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Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum
Intron lariats excised during the splicing process are rapidly degraded by RNA lariat debranching enzyme (Dbr1) and several exonucleases. Rapid turnover of lariat RNA is essential to cellular RNA homeostasis. However, the functions of Dbr1 have not been investigated in filamentous fungi. Here, we ch...
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/PMC9606315/ https://www.ncbi.nlm.nih.gov/pubmed/36289323 http://dx.doi.org/10.1038/s42003-022-04111-3 |
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author | Choi, Yejin Lee, Hyun-Hee Park, Jiyeun Kim, Sieun Choi, Soyoung Moon, Heeji Shin, Jiyoung Kim, Jung-Eun Choi, Gyung Ja Seo, Young-Su Son, Hokyoung |
author_facet | Choi, Yejin Lee, Hyun-Hee Park, Jiyeun Kim, Sieun Choi, Soyoung Moon, Heeji Shin, Jiyoung Kim, Jung-Eun Choi, Gyung Ja Seo, Young-Su Son, Hokyoung |
author_sort | Choi, Yejin |
collection | PubMed |
description | Intron lariats excised during the splicing process are rapidly degraded by RNA lariat debranching enzyme (Dbr1) and several exonucleases. Rapid turnover of lariat RNA is essential to cellular RNA homeostasis. However, the functions of Dbr1 have not been investigated in filamentous fungi. Here, we characterized the molecular functions of Dbr1 in Fusarium graminearum, a major fungal plant pathogen. Deletion of FgDBR1 resulted in pleiotropic defects in hyphal growth, conidiation, sexual reproduction, and virulence. Through transcriptome analysis, we revealed that the deletion mutant exhibited global accumulation of intron lariats and upregulation of ribosome-related genes. Excessive accumulation of lariat RNA led to reduced overall protein synthesis, causing various phenotypic defects in the absence of FgDBR1. The results of this study demonstrate that a compromised intron turnover process affects development and pathogenesis in this fungus and that Dbr1 function is critical to plant pathogenic fungi. |
format | Online Article Text |
id | pubmed-9606315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96063152022-10-28 Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum Choi, Yejin Lee, Hyun-Hee Park, Jiyeun Kim, Sieun Choi, Soyoung Moon, Heeji Shin, Jiyoung Kim, Jung-Eun Choi, Gyung Ja Seo, Young-Su Son, Hokyoung Commun Biol Article Intron lariats excised during the splicing process are rapidly degraded by RNA lariat debranching enzyme (Dbr1) and several exonucleases. Rapid turnover of lariat RNA is essential to cellular RNA homeostasis. However, the functions of Dbr1 have not been investigated in filamentous fungi. Here, we characterized the molecular functions of Dbr1 in Fusarium graminearum, a major fungal plant pathogen. Deletion of FgDBR1 resulted in pleiotropic defects in hyphal growth, conidiation, sexual reproduction, and virulence. Through transcriptome analysis, we revealed that the deletion mutant exhibited global accumulation of intron lariats and upregulation of ribosome-related genes. Excessive accumulation of lariat RNA led to reduced overall protein synthesis, causing various phenotypic defects in the absence of FgDBR1. The results of this study demonstrate that a compromised intron turnover process affects development and pathogenesis in this fungus and that Dbr1 function is critical to plant pathogenic fungi. Nature Publishing Group UK 2022-10-26 /pmc/articles/PMC9606315/ /pubmed/36289323 http://dx.doi.org/10.1038/s42003-022-04111-3 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 Choi, Yejin Lee, Hyun-Hee Park, Jiyeun Kim, Sieun Choi, Soyoung Moon, Heeji Shin, Jiyoung Kim, Jung-Eun Choi, Gyung Ja Seo, Young-Su Son, Hokyoung Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum |
title | Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum |
title_full | Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum |
title_fullStr | Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum |
title_full_unstemmed | Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum |
title_short | Intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus Fusarium graminearum |
title_sort | intron turnover is essential to the development and pathogenicity of the plant pathogenic fungus fusarium graminearum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9606315/ https://www.ncbi.nlm.nih.gov/pubmed/36289323 http://dx.doi.org/10.1038/s42003-022-04111-3 |
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