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SRX26602031: RNA-Seq of myxococcus xanthus: 24h submerged culture monolayer
1 ILLUMINA (Illumina HiSeq 4000) run: 19.4M spots, 968.1M bases, 387.1Mb downloads

Design: Briefly, 2-3 g of RNA was mixed in hybridization buffer (0.1 M Tris-HCl [pH 7.0], 0.2 M NaCl) with 76 DNA oligonucleotides (0.17 M/oligo) that anneal to M. xanthus 16S and 23S rRNAs, the mixture was incubated in a thermocycler at 95C for 2 min, then ramped down to 45C at a rate of 0.1C/s, followed by additional incubation at 45C for 5 min. The annealed samples were treated with Hybridase Thermostable RNase H (Epicentre) in order to hydrolyze RNA-DNA hybrids and digested with DNase I (Roche) to remove remaining oligos. Agencourt RNAClean XP beads (Beckman Coulter) were used for cleanup of the rRNA-depleted RNA samples. qPCR verification was performed to confirm successful (i.e., ~90%) rRNA depletion. The KAPA RNA HyperPrep kit (KAPA Biosystems) was used as described in the product manual to generate adapter-ligated libraries for multiplex sequencing. The Qubit 1X dsDNA HS (High-Sensitivity) Assay Kit (ThermoFisher Scientific) was used to measure library concentration.
Submitted by: Michigan State Univeristy
Study: Transcriptomic analysis of Myxococcus xanthus DK1622, csgA, fruA, and mrpC developing mutants in submerged culture
show Abstracthide Abstract
The bacterium Myxococcus xanthus provides an important multicellular model for understanding stress responses. The regulatory proteins CsgA, FruA, and MrpC are essential to survive prolonged starvation by forming fruiting bodies, which are mounds containing hardy round spores formed from vegetative rods, but the genome-wide pathways affected by these proteins remain poorly understood. Only a fruA mutant transcriptome and MrpC ChIP-seq have been reported. We describe RNA-seq transcriptome analysis of csgA, fruA, and mrpC mutants relative to a wild-type laboratory strain midway during the starvation-induced developmental process, when mounds, but not spores, have formed. The primary goal is to identify processes which are regulated by one or more of these genes during development.
Sample:
SAMN44442057 • SRS23006656 • All experiments • All runs
Library:
Name: DK1622(frua2)
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: Hybrid Selection
Layout: SINGLE
Runs: 1 run, 19.4M spots, 968.1M bases, 387.1Mb
Run# of Spots# of BasesSizePublished
SRR3122146619,362,562968.1M387.1Mb2024-11-04

ID:
35942240

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