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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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