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Blood Transcriptome Analysis of Septic Patients Reveals a Long Non-Coding Alu-RNA in the Complement C5a Receptor 1 Gene

Permanent lenke
https://hdl.handle.net/10037/26299
DOI
https://doi.org/10.3390/ncrna8020024
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article.pdf (2.466Mb)
Publisert versjon (PDF)
Dato
2022-03-29
Type
Journal article
Tidsskriftartikkel
Peer reviewed

Forfatter
Emblem, Åse; Knutsen, Erik; Jørgensen, Tor Erik; Fure, Hilde; Johansen, Steinar Daae; Brekke, Ole Lars; Mollnes, Tom Eirik; Karlsen, Bård Ove
Sammendrag
Many severe inflammation conditions are complement-dependent with the complement component C5a-C5aR1 axis as an important driver. At the RNA level, the blood transcriptome undergoes programmed expression of coding and long non-coding RNAs to combat invading microorganisms. Understanding the expression of long non-coding RNAs containing Alu elements in inflammation is important for reconstructing cell fate trajectories leading to severe disease. We have assembled a pipeline for computation mining of new Alu-containing long non-coding RNAs by intersecting immune genes with known Alu coordinates in the human genome. By applying the pipeline to patient bulk RNA-seq data with sepsis, we found immune genes containing 48 Alu insertion as robust candidates for further study. Interestingly, 1 of the 48 candidates was located within the complement system receptor gene C5aR1 and holds promise as a target for RNA therapeutics.
Forlag
MDPI
Sitering
Emblem Å, Knutsen E, Jørgensen TE, Fure H, Johansen S.D., Brekke O.L., Mollnes TE, Karlsen B. Blood Transcriptome Analysis of Septic Patients Reveals a Long Non-Coding Alu-RNA in the Complement C5a Receptor 1 Gene . Non-coding RNA. 2022
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  • Artikler, rapporter og annet (medisinsk biologi) [1103]
Copyright 2022 The Author(s)

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