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Mitochondrial small heat shock protein mediates seed germination via thermal sensing

Seed germination is an energy demanding process that requires functional mitochondria upon imbibition. However, how mitochondria fine tune seed germination, especially in response to the dynamics of environmental temperature, remains largely unknown at the molecular level. Here, we report a mitochon...

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Autores principales: Ma, Wei, Guan, Xueying, Li, Jie, Pan, Ronghui, Wang, Luyao, Liu, Fengjun, Ma, Hongyu, Zhu, Shuijin, Hu, Jin, Ruan, Yong-Ling, Chen, Xiaoya, Zhang, Tianzhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410843/
https://www.ncbi.nlm.nih.gov/pubmed/30765516
http://dx.doi.org/10.1073/pnas.1815790116
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author Ma, Wei
Guan, Xueying
Li, Jie
Pan, Ronghui
Wang, Luyao
Liu, Fengjun
Ma, Hongyu
Zhu, Shuijin
Hu, Jin
Ruan, Yong-Ling
Chen, Xiaoya
Zhang, Tianzhen
author_facet Ma, Wei
Guan, Xueying
Li, Jie
Pan, Ronghui
Wang, Luyao
Liu, Fengjun
Ma, Hongyu
Zhu, Shuijin
Hu, Jin
Ruan, Yong-Ling
Chen, Xiaoya
Zhang, Tianzhen
author_sort Ma, Wei
collection PubMed
description Seed germination is an energy demanding process that requires functional mitochondria upon imbibition. However, how mitochondria fine tune seed germination, especially in response to the dynamics of environmental temperature, remains largely unknown at the molecular level. Here, we report a mitochondrial matrix-localized heat shock protein GhHSP24.7, that regulates seed germination in a temperature-dependent manner. Suppression of GhHSP24.7 renders the seed insensitive to temperature changes and delays germination. We show that GhHSP24.7 competes with GhCCMH to bind to the maturation subunit protein GhCcmF(c) to form cytochrome C/C(1) (CytC/C(1)) in the mitochondrial electron transport chain. GhHSP24.7 modulates CytC/C(1) production to induce reactive oxygen species (ROS) generation, which consequently accelerates endosperm rupture and promotes seed germination. Overexpression of GhHSP24.7’s homologous genes can accelerate seed germination in Arabidopsis and tomato, indicating its conserved function across plant species. Therefore, HSP24.7 is a critical factor that positively controls seed germination via temperature-dependent ROS generation.
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spelling pubmed-64108432019-03-13 Mitochondrial small heat shock protein mediates seed germination via thermal sensing Ma, Wei Guan, Xueying Li, Jie Pan, Ronghui Wang, Luyao Liu, Fengjun Ma, Hongyu Zhu, Shuijin Hu, Jin Ruan, Yong-Ling Chen, Xiaoya Zhang, Tianzhen Proc Natl Acad Sci U S A Biological Sciences Seed germination is an energy demanding process that requires functional mitochondria upon imbibition. However, how mitochondria fine tune seed germination, especially in response to the dynamics of environmental temperature, remains largely unknown at the molecular level. Here, we report a mitochondrial matrix-localized heat shock protein GhHSP24.7, that regulates seed germination in a temperature-dependent manner. Suppression of GhHSP24.7 renders the seed insensitive to temperature changes and delays germination. We show that GhHSP24.7 competes with GhCCMH to bind to the maturation subunit protein GhCcmF(c) to form cytochrome C/C(1) (CytC/C(1)) in the mitochondrial electron transport chain. GhHSP24.7 modulates CytC/C(1) production to induce reactive oxygen species (ROS) generation, which consequently accelerates endosperm rupture and promotes seed germination. Overexpression of GhHSP24.7’s homologous genes can accelerate seed germination in Arabidopsis and tomato, indicating its conserved function across plant species. Therefore, HSP24.7 is a critical factor that positively controls seed germination via temperature-dependent ROS generation. National Academy of Sciences 2019-03-05 2019-02-14 /pmc/articles/PMC6410843/ /pubmed/30765516 http://dx.doi.org/10.1073/pnas.1815790116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Ma, Wei
Guan, Xueying
Li, Jie
Pan, Ronghui
Wang, Luyao
Liu, Fengjun
Ma, Hongyu
Zhu, Shuijin
Hu, Jin
Ruan, Yong-Ling
Chen, Xiaoya
Zhang, Tianzhen
Mitochondrial small heat shock protein mediates seed germination via thermal sensing
title Mitochondrial small heat shock protein mediates seed germination via thermal sensing
title_full Mitochondrial small heat shock protein mediates seed germination via thermal sensing
title_fullStr Mitochondrial small heat shock protein mediates seed germination via thermal sensing
title_full_unstemmed Mitochondrial small heat shock protein mediates seed germination via thermal sensing
title_short Mitochondrial small heat shock protein mediates seed germination via thermal sensing
title_sort mitochondrial small heat shock protein mediates seed germination via thermal sensing
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410843/
https://www.ncbi.nlm.nih.gov/pubmed/30765516
http://dx.doi.org/10.1073/pnas.1815790116
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