Cargando…

Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus

Newly emerged wheat blast disease is a serious threat to global wheat production. Wheat blast is caused by a distinct, exceptionally diverse lineage of the fungus causing rice blast disease. Through sequencing a recent field isolate, we report a reference genome that includes seven core chromosomes...

Descripción completa

Detalles Bibliográficos
Autores principales: Peng, Zhao, Oliveira-Garcia, Ely, Lin, Guifang, Hu, Ying, Dalby, Melinda, Migeon, Pierre, Tang, Haibao, Farman, Mark, Cook, David, White, Frank F., Valent, Barbara, Liu, Sanzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741851/
https://www.ncbi.nlm.nih.gov/pubmed/31513573
http://dx.doi.org/10.1371/journal.pgen.1008272
_version_ 1783451083864014848
author Peng, Zhao
Oliveira-Garcia, Ely
Lin, Guifang
Hu, Ying
Dalby, Melinda
Migeon, Pierre
Tang, Haibao
Farman, Mark
Cook, David
White, Frank F.
Valent, Barbara
Liu, Sanzhen
author_facet Peng, Zhao
Oliveira-Garcia, Ely
Lin, Guifang
Hu, Ying
Dalby, Melinda
Migeon, Pierre
Tang, Haibao
Farman, Mark
Cook, David
White, Frank F.
Valent, Barbara
Liu, Sanzhen
author_sort Peng, Zhao
collection PubMed
description Newly emerged wheat blast disease is a serious threat to global wheat production. Wheat blast is caused by a distinct, exceptionally diverse lineage of the fungus causing rice blast disease. Through sequencing a recent field isolate, we report a reference genome that includes seven core chromosomes and mini-chromosome sequences that harbor effector genes normally found on ends of core chromosomes in other strains. No mini-chromosomes were observed in an early field strain, and at least two from another isolate each contain different effector genes and core chromosome end sequences. The mini-chromosome is enriched in transposons occurring most frequently at core chromosome ends. Additionally, transposons in mini-chromosomes lack the characteristic signature for inactivation by repeat-induced point (RIP) mutation genome defenses. Our results, collectively, indicate that dispensable mini-chromosomes and core chromosomes undergo divergent evolutionary trajectories, and mini-chromosomes and core chromosome ends are coupled as a mobile, fast-evolving effector compartment in the wheat pathogen genome.
format Online
Article
Text
id pubmed-6741851
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-67418512019-09-20 Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus Peng, Zhao Oliveira-Garcia, Ely Lin, Guifang Hu, Ying Dalby, Melinda Migeon, Pierre Tang, Haibao Farman, Mark Cook, David White, Frank F. Valent, Barbara Liu, Sanzhen PLoS Genet Research Article Newly emerged wheat blast disease is a serious threat to global wheat production. Wheat blast is caused by a distinct, exceptionally diverse lineage of the fungus causing rice blast disease. Through sequencing a recent field isolate, we report a reference genome that includes seven core chromosomes and mini-chromosome sequences that harbor effector genes normally found on ends of core chromosomes in other strains. No mini-chromosomes were observed in an early field strain, and at least two from another isolate each contain different effector genes and core chromosome end sequences. The mini-chromosome is enriched in transposons occurring most frequently at core chromosome ends. Additionally, transposons in mini-chromosomes lack the characteristic signature for inactivation by repeat-induced point (RIP) mutation genome defenses. Our results, collectively, indicate that dispensable mini-chromosomes and core chromosomes undergo divergent evolutionary trajectories, and mini-chromosomes and core chromosome ends are coupled as a mobile, fast-evolving effector compartment in the wheat pathogen genome. Public Library of Science 2019-09-12 /pmc/articles/PMC6741851/ /pubmed/31513573 http://dx.doi.org/10.1371/journal.pgen.1008272 Text en © 2019 Peng et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Peng, Zhao
Oliveira-Garcia, Ely
Lin, Guifang
Hu, Ying
Dalby, Melinda
Migeon, Pierre
Tang, Haibao
Farman, Mark
Cook, David
White, Frank F.
Valent, Barbara
Liu, Sanzhen
Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
title Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
title_full Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
title_fullStr Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
title_full_unstemmed Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
title_short Effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
title_sort effector gene reshuffling involves dispensable mini-chromosomes in the wheat blast fungus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741851/
https://www.ncbi.nlm.nih.gov/pubmed/31513573
http://dx.doi.org/10.1371/journal.pgen.1008272
work_keys_str_mv AT pengzhao effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT oliveiragarciaely effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT linguifang effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT huying effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT dalbymelinda effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT migeonpierre effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT tanghaibao effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT farmanmark effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT cookdavid effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT whitefrankf effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT valentbarbara effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus
AT liusanzhen effectorgenereshufflinginvolvesdispensableminichromosomesinthewheatblastfungus