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Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection
Small RNA (sRNA) plays a central role in RNA silencing in fungi. The genome of Fusarium graminearum gemytripvirus 1 (FgGMTV1) is comprised of three DNA segments: DNA-A, DNA-B, and DNA-C. DNA-A and DNA-B are associated with fungal growth and virulence reduction. To elucidate the role of RNA silencing...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781238/ https://www.ncbi.nlm.nih.gov/pubmed/36547570 http://dx.doi.org/10.3390/jof8121237 |
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author | Wang, Shuangchao Ruan, Shaojian Zhang, Mingming Nie, Jianhua Nzabanita, Clement Guo, Lihua |
author_facet | Wang, Shuangchao Ruan, Shaojian Zhang, Mingming Nie, Jianhua Nzabanita, Clement Guo, Lihua |
author_sort | Wang, Shuangchao |
collection | PubMed |
description | Small RNA (sRNA) plays a central role in RNA silencing in fungi. The genome of Fusarium graminearum gemytripvirus 1 (FgGMTV1) is comprised of three DNA segments: DNA-A, DNA-B, and DNA-C. DNA-A and DNA-B are associated with fungal growth and virulence reduction. To elucidate the role of RNA silencing during the interactions of fungi and viruses, the sRNA profiles of F. graminearum in association with FgGMTV1 were established, using an FgGMTV1-free library (S-S), a library for infection with the DNA-A and DNA-B segments (S-AB), and a library for infection with the DNA-A, DNA-B, and DNA-C segments (S-ABC). A large amount of virus-derived sRNA (vsiRNA) was detected in the S-AB and S-ABC libraries, accounting for 9.9% and 13.8% of the total sRNA, respectively, indicating that FgGMTV1 triggers host RNA silencing. The total numbers of sRNA reads differed among the three libraries, suggesting that FgGMTV1 infection interferes with host RNA silencing. In addition, the relative proportions of the different sRNA lengths were altered in the S-AB and S-ABC libraries. The genome distribution patterns of the mapping of vsiRNA to DNA-A and DNA-B in the S-AB and S-ABC libraries were also different. These results suggest the influence of DNA-C on host RNA silencing. Transcripts targeted by vsiRNAs were enriched in pathways that included flavin adenine dinucleotide binding, protein folding, and filamentous growth. |
format | Online Article Text |
id | pubmed-9781238 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97812382022-12-24 Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection Wang, Shuangchao Ruan, Shaojian Zhang, Mingming Nie, Jianhua Nzabanita, Clement Guo, Lihua J Fungi (Basel) Article Small RNA (sRNA) plays a central role in RNA silencing in fungi. The genome of Fusarium graminearum gemytripvirus 1 (FgGMTV1) is comprised of three DNA segments: DNA-A, DNA-B, and DNA-C. DNA-A and DNA-B are associated with fungal growth and virulence reduction. To elucidate the role of RNA silencing during the interactions of fungi and viruses, the sRNA profiles of F. graminearum in association with FgGMTV1 were established, using an FgGMTV1-free library (S-S), a library for infection with the DNA-A and DNA-B segments (S-AB), and a library for infection with the DNA-A, DNA-B, and DNA-C segments (S-ABC). A large amount of virus-derived sRNA (vsiRNA) was detected in the S-AB and S-ABC libraries, accounting for 9.9% and 13.8% of the total sRNA, respectively, indicating that FgGMTV1 triggers host RNA silencing. The total numbers of sRNA reads differed among the three libraries, suggesting that FgGMTV1 infection interferes with host RNA silencing. In addition, the relative proportions of the different sRNA lengths were altered in the S-AB and S-ABC libraries. The genome distribution patterns of the mapping of vsiRNA to DNA-A and DNA-B in the S-AB and S-ABC libraries were also different. These results suggest the influence of DNA-C on host RNA silencing. Transcripts targeted by vsiRNAs were enriched in pathways that included flavin adenine dinucleotide binding, protein folding, and filamentous growth. MDPI 2022-11-22 /pmc/articles/PMC9781238/ /pubmed/36547570 http://dx.doi.org/10.3390/jof8121237 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Shuangchao Ruan, Shaojian Zhang, Mingming Nie, Jianhua Nzabanita, Clement Guo, Lihua Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection |
title | Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection |
title_full | Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection |
title_fullStr | Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection |
title_full_unstemmed | Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection |
title_short | Interference of Small RNAs in Fusarium graminearum through FgGMTV1 Infection |
title_sort | interference of small rnas in fusarium graminearum through fggmtv1 infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9781238/ https://www.ncbi.nlm.nih.gov/pubmed/36547570 http://dx.doi.org/10.3390/jof8121237 |
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