Cargando…

Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits

Plant shoot systems derive from the shoot apical meristems (SAMs), pools of stems cells that are regulated by a feedback between the WUSCHEL (WUS) homeobox protein and CLAVATA (CLV) peptides and receptors. The maize heterotrimeric G protein α subunit COMPACT PLANT2 (CT2) functions with CLV receptors...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Qingyu, Regan, Michael, Furukawa, Hiro, Jackson, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945058/
https://www.ncbi.nlm.nih.gov/pubmed/29708966
http://dx.doi.org/10.1371/journal.pgen.1007374
_version_ 1783321936694083584
author Wu, Qingyu
Regan, Michael
Furukawa, Hiro
Jackson, David
author_facet Wu, Qingyu
Regan, Michael
Furukawa, Hiro
Jackson, David
author_sort Wu, Qingyu
collection PubMed
description Plant shoot systems derive from the shoot apical meristems (SAMs), pools of stems cells that are regulated by a feedback between the WUSCHEL (WUS) homeobox protein and CLAVATA (CLV) peptides and receptors. The maize heterotrimeric G protein α subunit COMPACT PLANT2 (CT2) functions with CLV receptors to regulate meristem development. In addition to the sole canonical Gα CT2, maize also contains three eXtra Large GTP-binding proteins (XLGs), which have a domain with homology to Gα as well as additional domains. By either forcing CT2 to be constitutively active, or by depleting XLGs using CRISPR-Cas9, here we show that both CT2 and XLGs play important roles in maize meristem regulation, and their manipulation improved agronomic traits. For example, we show that expression of a constitutively active CT2 resulted in higher spikelet density and kernel row number, larger ear inflorescence meristems (IMs) and more upright leaves, all beneficial traits selected during maize improvement. Our findings suggest that both the canonical Gα, CT2 and the non-canonical XLGs play important roles in maize meristem regulation and further demonstrate that weak alleles of plant stem cell regulatory genes have the capacity to improve agronomic traits.
format Online
Article
Text
id pubmed-5945058
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-59450582018-05-25 Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits Wu, Qingyu Regan, Michael Furukawa, Hiro Jackson, David PLoS Genet Research Article Plant shoot systems derive from the shoot apical meristems (SAMs), pools of stems cells that are regulated by a feedback between the WUSCHEL (WUS) homeobox protein and CLAVATA (CLV) peptides and receptors. The maize heterotrimeric G protein α subunit COMPACT PLANT2 (CT2) functions with CLV receptors to regulate meristem development. In addition to the sole canonical Gα CT2, maize also contains three eXtra Large GTP-binding proteins (XLGs), which have a domain with homology to Gα as well as additional domains. By either forcing CT2 to be constitutively active, or by depleting XLGs using CRISPR-Cas9, here we show that both CT2 and XLGs play important roles in maize meristem regulation, and their manipulation improved agronomic traits. For example, we show that expression of a constitutively active CT2 resulted in higher spikelet density and kernel row number, larger ear inflorescence meristems (IMs) and more upright leaves, all beneficial traits selected during maize improvement. Our findings suggest that both the canonical Gα, CT2 and the non-canonical XLGs play important roles in maize meristem regulation and further demonstrate that weak alleles of plant stem cell regulatory genes have the capacity to improve agronomic traits. Public Library of Science 2018-04-30 /pmc/articles/PMC5945058/ /pubmed/29708966 http://dx.doi.org/10.1371/journal.pgen.1007374 Text en © 2018 Wu 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
Wu, Qingyu
Regan, Michael
Furukawa, Hiro
Jackson, David
Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits
title Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits
title_full Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits
title_fullStr Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits
title_full_unstemmed Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits
title_short Role of heterotrimeric Gα proteins in maize development and enhancement of agronomic traits
title_sort role of heterotrimeric gα proteins in maize development and enhancement of agronomic traits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945058/
https://www.ncbi.nlm.nih.gov/pubmed/29708966
http://dx.doi.org/10.1371/journal.pgen.1007374
work_keys_str_mv AT wuqingyu roleofheterotrimericgaproteinsinmaizedevelopmentandenhancementofagronomictraits
AT reganmichael roleofheterotrimericgaproteinsinmaizedevelopmentandenhancementofagronomictraits
AT furukawahiro roleofheterotrimericgaproteinsinmaizedevelopmentandenhancementofagronomictraits
AT jacksondavid roleofheterotrimericgaproteinsinmaizedevelopmentandenhancementofagronomictraits