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SRX3519697: GSM2907047: Nitrate replicate 3.2; Haloferax mediterranei; miRNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 27.6M spots, 1.4G bases, 898.6Mb downloads

Submitted by: NCBI (GEO)
Study: Are small RNAs involved in the regulation of nitrogen metabolism in haloarchaea?
show Abstracthide Abstract
Small RNAs have been studied in detail in Bacteria and Eukarya domain, but in the case of Archaea domain the knowledge is scarce and the physiological function of the majority is still uncertain. To extend the knowledge of sRNAs in Archaea domain and its possible role in the regulation of the nitrogen assimilation metabolism in haloarchaea, Haloferax mediterranei has been used as a model microorganism. Bioinformatic approach has allowed to predict 295 putative sRNAs genes in the genome of H. mediterranei, 88 of which have been verified by means of RNA-seq. The secondary structure of putative sRNAs and its possible targets have been identified. Curiously, some of them present as possible targets genes related to the nitrogen assimilation, as glutamate dehydrogenase or regulatory nitrogen protein PII. Analysis of RNA-seq data has also revealed differences in the expression pattern of 16 sRNAs according to the nitrogen source. Consequently, RNomic and the bioinformatic approaches used in this work have allowed the identification of new sRNAs in Hfx. mediterranei, some of which show different expression pattern depending on the nitrogen source. It suggests that these sRNAs could be involved in the regulation of nitrogen assimilation, being able to constitute important gene regulatory network. Overall design: microRNAs were isolated from Hfx. Mediterranei cultures grown in the presence of two different nitrogen sources, nitrate and ammonium, to mid-exponential phase.
Sample: Nitrate replicate 3.2
SAMN08274191 • SRS2796551 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: miRNA-Seq
Source: TRANSCRIPTOMIC
Selection: size fractionation
Layout: SINGLE
Construction protocol: microRNAs were isolated with mirVanaTM miRNA isolation kit (Ambion) following product specifications. Afterwards, the RNA samples were treated with Turbo DNase (Ambion). Size-selected RNA concentration was quantitated using the NanoDrop ND-100 Spectrophotometer (NanoDrop Technologies, Wilmington, DE) and size distribution visualized using Agilent 2200 Tapestation (Agilent Technologies, Palo Alto, CA, USA). microRNAs libraries were constructed using TruSeq Small RNA Library Prep Kit and the TruSeq Small RNA Library Prep Guide, Part #15004197 Rev. G protocol.
Experiment attributes:
GEO Accession: GSM2907047
Links:
Runs: 1 run, 27.6M spots, 1.4G bases, 898.6Mb
Run# of Spots# of BasesSizePublished
SRR642747427,561,2001.4G898.6Mb2018-02-20

ID:
4888922

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