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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
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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. |
format | Online Article Text |
id | pubmed-6410843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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