Cargando…

Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility

Sustainable utilization of lignocellulosic perennial grass feedstocks will be enabled by high biomass production and optimized cell wall chemistry for efficient conversion into biofuels. MicroRNAs are regulatory elements that modulate the expression of genes involved in various biological functions...

Descripción completa

Detalles Bibliográficos
Autores principales: Baxter, Holly L., Mazarei, Mitra, Dumitrache, Alexandru, Natzke, Jace M., Rodriguez, Miguel, Gou, Jiqing, Fu, Chunxiang, Sykes, Robert W., Turner, Geoffrey B., Davis, Mark F., Brown, Steven D., Davison, Brian H., Wang, Zeng‐Yu, Stewart, C. Neal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785337/
https://www.ncbi.nlm.nih.gov/pubmed/28436149
http://dx.doi.org/10.1111/pbi.12747
_version_ 1783295600511418368
author Baxter, Holly L.
Mazarei, Mitra
Dumitrache, Alexandru
Natzke, Jace M.
Rodriguez, Miguel
Gou, Jiqing
Fu, Chunxiang
Sykes, Robert W.
Turner, Geoffrey B.
Davis, Mark F.
Brown, Steven D.
Davison, Brian H.
Wang, Zeng‐Yu
Stewart, C. Neal
author_facet Baxter, Holly L.
Mazarei, Mitra
Dumitrache, Alexandru
Natzke, Jace M.
Rodriguez, Miguel
Gou, Jiqing
Fu, Chunxiang
Sykes, Robert W.
Turner, Geoffrey B.
Davis, Mark F.
Brown, Steven D.
Davison, Brian H.
Wang, Zeng‐Yu
Stewart, C. Neal
author_sort Baxter, Holly L.
collection PubMed
description Sustainable utilization of lignocellulosic perennial grass feedstocks will be enabled by high biomass production and optimized cell wall chemistry for efficient conversion into biofuels. MicroRNAs are regulatory elements that modulate the expression of genes involved in various biological functions in plants, including growth and development. In greenhouse studies, overexpressing a microRNA (miR156) gene in switchgrass had dramatic effects on plant architecture and flowering, which appeared to be driven by transgene expression levels. High expressing lines were extremely dwarfed, whereas low and moderate‐expressing lines had higher biomass yields, improved sugar release and delayed flowering. Four lines with moderate or low miR156 overexpression from the prior greenhouse study were selected for a field experiment to assess the relationship between miR156 expression and biomass production over three years. We also analysed important bioenergy feedstock traits such as flowering, disease resistance, cell wall chemistry and biofuel production. Phenotypes of the transgenic lines were inconsistent between the greenhouse and the field as well as among different field growing seasons. One low expressing transgenic line consistently produced more biomass (25%–56%) than the control across all three seasons, which translated to the production of 30% more biofuel per plant during the final season. The other three transgenic lines produced less biomass than the control by the final season, and the two lines with moderate expression levels also exhibited altered disease susceptibilities. Results of this study emphasize the importance of performing multiyear field studies for plants with altered regulatory transgenes that target plant growth and development.
format Online
Article
Text
id pubmed-5785337
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-57853372018-02-02 Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility Baxter, Holly L. Mazarei, Mitra Dumitrache, Alexandru Natzke, Jace M. Rodriguez, Miguel Gou, Jiqing Fu, Chunxiang Sykes, Robert W. Turner, Geoffrey B. Davis, Mark F. Brown, Steven D. Davison, Brian H. Wang, Zeng‐Yu Stewart, C. Neal Plant Biotechnol J Research Articles Sustainable utilization of lignocellulosic perennial grass feedstocks will be enabled by high biomass production and optimized cell wall chemistry for efficient conversion into biofuels. MicroRNAs are regulatory elements that modulate the expression of genes involved in various biological functions in plants, including growth and development. In greenhouse studies, overexpressing a microRNA (miR156) gene in switchgrass had dramatic effects on plant architecture and flowering, which appeared to be driven by transgene expression levels. High expressing lines were extremely dwarfed, whereas low and moderate‐expressing lines had higher biomass yields, improved sugar release and delayed flowering. Four lines with moderate or low miR156 overexpression from the prior greenhouse study were selected for a field experiment to assess the relationship between miR156 expression and biomass production over three years. We also analysed important bioenergy feedstock traits such as flowering, disease resistance, cell wall chemistry and biofuel production. Phenotypes of the transgenic lines were inconsistent between the greenhouse and the field as well as among different field growing seasons. One low expressing transgenic line consistently produced more biomass (25%–56%) than the control across all three seasons, which translated to the production of 30% more biofuel per plant during the final season. The other three transgenic lines produced less biomass than the control by the final season, and the two lines with moderate expression levels also exhibited altered disease susceptibilities. Results of this study emphasize the importance of performing multiyear field studies for plants with altered regulatory transgenes that target plant growth and development. John Wiley and Sons Inc. 2017-06-20 2018-01 /pmc/articles/PMC5785337/ /pubmed/28436149 http://dx.doi.org/10.1111/pbi.12747 Text en © 2017 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Baxter, Holly L.
Mazarei, Mitra
Dumitrache, Alexandru
Natzke, Jace M.
Rodriguez, Miguel
Gou, Jiqing
Fu, Chunxiang
Sykes, Robert W.
Turner, Geoffrey B.
Davis, Mark F.
Brown, Steven D.
Davison, Brian H.
Wang, Zeng‐Yu
Stewart, C. Neal
Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility
title Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility
title_full Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility
title_fullStr Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility
title_full_unstemmed Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility
title_short Transgenic miR156 switchgrass in the field: growth, recalcitrance and rust susceptibility
title_sort transgenic mir156 switchgrass in the field: growth, recalcitrance and rust susceptibility
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785337/
https://www.ncbi.nlm.nih.gov/pubmed/28436149
http://dx.doi.org/10.1111/pbi.12747
work_keys_str_mv AT baxterhollyl transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT mazareimitra transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT dumitrachealexandru transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT natzkejacem transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT rodriguezmiguel transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT goujiqing transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT fuchunxiang transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT sykesrobertw transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT turnergeoffreyb transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT davismarkf transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT brownstevend transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT davisonbrianh transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT wangzengyu transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility
AT stewartcneal transgenicmir156switchgrassinthefieldgrowthrecalcitranceandrustsusceptibility