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Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis

Macroautophagy/autophagy, a major catabolic pathway in eukaryotes, participates in plant sexual reproduction including the processes of male gametogenesis and the self-incompatibility response. Rapid pollen tube growth is another essential reproductive process that is metabolically highly demanding...

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Autores principales: Yan, He, Zhuang, Menglong, Xu, Xiaoyu, Li, Shanshan, Yang, Mingkang, Li, Nianle, Du, Xiaojuan, Hu, Kangwei, Peng, Xiaomin, Huang, Wei, Wu, Hong, Tse, Yu Chung, Zhao, Lifeng, Wang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980518/
https://www.ncbi.nlm.nih.gov/pubmed/35786359
http://dx.doi.org/10.1080/15548627.2022.2095838
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author Yan, He
Zhuang, Menglong
Xu, Xiaoyu
Li, Shanshan
Yang, Mingkang
Li, Nianle
Du, Xiaojuan
Hu, Kangwei
Peng, Xiaomin
Huang, Wei
Wu, Hong
Tse, Yu Chung
Zhao, Lifeng
Wang, Hao
author_facet Yan, He
Zhuang, Menglong
Xu, Xiaoyu
Li, Shanshan
Yang, Mingkang
Li, Nianle
Du, Xiaojuan
Hu, Kangwei
Peng, Xiaomin
Huang, Wei
Wu, Hong
Tse, Yu Chung
Zhao, Lifeng
Wang, Hao
author_sort Yan, He
collection PubMed
description Macroautophagy/autophagy, a major catabolic pathway in eukaryotes, participates in plant sexual reproduction including the processes of male gametogenesis and the self-incompatibility response. Rapid pollen tube growth is another essential reproductive process that is metabolically highly demanding to drive the vigorous cell growth for delivery of male gametes for fertilization in angiosperms. Whether and how autophagy operates to maintain the homeostasis of pollen tubes remains unknown. Here, we provide evidence that autophagy is elevated in growing pollen tubes and critically required during pollen tube growth and male fertility in Arabidopsis. We demonstrate that SH3P2, a critical non-ATG regulator of plant autophagy, colocalizes with representative ATG proteins during autophagosome biogenesis in growing pollen tubes. Downregulation of SH3P2 expression significantly disrupts Arabidopsis pollen germination and pollen tube growth. Further analysis of organelle dynamics reveals crosstalk between autophagosomes and prevacuolar compartments following the inhibition of phosphatidylinositol 3-kinase. In addition, time-lapse imaging and tracking of ATG8e-labeled autophagosomes and depolarized mitochondria demonstrate that they interact specifically via the ATG8-family interacting motif (AIM)-docking site to mediate mitophagy. Ultrastructural identification of mitophagosomes and two additional forms of autophagosomes imply that multiple types of autophagy are likely to function simultaneously within pollen tubes. Altogether, our results suggest that autophagy is functionally crucial for mediating mitochondrial quality control and canonical cytoplasm recycling during pollen tube growth. Abbreviations: AIM: ATG8-family interacting motif; ATG8: autophagy related 8; ATG5: autophagy related 5; ATG7: autophagy related 7; BTH: acibenzolar-S-methyl; DEX: dexamethasone; DNP: 2,4-dinitrophenol; GFP: green fluorescent protein; YFP: yellow fluorescent protein; PtdIns3K: phosphatidylinositol 3-kinase; PtdIns3P: phosphatidylinositol-3-phosphate; PVC: prevacuolar compartment; SH3P2: SH3 domain-containing protein 2.
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spelling pubmed-99805182023-03-03 Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis Yan, He Zhuang, Menglong Xu, Xiaoyu Li, Shanshan Yang, Mingkang Li, Nianle Du, Xiaojuan Hu, Kangwei Peng, Xiaomin Huang, Wei Wu, Hong Tse, Yu Chung Zhao, Lifeng Wang, Hao Autophagy Research Paper Macroautophagy/autophagy, a major catabolic pathway in eukaryotes, participates in plant sexual reproduction including the processes of male gametogenesis and the self-incompatibility response. Rapid pollen tube growth is another essential reproductive process that is metabolically highly demanding to drive the vigorous cell growth for delivery of male gametes for fertilization in angiosperms. Whether and how autophagy operates to maintain the homeostasis of pollen tubes remains unknown. Here, we provide evidence that autophagy is elevated in growing pollen tubes and critically required during pollen tube growth and male fertility in Arabidopsis. We demonstrate that SH3P2, a critical non-ATG regulator of plant autophagy, colocalizes with representative ATG proteins during autophagosome biogenesis in growing pollen tubes. Downregulation of SH3P2 expression significantly disrupts Arabidopsis pollen germination and pollen tube growth. Further analysis of organelle dynamics reveals crosstalk between autophagosomes and prevacuolar compartments following the inhibition of phosphatidylinositol 3-kinase. In addition, time-lapse imaging and tracking of ATG8e-labeled autophagosomes and depolarized mitochondria demonstrate that they interact specifically via the ATG8-family interacting motif (AIM)-docking site to mediate mitophagy. Ultrastructural identification of mitophagosomes and two additional forms of autophagosomes imply that multiple types of autophagy are likely to function simultaneously within pollen tubes. Altogether, our results suggest that autophagy is functionally crucial for mediating mitochondrial quality control and canonical cytoplasm recycling during pollen tube growth. Abbreviations: AIM: ATG8-family interacting motif; ATG8: autophagy related 8; ATG5: autophagy related 5; ATG7: autophagy related 7; BTH: acibenzolar-S-methyl; DEX: dexamethasone; DNP: 2,4-dinitrophenol; GFP: green fluorescent protein; YFP: yellow fluorescent protein; PtdIns3K: phosphatidylinositol 3-kinase; PtdIns3P: phosphatidylinositol-3-phosphate; PVC: prevacuolar compartment; SH3P2: SH3 domain-containing protein 2. Taylor & Francis 2022-07-11 /pmc/articles/PMC9980518/ /pubmed/35786359 http://dx.doi.org/10.1080/15548627.2022.2095838 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Yan, He
Zhuang, Menglong
Xu, Xiaoyu
Li, Shanshan
Yang, Mingkang
Li, Nianle
Du, Xiaojuan
Hu, Kangwei
Peng, Xiaomin
Huang, Wei
Wu, Hong
Tse, Yu Chung
Zhao, Lifeng
Wang, Hao
Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis
title Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis
title_full Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis
title_fullStr Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis
title_full_unstemmed Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis
title_short Autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in Arabidopsis
title_sort autophagy and its mediated mitochondrial quality control maintain pollen tube growth and male fertility in arabidopsis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980518/
https://www.ncbi.nlm.nih.gov/pubmed/35786359
http://dx.doi.org/10.1080/15548627.2022.2095838
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