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Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution
BACKGROUND: The fungus Marssonina brunnea is a causal pathogen of Marssonina leaf spot that devastates poplar plantations by defoliating susceptible trees before normal fall leaf drop. RESULTS: We sequence the genome of M. brunnea with a size of 52 Mb assembled into 89 scaffolds, representing the fi...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484023/ https://www.ncbi.nlm.nih.gov/pubmed/22876864 http://dx.doi.org/10.1186/1471-2164-13-382 |
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author | Zhu, Sheng Cao, You-Zhi Jiang, Cong Tan, Bi-Yue Wang, Zhong Feng, Sisi Zhang, Liang Su, Xiao-Hua Brejova, Brona Vinar, Tomas Xu, Meng Wang, Ming-Xiu Zhang, Shou-Gong Huang, Min-Ren Wu, Rongling Zhou, Yan |
author_facet | Zhu, Sheng Cao, You-Zhi Jiang, Cong Tan, Bi-Yue Wang, Zhong Feng, Sisi Zhang, Liang Su, Xiao-Hua Brejova, Brona Vinar, Tomas Xu, Meng Wang, Ming-Xiu Zhang, Shou-Gong Huang, Min-Ren Wu, Rongling Zhou, Yan |
author_sort | Zhu, Sheng |
collection | PubMed |
description | BACKGROUND: The fungus Marssonina brunnea is a causal pathogen of Marssonina leaf spot that devastates poplar plantations by defoliating susceptible trees before normal fall leaf drop. RESULTS: We sequence the genome of M. brunnea with a size of 52 Mb assembled into 89 scaffolds, representing the first sequenced Dermateaceae genome. By inoculating this fungus onto a poplar hybrid clone, we investigate how M. brunnea interacts and co-evolves with its host to colonize poplar leaves. While a handful of virulence genes in M. brunnea, mostly from the LysM family, are detected to up-regulate during infection, the poplar down-regulates its resistance genes, such as nucleotide binding site domains and leucine rich repeats, in response to infection. From 10,027 predicted proteins of M. brunnea in a comparison with those from poplar, we identify four poplar transferases that stimulate the host to resist M. brunnea. These transferas-encoding genes may have driven the co-evolution of M. brunnea and Populus during the process of infection and anti-infection. CONCLUSIONS: Our results from the draft sequence of the M. brunnea genome provide evidence for genome-genome interactions that play an important role in poplar-pathogen co-evolution. This knowledge could help to design effective strategies for controlling Marssonina leaf spot in poplar. |
format | Online Article Text |
id | pubmed-3484023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34840232012-10-31 Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution Zhu, Sheng Cao, You-Zhi Jiang, Cong Tan, Bi-Yue Wang, Zhong Feng, Sisi Zhang, Liang Su, Xiao-Hua Brejova, Brona Vinar, Tomas Xu, Meng Wang, Ming-Xiu Zhang, Shou-Gong Huang, Min-Ren Wu, Rongling Zhou, Yan BMC Genomics Research Article BACKGROUND: The fungus Marssonina brunnea is a causal pathogen of Marssonina leaf spot that devastates poplar plantations by defoliating susceptible trees before normal fall leaf drop. RESULTS: We sequence the genome of M. brunnea with a size of 52 Mb assembled into 89 scaffolds, representing the first sequenced Dermateaceae genome. By inoculating this fungus onto a poplar hybrid clone, we investigate how M. brunnea interacts and co-evolves with its host to colonize poplar leaves. While a handful of virulence genes in M. brunnea, mostly from the LysM family, are detected to up-regulate during infection, the poplar down-regulates its resistance genes, such as nucleotide binding site domains and leucine rich repeats, in response to infection. From 10,027 predicted proteins of M. brunnea in a comparison with those from poplar, we identify four poplar transferases that stimulate the host to resist M. brunnea. These transferas-encoding genes may have driven the co-evolution of M. brunnea and Populus during the process of infection and anti-infection. CONCLUSIONS: Our results from the draft sequence of the M. brunnea genome provide evidence for genome-genome interactions that play an important role in poplar-pathogen co-evolution. This knowledge could help to design effective strategies for controlling Marssonina leaf spot in poplar. BioMed Central 2012-08-09 /pmc/articles/PMC3484023/ /pubmed/22876864 http://dx.doi.org/10.1186/1471-2164-13-382 Text en Copyright ©2012 Zhu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhu, Sheng Cao, You-Zhi Jiang, Cong Tan, Bi-Yue Wang, Zhong Feng, Sisi Zhang, Liang Su, Xiao-Hua Brejova, Brona Vinar, Tomas Xu, Meng Wang, Ming-Xiu Zhang, Shou-Gong Huang, Min-Ren Wu, Rongling Zhou, Yan Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution |
title | Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution |
title_full | Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution |
title_fullStr | Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution |
title_full_unstemmed | Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution |
title_short | Sequencing the genome of Marssonina brunnea reveals fungus-poplar co-evolution |
title_sort | sequencing the genome of marssonina brunnea reveals fungus-poplar co-evolution |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484023/ https://www.ncbi.nlm.nih.gov/pubmed/22876864 http://dx.doi.org/10.1186/1471-2164-13-382 |
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