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Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens

In higher plants, the Dof transcription factors that harbour a conserved plant-specific DNA-binding domain function in the regulation of diverse biological processes that are unique to plants. Although these factors are present in both higher and lower plants, they have not yet been characterized in...

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Autores principales: Sugiyama, Takumi, Ishida, Tetsuya, Tabei, Nobumitsu, Shigyo, Mikao, Konishi, Mineko, Yoneyama, Tadakatsu, Yanagisawa, Shuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350930/
https://www.ncbi.nlm.nih.gov/pubmed/22345635
http://dx.doi.org/10.1093/jxb/ers042
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author Sugiyama, Takumi
Ishida, Tetsuya
Tabei, Nobumitsu
Shigyo, Mikao
Konishi, Mineko
Yoneyama, Tadakatsu
Yanagisawa, Shuichi
author_facet Sugiyama, Takumi
Ishida, Tetsuya
Tabei, Nobumitsu
Shigyo, Mikao
Konishi, Mineko
Yoneyama, Tadakatsu
Yanagisawa, Shuichi
author_sort Sugiyama, Takumi
collection PubMed
description In higher plants, the Dof transcription factors that harbour a conserved plant-specific DNA-binding domain function in the regulation of diverse biological processes that are unique to plants. Although these factors are present in both higher and lower plants, they have not yet been characterized in lower plants. Here six genes encoding Dof transcription factors in the moss Physcomitrella patens are characterized and two of these genes, PpDof1 and PpDof2, are functionally analysed. The targeted disruption of PpDof1 caused delayed or reduced gametophore formation, accompanied by an effect on development of the caulonema from the chloronema. Furthermore, the ppdof1 disruptants were found to form smaller colonies with a reduced frequency of branching of protonemal filaments, depending on the nutrients in the media. Most of these phenotypes were not apparent in the ppdof2 disruptant, although the ppdof2 disruptants also formed smaller colonies on a particular medium. Transcriptional repressor activity of PpDof1 and PpDof2 and modified expression of a number of genes in the ppdof disruptant lines were also shown. These results thus suggest that the PpDof1 transcriptional repressor has a role in controlling nutrient-dependent filament growth.
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spelling pubmed-33509302012-05-14 Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens Sugiyama, Takumi Ishida, Tetsuya Tabei, Nobumitsu Shigyo, Mikao Konishi, Mineko Yoneyama, Tadakatsu Yanagisawa, Shuichi J Exp Bot Research Papers In higher plants, the Dof transcription factors that harbour a conserved plant-specific DNA-binding domain function in the regulation of diverse biological processes that are unique to plants. Although these factors are present in both higher and lower plants, they have not yet been characterized in lower plants. Here six genes encoding Dof transcription factors in the moss Physcomitrella patens are characterized and two of these genes, PpDof1 and PpDof2, are functionally analysed. The targeted disruption of PpDof1 caused delayed or reduced gametophore formation, accompanied by an effect on development of the caulonema from the chloronema. Furthermore, the ppdof1 disruptants were found to form smaller colonies with a reduced frequency of branching of protonemal filaments, depending on the nutrients in the media. Most of these phenotypes were not apparent in the ppdof2 disruptant, although the ppdof2 disruptants also formed smaller colonies on a particular medium. Transcriptional repressor activity of PpDof1 and PpDof2 and modified expression of a number of genes in the ppdof disruptant lines were also shown. These results thus suggest that the PpDof1 transcriptional repressor has a role in controlling nutrient-dependent filament growth. Oxford University Press 2012-05 2012-02-15 /pmc/articles/PMC3350930/ /pubmed/22345635 http://dx.doi.org/10.1093/jxb/ers042 Text en © 2012 The Author(s). http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)
spellingShingle Research Papers
Sugiyama, Takumi
Ishida, Tetsuya
Tabei, Nobumitsu
Shigyo, Mikao
Konishi, Mineko
Yoneyama, Tadakatsu
Yanagisawa, Shuichi
Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens
title Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens
title_full Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens
title_fullStr Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens
title_full_unstemmed Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens
title_short Involvement of PpDof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in Physcomitrella patens
title_sort involvement of ppdof1 transcriptional repressor in the nutrient condition-dependent growth control of protonemal filaments in physcomitrella patens
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350930/
https://www.ncbi.nlm.nih.gov/pubmed/22345635
http://dx.doi.org/10.1093/jxb/ers042
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