Amyloplast displacement is necessary for gravisensing in Arabidopsis shoots as revealed by a centrifuge microscope
Summary The starch‐statolith hypothesis proposes that starch‐filled amyloplasts act as statoliths in plant gravisensing, moving in response to the gravity vector and signaling its direction. However, recent studies suggest that amyloplasts show continuous, complex movements in Arabidopsis shoots, co...
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Veröffentlicht in: | The Plant journal : for cell and molecular biology 2013-11, Vol.76 (4), p.648-660 |
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creator | Toyota, Masatsugu Ikeda, Norifumi Sawai‐Toyota, Satoe Kato, Takehide Gilroy, Simon Tasaka, Masao Morita, Miyo Terao |
description | Summary
The starch‐statolith hypothesis proposes that starch‐filled amyloplasts act as statoliths in plant gravisensing, moving in response to the gravity vector and signaling its direction. However, recent studies suggest that amyloplasts show continuous, complex movements in Arabidopsis shoots, contradicting the idea of a so‐called ‘static’ or ‘settled’ statolith. Here, we show that amyloplast movement underlies shoot gravisensing by using a custom‐designed centrifuge microscope in combination with analysis of gravitropic mutants. The centrifuge microscope revealed that sedimentary movements of amyloplasts under hypergravity conditions are linearly correlated with gravitropic curvature in wild‐type stems. We next analyzed the hypergravity response in the shoot gravitropism 2 (sgr2) mutant, which exhibits neither a shoot gravitropic response nor amyloplast sedimentation at 1 g. sgr2 mutants were able to sense and respond to gravity under 30 g conditions, during which the amyloplasts sedimented. These findings are consistent with amyloplast redistribution resulting from gravity‐driven movements triggering shoot gravisensing. To further support this idea, we examined two additional gravitropic mutants, phosphoglucomutase (pgm) and sgr9, which show abnormal amyloplast distribution and reduced gravitropism at 1 g. We found that the correlation between hypergravity‐induced amyloplast sedimentation and gravitropic curvature of these mutants was identical to that of wild‐type plants. These observations suggest that Arabidopsis shoots have a gravisensing mechanism that linearly converts the number of amyloplasts that settle to the ‘bottom’ of the cell into gravitropic signals. Further, the restoration of the gravitropic response by hypergravity in the gravitropic mutants that we tested indicates that these lines probably have a functional gravisensing mechanism that is not triggered at 1 g. |
doi_str_mv | 10.1111/tpj.12324 |
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The starch‐statolith hypothesis proposes that starch‐filled amyloplasts act as statoliths in plant gravisensing, moving in response to the gravity vector and signaling its direction. However, recent studies suggest that amyloplasts show continuous, complex movements in Arabidopsis shoots, contradicting the idea of a so‐called ‘static’ or ‘settled’ statolith. Here, we show that amyloplast movement underlies shoot gravisensing by using a custom‐designed centrifuge microscope in combination with analysis of gravitropic mutants. The centrifuge microscope revealed that sedimentary movements of amyloplasts under hypergravity conditions are linearly correlated with gravitropic curvature in wild‐type stems. We next analyzed the hypergravity response in the shoot gravitropism 2 (sgr2) mutant, which exhibits neither a shoot gravitropic response nor amyloplast sedimentation at 1 g. sgr2 mutants were able to sense and respond to gravity under 30 g conditions, during which the amyloplasts sedimented. These findings are consistent with amyloplast redistribution resulting from gravity‐driven movements triggering shoot gravisensing. To further support this idea, we examined two additional gravitropic mutants, phosphoglucomutase (pgm) and sgr9, which show abnormal amyloplast distribution and reduced gravitropism at 1 g. We found that the correlation between hypergravity‐induced amyloplast sedimentation and gravitropic curvature of these mutants was identical to that of wild‐type plants. These observations suggest that Arabidopsis shoots have a gravisensing mechanism that linearly converts the number of amyloplasts that settle to the ‘bottom’ of the cell into gravitropic signals. Further, the restoration of the gravitropic response by hypergravity in the gravitropic mutants that we tested indicates that these lines probably have a functional gravisensing mechanism that is not triggered at 1 g.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.12324</identifier><identifier>PMID: 24004104</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>amyloplast ; Arabidopsis ; Arabidopsis - chemistry ; Arabidopsis - genetics ; Arabidopsis - physiology ; Arabidopsis Proteins - chemistry ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - physiology ; Biophysics ; Cells ; Centrifugation ; centrifuge microscope ; gravisensing ; Gravitropism - genetics ; Hypergravity ; Microscopy ; Microscopy, Polarization ; Mutation ; Phosphoglucomutase - chemistry ; Phosphoglucomutase - genetics ; Phosphoglucomutase - physiology ; Phospholipases - chemistry ; Phospholipases - genetics ; Phospholipases - physiology ; Plant biology ; Plant Shoots - chemistry ; Plant Shoots - genetics ; Plant Shoots - physiology ; Plastids - chemistry ; Plastids - genetics ; Plastids - physiology ; RING Finger Domains - genetics ; RING Finger Domains - physiology ; starch‐statolith hypothesis ; Ubiquitin-Protein Ligases - chemistry ; Ubiquitin-Protein Ligases - genetics ; Ubiquitin-Protein Ligases - physiology</subject><ispartof>The Plant journal : for cell and molecular biology, 2013-11, Vol.76 (4), p.648-660</ispartof><rights>2013 The Authors The Plant Journal © 2013 John Wiley & Sons Ltd</rights><rights>2013 The Authors The Plant Journal © 2013 John Wiley & Sons Ltd.</rights><rights>Copyright © 2013 John Wiley & Sons Ltd and the Society for Experimental Biology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4194-d2e73c7b544e9cda34828b80a19715129be32c9a0ccf03795f81fc99472eb7cc3</citedby><cites>FETCH-LOGICAL-c4194-d2e73c7b544e9cda34828b80a19715129be32c9a0ccf03795f81fc99472eb7cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftpj.12324$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftpj.12324$$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/24004104$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Toyota, Masatsugu</creatorcontrib><creatorcontrib>Ikeda, Norifumi</creatorcontrib><creatorcontrib>Sawai‐Toyota, Satoe</creatorcontrib><creatorcontrib>Kato, Takehide</creatorcontrib><creatorcontrib>Gilroy, Simon</creatorcontrib><creatorcontrib>Tasaka, Masao</creatorcontrib><creatorcontrib>Morita, Miyo Terao</creatorcontrib><title>Amyloplast displacement is necessary for gravisensing in Arabidopsis shoots as revealed by a centrifuge microscope</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>Summary
The starch‐statolith hypothesis proposes that starch‐filled amyloplasts act as statoliths in plant gravisensing, moving in response to the gravity vector and signaling its direction. However, recent studies suggest that amyloplasts show continuous, complex movements in Arabidopsis shoots, contradicting the idea of a so‐called ‘static’ or ‘settled’ statolith. Here, we show that amyloplast movement underlies shoot gravisensing by using a custom‐designed centrifuge microscope in combination with analysis of gravitropic mutants. The centrifuge microscope revealed that sedimentary movements of amyloplasts under hypergravity conditions are linearly correlated with gravitropic curvature in wild‐type stems. We next analyzed the hypergravity response in the shoot gravitropism 2 (sgr2) mutant, which exhibits neither a shoot gravitropic response nor amyloplast sedimentation at 1 g. sgr2 mutants were able to sense and respond to gravity under 30 g conditions, during which the amyloplasts sedimented. These findings are consistent with amyloplast redistribution resulting from gravity‐driven movements triggering shoot gravisensing. To further support this idea, we examined two additional gravitropic mutants, phosphoglucomutase (pgm) and sgr9, which show abnormal amyloplast distribution and reduced gravitropism at 1 g. We found that the correlation between hypergravity‐induced amyloplast sedimentation and gravitropic curvature of these mutants was identical to that of wild‐type plants. These observations suggest that Arabidopsis shoots have a gravisensing mechanism that linearly converts the number of amyloplasts that settle to the ‘bottom’ of the cell into gravitropic signals. Further, the restoration of the gravitropic response by hypergravity in the gravitropic mutants that we tested indicates that these lines probably have a functional gravisensing mechanism that is not triggered at 1 g.</description><subject>amyloplast</subject><subject>Arabidopsis</subject><subject>Arabidopsis - chemistry</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - physiology</subject><subject>Arabidopsis Proteins - chemistry</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - physiology</subject><subject>Biophysics</subject><subject>Cells</subject><subject>Centrifugation</subject><subject>centrifuge microscope</subject><subject>gravisensing</subject><subject>Gravitropism - genetics</subject><subject>Hypergravity</subject><subject>Microscopy</subject><subject>Microscopy, Polarization</subject><subject>Mutation</subject><subject>Phosphoglucomutase - chemistry</subject><subject>Phosphoglucomutase - genetics</subject><subject>Phosphoglucomutase - physiology</subject><subject>Phospholipases - chemistry</subject><subject>Phospholipases - genetics</subject><subject>Phospholipases - physiology</subject><subject>Plant biology</subject><subject>Plant Shoots - chemistry</subject><subject>Plant Shoots - genetics</subject><subject>Plant Shoots - physiology</subject><subject>Plastids - chemistry</subject><subject>Plastids - genetics</subject><subject>Plastids - physiology</subject><subject>RING Finger Domains - genetics</subject><subject>RING Finger Domains - physiology</subject><subject>starch‐statolith hypothesis</subject><subject>Ubiquitin-Protein Ligases - chemistry</subject><subject>Ubiquitin-Protein Ligases - genetics</subject><subject>Ubiquitin-Protein Ligases - physiology</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10btu2zAUBmCiaBA7boa-QEGgSzIo4U2mOBpGLg0CJEMKdBMo6silIYkqj-TCbx-6TjsUCJfD4cMP8vyEfObsiqdzPQ7bKy6kUB_InMtlnkkuf3wkc2aWLNOKixk5Q9wyxrVcqlMyE4oxxZmak7jq9m0YWosjrT2mi4MO-pF6pD04QLRxT5sQ6SbanUfo0fcb6nu6irbydRgwSfwZwojUIo2wA9tCTas9tdSlpOibaQO08y4GdGGAT-SksS3C-dtckO-3Ny_r--zx6e7bevWYOcWNymoBWjpd5UqBcbWVqhBFVTDLjeY5F6YCKZyxzLmGSW3ypuCNM0ZpAZV2Ti7IxTF3iOHXBDiWnUcHbWt7CBOWXCnNWaGETPTrf3Qbptin1x1Uro3WrEjq8qgOP8EITTlE36X9lJyVhyLKVET5p4hkv7wlTlUH9T_5d_MJXB_Bb9_C_v2k8uX54Rj5Ch1Gk2A</recordid><startdate>201311</startdate><enddate>201311</enddate><creator>Toyota, Masatsugu</creator><creator>Ikeda, Norifumi</creator><creator>Sawai‐Toyota, Satoe</creator><creator>Kato, Takehide</creator><creator>Gilroy, Simon</creator><creator>Tasaka, Masao</creator><creator>Morita, Miyo Terao</creator><general>Blackwell Publishing Ltd</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>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201311</creationdate><title>Amyloplast displacement is necessary for gravisensing in Arabidopsis shoots as revealed by a centrifuge microscope</title><author>Toyota, Masatsugu ; Ikeda, Norifumi ; Sawai‐Toyota, Satoe ; Kato, Takehide ; Gilroy, Simon ; Tasaka, Masao ; Morita, Miyo Terao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4194-d2e73c7b544e9cda34828b80a19715129be32c9a0ccf03795f81fc99472eb7cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>amyloplast</topic><topic>Arabidopsis</topic><topic>Arabidopsis - chemistry</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - physiology</topic><topic>Arabidopsis Proteins - chemistry</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - physiology</topic><topic>Biophysics</topic><topic>Cells</topic><topic>Centrifugation</topic><topic>centrifuge microscope</topic><topic>gravisensing</topic><topic>Gravitropism - genetics</topic><topic>Hypergravity</topic><topic>Microscopy</topic><topic>Microscopy, Polarization</topic><topic>Mutation</topic><topic>Phosphoglucomutase - chemistry</topic><topic>Phosphoglucomutase - genetics</topic><topic>Phosphoglucomutase - physiology</topic><topic>Phospholipases - chemistry</topic><topic>Phospholipases - genetics</topic><topic>Phospholipases - physiology</topic><topic>Plant biology</topic><topic>Plant Shoots - chemistry</topic><topic>Plant Shoots - genetics</topic><topic>Plant Shoots - physiology</topic><topic>Plastids - chemistry</topic><topic>Plastids - genetics</topic><topic>Plastids - physiology</topic><topic>RING Finger Domains - genetics</topic><topic>RING Finger Domains - physiology</topic><topic>starch‐statolith hypothesis</topic><topic>Ubiquitin-Protein Ligases - chemistry</topic><topic>Ubiquitin-Protein Ligases - genetics</topic><topic>Ubiquitin-Protein Ligases - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Toyota, Masatsugu</creatorcontrib><creatorcontrib>Ikeda, Norifumi</creatorcontrib><creatorcontrib>Sawai‐Toyota, Satoe</creatorcontrib><creatorcontrib>Kato, Takehide</creatorcontrib><creatorcontrib>Gilroy, Simon</creatorcontrib><creatorcontrib>Tasaka, Masao</creatorcontrib><creatorcontrib>Morita, Miyo Terao</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>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</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 Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Toyota, Masatsugu</au><au>Ikeda, Norifumi</au><au>Sawai‐Toyota, Satoe</au><au>Kato, Takehide</au><au>Gilroy, Simon</au><au>Tasaka, Masao</au><au>Morita, Miyo Terao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amyloplast displacement is necessary for gravisensing in Arabidopsis shoots as revealed by a centrifuge microscope</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2013-11</date><risdate>2013</risdate><volume>76</volume><issue>4</issue><spage>648</spage><epage>660</epage><pages>648-660</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Summary
The starch‐statolith hypothesis proposes that starch‐filled amyloplasts act as statoliths in plant gravisensing, moving in response to the gravity vector and signaling its direction. However, recent studies suggest that amyloplasts show continuous, complex movements in Arabidopsis shoots, contradicting the idea of a so‐called ‘static’ or ‘settled’ statolith. Here, we show that amyloplast movement underlies shoot gravisensing by using a custom‐designed centrifuge microscope in combination with analysis of gravitropic mutants. The centrifuge microscope revealed that sedimentary movements of amyloplasts under hypergravity conditions are linearly correlated with gravitropic curvature in wild‐type stems. We next analyzed the hypergravity response in the shoot gravitropism 2 (sgr2) mutant, which exhibits neither a shoot gravitropic response nor amyloplast sedimentation at 1 g. sgr2 mutants were able to sense and respond to gravity under 30 g conditions, during which the amyloplasts sedimented. These findings are consistent with amyloplast redistribution resulting from gravity‐driven movements triggering shoot gravisensing. To further support this idea, we examined two additional gravitropic mutants, phosphoglucomutase (pgm) and sgr9, which show abnormal amyloplast distribution and reduced gravitropism at 1 g. We found that the correlation between hypergravity‐induced amyloplast sedimentation and gravitropic curvature of these mutants was identical to that of wild‐type plants. These observations suggest that Arabidopsis shoots have a gravisensing mechanism that linearly converts the number of amyloplasts that settle to the ‘bottom’ of the cell into gravitropic signals. Further, the restoration of the gravitropic response by hypergravity in the gravitropic mutants that we tested indicates that these lines probably have a functional gravisensing mechanism that is not triggered at 1 g.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24004104</pmid><doi>10.1111/tpj.12324</doi><tpages>13</tpages></addata></record> |
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subjects | amyloplast Arabidopsis Arabidopsis - chemistry Arabidopsis - genetics Arabidopsis - physiology Arabidopsis Proteins - chemistry Arabidopsis Proteins - genetics Arabidopsis Proteins - physiology Biophysics Cells Centrifugation centrifuge microscope gravisensing Gravitropism - genetics Hypergravity Microscopy Microscopy, Polarization Mutation Phosphoglucomutase - chemistry Phosphoglucomutase - genetics Phosphoglucomutase - physiology Phospholipases - chemistry Phospholipases - genetics Phospholipases - physiology Plant biology Plant Shoots - chemistry Plant Shoots - genetics Plant Shoots - physiology Plastids - chemistry Plastids - genetics Plastids - physiology RING Finger Domains - genetics RING Finger Domains - physiology starch‐statolith hypothesis Ubiquitin-Protein Ligases - chemistry Ubiquitin-Protein Ligases - genetics Ubiquitin-Protein Ligases - physiology |
title | Amyloplast displacement is necessary for gravisensing in Arabidopsis shoots as revealed by a centrifuge microscope |
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