U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX556571: GSM1401488: Pabyssi_RNAseq; Pyrococcus abyssi; RNA-Seq
1 ILLUMINA (Illumina Genome Analyzer IIx) run: 51.3M spots, 2.1G bases, 1.1Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: RNA at 92 °C: the non-coding transcriptome of the hyperthermophilic archaeon Pyrococcus abyssi.
show Abstracthide Abstract
The non-coding transcriptome of the hyperthermophilic archaeon Pyrococcus abyssi is investigated using the RNA-seq technology. A dedicated computational pipeline analyzes RNA-seq reads and prior genome annotation to identify small RNAs, untranslated regions of mRNAs, and cis-encoded antisense transcripts. Unlike other archaea, such as Sulfolobus and Halobacteriales, P. abyssi produces few leaderless mRNA transcripts. Antisense transcription is widespread (215 transcripts) and targets protein-coding genes that are less conserved than average genes. We identify at least three novel H/ACA-like guide RNAs among the newly characterized non-coding RNAs. Long 5'' UTRs in mRNAs of ribosomal proteins and amino-acid biosynthesis genes strongly suggest the presence of cis-regulatory leaders in these mRNAs. We selected a high-interest subset of non-coding RNAs based on their strong promoters, high GC-content, phylogenetic conservation, or abundance. Some of the novel small RNAs and long 5'' UTRs display high GC contents, suggesting unknown structural RNA functions. However, we were surprised to observe that most of the high-interest RNAs are AU-rich, which suggests an absence of stable secondary structure in the high-temperature environment of P. abyssi. Yet, these transcripts display other hallmarks of functionality, such as high expression or high conservation, which leads us to consider possible RNA functions that do not require extensive secondary structure. Overall design: directional RNA-seq, Illumina GA-IIx
Sample: Pabyssi_RNAseq
SAMN02808713 • SRS623567 • All experiments • All runs
Library:
Instrument: Illumina Genome Analyzer IIx
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNAs were extracted using the TRIzol method (Invitrogen). A pool of equal amounts of each sample was checked for integrity by 2100 Bioanalyzer (Agilent Technologies Inc.) and treated to enrich in primary transcripts using a 5'-phosphate-dependent exonuclease (Terminator, Epicenter). RNA samples were subsequently purified and concentrated using the RNA Clean-Up and Concentration Kit (Norgen Biotek Corp). The strand-specific RNA-seq template library was prepared starting from a pool of total samples (50 ng) following the directional mRNA-seq library preparation protocol provided by Illumina Inc.
Experiment attributes:
GEO Accession: GSM1401488
Links:
External link:
Runs: 1 run, 51.3M spots, 2.1G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR130462051,342,7702.1G1.1Gb2014-06-02

ID:
795599

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...