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 |
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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. This result validates our in vitro system in vivo.</description><identifier>ISSN: 0021-9533</identifier><identifier>EISSN: 1477-9137</identifier><identifier>DOI: 10.1242/jcs.075077</identifier><identifier>PMID: 21098637</identifier><language>eng</language><publisher>England: The Company of Biologists Limited</publisher><subject>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</subject><ispartof>Journal of cell science, 2010-12, Vol.123 (24), p.4301-4309</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c342t-61628df1540c371e2a51d774ef25e6f8e185d12f1ff4237f4116792a223e8f803</citedby><cites>FETCH-LOGICAL-c342t-61628df1540c371e2a51d774ef25e6f8e185d12f1ff4237f4116792a223e8f803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3676,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21098637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Chun-Lei</creatorcontrib><creatorcontrib>Wu, Jun</creatorcontrib><creatorcontrib>Xu, Guo-Hua</creatorcontrib><creatorcontrib>Gao, Yong-bin</creatorcontrib><creatorcontrib>Chen, Gong</creatorcontrib><creatorcontrib>Wu, Ju-You</creatorcontrib><creatorcontrib>Wu, Hua-qing</creatorcontrib><creatorcontrib>Zhang, Shao-Ling</creatorcontrib><title>S-RNase disrupts tip-localized reactive oxygen species and induces nuclear DNA degradation in incompatible pollen tubes of Pyrus pyrifolia</title><title>Journal of cell science</title><addtitle>J Cell Sci</addtitle><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.</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 ; Wu, Jun ; Xu, Guo-Hua ; Gao, Yong-bin ; Chen, Gong ; Wu, Ju-You ; Wu, Hua-qing ; Zhang, Shao-Ling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c342t-61628df1540c371e2a51d774ef25e6f8e185d12f1ff4237f4116792a223e8f803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Calcium Signaling</topic><topic>Cell Nucleus - metabolism</topic><topic>Cytoskeleton - metabolism</topic><topic>DNA Fragmentation</topic><topic>Fluorescence</topic><topic>Hydrogen Peroxide - metabolism</topic><topic>NADP - metabolism</topic><topic>Pollen Tube - cytology</topic><topic>Pollen Tube - enzymology</topic><topic>Pollen Tube - ultrastructure</topic><topic>Pollination - physiology</topic><topic>Polymerization</topic><topic>Pyrus - cytology</topic><topic>Pyrus - enzymology</topic><topic>Pyrus - ultrastructure</topic><topic>Pyrus pyrifolia</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Ribonucleases - metabolism</topic><topic>Spheroplasts - cytology</topic><topic>Spheroplasts - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Chun-Lei</creatorcontrib><creatorcontrib>Wu, Jun</creatorcontrib><creatorcontrib>Xu, Guo-Hua</creatorcontrib><creatorcontrib>Gao, Yong-bin</creatorcontrib><creatorcontrib>Chen, Gong</creatorcontrib><creatorcontrib>Wu, Ju-You</creatorcontrib><creatorcontrib>Wu, Hua-qing</creatorcontrib><creatorcontrib>Zhang, Shao-Ling</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>Journal of cell science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Chun-Lei</au><au>Wu, Jun</au><au>Xu, Guo-Hua</au><au>Gao, Yong-bin</au><au>Chen, Gong</au><au>Wu, Ju-You</au><au>Wu, Hua-qing</au><au>Zhang, Shao-Ling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>S-RNase disrupts tip-localized reactive oxygen species and induces nuclear DNA degradation in incompatible pollen tubes of Pyrus pyrifolia</atitle><jtitle>Journal of cell science</jtitle><addtitle>J Cell Sci</addtitle><date>2010-12-15</date><risdate>2010</risdate><volume>123</volume><issue>24</issue><spage>4301</spage><epage>4309</epage><pages>4301-4309</pages><issn>0021-9533</issn><eissn>1477-9137</eissn><abstract>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.</abstract><cop>England</cop><pub>The Company of Biologists Limited</pub><pmid>21098637</pmid><doi>10.1242/jcs.075077</doi><tpages>9</tpages></addata></record> |
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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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