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Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica

Long non-coding (lnc)RNAs are a class of eukaryotic RNA that do not code for protein and are linked with transcriptional regulation, amongst a myriad of other functions. Using a custom in silico pipeline we have identified 6,436 putative lncRNA transcripts in the liver fluke parasite, Fasciola hepat...

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Autores principales: McVeigh, Paul, McCammick, Erin, Robb, Emily, Brophy, Peter, Morphew, Russell M., Marks, Nikki J., Maule, Aaron G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564125/
https://www.ncbi.nlm.nih.gov/pubmed/37769025
http://dx.doi.org/10.1371/journal.pntd.0011663
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author McVeigh, Paul
McCammick, Erin
Robb, Emily
Brophy, Peter
Morphew, Russell M.
Marks, Nikki J.
Maule, Aaron G.
author_facet McVeigh, Paul
McCammick, Erin
Robb, Emily
Brophy, Peter
Morphew, Russell M.
Marks, Nikki J.
Maule, Aaron G.
author_sort McVeigh, Paul
collection PubMed
description Long non-coding (lnc)RNAs are a class of eukaryotic RNA that do not code for protein and are linked with transcriptional regulation, amongst a myriad of other functions. Using a custom in silico pipeline we have identified 6,436 putative lncRNA transcripts in the liver fluke parasite, Fasciola hepatica, none of which are conserved with those previously described from Schistosoma mansoni. F. hepatica lncRNAs were distinct from F. hepatica mRNAs in transcript length, coding probability, exon/intron composition, expression patterns, and genome distribution. RNA-Seq and digital droplet PCR measurements demonstrated developmentally regulated expression of lncRNAs between intra-mammalian life stages; a similar proportion of lncRNAs (14.2%) and mRNAs (12.8%) were differentially expressed (p<0.001), supporting a functional role for lncRNAs in F. hepatica life stages. While most lncRNAs (81%) were intergenic, we identified some that overlapped protein coding loci in antisense (13%) or intronic (6%) configurations. We found no unequivocal evidence for correlated developmental expression within positionally correlated lncRNA:mRNA pairs, but global co-expression analysis identified five lncRNA that were inversely co-regulated with 89 mRNAs, including a large number of functionally essential proteases. The presence of micro (mi)RNA binding sites in 3135 lncRNAs indicates the potential for miRNA-based post-transcriptional regulation of lncRNA, and/or their function as competing endogenous (ce)RNAs. The same annotation pipeline identified 24,141 putative lncRNAs in F. gigantica. This first description of lncRNAs in F. hepatica provides an avenue to future functional and comparative genomics studies that will provide a new perspective on a poorly understood aspect of parasite biology.
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spelling pubmed-105641252023-10-11 Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica McVeigh, Paul McCammick, Erin Robb, Emily Brophy, Peter Morphew, Russell M. Marks, Nikki J. Maule, Aaron G. PLoS Negl Trop Dis Research Article Long non-coding (lnc)RNAs are a class of eukaryotic RNA that do not code for protein and are linked with transcriptional regulation, amongst a myriad of other functions. Using a custom in silico pipeline we have identified 6,436 putative lncRNA transcripts in the liver fluke parasite, Fasciola hepatica, none of which are conserved with those previously described from Schistosoma mansoni. F. hepatica lncRNAs were distinct from F. hepatica mRNAs in transcript length, coding probability, exon/intron composition, expression patterns, and genome distribution. RNA-Seq and digital droplet PCR measurements demonstrated developmentally regulated expression of lncRNAs between intra-mammalian life stages; a similar proportion of lncRNAs (14.2%) and mRNAs (12.8%) were differentially expressed (p<0.001), supporting a functional role for lncRNAs in F. hepatica life stages. While most lncRNAs (81%) were intergenic, we identified some that overlapped protein coding loci in antisense (13%) or intronic (6%) configurations. We found no unequivocal evidence for correlated developmental expression within positionally correlated lncRNA:mRNA pairs, but global co-expression analysis identified five lncRNA that were inversely co-regulated with 89 mRNAs, including a large number of functionally essential proteases. The presence of micro (mi)RNA binding sites in 3135 lncRNAs indicates the potential for miRNA-based post-transcriptional regulation of lncRNA, and/or their function as competing endogenous (ce)RNAs. The same annotation pipeline identified 24,141 putative lncRNAs in F. gigantica. This first description of lncRNAs in F. hepatica provides an avenue to future functional and comparative genomics studies that will provide a new perspective on a poorly understood aspect of parasite biology. Public Library of Science 2023-09-28 /pmc/articles/PMC10564125/ /pubmed/37769025 http://dx.doi.org/10.1371/journal.pntd.0011663 Text en © 2023 McVeigh et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
McVeigh, Paul
McCammick, Erin
Robb, Emily
Brophy, Peter
Morphew, Russell M.
Marks, Nikki J.
Maule, Aaron G.
Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica
title Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica
title_full Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica
title_fullStr Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica
title_full_unstemmed Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica
title_short Discovery of long non-coding RNAs in the liver fluke, Fasciola hepatica
title_sort discovery of long non-coding rnas in the liver fluke, fasciola hepatica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564125/
https://www.ncbi.nlm.nih.gov/pubmed/37769025
http://dx.doi.org/10.1371/journal.pntd.0011663
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