S-RNase disrupts tip-localized reactive oxygen species and induces nuclear DNA degradation in incompatible pollen tubes of Pyrus pyrifolia

Pear (Pyrus pyrifolia L.) has an S-RNase-based gametophytic self-incompatibility (SI) mechanism, and S-RNase has also been implicated in the rejection of self-pollen and genetically identical pollen. However, RNA degradation might be only the beginning of the SI response, not the end. Recent in vitr...

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Veröffentlicht in:Journal of cell science 2010-12, Vol.123 (24), p.4301-4309
Hauptverfasser: Wang, Chun-Lei, Wu, Jun, Xu, Guo-Hua, Gao, Yong-bin, Chen, Gong, Wu, Ju-You, Wu, Hua-qing, Zhang, Shao-Ling
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container_end_page 4309
container_issue 24
container_start_page 4301
container_title Journal of cell science
container_volume 123
creator Wang, Chun-Lei
Wu, Jun
Xu, Guo-Hua
Gao, Yong-bin
Chen, Gong
Wu, Ju-You
Wu, Hua-qing
Zhang, Shao-Ling
description Pear (Pyrus pyrifolia L.) has an S-RNase-based gametophytic self-incompatibility (SI) mechanism, and S-RNase has also been implicated in the rejection of self-pollen and genetically identical pollen. However, RNA degradation might be only the beginning of the SI response, not the end. Recent in vitro studies suggest that S-RNase triggers mitochondrial alteration and DNA degradation in the incompatible pollen tube of Pyrus pyrifolia, and it seems that a relationship exists between self S-RNase, actin depolymerization and DNA degradation. To further uncover the SI response in pear, the relationship between self S-RNase and tip-localized reactive oxygen species (ROS) was evaluated. Our results show that S-RNase specifically disrupted tip-localized ROS of incompatible pollen tubes via arrest of ROS formation in mitochondria and cell walls. The mitochondrial ROS disruption was related to mitochondrial alteration, whereas cell wall ROS disruption was related to a decrease in NADPH. Tip-localized ROS disruption not only decreased the Ca²⁺ current and depolymerized the actin cytoskeleton, but it also induced nuclear DNA degradation. These results indicate that tip-localized ROS disruption occurs in Pyrus pyrifolia SI. Importantly, we demonstrated nuclear DNA degradation in the incompatible pollen tube after pollination in vivo. This result validates our in vitro system in vivo.
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However, RNA degradation might be only the beginning of the SI response, not the end. Recent in vitro studies suggest that S-RNase triggers mitochondrial alteration and DNA degradation in the incompatible pollen tube of Pyrus pyrifolia, and it seems that a relationship exists between self S-RNase, actin depolymerization and DNA degradation. To further uncover the SI response in pear, the relationship between self S-RNase and tip-localized reactive oxygen species (ROS) was evaluated. Our results show that S-RNase specifically disrupted tip-localized ROS of incompatible pollen tubes via arrest of ROS formation in mitochondria and cell walls. The mitochondrial ROS disruption was related to mitochondrial alteration, whereas cell wall ROS disruption was related to a decrease in NADPH. Tip-localized ROS disruption not only decreased the Ca²⁺ current and depolymerized the actin cytoskeleton, but it also induced nuclear DNA degradation. These results indicate that tip-localized ROS disruption occurs in Pyrus pyrifolia SI. Importantly, we demonstrated nuclear DNA degradation in the incompatible pollen tube after pollination in vivo. 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This result validates our in vitro system in vivo.</description><subject>Calcium Signaling</subject><subject>Cell Nucleus - metabolism</subject><subject>Cytoskeleton - metabolism</subject><subject>DNA Fragmentation</subject><subject>Fluorescence</subject><subject>Hydrogen Peroxide - metabolism</subject><subject>NADP - metabolism</subject><subject>Pollen Tube - cytology</subject><subject>Pollen Tube - enzymology</subject><subject>Pollen Tube - ultrastructure</subject><subject>Pollination - physiology</subject><subject>Polymerization</subject><subject>Pyrus - cytology</subject><subject>Pyrus - enzymology</subject><subject>Pyrus - ultrastructure</subject><subject>Pyrus pyrifolia</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Ribonucleases - metabolism</subject><subject>Spheroplasts - cytology</subject><subject>Spheroplasts - metabolism</subject><issn>0021-9533</issn><issn>1477-9137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-KFDEQh4Mo7rh68QE0N0HoNZV0Op3jsus_WFZx3XPIJJUhS6bTJt3i-Ag-tZFZvQoFVUV99bt8hDwHdga852_uXD1jSjKlHpAN9Ep1GoR6SDaMcei0FOKEPKn1jjGmuFaPyQkHpsdBqA35ddN9ubYVqY-1rPNS6RLnLmVnU_yJnha0bonfkeYfhx1OtM7oIlZqJ0_j5FfX5ml1CW2hl9fn1OOuWG-XmKd2b-Xyfm7rNiGdc0otYlm37SkH-vlQ1krnQ4khp2ifkkfBporP7vspuX339uvFh-7q0_uPF-dXnRM9X7oBBj76ALJnTihAbiV4pXoMXOIQRoRReuABQui5UKEHGJTmlnOBYxiZOCWvjrlzyd9WrIvZx-owJTthXqsZh15LAKX-T4LUg5BMNvL1kXQl11owmLnEvS0HA8z8kWSaJHOU1OAX97Hrdo_-H_rXSgNeHoFgs7G7Equ5veEMBAMNgwYmfgNat5dJ</recordid><startdate>20101215</startdate><enddate>20101215</enddate><creator>Wang, Chun-Lei</creator><creator>Wu, Jun</creator><creator>Xu, Guo-Hua</creator><creator>Gao, Yong-bin</creator><creator>Chen, Gong</creator><creator>Wu, Ju-You</creator><creator>Wu, Hua-qing</creator><creator>Zhang, Shao-Ling</creator><general>The Company of Biologists Limited</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7TM</scope></search><sort><creationdate>20101215</creationdate><title>S-RNase disrupts tip-localized reactive oxygen species and induces nuclear DNA degradation in incompatible pollen tubes of Pyrus pyrifolia</title><author>Wang, Chun-Lei ; 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However, RNA degradation might be only the beginning of the SI response, not the end. Recent in vitro studies suggest that S-RNase triggers mitochondrial alteration and DNA degradation in the incompatible pollen tube of Pyrus pyrifolia, and it seems that a relationship exists between self S-RNase, actin depolymerization and DNA degradation. To further uncover the SI response in pear, the relationship between self S-RNase and tip-localized reactive oxygen species (ROS) was evaluated. Our results show that S-RNase specifically disrupted tip-localized ROS of incompatible pollen tubes via arrest of ROS formation in mitochondria and cell walls. The mitochondrial ROS disruption was related to mitochondrial alteration, whereas cell wall ROS disruption was related to a decrease in NADPH. Tip-localized ROS disruption not only decreased the Ca²⁺ current and depolymerized the actin cytoskeleton, but it also induced nuclear DNA degradation. 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subjects Calcium Signaling
Cell Nucleus - metabolism
Cytoskeleton - metabolism
DNA Fragmentation
Fluorescence
Hydrogen Peroxide - metabolism
NADP - metabolism
Pollen Tube - cytology
Pollen Tube - enzymology
Pollen Tube - ultrastructure
Pollination - physiology
Polymerization
Pyrus - cytology
Pyrus - enzymology
Pyrus - ultrastructure
Pyrus pyrifolia
Reactive Oxygen Species - metabolism
Ribonucleases - metabolism
Spheroplasts - cytology
Spheroplasts - metabolism
title S-RNase disrupts tip-localized reactive oxygen species and induces nuclear DNA degradation in incompatible pollen tubes of Pyrus pyrifolia
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