Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0122203
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dc.titleCharacterisation of the small RNAs in the biomedically important green-bottle blowfly Lucilia sericata
dc.contributor.authorBlenkiron C.
dc.contributor.authorTsai P.
dc.contributor.authorBrown L.A.
dc.contributor.authorTintinger V.
dc.contributor.authorAskelund K.J.
dc.contributor.authorWindsor J.A.
dc.contributor.authorPhillips A.R.
dc.date.accessioned2019-11-07T05:00:29Z
dc.date.available2019-11-07T05:00:29Z
dc.date.issued2015
dc.identifier.citationBlenkiron C., Tsai P., Brown L.A., Tintinger V., Askelund K.J., Windsor J.A., Phillips A.R. (2015). Characterisation of the small RNAs in the biomedically important green-bottle blowfly Lucilia sericata. PLoS ONE 10 (3) : e0122203. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0122203
dc.identifier.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161738
dc.description.abstractBackground: The green bottle fly maggot, Lucilia sericata, is a species with importance in medicine, agriculture and forensics. Improved understanding of this species' biology is of great potential benefit to many research communities. MicroRNAs (miRNA) are a short non-protein coding regulatory RNA, which directly regulate a host of protein coding genes at the translational level. They have been shown to have developmental and tissue specific distributions where they impact directly on gene regulation. In order to improve understanding of the biology of L. sericata maggots we have performed small RNA-sequencing of their secretions and tissue at different developmental stages. Results: We have successfully isolated RNA from the secretions of L. sericata maggots. Illumina small RNA-sequencing of these secretions and the three tissues (crop, salivary gland, gut) revealed that the most common small RNA fragments were derived from ribosomal RNA and transfer RNAs of both insect and bacterial origins. These RNA fragments were highly specific, with the most common tRNAs, such as GlyGCC, predominantly represented by reads derived from the 5' end of the mature maggot tRNA. Each library also had a unique profile of miRNAs with a high abundance of miR-10-5p in the maggot secretions and gut and miR-8 in the food storage organ the crop and salivary glands. The pattern of small RNAs in the bioactive maggot secretions suggests they originate from a combination of saliva, foregut and hindgut tissues. Droplet digital RT-PCR validation of the RNA-sequencing data shows that not only are there differences in the tissue profiles for miRNAs and small RNA fragments but that these are also modulated through developmental stages of the insect. Conclusions: We have identified the small-RNAome of the medicinal maggots L. sericata and shown that there are distinct subsets of miRNAs expressed in specific tissues that also alter during the development of the insect. Furthermore there are very specific RNA fragments derived from other non-coding RNAs present in tissues and in the secretions. This new knowledge has applicability in diverse research fields including wound healing, agriculture and forensics. © 2015 Blenkiron et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectmicroRNA
dc.subjectmicroRNA 10 5p
dc.subjectmicroRNA 8
dc.subjectribosome RNA
dc.subjectRNA
dc.subjectsmall RNA
dc.subjecttransfer RNA
dc.subjectunclassified drug
dc.subjectuntranslated RNA
dc.subjectmicroRNA
dc.subjectribosome RNA
dc.subjecttransfer RNA
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectCalliphoridae
dc.subjectdevelopmental stage
dc.subjectintestine
dc.subjectLucilia sericata
dc.subjectnonhuman
dc.subjectreverse transcription polymerase chain reaction
dc.subjectRNA sequence
dc.subjectsalivary gland
dc.subjectsecretion (process)
dc.subjecttissue distribution
dc.subjectanimal
dc.subjectbodily secretions
dc.subjectchemistry
dc.subjectDiptera
dc.subjectgastrointestinal tract
dc.subjectgene expression regulation
dc.subjectgene library
dc.subjectgenetics
dc.subjectlarva
dc.subjectmolecular genetics
dc.subjectnucleotide sequence
dc.subjectsequence analysis
dc.subjectBacteria (microorganisms)
dc.subjectHexapoda
dc.subjectLucilia sericata
dc.subjectAnimals
dc.subjectBase Sequence
dc.subjectBodily Secretions
dc.subjectDiptera
dc.subjectGastrointestinal Tract
dc.subjectGene Expression Regulation
dc.subjectGene Library
dc.subjectLarva
dc.subjectMicroRNAs
dc.subjectMolecular Sequence Data
dc.subjectReverse Transcriptase Polymerase Chain Reaction
dc.subjectRNA, Ribosomal
dc.subjectRNA, Transfer
dc.subjectSequence Analysis, RNA
dc.typeArticle
dc.contributor.departmentSURGERY
dc.description.doi10.1371/journal.pone.0122203
dc.description.sourcetitlePLoS ONE
dc.description.volume10
dc.description.issue3
dc.description.pagee0122203
dc.published.statePublished
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