Origins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology
Long non-coding RNAs (lncRNAs) have emerged during the post-genomic era as significant epigenetic regulators. Viral-like 30 elements (VL30s) are a family of mouse retrotransposons that are transcribed into functional lncRNAs. Recent data suggest that VL30 RNAs are efficiently packaged in small extra...
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oai:doaj.org-article:546462aa2503468db0f0bbf1f8f26b732021-11-25T16:51:38ZOrigins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology10.3390/biomedicines91117422227-9059https://doaj.org/article/546462aa2503468db0f0bbf1f8f26b732021-11-01T00:00:00Zhttps://www.mdpi.com/2227-9059/9/11/1742https://doaj.org/toc/2227-9059Long non-coding RNAs (lncRNAs) have emerged during the post-genomic era as significant epigenetic regulators. Viral-like 30 elements (VL30s) are a family of mouse retrotransposons that are transcribed into functional lncRNAs. Recent data suggest that VL30 RNAs are efficiently packaged in small extracellular vesicles (SEVs) through an SEV enrichment sequence. We analysed VL30 elements for the presence of the distinct 26 nt SEV enrichment motif and found that SEV enrichment is an inherent hallmark of the VL30 family, contained in 36 full-length elements, with a widespread chromosomal distribution. Among them, 25 elements represent active, present-day integrations and contain an abundance of regulatory sequences. Phylogenetic analysis revealed a recent spread of SEV-VL30s from 4.4 million years ago till today. Importantly, 39 elements contain an SFPQ-binding motif, associated with the transcriptional induction of oncogenes. Most SEV-VL30s reside in transcriptionally active regions, as characterised by their distribution adjacent to candidate cis-regulatory elements (cCREs). Network analysis of SEV-VL30-associated genes suggests a distinct transcriptional footprint associated with embryonal abnormalities and neoplasia. Given the established role of VL30s in oncogenesis, we conclude that their potential to spread through SEVs represents a novel mechanism for non-coding RNA biology with numerous implications for cellular homeostasis and disease.Stefania MantziouGeorgios S. MarkopoulosMDPI AGarticlesmall extracellular vesiclesVL30 lncRNAnon-coding RNAscancerSFPQBiology (General)QH301-705.5ENBiomedicines, Vol 9, Iss 1742, p 1742 (2021) |
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small extracellular vesicles VL30 lncRNA non-coding RNAs cancer SFPQ Biology (General) QH301-705.5 |
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small extracellular vesicles VL30 lncRNA non-coding RNAs cancer SFPQ Biology (General) QH301-705.5 Stefania Mantziou Georgios S. Markopoulos Origins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology |
description |
Long non-coding RNAs (lncRNAs) have emerged during the post-genomic era as significant epigenetic regulators. Viral-like 30 elements (VL30s) are a family of mouse retrotransposons that are transcribed into functional lncRNAs. Recent data suggest that VL30 RNAs are efficiently packaged in small extracellular vesicles (SEVs) through an SEV enrichment sequence. We analysed VL30 elements for the presence of the distinct 26 nt SEV enrichment motif and found that SEV enrichment is an inherent hallmark of the VL30 family, contained in 36 full-length elements, with a widespread chromosomal distribution. Among them, 25 elements represent active, present-day integrations and contain an abundance of regulatory sequences. Phylogenetic analysis revealed a recent spread of SEV-VL30s from 4.4 million years ago till today. Importantly, 39 elements contain an SFPQ-binding motif, associated with the transcriptional induction of oncogenes. Most SEV-VL30s reside in transcriptionally active regions, as characterised by their distribution adjacent to candidate cis-regulatory elements (cCREs). Network analysis of SEV-VL30-associated genes suggests a distinct transcriptional footprint associated with embryonal abnormalities and neoplasia. Given the established role of VL30s in oncogenesis, we conclude that their potential to spread through SEVs represents a novel mechanism for non-coding RNA biology with numerous implications for cellular homeostasis and disease. |
format |
article |
author |
Stefania Mantziou Georgios S. Markopoulos |
author_facet |
Stefania Mantziou Georgios S. Markopoulos |
author_sort |
Stefania Mantziou |
title |
Origins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology |
title_short |
Origins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology |
title_full |
Origins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology |
title_fullStr |
Origins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology |
title_full_unstemmed |
Origins and Function of VL30 lncRNA Packaging in Small Extracellular Vesicles: Implications for Cellular Physiology and Pathology |
title_sort |
origins and function of vl30 lncrna packaging in small extracellular vesicles: implications for cellular physiology and pathology |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/546462aa2503468db0f0bbf1f8f26b73 |
work_keys_str_mv |
AT stefaniamantziou originsandfunctionofvl30lncrnapackaginginsmallextracellularvesiclesimplicationsforcellularphysiologyandpathology AT georgiossmarkopoulos originsandfunctionofvl30lncrnapackaginginsmallextracellularvesiclesimplicationsforcellularphysiologyandpathology |
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1718412895431163904 |