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Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants
It is challenging to identify the smallest microexons (≤15-nt) due to their small size. Consequently, these microexons are often misannotated or missed entirely during genome annotation. Here, we develop a pipeline to accurately identify 2,398 small microexons in 10 diverse plant species using 990 R...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831610/ https://www.ncbi.nlm.nih.gov/pubmed/35145097 http://dx.doi.org/10.1038/s41467-022-28449-8 |
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author | Yu, Huihui Li, Mu Sandhu, Jaspreet Sun, Guangchao Schnable, James C. Walia, Harkamal Xie, Weibo Yu, Bin Mower, Jeffrey P. Zhang, Chi |
author_facet | Yu, Huihui Li, Mu Sandhu, Jaspreet Sun, Guangchao Schnable, James C. Walia, Harkamal Xie, Weibo Yu, Bin Mower, Jeffrey P. Zhang, Chi |
author_sort | Yu, Huihui |
collection | PubMed |
description | It is challenging to identify the smallest microexons (≤15-nt) due to their small size. Consequently, these microexons are often misannotated or missed entirely during genome annotation. Here, we develop a pipeline to accurately identify 2,398 small microexons in 10 diverse plant species using 990 RNA-seq datasets, and most of them have not been annotated in the reference genomes. Analysis reveals that microexons tend to have increased detained flanking introns that require post-transcriptional splicing after polyadenylation. Examination of 45 conserved microexon clusters demonstrates that microexons and associated gene structures can be traced back to the origin of land plants. Based on these clusters, we develop an algorithm to genome-wide model coding microexons in 132 plants and find that microexons provide a strong phylogenetic signal for plant organismal relationships. Microexon modeling reveals diverse evolutionary trajectories, involving microexon gain and loss and alternative splicing. Our work provides a comprehensive view of microexons in plants. |
format | Online Article Text |
id | pubmed-8831610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88316102022-03-04 Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants Yu, Huihui Li, Mu Sandhu, Jaspreet Sun, Guangchao Schnable, James C. Walia, Harkamal Xie, Weibo Yu, Bin Mower, Jeffrey P. Zhang, Chi Nat Commun Article It is challenging to identify the smallest microexons (≤15-nt) due to their small size. Consequently, these microexons are often misannotated or missed entirely during genome annotation. Here, we develop a pipeline to accurately identify 2,398 small microexons in 10 diverse plant species using 990 RNA-seq datasets, and most of them have not been annotated in the reference genomes. Analysis reveals that microexons tend to have increased detained flanking introns that require post-transcriptional splicing after polyadenylation. Examination of 45 conserved microexon clusters demonstrates that microexons and associated gene structures can be traced back to the origin of land plants. Based on these clusters, we develop an algorithm to genome-wide model coding microexons in 132 plants and find that microexons provide a strong phylogenetic signal for plant organismal relationships. Microexon modeling reveals diverse evolutionary trajectories, involving microexon gain and loss and alternative splicing. Our work provides a comprehensive view of microexons in plants. Nature Publishing Group UK 2022-02-10 /pmc/articles/PMC8831610/ /pubmed/35145097 http://dx.doi.org/10.1038/s41467-022-28449-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yu, Huihui Li, Mu Sandhu, Jaspreet Sun, Guangchao Schnable, James C. Walia, Harkamal Xie, Weibo Yu, Bin Mower, Jeffrey P. Zhang, Chi Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants |
title | Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants |
title_full | Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants |
title_fullStr | Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants |
title_full_unstemmed | Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants |
title_short | Pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants |
title_sort | pervasive misannotation of microexons that are evolutionarily conserved and crucial for gene function in plants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831610/ https://www.ncbi.nlm.nih.gov/pubmed/35145097 http://dx.doi.org/10.1038/s41467-022-28449-8 |
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