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RNA-Seq Data-Mining Allows the Discovery of Two Long Non-Coding RNA Biomarkers of Viral Infection in Humans. | LitMetric

RNA-Seq Data-Mining Allows the Discovery of Two Long Non-Coding RNA Biomarkers of Viral Infection in Humans.

Int J Mol Sci

Unidade de Xenética, Instituto de Ciencias Forenses (INCIFOR), Facultade de Medicina, Universidade de Santiago de Compostela, 15782 Galicia, Spain.

Published: April 2020

AI Article Synopsis

  • There is an increasing focus on understanding how gene expression affects viral infections and their progression.
  • Recent research shows that long non-coding RNAs (lncRNAs) play a crucial role in regulating the immune response by affecting gene expression in various ways.
  • Two specific lncRNAs, which are notably downregulated during viral infections, have been identified as potential biomarkers for diagnosing these infections in patients compared to healthy controls.

Article Abstract

There is a growing interest in unraveling gene expression mechanisms leading to viral host invasion and infection progression. Current findings reveal that long non-coding RNAs (lncRNAs) are implicated in the regulation of the immune system by influencing gene expression through a wide range of mechanisms. By mining whole-transcriptome shotgun sequencing (RNA-seq) data using machine learning approaches, we detected two lncRNAs (ENSG00000254680 and ENSG00000273149) that are downregulated in a wide range of viral infections and different cell types, including blood monocluclear cells, umbilical vein endothelial cells, and dermal fibroblasts. The efficiency of these two lncRNAs was positively validated in different viral phenotypic scenarios. These two lncRNAs showed a strong downregulation in virus-infected patients when compared to healthy control transcriptomes, indicating that these biomarkers are promising targets for infection diagnosis. To the best of our knowledge, this is the very first study using host lncRNAs biomarkers for the diagnosis of human viral infections.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215422PMC
http://dx.doi.org/10.3390/ijms21082748DOI Listing

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