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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
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.
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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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