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SRX8999046: GSM4743706: cholinium chloride_rep1 - CholCl_R1; Daphnia magna; RNA-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 29.9M spots, 9G bases, 3.3Gb downloads

Submitted by: NCBI (GEO)
Study: Transcriptional toxicity of imidazolium- and cholinium-based ionic liquids
show Abstracthide Abstract
Ionic Liquids are a broad group of salts with low melting points that can be specifically tuned for a broad range of applications. Despite being initially considered “green” solvents, their better environmental friendliness compared to traditional solvents has been increasingly challenged. In this study, we aimed to investigate the molecular effects of ILs exposure by using RNA-sequencing to study differential gene expression patterns. Thus, we exposed Daphnia magna to 1-ethyl-3-methylimidazolium chloride ([C2mim]Cl), 1-dodecyl chloride-3-methylimidazolium ([C12mim]Cl) and cholinium chloride ([Chol]Cl). Results suggest that the three ILs share several mechanisms of toxicity, including cellular membrane and cytoskeleton damage, oxidative stress, inhibition of antioxidant enzymes, mitochondrial affectation, changes in protein biosynthesis and energy production, DNA damage, and ultimately, programmed cell death and disease initiation. Overall, the dataset revealed that [C2mim]Cl and [C12mim]Cl were, respectively, the least and the most toxic ILs at the transcriptional level. Also, it is reinforced that [Chol]Cl is not devoid of environmental hazardous potential. Unique gene expression signatures could also be identified for each IL. Overall design: 12 samples of whole-body mRNA profiles of 48-hours old Daphnia magna: control (3 replicates), exposure to 1-ethyl-3-methylimidazolium chloride (3 replicates), exposure to 1-dodecyl chloride-3-methylimidazolium (3 replicates) and exposure to cholinium chloride (3 replicates)
Sample: cholinium chloride_rep1 - CholCl_R1
SAMN15894659 • SRS7251773 • All experiments • All runs
Organism: Daphnia magna
Library:
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: After exposure, active organisms were randomly collected from each replicate into RNAlater® for further storage at -80 °C. Pools of 90 individuals collected from each replicate were used for extraction. Organisms were homogenized with a disposable pestle before RNA extraction with the RNeasy kit and Qiashredder by Qiagen (Venlo, Netherlands) following the manufacturer's protocol. The library construction of cDNA molecules was carried out using the Kapa Stranded mRNA Library Preparation Kit (Kapa Biosystems) and the generated DNA fragments were sequenced in an lllumina HiSeq 4000 platform, using 150 bp paired-end sequencing reads
Experiment attributes:
GEO Accession: GSM4743706
Links:
Runs: 1 run, 29.9M spots, 9G bases, 3.3Gb
Run# of Spots# of BasesSizePublished
SRR1250827129,891,9809G3.3Gb2021-08-14

ID:
11695591

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