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Survey of 800+data sets from human tissue and body fluid reveals xenomiRs are likely artifacts
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Stockholm University, Science for Life Laboratory (SciLifeLab).
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Number of Authors: 92017 (English)In: RNA: A publication of the RNA Society, ISSN 1355-8382, E-ISSN 1469-9001, Vol. 23, no 4, p. 433-445Article in journal (Refereed) Published
Abstract [en]

miRNAs are small 22-nucleotide RNAs that can post-transcriptionally regulate gene expression. It has been proposed that dietary plant miRNAs can enter the human bloodstream and regulate host transcripts; however, these findings have been widely disputed. We here conduct the first comprehensive meta-study in the field, surveying the presence and abundances of cross-species miRNAs (xenomiRs) in 824 sequencing data sets from various human tissues and body fluids. We find that xenomiRs are commonly present in tissues (17%) and body fluids (69%); however, the abundances are low, comprising 0.001% of host human miRNA counts. Further, we do not detect a significant enrichment of xenomiRs in sequencing data originating from tissues and body fluids that are exposed to dietary intake (such as liver). Likewise, there is no significant depletion of xenomiRs in tissues and body fluids that are relatively separated from the main bloodstream (such as brain and cerebro-spinal fluids). Interestingly, the majority (81%) of body fluid xenomiRs stem from rodents, which are a rare human dietary contribution but common laboratory animals. Body fluid samples from the same studies tend to group together when clustered by xenomiR compositions, suggesting technical batch effects. Last, we performed carefully designed and controlled animal feeding studies, in which we detected no transfer of plant miRNAs into rat blood, or bovine milk sequences into piglet blood. In summary, our comprehensive computational and experimental results indicate that xenomiRs originate from technical artifacts rather than dietary intake.

Place, publisher, year, edition, pages
2017. Vol. 23, no 4, p. 433-445
Keywords [en]
miRNA, microRNA, meta-study, exogenous miRNAs, next-generation sequencing, contamination, artifacts
National Category
Biological Sciences
Identifiers
URN: urn:nbn:se:su:diva-142631DOI: 10.1261/rna.059725.116ISI: 000396786100001PubMedID: 28062594OAI: oai:DiVA.org:su-142631DiVA, id: diva2:1096007
Available from: 2017-05-16 Created: 2017-05-16 Last updated: 2022-03-23Bibliographically approved
In thesis
1. microRNAs: from biogenesis to organismal tracing
Open this publication in new window or tab >>microRNAs: from biogenesis to organismal tracing
2020 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

MicroRNAs (miRNAs) are short noncoding RNAs of around 22 nucleotides in length, which help to shape the expression of most mRNAs. Perturbation of miRNA expression has revealed a variety of defects in development, cell specification, physiology and behavior. This thesis focuses on two topics of miRNA: identification of structural features that influence miRNA biogenesis (Paper I) and application of taxonomical marker miRNAs to resolve organismal origin of samples (Paper II and III).

The current model of miRNA hairpin biogenesis has limited information content and appears to be incomplete. In paper I, we apply a novel high-throughput screening method to profile the optimal structure of miRNA hairpins for efficient and precise miRNA biogenesis. The optimal structure consists of tight and loose local structures across the hairpin, which reflects the constraints of biogenesis proteins. We find that miRNA hairpins with stable lower basal stem are more efficiently processed and have a higher expression level in tissues of 20 animal species. We address that the structural features - which have been largely neglected in the current model - are in fact as important as the well-known sequence motifs.

New miRNAs are continuously added over evolutionary time and are rarely secondarily lost, making them ideal taxonomical markers. In paper II, we demonstrate as a proof-of-principle that miRNAs can be used to trace biological sample back to the lineage or even species of origin. Based on the marker miRNAs, we develop miRTrace, the first software to accurately trace miRNA sequences back to their taxonomical origin. The method can sensitively identify the origin of single cells and detect parasitic nematode RNA in mammalian host blood sample. In paper III, we apply miRNA tracing to address a controversial question about the origin of the exogenous plant miRNAs (xenomiRs) found in human samples, and which have been proposed to regulate human gene expression. Our computational and experimental results provide evidence that xenomiRs are derived from technical artifacts rather than dietary intake.

Place, publisher, year, edition, pages
Stockholm: Institutionen för molekylär biovetenskap, Wenner-Grens institut, Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, 2020. p. 46
Keywords
microRNA, microRNA biogenesis, taxonomical identification, high throughput sequencing, xenomiRs, RNA structure, high throughput screening
National Category
Bioinformatics and Computational Biology Evolutionary Biology Structural Biology Biochemistry Molecular Biology
Research subject
Molecular Bioscience
Identifiers
urn:nbn:se:su:diva-185709 (URN)978-91-7911-306-3 (ISBN)978-91-7911-307-0 (ISBN)
Public defence
2020-11-18, online via Zoom, public link is available at the department web site, Stockholm, 09:00 (English)
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Supervisors
Available from: 2020-10-26 Created: 2020-10-05 Last updated: 2025-02-20Bibliographically approved

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Kang, WenjingFriedländer, Marc R.

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