conditions. It is our interest to identify small regulatory RNAs using microarray expression data (GSE26043) obtained from B. cereus ATCC 14579 in AgNO3 stress. By definition, expression of transcripts from the Intergenic Regions (IGR) with >=2 fold under silver stress is predicted as novel small RNAs. Computational analysis of the IGR expression levels extracted from the available microarray data help in the identification of stress responsive sRNAs with rare promoters (Sigma 24, 28, 32, 54 and 70) followed by terminator signals predicted using the sRNAscanner tool. We predicted 1512 sRNA specific regions on both positive and negative strands collectively. Thus, a non-redundant high scoring unique 860 sRNAs with distinct promoter (S24: 83, S28: 86, S32: 31, S54: 57, S70: 223, sRNA_specific_S70: 380) and terminator signals are reported. These unique computationally predicted sRNA regions were verified with the highly expressing IGRs from the microarray data. It should be noted that 14 sRNAs reported in earlier studies were also found in this dataset. This study has reported 71 additional sRNAs from the transcriptome under metal stress response. Hence, we use global transcriptomics data for the identification of novel sRNAs in B. cereus. We described a general model using a procedure for the identification of small regulatory RNAs using microarray expression data with appropriate cross validation modules. It is found that some sRNAs reported in this study were found to have multiple rare promoters. This opens the possibility of sRNA activation under multiple stress condition. These sRNA data reported in this study should be characterized for their mRNA targets and molecular functional networks in future investigations.

摘要

微生物会根据不断变化的环境条件调节其代谢和生理机制。我们感兴趣的是利用从蜡状芽孢杆菌ATCC 14579在硝酸银胁迫下获得的微阵列表达数据(GSE26043)来鉴定小调控RNA。根据定义,在银胁迫下基因间区域(IGR)转录本表达增加≥2倍的被预测为新型小RNA。对从现有微阵列数据中提取的IGR表达水平进行计算分析,有助于鉴定具有罕见启动子(西格玛24、28、32、54和70)的应激反应性sRNA,随后使用sRNAscanner工具预测终止子信号。我们总共在正链和负链上预测了1512个sRNA特异性区域。因此,报告了860个具有不同启动子(S24:83,S28:86,S32:31,S54:57,S70:223,sRNA_specific_S70:380)和终止子信号的非冗余高分独特sRNA。这些独特的通过计算预测的sRNA区域用微阵列数据中高表达的IGR进行了验证。应该注意的是,在该数据集中也发现了早期研究中报道的14个sRNA。本研究报告了在金属应激反应下转录组中的另外71个sRNA。因此,我们使用全局转录组学数据来鉴定蜡状芽孢杆菌中的新型sRNA。我们描述了一个通用模型,该模型使用一种程序,通过带有适当交叉验证模块的微阵列表达数据来鉴定小调控RNA。结果发现,本研究中报道的一些sRNA具有多个罕见启动子。这开启了在多重应激条件下sRNA激活的可能性。本研究报告的这些sRNA数据在未来的研究中应针对其mRNA靶标和分子功能网络进行表征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/747f/6704327/51da83c63cb3/97320630015474F1.jpg

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