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TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome
LncRNAs are not only well-known as non-coding elements, but also serve as templates for peptide translation, playing important roles in fundamental cellular processes and diseases. Here, we describe a database, TransLnc (http://bio-bigdata.hrbmu.edu.cn/TransLnc/), which aims to provide comprehensive...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728190/ https://www.ncbi.nlm.nih.gov/pubmed/34570220 http://dx.doi.org/10.1093/nar/gkab847 |
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author | Lv, Dezhong Chang, Zhenghong Cai, Yangyang Li, Junyi Wang, Liping Jiang, Qiushuang Xu, Kang Ding, Na Li, Xia Xu, Juan Li, Yongsheng |
author_facet | Lv, Dezhong Chang, Zhenghong Cai, Yangyang Li, Junyi Wang, Liping Jiang, Qiushuang Xu, Kang Ding, Na Li, Xia Xu, Juan Li, Yongsheng |
author_sort | Lv, Dezhong |
collection | PubMed |
description | LncRNAs are not only well-known as non-coding elements, but also serve as templates for peptide translation, playing important roles in fundamental cellular processes and diseases. Here, we describe a database, TransLnc (http://bio-bigdata.hrbmu.edu.cn/TransLnc/), which aims to provide comprehensive experimentally supported and predicted lncRNA peptides in multiple species. TransLnc currently documents approximate 583 840 peptides encoded by 33 094 lncRNAs. Six types of direct and indirect evidences supporting the coding potential of lncRNAs were integrated, and 65.28% peptides entries were with at least one type of evidence. Considering the strong tissue-specific expression of lncRNAs, TransLnc allows users to access lncRNA peptides in any of the 34 tissues involved in. In addition, both the unique characteristic and homology relationship were also predicted and provided. Importantly, TransLnc provides computationally predicted tumour neoantigens from peptides encoded by lncRNAs, which would provide novel insights into cancer immunotherapy. There were 220 791 and 237 915 candidate neoantigens binding by major histocompatibility complex (MHC) class I or II molecules, respectively. Several flexible tools were developed to aid retrieve and analyse, particularly lncRNAs tissue expression patterns, clinical relevance across cancer types. TransLnc will serve as a valuable resource for investigating the translation capacity of lncRNAs and greatly extends the cancer immunopeptidome. |
format | Online Article Text |
id | pubmed-8728190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-87281902022-01-05 TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome Lv, Dezhong Chang, Zhenghong Cai, Yangyang Li, Junyi Wang, Liping Jiang, Qiushuang Xu, Kang Ding, Na Li, Xia Xu, Juan Li, Yongsheng Nucleic Acids Res Database Issue LncRNAs are not only well-known as non-coding elements, but also serve as templates for peptide translation, playing important roles in fundamental cellular processes and diseases. Here, we describe a database, TransLnc (http://bio-bigdata.hrbmu.edu.cn/TransLnc/), which aims to provide comprehensive experimentally supported and predicted lncRNA peptides in multiple species. TransLnc currently documents approximate 583 840 peptides encoded by 33 094 lncRNAs. Six types of direct and indirect evidences supporting the coding potential of lncRNAs were integrated, and 65.28% peptides entries were with at least one type of evidence. Considering the strong tissue-specific expression of lncRNAs, TransLnc allows users to access lncRNA peptides in any of the 34 tissues involved in. In addition, both the unique characteristic and homology relationship were also predicted and provided. Importantly, TransLnc provides computationally predicted tumour neoantigens from peptides encoded by lncRNAs, which would provide novel insights into cancer immunotherapy. There were 220 791 and 237 915 candidate neoantigens binding by major histocompatibility complex (MHC) class I or II molecules, respectively. Several flexible tools were developed to aid retrieve and analyse, particularly lncRNAs tissue expression patterns, clinical relevance across cancer types. TransLnc will serve as a valuable resource for investigating the translation capacity of lncRNAs and greatly extends the cancer immunopeptidome. Oxford University Press 2021-09-27 /pmc/articles/PMC8728190/ /pubmed/34570220 http://dx.doi.org/10.1093/nar/gkab847 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Lv, Dezhong Chang, Zhenghong Cai, Yangyang Li, Junyi Wang, Liping Jiang, Qiushuang Xu, Kang Ding, Na Li, Xia Xu, Juan Li, Yongsheng TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome |
title | TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome |
title_full | TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome |
title_fullStr | TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome |
title_full_unstemmed | TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome |
title_short | TransLnc: a comprehensive resource for translatable lncRNAs extends immunopeptidome |
title_sort | translnc: a comprehensive resource for translatable lncrnas extends immunopeptidome |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728190/ https://www.ncbi.nlm.nih.gov/pubmed/34570220 http://dx.doi.org/10.1093/nar/gkab847 |
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