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Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure
Understanding the genetic regulatory code governing gene expression is an important challenge in molecular biology. However, how individual coding and non-coding regions of the gene regulatory structure interact and contribute to mRNA expression levels remains unclear. Here we apply deep learning on...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708451/ https://www.ncbi.nlm.nih.gov/pubmed/33262328 http://dx.doi.org/10.1038/s41467-020-19921-4 |
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author | Zrimec, Jan Börlin, Christoph S. Buric, Filip Muhammad, Azam Sheikh Chen, Rhongzen Siewers, Verena Verendel, Vilhelm Nielsen, Jens Töpel, Mats Zelezniak, Aleksej |
author_facet | Zrimec, Jan Börlin, Christoph S. Buric, Filip Muhammad, Azam Sheikh Chen, Rhongzen Siewers, Verena Verendel, Vilhelm Nielsen, Jens Töpel, Mats Zelezniak, Aleksej |
author_sort | Zrimec, Jan |
collection | PubMed |
description | Understanding the genetic regulatory code governing gene expression is an important challenge in molecular biology. However, how individual coding and non-coding regions of the gene regulatory structure interact and contribute to mRNA expression levels remains unclear. Here we apply deep learning on over 20,000 mRNA datasets to examine the genetic regulatory code controlling mRNA abundance in 7 model organisms ranging from bacteria to Human. In all organisms, we can predict mRNA abundance directly from DNA sequence, with up to 82% of the variation of transcript levels encoded in the gene regulatory structure. By searching for DNA regulatory motifs across the gene regulatory structure, we discover that motif interactions could explain the whole dynamic range of mRNA levels. Co-evolution across coding and non-coding regions suggests that it is not single motifs or regions, but the entire gene regulatory structure and specific combination of regulatory elements that define gene expression levels. |
format | Online Article Text |
id | pubmed-7708451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77084512020-12-03 Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure Zrimec, Jan Börlin, Christoph S. Buric, Filip Muhammad, Azam Sheikh Chen, Rhongzen Siewers, Verena Verendel, Vilhelm Nielsen, Jens Töpel, Mats Zelezniak, Aleksej Nat Commun Article Understanding the genetic regulatory code governing gene expression is an important challenge in molecular biology. However, how individual coding and non-coding regions of the gene regulatory structure interact and contribute to mRNA expression levels remains unclear. Here we apply deep learning on over 20,000 mRNA datasets to examine the genetic regulatory code controlling mRNA abundance in 7 model organisms ranging from bacteria to Human. In all organisms, we can predict mRNA abundance directly from DNA sequence, with up to 82% of the variation of transcript levels encoded in the gene regulatory structure. By searching for DNA regulatory motifs across the gene regulatory structure, we discover that motif interactions could explain the whole dynamic range of mRNA levels. Co-evolution across coding and non-coding regions suggests that it is not single motifs or regions, but the entire gene regulatory structure and specific combination of regulatory elements that define gene expression levels. Nature Publishing Group UK 2020-12-01 /pmc/articles/PMC7708451/ /pubmed/33262328 http://dx.doi.org/10.1038/s41467-020-19921-4 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zrimec, Jan Börlin, Christoph S. Buric, Filip Muhammad, Azam Sheikh Chen, Rhongzen Siewers, Verena Verendel, Vilhelm Nielsen, Jens Töpel, Mats Zelezniak, Aleksej Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure |
title | Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure |
title_full | Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure |
title_fullStr | Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure |
title_full_unstemmed | Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure |
title_short | Deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure |
title_sort | deep learning suggests that gene expression is encoded in all parts of a co-evolving interacting gene regulatory structure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708451/ https://www.ncbi.nlm.nih.gov/pubmed/33262328 http://dx.doi.org/10.1038/s41467-020-19921-4 |
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