Canonical Rab5 GTPases are essential for pollen tube growth through style in Arabidopsis
Summary Pollen tubes have dynamic tubular vacuoles. Functional loss of AP‐3, a regulator of one vacuolar trafficking route, reduces pollen tube growth. However, the role of canonical Rab5 GTPases that are responsible for two other vacuolar trafficking routes in Arabidopsis pollen tubes is obscure. B...
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Veröffentlicht in: | The New phytologist 2023-09, Vol.239 (5), p.1740-1753 |
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creator | Hao, Guang‐Jiu Li, Lu‐Shen Zhao, Xin‐Ying Ying, Jun Zhang, Miao‐Miao Cui, Xue‐Chun Sun, Tiantian Li, En Su, Le‐Yan Shen, Jinbo Zhou, Xiang Zhu, Xiaoyue Li, Sha Zhang, Yan |
description | Summary
Pollen tubes have dynamic tubular vacuoles. Functional loss of AP‐3, a regulator of one vacuolar trafficking route, reduces pollen tube growth. However, the role of canonical Rab5 GTPases that are responsible for two other vacuolar trafficking routes in Arabidopsis pollen tubes is obscure.
By using genomic editing, confocal microscopy, pollen tube growth assays, and transmission electron microscopy, we demonstrate that functional loss of canonical Rab5s in Arabidopsis, RHA1 and ARA7, causes the failure of pollen tubes to grow through style and thus impairs male transmission.
Functional loss of canonical Rab5s compromises vacuolar trafficking of tonoplast proteins, vacuolar biogenesis, and turgor regulation. However, rha1;ara7 pollen tubes are comparable to those of wild‐type in growing through narrow passages by microfluidic assays.
We demonstrate that functional loss of canonical Rab5s compromises endocytic and secretory trafficking at the plasma membrane (PM), whereas the targeting of PM‐associated ATPases is largely unaffected. Despite that, rha1;ara7 pollen tubes contain a reduced cytosolic pH and disrupted actin microfilaments, correlating with the mis‐targeting of vacuolar ATPases (VHA). These results imply a key role of vacuoles in maintaining cytoplasmic proton homeostasis and in pollen tube penetrative growth through style. |
doi_str_mv | 10.1111/nph.19059 |
format | Article |
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Pollen tubes have dynamic tubular vacuoles. Functional loss of AP‐3, a regulator of one vacuolar trafficking route, reduces pollen tube growth. However, the role of canonical Rab5 GTPases that are responsible for two other vacuolar trafficking routes in Arabidopsis pollen tubes is obscure.
By using genomic editing, confocal microscopy, pollen tube growth assays, and transmission electron microscopy, we demonstrate that functional loss of canonical Rab5s in Arabidopsis, RHA1 and ARA7, causes the failure of pollen tubes to grow through style and thus impairs male transmission.
Functional loss of canonical Rab5s compromises vacuolar trafficking of tonoplast proteins, vacuolar biogenesis, and turgor regulation. However, rha1;ara7 pollen tubes are comparable to those of wild‐type in growing through narrow passages by microfluidic assays.
We demonstrate that functional loss of canonical Rab5s compromises endocytic and secretory trafficking at the plasma membrane (PM), whereas the targeting of PM‐associated ATPases is largely unaffected. Despite that, rha1;ara7 pollen tubes contain a reduced cytosolic pH and disrupted actin microfilaments, correlating with the mis‐targeting of vacuolar ATPases (VHA). These results imply a key role of vacuoles in maintaining cytoplasmic proton homeostasis and in pollen tube penetrative growth through style.</description><identifier>ISSN: 0028-646X</identifier><identifier>EISSN: 1469-8137</identifier><identifier>DOI: 10.1111/nph.19059</identifier><identifier>PMID: 37301984</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Actin ; Adenosine Triphosphatases - metabolism ; Arabidopsis ; Arabidopsis - metabolism ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Biogenesis ; cell wall ; Confocal microscopy ; Electron microscopy ; Growth ; GTP Phosphohydrolases - metabolism ; Homeostasis ; membrane homeostasis ; Membrane trafficking ; Microfilaments ; Microfluidics ; Microscopy ; Pollen ; Pollen Tube ; pollen tube growth ; Pollen tubes ; proton ; style penetration ; Transmission electron microscopy ; Turgor ; vacuole ; Vacuoles</subject><ispartof>The New phytologist, 2023-09, Vol.239 (5), p.1740-1753</ispartof><rights>2023 The Authors. © 2023 New Phytologist Foundation</rights><rights>2023 The Authors. New Phytologist © 2023 New Phytologist Foundation.</rights><rights>Copyright © 2023 New Phytologist Trust</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3539-1bbb042f84699b43b95483f31e943b95b659f9c6251af7f364e79b638a0323593</citedby><cites>FETCH-LOGICAL-c3539-1bbb042f84699b43b95483f31e943b95b659f9c6251af7f364e79b638a0323593</cites><orcidid>0000-0002-7197-0181 ; 0000-0002-0858-0375 ; 0000-0001-9725-2914 ; 0009-0003-2944-8028 ; 0009-0007-7322-2658 ; 0009-0002-8891-313X ; 0000-0002-3501-5857 ; 0000-0001-7848-367X ; 0009-0006-0742-5185 ; 0000-0002-0412-5586 ; 0000-0002-7308-6584</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fnph.19059$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fnph.19059$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37301984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hao, Guang‐Jiu</creatorcontrib><creatorcontrib>Li, Lu‐Shen</creatorcontrib><creatorcontrib>Zhao, Xin‐Ying</creatorcontrib><creatorcontrib>Ying, Jun</creatorcontrib><creatorcontrib>Zhang, Miao‐Miao</creatorcontrib><creatorcontrib>Cui, Xue‐Chun</creatorcontrib><creatorcontrib>Sun, Tiantian</creatorcontrib><creatorcontrib>Li, En</creatorcontrib><creatorcontrib>Su, Le‐Yan</creatorcontrib><creatorcontrib>Shen, Jinbo</creatorcontrib><creatorcontrib>Zhou, Xiang</creatorcontrib><creatorcontrib>Zhu, Xiaoyue</creatorcontrib><creatorcontrib>Li, Sha</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><title>Canonical Rab5 GTPases are essential for pollen tube growth through style in Arabidopsis</title><title>The New phytologist</title><addtitle>New Phytol</addtitle><description>Summary
Pollen tubes have dynamic tubular vacuoles. Functional loss of AP‐3, a regulator of one vacuolar trafficking route, reduces pollen tube growth. However, the role of canonical Rab5 GTPases that are responsible for two other vacuolar trafficking routes in Arabidopsis pollen tubes is obscure.
By using genomic editing, confocal microscopy, pollen tube growth assays, and transmission electron microscopy, we demonstrate that functional loss of canonical Rab5s in Arabidopsis, RHA1 and ARA7, causes the failure of pollen tubes to grow through style and thus impairs male transmission.
Functional loss of canonical Rab5s compromises vacuolar trafficking of tonoplast proteins, vacuolar biogenesis, and turgor regulation. However, rha1;ara7 pollen tubes are comparable to those of wild‐type in growing through narrow passages by microfluidic assays.
We demonstrate that functional loss of canonical Rab5s compromises endocytic and secretory trafficking at the plasma membrane (PM), whereas the targeting of PM‐associated ATPases is largely unaffected. Despite that, rha1;ara7 pollen tubes contain a reduced cytosolic pH and disrupted actin microfilaments, correlating with the mis‐targeting of vacuolar ATPases (VHA). These results imply a key role of vacuoles in maintaining cytoplasmic proton homeostasis and in pollen tube penetrative growth through style.</description><subject>Actin</subject><subject>Adenosine Triphosphatases - metabolism</subject><subject>Arabidopsis</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Biogenesis</subject><subject>cell wall</subject><subject>Confocal microscopy</subject><subject>Electron microscopy</subject><subject>Growth</subject><subject>GTP Phosphohydrolases - metabolism</subject><subject>Homeostasis</subject><subject>membrane homeostasis</subject><subject>Membrane trafficking</subject><subject>Microfilaments</subject><subject>Microfluidics</subject><subject>Microscopy</subject><subject>Pollen</subject><subject>Pollen Tube</subject><subject>pollen tube growth</subject><subject>Pollen tubes</subject><subject>proton</subject><subject>style penetration</subject><subject>Transmission electron microscopy</subject><subject>Turgor</subject><subject>vacuole</subject><subject>Vacuoles</subject><issn>0028-646X</issn><issn>1469-8137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1Kw0AURgdRbK0ufAEZcKOLtPPfzLIUbYWiRSp0F2bSSZuSZuJMQunbOzbVheDdXC73cPj4ALjFqI_DDMpq08cScXkGupgJGcWYDs9BFyESR4KJZQdceb9FCEkuyCXo0CFFWMasC5ZjVdoyT1UB35XmcLKYK288VM5A470p6zy8MutgZYvClLButIFrZ_f1BtYbZ5v1Bvr6UBiYl3DklM5XtvK5vwYXmSq8uTntHvh4flqMp9HsbfIyHs2ilHIqI6y1RoxkcYgtNaNachbTjGIjj4cWXGYyFYRjlQ0zKpgZSi1orBAllEvaAw-tt3L2szG-Tna5T01RqNLYxickJkHNCSMBvf-Dbm3jypAuUIwxTgTFgXpsqdRZ753JksrlO-UOCUbJd91JqDs51h3Yu5Ox0Tuz-iV_-g3AoAX2eWEO_5uS1_m0VX4BSvGHfQ</recordid><startdate>202309</startdate><enddate>202309</enddate><creator>Hao, Guang‐Jiu</creator><creator>Li, Lu‐Shen</creator><creator>Zhao, Xin‐Ying</creator><creator>Ying, Jun</creator><creator>Zhang, Miao‐Miao</creator><creator>Cui, Xue‐Chun</creator><creator>Sun, Tiantian</creator><creator>Li, En</creator><creator>Su, Le‐Yan</creator><creator>Shen, Jinbo</creator><creator>Zhou, Xiang</creator><creator>Zhu, Xiaoyue</creator><creator>Li, Sha</creator><creator>Zhang, Yan</creator><general>Wiley Subscription Services, Inc</general><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>7QO</scope><scope>7SN</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7197-0181</orcidid><orcidid>https://orcid.org/0000-0002-0858-0375</orcidid><orcidid>https://orcid.org/0000-0001-9725-2914</orcidid><orcidid>https://orcid.org/0009-0003-2944-8028</orcidid><orcidid>https://orcid.org/0009-0007-7322-2658</orcidid><orcidid>https://orcid.org/0009-0002-8891-313X</orcidid><orcidid>https://orcid.org/0000-0002-3501-5857</orcidid><orcidid>https://orcid.org/0000-0001-7848-367X</orcidid><orcidid>https://orcid.org/0009-0006-0742-5185</orcidid><orcidid>https://orcid.org/0000-0002-0412-5586</orcidid><orcidid>https://orcid.org/0000-0002-7308-6584</orcidid></search><sort><creationdate>202309</creationdate><title>Canonical Rab5 GTPases are essential for pollen tube growth through style in Arabidopsis</title><author>Hao, Guang‐Jiu ; Li, Lu‐Shen ; Zhao, Xin‐Ying ; Ying, Jun ; Zhang, Miao‐Miao ; Cui, Xue‐Chun ; Sun, Tiantian ; Li, En ; Su, Le‐Yan ; Shen, Jinbo ; Zhou, Xiang ; Zhu, Xiaoyue ; Li, Sha ; Zhang, Yan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3539-1bbb042f84699b43b95483f31e943b95b659f9c6251af7f364e79b638a0323593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Actin</topic><topic>Adenosine Triphosphatases - metabolism</topic><topic>Arabidopsis</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Biogenesis</topic><topic>cell wall</topic><topic>Confocal microscopy</topic><topic>Electron microscopy</topic><topic>Growth</topic><topic>GTP Phosphohydrolases - metabolism</topic><topic>Homeostasis</topic><topic>membrane homeostasis</topic><topic>Membrane trafficking</topic><topic>Microfilaments</topic><topic>Microfluidics</topic><topic>Microscopy</topic><topic>Pollen</topic><topic>Pollen Tube</topic><topic>pollen tube growth</topic><topic>Pollen tubes</topic><topic>proton</topic><topic>style penetration</topic><topic>Transmission electron microscopy</topic><topic>Turgor</topic><topic>vacuole</topic><topic>Vacuoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hao, Guang‐Jiu</creatorcontrib><creatorcontrib>Li, Lu‐Shen</creatorcontrib><creatorcontrib>Zhao, Xin‐Ying</creatorcontrib><creatorcontrib>Ying, Jun</creatorcontrib><creatorcontrib>Zhang, Miao‐Miao</creatorcontrib><creatorcontrib>Cui, Xue‐Chun</creatorcontrib><creatorcontrib>Sun, Tiantian</creatorcontrib><creatorcontrib>Li, En</creatorcontrib><creatorcontrib>Su, Le‐Yan</creatorcontrib><creatorcontrib>Shen, Jinbo</creatorcontrib><creatorcontrib>Zhou, Xiang</creatorcontrib><creatorcontrib>Zhu, Xiaoyue</creatorcontrib><creatorcontrib>Li, Sha</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The New phytologist</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hao, Guang‐Jiu</au><au>Li, Lu‐Shen</au><au>Zhao, Xin‐Ying</au><au>Ying, Jun</au><au>Zhang, Miao‐Miao</au><au>Cui, Xue‐Chun</au><au>Sun, Tiantian</au><au>Li, En</au><au>Su, Le‐Yan</au><au>Shen, Jinbo</au><au>Zhou, Xiang</au><au>Zhu, Xiaoyue</au><au>Li, Sha</au><au>Zhang, Yan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Canonical Rab5 GTPases are essential for pollen tube growth through style in Arabidopsis</atitle><jtitle>The New phytologist</jtitle><addtitle>New Phytol</addtitle><date>2023-09</date><risdate>2023</risdate><volume>239</volume><issue>5</issue><spage>1740</spage><epage>1753</epage><pages>1740-1753</pages><issn>0028-646X</issn><eissn>1469-8137</eissn><abstract>Summary
Pollen tubes have dynamic tubular vacuoles. Functional loss of AP‐3, a regulator of one vacuolar trafficking route, reduces pollen tube growth. However, the role of canonical Rab5 GTPases that are responsible for two other vacuolar trafficking routes in Arabidopsis pollen tubes is obscure.
By using genomic editing, confocal microscopy, pollen tube growth assays, and transmission electron microscopy, we demonstrate that functional loss of canonical Rab5s in Arabidopsis, RHA1 and ARA7, causes the failure of pollen tubes to grow through style and thus impairs male transmission.
Functional loss of canonical Rab5s compromises vacuolar trafficking of tonoplast proteins, vacuolar biogenesis, and turgor regulation. However, rha1;ara7 pollen tubes are comparable to those of wild‐type in growing through narrow passages by microfluidic assays.
We demonstrate that functional loss of canonical Rab5s compromises endocytic and secretory trafficking at the plasma membrane (PM), whereas the targeting of PM‐associated ATPases is largely unaffected. Despite that, rha1;ara7 pollen tubes contain a reduced cytosolic pH and disrupted actin microfilaments, correlating with the mis‐targeting of vacuolar ATPases (VHA). These results imply a key role of vacuoles in maintaining cytoplasmic proton homeostasis and in pollen tube penetrative growth through style.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37301984</pmid><doi>10.1111/nph.19059</doi><tpages>1753</tpages><orcidid>https://orcid.org/0000-0002-7197-0181</orcidid><orcidid>https://orcid.org/0000-0002-0858-0375</orcidid><orcidid>https://orcid.org/0000-0001-9725-2914</orcidid><orcidid>https://orcid.org/0009-0003-2944-8028</orcidid><orcidid>https://orcid.org/0009-0007-7322-2658</orcidid><orcidid>https://orcid.org/0009-0002-8891-313X</orcidid><orcidid>https://orcid.org/0000-0002-3501-5857</orcidid><orcidid>https://orcid.org/0000-0001-7848-367X</orcidid><orcidid>https://orcid.org/0009-0006-0742-5185</orcidid><orcidid>https://orcid.org/0000-0002-0412-5586</orcidid><orcidid>https://orcid.org/0000-0002-7308-6584</orcidid></addata></record> |
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subjects | Actin Adenosine Triphosphatases - metabolism Arabidopsis Arabidopsis - metabolism Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Biogenesis cell wall Confocal microscopy Electron microscopy Growth GTP Phosphohydrolases - metabolism Homeostasis membrane homeostasis Membrane trafficking Microfilaments Microfluidics Microscopy Pollen Pollen Tube pollen tube growth Pollen tubes proton style penetration Transmission electron microscopy Turgor vacuole Vacuoles |
title | Canonical Rab5 GTPases are essential for pollen tube growth through style in Arabidopsis |
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