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RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants

The environmentally responsive signaling pathways that link global transcriptomic changes through alternative splicing (AS) to plant fitness remain unclear. Here, we found that the interaction of the extracellular rapid alkalinization FACTOR 1 (RALF1) peptide with its receptor FERONIA (FER) triggere...

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Autores principales: Wang, Long, Yang, Tao, Wang, Bingqian, Lin, Qinlu, Zhu, Sirui, Li, Chiyu, Ma, Youchu, Tang, Jing, Xing, Junjie, Li, Xiushan, Liao, Hongdong, Staiger, Dorothee, Hu, Zhiqiang, Yu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314565/
https://www.ncbi.nlm.nih.gov/pubmed/32671204
http://dx.doi.org/10.1126/sciadv.aaz1622
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author Wang, Long
Yang, Tao
Wang, Bingqian
Lin, Qinlu
Zhu, Sirui
Li, Chiyu
Ma, Youchu
Tang, Jing
Xing, Junjie
Li, Xiushan
Liao, Hongdong
Staiger, Dorothee
Hu, Zhiqiang
Yu, Feng
author_facet Wang, Long
Yang, Tao
Wang, Bingqian
Lin, Qinlu
Zhu, Sirui
Li, Chiyu
Ma, Youchu
Tang, Jing
Xing, Junjie
Li, Xiushan
Liao, Hongdong
Staiger, Dorothee
Hu, Zhiqiang
Yu, Feng
author_sort Wang, Long
collection PubMed
description The environmentally responsive signaling pathways that link global transcriptomic changes through alternative splicing (AS) to plant fitness remain unclear. Here, we found that the interaction of the extracellular rapid alkalinization FACTOR 1 (RALF1) peptide with its receptor FERONIA (FER) triggered a rapid and massive RNA AS response by interacting with and phosphorylating glycine-rich RNA binding protein7 (GRP7) to elevate GRP7 nuclear accumulation in Arabidopsis thaliana. FER-dependent GRP7 phosphorylation enhanced its mRNA binding ability and its association with the spliceosome component U1-70K to enable splice site selection, modulating dynamic AS. Genetic reversal of a RALF1-FER–dependent splicing target partly rescued mutants deficient in GRP7. AS of GRP7 itself induced nonsense-mediated decay feedback to the RALF1-FER-GRP7 module, fine-tuning stress responses, and cell growth. The RALF1-FER-GRP7 module provides a paradigm for regulatory mechanisms of RNA splicing in response to external stimuli.
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spelling pubmed-73145652020-07-14 RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants Wang, Long Yang, Tao Wang, Bingqian Lin, Qinlu Zhu, Sirui Li, Chiyu Ma, Youchu Tang, Jing Xing, Junjie Li, Xiushan Liao, Hongdong Staiger, Dorothee Hu, Zhiqiang Yu, Feng Sci Adv Research Articles The environmentally responsive signaling pathways that link global transcriptomic changes through alternative splicing (AS) to plant fitness remain unclear. Here, we found that the interaction of the extracellular rapid alkalinization FACTOR 1 (RALF1) peptide with its receptor FERONIA (FER) triggered a rapid and massive RNA AS response by interacting with and phosphorylating glycine-rich RNA binding protein7 (GRP7) to elevate GRP7 nuclear accumulation in Arabidopsis thaliana. FER-dependent GRP7 phosphorylation enhanced its mRNA binding ability and its association with the spliceosome component U1-70K to enable splice site selection, modulating dynamic AS. Genetic reversal of a RALF1-FER–dependent splicing target partly rescued mutants deficient in GRP7. AS of GRP7 itself induced nonsense-mediated decay feedback to the RALF1-FER-GRP7 module, fine-tuning stress responses, and cell growth. The RALF1-FER-GRP7 module provides a paradigm for regulatory mechanisms of RNA splicing in response to external stimuli. American Association for the Advancement of Science 2020-05-20 /pmc/articles/PMC7314565/ /pubmed/32671204 http://dx.doi.org/10.1126/sciadv.aaz1622 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Wang, Long
Yang, Tao
Wang, Bingqian
Lin, Qinlu
Zhu, Sirui
Li, Chiyu
Ma, Youchu
Tang, Jing
Xing, Junjie
Li, Xiushan
Liao, Hongdong
Staiger, Dorothee
Hu, Zhiqiang
Yu, Feng
RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants
title RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants
title_full RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants
title_fullStr RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants
title_full_unstemmed RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants
title_short RALF1-FERONIA complex affects splicing dynamics to modulate stress responses and growth in plants
title_sort ralf1-feronia complex affects splicing dynamics to modulate stress responses and growth in plants
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314565/
https://www.ncbi.nlm.nih.gov/pubmed/32671204
http://dx.doi.org/10.1126/sciadv.aaz1622
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