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A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens

Gravity is a critical environmental factor regulating directional growth and morphogenesis in plants, and gravitropism is the process by which plants perceive and respond to the gravity vector. The cytoskeleton is proposed to play important roles in gravitropism, but the underlying mechanisms are ob...

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Autores principales: Li, Yufan, Deng, Zhaoguo, Kamisugi, Yasuko, Chen, Zhiren, Wang, Jiajun, Han, Xue, Wei, Yuxiao, He, Hang, Terzaghi, William, Cove, David J., Cuming, Andrew C., Chen, Haodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298521/
https://www.ncbi.nlm.nih.gov/pubmed/34294690
http://dx.doi.org/10.1038/s41467-021-24546-2
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author Li, Yufan
Deng, Zhaoguo
Kamisugi, Yasuko
Chen, Zhiren
Wang, Jiajun
Han, Xue
Wei, Yuxiao
He, Hang
Terzaghi, William
Cove, David J.
Cuming, Andrew C.
Chen, Haodong
author_facet Li, Yufan
Deng, Zhaoguo
Kamisugi, Yasuko
Chen, Zhiren
Wang, Jiajun
Han, Xue
Wei, Yuxiao
He, Hang
Terzaghi, William
Cove, David J.
Cuming, Andrew C.
Chen, Haodong
author_sort Li, Yufan
collection PubMed
description Gravity is a critical environmental factor regulating directional growth and morphogenesis in plants, and gravitropism is the process by which plants perceive and respond to the gravity vector. The cytoskeleton is proposed to play important roles in gravitropism, but the underlying mechanisms are obscure. Here we use genetic screening in Physcomitrella patens, to identify a locus GTRC, that when mutated, reverses the direction of protonemal gravitropism. GTRC encodes a processive minus-end-directed KCHb kinesin, and its N-terminal, C-terminal and motor domains are all essential for transducing the gravity signal. Chimeric analysis between GTRC/KCHb and KCHa reveal a unique role for the N-terminus of GTRC in gravitropism. Further study shows that gravity-triggered normal asymmetric distribution of actin filaments in the tip of protonema is dependent on GTRC. Thus, our work identifies a microtubule-based cellular motor that determines the direction of plant gravitropism via mediating the asymmetric distribution of actin filaments.
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spelling pubmed-82985212021-08-12 A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens Li, Yufan Deng, Zhaoguo Kamisugi, Yasuko Chen, Zhiren Wang, Jiajun Han, Xue Wei, Yuxiao He, Hang Terzaghi, William Cove, David J. Cuming, Andrew C. Chen, Haodong Nat Commun Article Gravity is a critical environmental factor regulating directional growth and morphogenesis in plants, and gravitropism is the process by which plants perceive and respond to the gravity vector. The cytoskeleton is proposed to play important roles in gravitropism, but the underlying mechanisms are obscure. Here we use genetic screening in Physcomitrella patens, to identify a locus GTRC, that when mutated, reverses the direction of protonemal gravitropism. GTRC encodes a processive minus-end-directed KCHb kinesin, and its N-terminal, C-terminal and motor domains are all essential for transducing the gravity signal. Chimeric analysis between GTRC/KCHb and KCHa reveal a unique role for the N-terminus of GTRC in gravitropism. Further study shows that gravity-triggered normal asymmetric distribution of actin filaments in the tip of protonema is dependent on GTRC. Thus, our work identifies a microtubule-based cellular motor that determines the direction of plant gravitropism via mediating the asymmetric distribution of actin filaments. Nature Publishing Group UK 2021-07-22 /pmc/articles/PMC8298521/ /pubmed/34294690 http://dx.doi.org/10.1038/s41467-021-24546-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Yufan
Deng, Zhaoguo
Kamisugi, Yasuko
Chen, Zhiren
Wang, Jiajun
Han, Xue
Wei, Yuxiao
He, Hang
Terzaghi, William
Cove, David J.
Cuming, Andrew C.
Chen, Haodong
A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens
title A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens
title_full A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens
title_fullStr A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens
title_full_unstemmed A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens
title_short A minus-end directed kinesin motor directs gravitropism in Physcomitrella patens
title_sort minus-end directed kinesin motor directs gravitropism in physcomitrella patens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298521/
https://www.ncbi.nlm.nih.gov/pubmed/34294690
http://dx.doi.org/10.1038/s41467-021-24546-2
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