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Genomic competition for noise reduction shaped evolutionary landscape of mir-4673
The genomic platform that informs evolution of microRNA cascades remains unknown. Here we capitalised on the recent evolutionary trajectory of hominin-specific miRNA-4673, encoded in intron 4 of notch-1, to uncover the identity of one such precursor genomic element and the selective forces acting up...
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/PMC7203229/ https://www.ncbi.nlm.nih.gov/pubmed/32376854 http://dx.doi.org/10.1038/s41540-020-0131-2 |
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author | Farahani, Ramin M. Rezaei-Lotfi, Saba Hunter, Neil |
author_facet | Farahani, Ramin M. Rezaei-Lotfi, Saba Hunter, Neil |
author_sort | Farahani, Ramin M. |
collection | PubMed |
description | The genomic platform that informs evolution of microRNA cascades remains unknown. Here we capitalised on the recent evolutionary trajectory of hominin-specific miRNA-4673, encoded in intron 4 of notch-1, to uncover the identity of one such precursor genomic element and the selective forces acting upon it. The miRNA targets genes that regulate Wnt/β-catenin signalling cascade. Primary sequence of the microRNA and its target region in Wnt modulating genes evolved from homologous signatures mapped to homotypic cis-clusters recognised by TCF3/4 and TFAP2A/B/C families. Integration of homologous TFAP2A/B/C cis-clusters (short range inhibitor of β-catenin) into the transcriptional landscape of Wnt cascade genes can reduce noise in gene expression. Probabilistic adoption of miRNA secondary structure by one such cis-signature in notch-1 reflected selection for superhelical curvature symmetry of precursor DNA to localise a nucleosome that overlapped the latter cis-cluster. By replicating the cis-cluster signature, non-random interactions of the miRNA with key Wnt modulator genes expanded the transcriptional noise buffering capacity via a coherent feed-forward loop mechanism. In consequence, an autonomous transcriptional noise dampener (the cis-cluster/nucleosome) evolved into a post-transcriptional one (the miRNA). The findings suggest a latent potential for remodelling of transcriptional landscape by miRNAs that capitalise on non-random distribution of genomic cis-signatures. |
format | Online Article Text |
id | pubmed-7203229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72032292020-05-14 Genomic competition for noise reduction shaped evolutionary landscape of mir-4673 Farahani, Ramin M. Rezaei-Lotfi, Saba Hunter, Neil NPJ Syst Biol Appl Article The genomic platform that informs evolution of microRNA cascades remains unknown. Here we capitalised on the recent evolutionary trajectory of hominin-specific miRNA-4673, encoded in intron 4 of notch-1, to uncover the identity of one such precursor genomic element and the selective forces acting upon it. The miRNA targets genes that regulate Wnt/β-catenin signalling cascade. Primary sequence of the microRNA and its target region in Wnt modulating genes evolved from homologous signatures mapped to homotypic cis-clusters recognised by TCF3/4 and TFAP2A/B/C families. Integration of homologous TFAP2A/B/C cis-clusters (short range inhibitor of β-catenin) into the transcriptional landscape of Wnt cascade genes can reduce noise in gene expression. Probabilistic adoption of miRNA secondary structure by one such cis-signature in notch-1 reflected selection for superhelical curvature symmetry of precursor DNA to localise a nucleosome that overlapped the latter cis-cluster. By replicating the cis-cluster signature, non-random interactions of the miRNA with key Wnt modulator genes expanded the transcriptional noise buffering capacity via a coherent feed-forward loop mechanism. In consequence, an autonomous transcriptional noise dampener (the cis-cluster/nucleosome) evolved into a post-transcriptional one (the miRNA). The findings suggest a latent potential for remodelling of transcriptional landscape by miRNAs that capitalise on non-random distribution of genomic cis-signatures. Nature Publishing Group UK 2020-05-06 /pmc/articles/PMC7203229/ /pubmed/32376854 http://dx.doi.org/10.1038/s41540-020-0131-2 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 Farahani, Ramin M. Rezaei-Lotfi, Saba Hunter, Neil Genomic competition for noise reduction shaped evolutionary landscape of mir-4673 |
title | Genomic competition for noise reduction shaped evolutionary landscape of mir-4673 |
title_full | Genomic competition for noise reduction shaped evolutionary landscape of mir-4673 |
title_fullStr | Genomic competition for noise reduction shaped evolutionary landscape of mir-4673 |
title_full_unstemmed | Genomic competition for noise reduction shaped evolutionary landscape of mir-4673 |
title_short | Genomic competition for noise reduction shaped evolutionary landscape of mir-4673 |
title_sort | genomic competition for noise reduction shaped evolutionary landscape of mir-4673 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203229/ https://www.ncbi.nlm.nih.gov/pubmed/32376854 http://dx.doi.org/10.1038/s41540-020-0131-2 |
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