Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0017537
Title: Identification and characterization of 63 microRNAs in the Asian seabass Lates calcarifer
Authors: Xia J.H.
He X.P.
Bai Z.Y.
Yue G.H. 
Keywords: microRNA
microRNA 1
microRNA 103
microRNA 125
microRNA 183
microRNA 184
microrna 192
microRNA 21
microRNA 29
RNA
unclassified drug
lipopolysaccharide
microRNA
RNA precursor
animal experiment
animal model
animal tissue
article
controlled study
gene expression
Lates calcarifer
molecular evolution
nonhuman
nucleotide sequence
Perciformes
quantitative analysis
reverse transcription polymerase chain reaction
RNA analysis
RNA sequence
tissue distribution
transcription regulation
upregulation
animal
Asia
bass
drug effect
gene expression profiling
gene expression regulation
genetics
inflammation
metabolism
microbiology
molecular genetics
species difference
Vibrio
Lates calcarifer
Animals
Asia
Base Sequence
Bass
Conserved Sequence
Evolution, Molecular
Gene Expression Profiling
Gene Expression Regulation
Inflammation
Lipopolysaccharides
MicroRNAs
Molecular Sequence Data
RNA Precursors
Species Specificity
Vibrio
Issue Date: 2011
Publisher: Public Library of Science
Citation: Xia J.H., He X.P., Bai Z.Y., Yue G.H. (2011). Identification and characterization of 63 microRNAs in the Asian seabass Lates calcarifer. PLoS ONE 6 (3) : e17537. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0017537
Abstract: Background: MicroRNAs (miRNAs) play an important role in the regulation of many fundamental biological processes. So far miRNAs have been only identified in a few fish species, although there are over 30,000 fish species living under different environmental conditions on the earth. Here, we described an approach to identify conserved miRNAs and characterized their expression patterns in different tissues for the first time in a food fish species Asian seabass (Lates calcarifer). Methodology/Principal Findings: By combining a bioinformatics analysis with an approach of homolog-based PCR amplification and sequencing, 63 novel miRNAs belonging to 29 conserved miRNA families were identified. Of which, 59 miRNAs were conserved across 10-86 species (E value≤10-4) and 4 miRNAs were conserved only in fish species. qRT-PCR analysis showed that miR-29, miR-103, miR-125 and several let-7 family members were strongly and ubiquitously expressed in all tissues tested. Interestingly, miR-1, miR-21, miR-183, miR-184 and miR-192 showed highly conserved tissue-specific expression patterns. Exposure of the Asian seabass to lipopolysaccharide (LPS) resulted in up-regulation of over 50% of the identified miRNAs in spleen suggesting the importance of the miRNAs in acute inflammatory immune responses. Conclusions/Significance: The approach used in this study is highly effective for identification of conserved miRNAs. The identification of 63 miRNAs and determination of the spatial expression patterns of these miRNAs are valuable resources for further studies on post-transcriptional gene regulation in Asian seabass and other fish species. Further identification of the target genes of these miRNAs would shed new light on their regulatory roles of microRNAs in fish. © 2011 Xia et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/165594
ISSN: 19326203
DOI: 10.1371/journal.pone.0017537
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