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SRX9510403: GSM4908794: Aus0004 wild-type strain - sample 1; Enterococcus faecium; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 25.5M spots, 1.9G bases, 831.9Mb downloads

Submitted by: NCBI (GEO)
Study: A dual T-box riboswitch in Enterococcus faecium binds two tRNAs
show Abstracthide Abstract
A set of small RNAs was identified in Vancomycin-resistant Enterococcus faecium, a leading cause of MDR infections. We described here the function of srn_2050, acting as a T-box riboswitch to regulate expression of downstream genes encoding the HisRS and AspRS aminoacyl-tRNA synthetases. Comparative RNAseq between Aus0004 and isogenic srn_2050 mutant identified the genes whose expression is impacted by the RNA. srn_2050 structure in its 'off state' was deciphered by in-line probing, containing T-box consensus sequences, a pseudoknot, a specifier loop and a terminator. Transcription binding assays between the riboswitch and either tRNAAsp or tRNAHis indicate that each deacylated tRNA interacts with the T-box. Their anticodons bind to a GACAC sequence within the specifier loop (GAC and CAC are Asp and His codons, respectively), whereas tRNATyr (UA/C-U) does not. A pioneering evaluation of E. faecium amino acid auxotrophy, with emphasis on E. faecium strain Aus0004, revealed auxotrophy for Histidine but not for Aspartic acid. Based on comparative growths and RNAseq between Aus004 and Aus004-?srn2050, the riboswitch is shown essential for growth under aspartate starvation. This is the first example of a functional riboswitch in E. faecium with two overlapping codons allowing a dual tRNA-dependent regulation at transcriptional level. Overall design: Transcriptome analysis by RNA-seq to compare the levels of all transcripts in srn2050-deleted E. faecium Aus0004 mutant versus wild-type strain and in trans-complemented srn2050-deleted E. faecium Aus0004 mutant versus srn2050-deleted E. faecium Aus0004 mutant with empty plasmid
Sample: Aus0004 wild-type strain - sample 1
SAMN16803222 • SRS7718899 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was extracted from using the phenol/chloroform method. Residual chromosomal DNA was removed by treating samples with the TURBO DNA-free kit (Life Technologies). The strand-specific library preparation was performed using the Ovation Universal Prokaryotic RNA-Seq kit (Nugen) with custom depletion (Anydeplete rRNA design Enterococcus faecium) and the samples were sequenced using the Illumina NextSeq500 instrument (multiplex protocol, single-end 75-bp reads).
Experiment attributes:
GEO Accession: GSM4908794
Links:
Runs: 1 run, 25.5M spots, 1.9G bases, 831.9Mb
Run# of Spots# of BasesSizePublished
SRR1306239225,451,2301.9G831.9Mb2020-11-16

ID:
12429541

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