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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...

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Autores principales: Yu, Huihui, Li, Mu, Sandhu, Jaspreet, Sun, Guangchao, Schnable, James C., Walia, Harkamal, Xie, Weibo, Yu, Bin, Mower, Jeffrey P., Zhang, Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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