Cargando…

The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development

Ovules are essential for plant reproduction and develop into seeds after fertilization. SPOROCYTELESS/NOZZLE (SPL/NZZ) has been known for more than 15 years as an essential factor for ovule development in Arabidopsis, but the biochemical nature of SPL function has remained unsolved. Here, we demonst...

Descripción completa

Detalles Bibliográficos
Autores principales: Wei, Baoye, Zhang, Jinzhe, Pang, Changxu, Yu, Hao, Guo, Dongshu, Jiang, Hao, Ding, Mingxin, Chen, Zhuoyao, Tao, Qing, Gu, Hongya, Qu, Li-Jia, Qin, Genji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650584/
https://www.ncbi.nlm.nih.gov/pubmed/25378179
http://dx.doi.org/10.1038/cr.2014.145
_version_ 1782401518149828608
author Wei, Baoye
Zhang, Jinzhe
Pang, Changxu
Yu, Hao
Guo, Dongshu
Jiang, Hao
Ding, Mingxin
Chen, Zhuoyao
Tao, Qing
Gu, Hongya
Qu, Li-Jia
Qin, Genji
author_facet Wei, Baoye
Zhang, Jinzhe
Pang, Changxu
Yu, Hao
Guo, Dongshu
Jiang, Hao
Ding, Mingxin
Chen, Zhuoyao
Tao, Qing
Gu, Hongya
Qu, Li-Jia
Qin, Genji
author_sort Wei, Baoye
collection PubMed
description Ovules are essential for plant reproduction and develop into seeds after fertilization. SPOROCYTELESS/NOZZLE (SPL/NZZ) has been known for more than 15 years as an essential factor for ovule development in Arabidopsis, but the biochemical nature of SPL function has remained unsolved. Here, we demonstrate that SPL functions as an adaptor-like transcriptional repressor. We show that SPL recruits TOPLESS/TOPLESS-RELATED (TPL/TPR) co-repressors to inhibit the CINCINNATA (CIN)-like TEOSINTE BRANCHED1/CYCLOIDEA/PCF (TCP) transcription factors. We reveal that SPL uses its EAR motif at the C-terminal end to recruit TPL/TPRs and its N-terminal part to bind and inhibit the TCPs. We demonstrate that either disruption of TPL/TPRs or overexpression of TCPs partially phenocopies the defects of megasporogenesis in spl. Moreover, disruption of TCPs causes phenotypes that resemble spl-D gain-of-function mutants. These results define the action mechanism for SPL, which along with TPL/TPRs controls ovule development by repressing the activities of key transcription factors. Our findings suggest that a similar gene repression strategy is employed by both plants and fungi to control sporogenesis.
format Online
Article
Text
id pubmed-4650584
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-46505842015-12-01 The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development Wei, Baoye Zhang, Jinzhe Pang, Changxu Yu, Hao Guo, Dongshu Jiang, Hao Ding, Mingxin Chen, Zhuoyao Tao, Qing Gu, Hongya Qu, Li-Jia Qin, Genji Cell Res Original Article Ovules are essential for plant reproduction and develop into seeds after fertilization. SPOROCYTELESS/NOZZLE (SPL/NZZ) has been known for more than 15 years as an essential factor for ovule development in Arabidopsis, but the biochemical nature of SPL function has remained unsolved. Here, we demonstrate that SPL functions as an adaptor-like transcriptional repressor. We show that SPL recruits TOPLESS/TOPLESS-RELATED (TPL/TPR) co-repressors to inhibit the CINCINNATA (CIN)-like TEOSINTE BRANCHED1/CYCLOIDEA/PCF (TCP) transcription factors. We reveal that SPL uses its EAR motif at the C-terminal end to recruit TPL/TPRs and its N-terminal part to bind and inhibit the TCPs. We demonstrate that either disruption of TPL/TPRs or overexpression of TCPs partially phenocopies the defects of megasporogenesis in spl. Moreover, disruption of TCPs causes phenotypes that resemble spl-D gain-of-function mutants. These results define the action mechanism for SPL, which along with TPL/TPRs controls ovule development by repressing the activities of key transcription factors. Our findings suggest that a similar gene repression strategy is employed by both plants and fungi to control sporogenesis. Nature Publishing Group 2015-01 2014-11-07 /pmc/articles/PMC4650584/ /pubmed/25378179 http://dx.doi.org/10.1038/cr.2014.145 Text en Copyright © 2015 Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This work is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0
spellingShingle Original Article
Wei, Baoye
Zhang, Jinzhe
Pang, Changxu
Yu, Hao
Guo, Dongshu
Jiang, Hao
Ding, Mingxin
Chen, Zhuoyao
Tao, Qing
Gu, Hongya
Qu, Li-Jia
Qin, Genji
The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development
title The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development
title_full The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development
title_fullStr The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development
title_full_unstemmed The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development
title_short The molecular mechanism of SPOROCYTELESS/NOZZLE in controlling Arabidopsis ovule development
title_sort molecular mechanism of sporocyteless/nozzle in controlling arabidopsis ovule development
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4650584/
https://www.ncbi.nlm.nih.gov/pubmed/25378179
http://dx.doi.org/10.1038/cr.2014.145
work_keys_str_mv AT weibaoye themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT zhangjinzhe themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT pangchangxu themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT yuhao themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT guodongshu themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT jianghao themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT dingmingxin themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT chenzhuoyao themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT taoqing themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT guhongya themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT qulijia themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT qingenji themolecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT weibaoye molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT zhangjinzhe molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT pangchangxu molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT yuhao molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT guodongshu molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT jianghao molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT dingmingxin molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT chenzhuoyao molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT taoqing molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT guhongya molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT qulijia molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment
AT qingenji molecularmechanismofsporocytelessnozzleincontrollingarabidopsisovuledevelopment