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Series GSE32632 Query DataSets for GSE32632
Status Public on Jun 18, 2012
Title Ethanol alters microNA expression in zebrafish embryos
Platform organisms Caenorhabditis elegans; Drosophila melanogaster; Danio rerio; Gallus gallus; Homo sapiens; Mus musculus; Rattus norvegicus; Takifugu rubripes
Sample organism Danio rerio
Experiment type Non-coding RNA profiling by array
Summary Prenatal exposure to ethanol leads to a myriad of developmental disorders known as fetal alcohol spectrum disorder, often characterized by growth and mental retardation, central nervous system damage and specific craniofacial dysmorphic features. Although the exact mechanisms of ethanol toxicity are not well understood it is known that ethanol exposure during development affects the expression of several genes involved in cell cycle control, apoptosis and transcription. MicroRNAs (miRNAs) are implicated in some of these processes however it is unclear if they are involved in ethanol-induced toxicity. Here we tested whether ethanol deregulates miRNA expression in zebrafish embryos and if a miRNA deregulation signature could be inferred. For this, zebrafish embryos were exposed to two different ethanol concentrations (1% and 1.5%) from 4 hours post-fertilization (hpf) to 24hpf. MicroRNA expression profiles revealed that ethanol exposure induces deregulation of miRNA expression significantly. Seven miRNAs are commonly up-regulated after both ethanol treatments, namely miR-153a, miR-725, miR-30d, let-7k, miR-100, miR-738 and miR-732, whereas downregulation of miR-23a, miR-203, let-7c, miR-128 and miR-193b is detected after 1% ethanol exposure only. Target prediction of deregulated miRNAs shows that putative targets are involved in cell cycle control, apoptosis and transcription, which are the main processes affected by ethanol toxicity. The overall study shows that the effects of ethanol on miRNA deregulation are dose-dependent and that miRNAs are relevant in the context of alcohol toxicity. Moreover, a miRNA toxicity signature for embryonic ethanol exposure was obtained.
 
Overall design Zebrafish embryos were obtained from spawning adults in groups of about 10 males and 10 females. Zebrafish embryos were collected and Petri dishes with approximately 250 eggs each were incubated at 28ºC to allow normal zebrafish development until 4hpf, when blastula is reached. At this stage, embryos were examined under a dissecting microscope and those that had developed normally were selected for EtOH exposure (approximately 200 eggs). Briefly, 200 embryos were randomly distributed into plastic Petri dishes containing 20 mL of EtOH test solutions (1% EtOH, 1.5% EtOH). All solutions were made by dilution of absolute EtOH in system water. Exposure was from 4hpf to 24hpf. At this stage, solutions were changed by system water and embryos were allowed to grow until 24hpf. The control group was allowed to grow in plain system water. Zebrafish embryos were collected at 24hpf for microarray analysis. Two biological replicates were performed for each assay.
 
Contributor(s) Soares AR, Pereira PM, Ferreira V, Reverendo M, Simões J, Bezerra AR, Moura G, Santos MA
Citation(s) 22298809
Submission date Oct 05, 2011
Last update date Jun 20, 2012
Contact name Patrícia Matos Pereira
E-mail(s) pereirap@ua.pt
Organization name University of Aveiro
Department Biology
Lab RNA biology
Street address Campus Universitário de Santiago
City Aveiro
ZIP/Postal code 3810-183
Country Portugal
 
Platforms (1)
GPL14672 miRNAChip_MS_V1
Samples (6)
GSM808869 Embryos_Ctrl_24hpf_R1
GSM808870 Embryos_Ctrl_24hpf_R2
GSM808871 Embryos_EtOH1%_24hpf_R1
Relations
BioProject PRJNA146975

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE32632_RAW.tar 1.2 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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