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Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants

Transposable element (TE)-derived genes are increasingly recognized as major sources conferring essential traits in agriculturally important crops but underlying evolutionary mechanisms remain obscure. We updated previous annotations and constructed 18,744 FAR-RED IMPAIRED RESPONSE1 (FAR1) genes, a...

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Autores principales: Young Chae, Geun, Hong, Woo-Jong, Jeong Jang, Min, Jung, Ki-Hong, Kim, Seungill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599713/
https://www.ncbi.nlm.nih.gov/pubmed/34725701
http://dx.doi.org/10.1093/nar/gkab932
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author Young Chae, Geun
Hong, Woo-Jong
Jeong Jang, Min
Jung, Ki-Hong
Kim, Seungill
author_facet Young Chae, Geun
Hong, Woo-Jong
Jeong Jang, Min
Jung, Ki-Hong
Kim, Seungill
author_sort Young Chae, Geun
collection PubMed
description Transposable element (TE)-derived genes are increasingly recognized as major sources conferring essential traits in agriculturally important crops but underlying evolutionary mechanisms remain obscure. We updated previous annotations and constructed 18,744 FAR-RED IMPAIRED RESPONSE1 (FAR1) genes, a transcription factor family derived from Mutator-like elements (MULEs), from 80 plant species, including 15,546 genes omitted in previous annotations. In-depth sequence comparison of the updated gene repertoire revealed that FAR1 genes underwent continuous structural divergence via frameshift and nonsense mutations that caused premature translation termination or specific domain truncations. CRISPR/Cas9-based genome editing and transcriptome analysis determined a novel gene involved in fertility-regulating transcription of rice pollen, denoting the functional capacity of our re-annotated gene models especially in monocots which had the highest copy numbers. Genomic evidence showed that the functional gene adapted by obtaining a shortened form through a frameshift mutation caused by a tandem duplication of a 79-bp sequence resulting in premature translation termination. Our findings provide improved resources for comprehensive studies of FAR1 genes with beneficial agricultural traits and unveil novel evolutionary mechanisms generating structural divergence and subsequent adaptation of TE-derived genes in plants.
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spelling pubmed-85997132021-11-18 Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants Young Chae, Geun Hong, Woo-Jong Jeong Jang, Min Jung, Ki-Hong Kim, Seungill Nucleic Acids Res Genomics Transposable element (TE)-derived genes are increasingly recognized as major sources conferring essential traits in agriculturally important crops but underlying evolutionary mechanisms remain obscure. We updated previous annotations and constructed 18,744 FAR-RED IMPAIRED RESPONSE1 (FAR1) genes, a transcription factor family derived from Mutator-like elements (MULEs), from 80 plant species, including 15,546 genes omitted in previous annotations. In-depth sequence comparison of the updated gene repertoire revealed that FAR1 genes underwent continuous structural divergence via frameshift and nonsense mutations that caused premature translation termination or specific domain truncations. CRISPR/Cas9-based genome editing and transcriptome analysis determined a novel gene involved in fertility-regulating transcription of rice pollen, denoting the functional capacity of our re-annotated gene models especially in monocots which had the highest copy numbers. Genomic evidence showed that the functional gene adapted by obtaining a shortened form through a frameshift mutation caused by a tandem duplication of a 79-bp sequence resulting in premature translation termination. Our findings provide improved resources for comprehensive studies of FAR1 genes with beneficial agricultural traits and unveil novel evolutionary mechanisms generating structural divergence and subsequent adaptation of TE-derived genes in plants. Oxford University Press 2021-11-02 /pmc/articles/PMC8599713/ /pubmed/34725701 http://dx.doi.org/10.1093/nar/gkab932 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Young Chae, Geun
Hong, Woo-Jong
Jeong Jang, Min
Jung, Ki-Hong
Kim, Seungill
Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants
title Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants
title_full Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants
title_fullStr Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants
title_full_unstemmed Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants
title_short Recurrent mutations promote widespread structural and functional divergence of MULE-derived genes in plants
title_sort recurrent mutations promote widespread structural and functional divergence of mule-derived genes in plants
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599713/
https://www.ncbi.nlm.nih.gov/pubmed/34725701
http://dx.doi.org/10.1093/nar/gkab932
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