U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from BioSample

SRX19494937: GSM7061723: S.islandicus.REY15A.E234.Cappable-seq.replicate1; Sulfolobus islandicus REY15A; OTHER
1 ILLUMINA (NextSeq 500) run: 11.9M spots, 891.7M bases, 339.5Mb downloads

External Id: GSM7061723_r1
Submitted by: Institute of Structural and Molecular Biology, University College London
Study: Cappable-seq data for Sulfolobus islandicus REY15A and cbp1 deletion strains
show Abstracthide Abstract
Chromatin proteins competes with the transcription machinery for access to genomic DNA and suppress cryptic promoters. CRISPR arrays form the physical memory of CRISPR adaptive immune systems. The incorporation of virus-derived AT-rich DNA into CRISPR arrays renders them prone to harbouring cryptic promoters. Sulfolobales feature extremely long CRISPR arrays spanning several kilobases as well as a CRISPR-specific chromatin protein termed Cbp1. Altered Cbp1 expression affects transcription from CRISPR arrays in multiple ways, but the mechanistic basis remains to be understood. Here, we show that Cbp1 recruits the general chromatin protein Cren7 to form a heteromeric chromatin complex at CRISPR arrays. Cbp1-CreN7 chromatinisation plays a dual role in the transcription of CRISPR array. It suppresses spurious transcription from cryptic CRISPR array-internal promoters via steric occlusion of the transcription machinery while enhancing transcription from promoters in the CRISPR leaders. Our results show that Cbp1-CreN7 chromatinization drives the coordinated transcription of long CRISPR arrays. Additional binding sites of Cbp1 associated with transposases and the leaders of alternative CRISPR arrays hint on a wider regulatory function of Cbp1 linking defense systems and mobile genetic elements. Overall design: Cappable-seq data for Sulfolobus islandicus REY15A ?cbp1 strain and the parental strain E234 to map 5'-ends of small (20-200 nt) 5'-triphosphorylated RNAs
Sample: S.islandicus.REY15A.E234.Cappable-seq.replicate1
SAMN33434657 • SRS16885011 • All experiments • All runs
Library:
Name: GSM7061723
Instrument: NextSeq 500
Strategy: OTHER
Source: TRANSCRIPTOMIC
Selection: other
Layout: SINGLE
Construction protocol: 15 ml cell culture was rapidly mixed with 30 ml pre-cooled RNAprotect Bacteria Reagent (Qiagen) placed in an ice bath. Cells were harvested by centrifugation (5 min at 4000 x g at 4 ºC). Pellets were immediately subjected to RNA isolation using the mirVana miRNA isolation kit (Ambion) with an initial resuspension buffer volume of 200 µl following the protocol for small RNAs (20-200 nt length). Library preparation and deep sequencing was conducted at Vertis Biotechnologie (Germany). In brief, 5'-triphosporylated RNA was capped with 3'-desthiobiotin-TEG-GTP (NEB)) using the Vaccinia virus Capping enzyme (NEB) and biotinylated RNA species were subsequently enriched by affinity purification using streptavidin beads yielding 0.6 to 1.3% of the sRNA preparation. The eluted RNA was poly-adenylated using E. coli Poly(A) polymerase and 5'-ends were converted to mono-phosphates by incubation with RNA 5' Pyrophosphohydrolase (NEB). Subsequently, an RNA adapter was ligated to the newly formed 5'-monophosphate structures. First-strand cDNA synthesis was performed using an oligo(dT)-adapter primer and the M- MLV reverse transcriptase at 42 ºC. The resulting cDNA was finally PCR-amplified (12 cycles) with TruSeq Dual Index sequencing primers (Illumina).
Runs: 1 run, 11.9M spots, 891.7M bases, 339.5Mb
Run# of Spots# of BasesSizePublished
SRR2361005311,888,886891.7M339.5Mb2023-03-24

ID:
26775825

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...