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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 |
Appears in Collections: | Elements Staff Publications |
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