Cargando…
Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer
Evidence for ancestral gene transfer between Epichloë fungal endophyte ancestors and their host grass species is described. From genomes of cool-season grasses (the Poeae tribe), two Epichloë-originated genes were identified through DNA sequence similarity analysis. The two genes showed 96% and 85%...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670438/ https://www.ncbi.nlm.nih.gov/pubmed/33199756 http://dx.doi.org/10.1038/s41598-020-76478-4 |
_version_ | 1783610737940234240 |
---|---|
author | Shinozuka, Hiroshi Shinozuka, Maiko de Vries, Ellen M. Sawbridge, Timothy I. Spangenberg, German C. Cocks, Benjamin G. |
author_facet | Shinozuka, Hiroshi Shinozuka, Maiko de Vries, Ellen M. Sawbridge, Timothy I. Spangenberg, German C. Cocks, Benjamin G. |
author_sort | Shinozuka, Hiroshi |
collection | PubMed |
description | Evidence for ancestral gene transfer between Epichloë fungal endophyte ancestors and their host grass species is described. From genomes of cool-season grasses (the Poeae tribe), two Epichloë-originated genes were identified through DNA sequence similarity analysis. The two genes showed 96% and 85% DNA sequence identities between the corresponding Epichloë genes. One of the genes was specific to the Loliinae sub-tribe. The other gene was more widely conserved in the Poeae and Triticeae tribes, including wheat (Triticum aestivum L.) and barley (Hordeum vulgare L.). The genes were independently transferred during the last 39 million years. The transferred genes were expressed in plant tissues, presumably retaining molecular functions. Multiple gene transfer events between the specific plant and fungal lineages are unique. A range of cereal crops is included in the Poeae and Triticeae tribes, and the Loliinae sub-tribe is consisted of economically important pasture and forage crops. Identification and characterisation of the 'natural' adaptation transgenes in the genomes of cereals, and pasture and forage grasses, that worldwide underpin the production of major foods, such as bread, meat, and milk, may change the ‘unnatural’ perception status of transgenic and gene-edited plants. |
format | Online Article Text |
id | pubmed-7670438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76704382020-11-18 Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer Shinozuka, Hiroshi Shinozuka, Maiko de Vries, Ellen M. Sawbridge, Timothy I. Spangenberg, German C. Cocks, Benjamin G. Sci Rep Article Evidence for ancestral gene transfer between Epichloë fungal endophyte ancestors and their host grass species is described. From genomes of cool-season grasses (the Poeae tribe), two Epichloë-originated genes were identified through DNA sequence similarity analysis. The two genes showed 96% and 85% DNA sequence identities between the corresponding Epichloë genes. One of the genes was specific to the Loliinae sub-tribe. The other gene was more widely conserved in the Poeae and Triticeae tribes, including wheat (Triticum aestivum L.) and barley (Hordeum vulgare L.). The genes were independently transferred during the last 39 million years. The transferred genes were expressed in plant tissues, presumably retaining molecular functions. Multiple gene transfer events between the specific plant and fungal lineages are unique. A range of cereal crops is included in the Poeae and Triticeae tribes, and the Loliinae sub-tribe is consisted of economically important pasture and forage crops. Identification and characterisation of the 'natural' adaptation transgenes in the genomes of cereals, and pasture and forage grasses, that worldwide underpin the production of major foods, such as bread, meat, and milk, may change the ‘unnatural’ perception status of transgenic and gene-edited plants. Nature Publishing Group UK 2020-11-16 /pmc/articles/PMC7670438/ /pubmed/33199756 http://dx.doi.org/10.1038/s41598-020-76478-4 Text en © Crown 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Shinozuka, Hiroshi Shinozuka, Maiko de Vries, Ellen M. Sawbridge, Timothy I. Spangenberg, German C. Cocks, Benjamin G. Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer |
title | Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer |
title_full | Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer |
title_fullStr | Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer |
title_full_unstemmed | Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer |
title_short | Fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer |
title_sort | fungus-originated genes in the genomes of cereal and pasture grasses acquired through ancient lateral transfer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670438/ https://www.ncbi.nlm.nih.gov/pubmed/33199756 http://dx.doi.org/10.1038/s41598-020-76478-4 |
work_keys_str_mv | AT shinozukahiroshi fungusoriginatedgenesinthegenomesofcerealandpasturegrassesacquiredthroughancientlateraltransfer AT shinozukamaiko fungusoriginatedgenesinthegenomesofcerealandpasturegrassesacquiredthroughancientlateraltransfer AT devriesellenm fungusoriginatedgenesinthegenomesofcerealandpasturegrassesacquiredthroughancientlateraltransfer AT sawbridgetimothyi fungusoriginatedgenesinthegenomesofcerealandpasturegrassesacquiredthroughancientlateraltransfer AT spangenberggermanc fungusoriginatedgenesinthegenomesofcerealandpasturegrassesacquiredthroughancientlateraltransfer AT cocksbenjaming fungusoriginatedgenesinthegenomesofcerealandpasturegrassesacquiredthroughancientlateraltransfer |