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Genetic variants associated mRNA stability in lung

BACKGROUND: Expression quantitative trait loci (eQTLs) analyses have been widely used to identify genetic variants associated with gene expression levels to understand what molecular mechanisms underlie genetic traits. The resultant eQTLs might affect the expression of associated genes through trans...

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Autores principales: Li, Jian-Rong, Tang, Mabel, Li, Yafang, Amos, Christopher I., Cheng, Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915503/
https://www.ncbi.nlm.nih.gov/pubmed/35272635
http://dx.doi.org/10.1186/s12864-022-08405-y
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author Li, Jian-Rong
Tang, Mabel
Li, Yafang
Amos, Christopher I.
Cheng, Chao
author_facet Li, Jian-Rong
Tang, Mabel
Li, Yafang
Amos, Christopher I.
Cheng, Chao
author_sort Li, Jian-Rong
collection PubMed
description BACKGROUND: Expression quantitative trait loci (eQTLs) analyses have been widely used to identify genetic variants associated with gene expression levels to understand what molecular mechanisms underlie genetic traits. The resultant eQTLs might affect the expression of associated genes through transcriptional or post-transcriptional regulation. In this study, we attempt to distinguish these two types of regulation by identifying genetic variants associated with mRNA stability of genes (stQTLs). RESULTS: Here, we presented a computational framework that takes advantage of recently developed methods to infer the mRNA stability of genes based on RNA-seq data and performed association analysis to identify stQTLs. Using the Genotype-Tissue Expression (GTEx) lung RNA-Seq data, we identified a total of 142,801 stQTLs for 3942 genes and 186,132 eQTLs for 4751 genes from 15,122,700 genetic variants for 13,476 genes on the autosomes, respectively. Interestingly, our results indicated that stQTLs were enriched in the CDS and 3’UTR regions, while eQTLs are enriched in the CDS, 3’UTR, 5’UTR, and upstream regions. We also found that stQTLs are more likely than eQTLs to overlap with RNA binding protein (RBP) and microRNA (miRNA) binding sites. Our analyses demonstrate that simultaneous identification of stQTLs and eQTLs can provide more mechanistic insight on the association between genetic variants and gene expression levels. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08405-y.
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spelling pubmed-89155032022-03-18 Genetic variants associated mRNA stability in lung Li, Jian-Rong Tang, Mabel Li, Yafang Amos, Christopher I. Cheng, Chao BMC Genomics Research BACKGROUND: Expression quantitative trait loci (eQTLs) analyses have been widely used to identify genetic variants associated with gene expression levels to understand what molecular mechanisms underlie genetic traits. The resultant eQTLs might affect the expression of associated genes through transcriptional or post-transcriptional regulation. In this study, we attempt to distinguish these two types of regulation by identifying genetic variants associated with mRNA stability of genes (stQTLs). RESULTS: Here, we presented a computational framework that takes advantage of recently developed methods to infer the mRNA stability of genes based on RNA-seq data and performed association analysis to identify stQTLs. Using the Genotype-Tissue Expression (GTEx) lung RNA-Seq data, we identified a total of 142,801 stQTLs for 3942 genes and 186,132 eQTLs for 4751 genes from 15,122,700 genetic variants for 13,476 genes on the autosomes, respectively. Interestingly, our results indicated that stQTLs were enriched in the CDS and 3’UTR regions, while eQTLs are enriched in the CDS, 3’UTR, 5’UTR, and upstream regions. We also found that stQTLs are more likely than eQTLs to overlap with RNA binding protein (RBP) and microRNA (miRNA) binding sites. Our analyses demonstrate that simultaneous identification of stQTLs and eQTLs can provide more mechanistic insight on the association between genetic variants and gene expression levels. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-022-08405-y. BioMed Central 2022-03-11 /pmc/articles/PMC8915503/ /pubmed/35272635 http://dx.doi.org/10.1186/s12864-022-08405-y 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 Research
Li, Jian-Rong
Tang, Mabel
Li, Yafang
Amos, Christopher I.
Cheng, Chao
Genetic variants associated mRNA stability in lung
title Genetic variants associated mRNA stability in lung
title_full Genetic variants associated mRNA stability in lung
title_fullStr Genetic variants associated mRNA stability in lung
title_full_unstemmed Genetic variants associated mRNA stability in lung
title_short Genetic variants associated mRNA stability in lung
title_sort genetic variants associated mrna stability in lung
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915503/
https://www.ncbi.nlm.nih.gov/pubmed/35272635
http://dx.doi.org/10.1186/s12864-022-08405-y
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