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SRX8417152: GSM4576391: pWM321 replicate 2; Methanosarcina mazei Go1; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 5.6M spots, 561.8M bases, 318.3Mb downloads

Submitted by: NCBI (GEO)
Study: MM_0565 orchestrates CRISPR-based immunity in Methanosarcina mazei by transcriptional regulation of components essential for the adaptation
show Abstracthide Abstract
CRISPR loci are found in bacterial and archaeal genomes where they provide the molecular machinery for acquisition of immunity against foreign DNA. In addition to the cas genes fundamentally required for CRISPR activity, a second class of genes is associated with the CRISPR loci, of which many have no reported function in CRISPR-mediated immunity. Here, we characterize MM_0565 of Methanosarcina mazei Gö1 associated to the type I-B CRISPR-locus providing evidence for its relevance in regulating this system. We show that MM_0565 is composed of a modified Rossmann-like fold and a winged helix-turn-helix domain and forms a dimer in solution. While direct effects on CRISPR-Cas transcription were not detected by genetic approaches, binding to the leader region of both CRISPR-Cas systems was observed by microscale thermophoresis and electromobility shift assays. Overexpression of MM_0565 however, strongly induced transcription of the cas1-solo gene located in the recently reported casposon, the gene product of which shows high similarity to classical Cas1 proteins. Based on our findings we hypothesize that Cas1-solo is involved in the adaptation of CRISPR-mediated immunity in M. mazei, and that MM_0565 modulates the activity of the CRISPR systems amongst potential other hypnotized actions by activating the transcription of the cas1-solo gene. Overall design: Investigation of differential-gene expression profiles of a MM565 overproduction M. mazei strain (OP_MM565) and a vector control strain (pWM321), using duplicates.
Sample: pWM321 replicate 2
SAMN15047729 • SRS6728973 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: RNA isolation was performed using TRI reagent following the manufacturer´s protocol followed by DNaseI treatment and phenol-chloroform precipitation cDNA libraries for Illumina sequencing were constructed by vertis Biotechnologie AG, Germany (http://www.vertis‐biotech.com/) as described previously for eukaryotic microRNA (Berezikov et al., 2006) but omitting the RNA size‐fractionation step prior to cDNA synthesis. In brief, equal amounts of RNA samples were poly(A)‐tailed using poly(A) polymerase. Then, the 5'PPP structures were removed using tobacco acid pyrophosphatase (TAP). Afterwards, an RNA adapter was ligated to the 5 ́‐phosphate of the RNA. First‐strand cDNA was synthesis by an oligo(dT)‐adapter primer and the M‐MLV reverse transcriptase. In a PCR‐based amplification step using a high fidelity DNA polymerase the cDNA concentration was increased to 20‐30 ng/μl. A library‐specific barcode for multiplex sequencing was part of a 3'‐sequencing adapter.
Experiment attributes:
GEO Accession: GSM4576391
Links:
Runs: 1 run, 5.6M spots, 561.8M bases, 318.3Mb
Run# of Spots# of BasesSizePublished
SRR118667875,619,405561.8M318.3Mb2020-09-08

ID:
10948917

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