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Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach
BACKGROUND: Long non-coding RNAs (lncRNAs) are involved in a variety of mechanisms related to tumorigenesis by functioning as oncogenes or tumor-suppressors or even harboring oncogenic and tumor-suppressing effects; representing a new class of cancer biomarkers and therapeutic targets. It is predict...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636742/ https://www.ncbi.nlm.nih.gov/pubmed/36333783 http://dx.doi.org/10.1186/s12935-022-02752-2 |
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author | Kerachian, Mohammad Amin Azghandi, Marjan |
author_facet | Kerachian, Mohammad Amin Azghandi, Marjan |
author_sort | Kerachian, Mohammad Amin |
collection | PubMed |
description | BACKGROUND: Long non-coding RNAs (lncRNAs) are involved in a variety of mechanisms related to tumorigenesis by functioning as oncogenes or tumor-suppressors or even harboring oncogenic and tumor-suppressing effects; representing a new class of cancer biomarkers and therapeutic targets. It is predicted that more than 35,000 ncRNA especially lncRNA are positioned at the intergenic regions of the human genome. Emerging research indicates that one of the key pathways controlling lncRNA expression and tissue specificity is epigenetic regulation. METHODS: In the current article, a novel approach for lncRNA discovery based on the intergenic position of most lncRNAs and a single CpG site methylation level representing epigenetic characteristics has been suggested. RESULTS: Using this method, a novel antisense lncRNA named LINC02892 presenting three transcripts without the capacity of coding a protein was found exhibiting nuclear, cytoplasmic, and exosome distributions. CONCLUSION: The current discovery strategy could be applied to identify novel non-coding RNAs influenced by methylation aberrations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02752-2. |
format | Online Article Text |
id | pubmed-9636742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96367422022-11-06 Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach Kerachian, Mohammad Amin Azghandi, Marjan Cancer Cell Int Primary Research BACKGROUND: Long non-coding RNAs (lncRNAs) are involved in a variety of mechanisms related to tumorigenesis by functioning as oncogenes or tumor-suppressors or even harboring oncogenic and tumor-suppressing effects; representing a new class of cancer biomarkers and therapeutic targets. It is predicted that more than 35,000 ncRNA especially lncRNA are positioned at the intergenic regions of the human genome. Emerging research indicates that one of the key pathways controlling lncRNA expression and tissue specificity is epigenetic regulation. METHODS: In the current article, a novel approach for lncRNA discovery based on the intergenic position of most lncRNAs and a single CpG site methylation level representing epigenetic characteristics has been suggested. RESULTS: Using this method, a novel antisense lncRNA named LINC02892 presenting three transcripts without the capacity of coding a protein was found exhibiting nuclear, cytoplasmic, and exosome distributions. CONCLUSION: The current discovery strategy could be applied to identify novel non-coding RNAs influenced by methylation aberrations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02752-2. BioMed Central 2022-11-04 /pmc/articles/PMC9636742/ /pubmed/36333783 http://dx.doi.org/10.1186/s12935-022-02752-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Primary Research Kerachian, Mohammad Amin Azghandi, Marjan Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach |
title | Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach |
title_full | Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach |
title_fullStr | Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach |
title_full_unstemmed | Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach |
title_short | Identification of long non-coding RNA using single nucleotide epimutation analysis: a novel gene discovery approach |
title_sort | identification of long non-coding rna using single nucleotide epimutation analysis: a novel gene discovery approach |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636742/ https://www.ncbi.nlm.nih.gov/pubmed/36333783 http://dx.doi.org/10.1186/s12935-022-02752-2 |
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