Genome-Wide Analyses of Repeat-Induced Point Mutations in the Ascomycota

The Repeat-Induced Point (RIP) mutation pathway is a fungus-specific genome defense mechanism that mitigates the deleterious consequences of repeated genomic regions and transposable elements (TEs). RIP mutates targeted sequences by introducing cytosine to thymine transitions. We investigated the ge...

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Main Authors: Stephanie van Wyk, Brenda D. Wingfield, Lieschen De Vos, Nicolaas A. van der Merwe, Emma T. Steenkamp
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Microbiology
Subjects:
RIP
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2020.622368/full
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spelling doaj-0e04ebe9f54e47ceb25e457a679c8e212021-02-01T04:56:59ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2021-02-011110.3389/fmicb.2020.622368622368Genome-Wide Analyses of Repeat-Induced Point Mutations in the AscomycotaStephanie van WykBrenda D. WingfieldLieschen De VosNicolaas A. van der MerweEmma T. SteenkampThe Repeat-Induced Point (RIP) mutation pathway is a fungus-specific genome defense mechanism that mitigates the deleterious consequences of repeated genomic regions and transposable elements (TEs). RIP mutates targeted sequences by introducing cytosine to thymine transitions. We investigated the genome-wide occurrence and extent of RIP with a sliding-window approach. Using genome-wide RIP data and two sets of control groups, the association between RIP, TEs, and GC content were contrasted in organisms capable and incapable of RIP. Based on these data, we then set out to determine the extent and occurrence of RIP in 58 representatives of the Ascomycota. The findings were summarized by placing each of the fungi investigated in one of six categories based on the extent of genome-wide RIP. In silico RIP analyses, using a sliding-window approach with stringent RIP parameters, implemented simultaneously within the same genetic context, on high quality genome assemblies, yielded superior results in determining the genome-wide RIP among the Ascomycota. Most Ascomycota had RIP and these mutations were particularly widespread among classes of the Pezizomycotina, including the early diverging Orbiliomycetes and the Pezizomycetes. The most extreme cases of RIP were limited to representatives of the Dothideomycetes and Sordariomycetes. By contrast, the genomes of the Taphrinomycotina and Saccharomycotina contained no detectable evidence of RIP. Also, recent losses in RIP combined with controlled TE proliferation in the Pezizomycotina subphyla may promote substantial genome enlargement as well as the formation of sub-genomic compartments. These findings have broadened our understanding of the taxonomic range and extent of RIP in Ascomycota and how this pathway affects the genomes of fungi harboring it.https://www.frontiersin.org/articles/10.3389/fmicb.2020.622368/fullrepeat-induced point mutationRIPAscomycotagenome evolutionGC content
collection DOAJ
language English
format Article
sources DOAJ
author Stephanie van Wyk
Brenda D. Wingfield
Lieschen De Vos
Nicolaas A. van der Merwe
Emma T. Steenkamp
spellingShingle Stephanie van Wyk
Brenda D. Wingfield
Lieschen De Vos
Nicolaas A. van der Merwe
Emma T. Steenkamp
Genome-Wide Analyses of Repeat-Induced Point Mutations in the Ascomycota
Frontiers in Microbiology
repeat-induced point mutation
RIP
Ascomycota
genome evolution
GC content
author_facet Stephanie van Wyk
Brenda D. Wingfield
Lieschen De Vos
Nicolaas A. van der Merwe
Emma T. Steenkamp
author_sort Stephanie van Wyk
title Genome-Wide Analyses of Repeat-Induced Point Mutations in the Ascomycota
title_short Genome-Wide Analyses of Repeat-Induced Point Mutations in the Ascomycota
title_full Genome-Wide Analyses of Repeat-Induced Point Mutations in the Ascomycota
title_fullStr Genome-Wide Analyses of Repeat-Induced Point Mutations in the Ascomycota
title_full_unstemmed Genome-Wide Analyses of Repeat-Induced Point Mutations in the Ascomycota
title_sort genome-wide analyses of repeat-induced point mutations in the ascomycota
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2021-02-01
description The Repeat-Induced Point (RIP) mutation pathway is a fungus-specific genome defense mechanism that mitigates the deleterious consequences of repeated genomic regions and transposable elements (TEs). RIP mutates targeted sequences by introducing cytosine to thymine transitions. We investigated the genome-wide occurrence and extent of RIP with a sliding-window approach. Using genome-wide RIP data and two sets of control groups, the association between RIP, TEs, and GC content were contrasted in organisms capable and incapable of RIP. Based on these data, we then set out to determine the extent and occurrence of RIP in 58 representatives of the Ascomycota. The findings were summarized by placing each of the fungi investigated in one of six categories based on the extent of genome-wide RIP. In silico RIP analyses, using a sliding-window approach with stringent RIP parameters, implemented simultaneously within the same genetic context, on high quality genome assemblies, yielded superior results in determining the genome-wide RIP among the Ascomycota. Most Ascomycota had RIP and these mutations were particularly widespread among classes of the Pezizomycotina, including the early diverging Orbiliomycetes and the Pezizomycetes. The most extreme cases of RIP were limited to representatives of the Dothideomycetes and Sordariomycetes. By contrast, the genomes of the Taphrinomycotina and Saccharomycotina contained no detectable evidence of RIP. Also, recent losses in RIP combined with controlled TE proliferation in the Pezizomycotina subphyla may promote substantial genome enlargement as well as the formation of sub-genomic compartments. These findings have broadened our understanding of the taxonomic range and extent of RIP in Ascomycota and how this pathway affects the genomes of fungi harboring it.
topic repeat-induced point mutation
RIP
Ascomycota
genome evolution
GC content
url https://www.frontiersin.org/articles/10.3389/fmicb.2020.622368/full
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