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A multi‐colour/multi‐affinity marker set to visualize phosphoinositide dynamics in A rabidopsis
Phosphatidylinositolphosphates ( PIP s) are phospholipids that contain a phosphorylated inositol head group. PIP s represent a minor fraction of total phospholipids, but are involved in many regulatory processes, such as cell signalling and intracellular trafficking. Membrane compartments are enrich...
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Published in: | The Plant journal : for cell and molecular biology 2014-01, Vol.77 (2), p.322-337 |
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container_end_page | 337 |
container_issue | 2 |
container_start_page | 322 |
container_title | The Plant journal : for cell and molecular biology |
container_volume | 77 |
creator | Simon, Mathilde Laetitia Audrey Platre, Matthieu Pierre Assil, Sonia van Wijk, Ringo Chen, William Yawei Chory, Joanne Dreux, Marlène Munnik, Teun Jaillais, Yvon |
description | Phosphatidylinositolphosphates (
PIP
s) are phospholipids that contain a phosphorylated inositol head group.
PIP
s represent a minor fraction of total phospholipids, but are involved in many regulatory processes, such as cell signalling and intracellular trafficking. Membrane compartments are enriched or depleted in specific
PIP
s, providing a unique composition for these compartments and contributing to their identity. The precise subcellular localization and dynamics of most
PIP
species is not fully understood in plants. Here, we designed genetically encoded biosensors with distinct relative affinities and expressed them stably in
A
rabidopsis thaliana
. Analysis of this multi‐affinity ‘
PIP
line’ marker set revealed previously unrecognized localization of various
PIP
s in root epidermis. Notably, we found that
PI
(4,5)P
2
is able to localize
PIP
2
‐interacting protein domains to the plasma membrane in non‐stressed root epidermal cells. Our analysis further revealed that there is a gradient of
PI
4P, with the highest concentration at the plasma membrane, intermediate concentration in post‐Golgi/endosomal compartments, and the lowest concentration in the Golgi. Finally, we also found a similar gradient of
PI
3P from high in late endosomes to low in the tonoplast. Our library extends the range of available
PIP
biosensors, and will allow rapid progress in our understanding of
PIP
dynamics in plants. |
doi_str_mv | 10.1111/tpj.12358 |
format | article |
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PIP
s) are phospholipids that contain a phosphorylated inositol head group.
PIP
s represent a minor fraction of total phospholipids, but are involved in many regulatory processes, such as cell signalling and intracellular trafficking. Membrane compartments are enriched or depleted in specific
PIP
s, providing a unique composition for these compartments and contributing to their identity. The precise subcellular localization and dynamics of most
PIP
species is not fully understood in plants. Here, we designed genetically encoded biosensors with distinct relative affinities and expressed them stably in
A
rabidopsis thaliana
. Analysis of this multi‐affinity ‘
PIP
line’ marker set revealed previously unrecognized localization of various
PIP
s in root epidermis. Notably, we found that
PI
(4,5)P
2
is able to localize
PIP
2
‐interacting protein domains to the plasma membrane in non‐stressed root epidermal cells. Our analysis further revealed that there is a gradient of
PI
4P, with the highest concentration at the plasma membrane, intermediate concentration in post‐Golgi/endosomal compartments, and the lowest concentration in the Golgi. Finally, we also found a similar gradient of
PI
3P from high in late endosomes to low in the tonoplast. Our library extends the range of available
PIP
biosensors, and will allow rapid progress in our understanding of
PIP
dynamics in plants.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.12358</identifier><language>eng</language><ispartof>The Plant journal : for cell and molecular biology, 2014-01, Vol.77 (2), p.322-337</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c748-ec7802f9f5bd832ed6820c92a0e1e7791ca62abb3ace4c1e7bdd398008a9a8133</citedby><cites>FETCH-LOGICAL-c748-ec7802f9f5bd832ed6820c92a0e1e7791ca62abb3ace4c1e7bdd398008a9a8133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Simon, Mathilde Laetitia Audrey</creatorcontrib><creatorcontrib>Platre, Matthieu Pierre</creatorcontrib><creatorcontrib>Assil, Sonia</creatorcontrib><creatorcontrib>van Wijk, Ringo</creatorcontrib><creatorcontrib>Chen, William Yawei</creatorcontrib><creatorcontrib>Chory, Joanne</creatorcontrib><creatorcontrib>Dreux, Marlène</creatorcontrib><creatorcontrib>Munnik, Teun</creatorcontrib><creatorcontrib>Jaillais, Yvon</creatorcontrib><title>A multi‐colour/multi‐affinity marker set to visualize phosphoinositide dynamics in A rabidopsis</title><title>The Plant journal : for cell and molecular biology</title><description>Phosphatidylinositolphosphates (
PIP
s) are phospholipids that contain a phosphorylated inositol head group.
PIP
s represent a minor fraction of total phospholipids, but are involved in many regulatory processes, such as cell signalling and intracellular trafficking. Membrane compartments are enriched or depleted in specific
PIP
s, providing a unique composition for these compartments and contributing to their identity. The precise subcellular localization and dynamics of most
PIP
species is not fully understood in plants. Here, we designed genetically encoded biosensors with distinct relative affinities and expressed them stably in
A
rabidopsis thaliana
. Analysis of this multi‐affinity ‘
PIP
line’ marker set revealed previously unrecognized localization of various
PIP
s in root epidermis. Notably, we found that
PI
(4,5)P
2
is able to localize
PIP
2
‐interacting protein domains to the plasma membrane in non‐stressed root epidermal cells. Our analysis further revealed that there is a gradient of
PI
4P, with the highest concentration at the plasma membrane, intermediate concentration in post‐Golgi/endosomal compartments, and the lowest concentration in the Golgi. Finally, we also found a similar gradient of
PI
3P from high in late endosomes to low in the tonoplast. Our library extends the range of available
PIP
biosensors, and will allow rapid progress in our understanding of
PIP
dynamics in plants.</description><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNo1kMtKxDAYhYMoWEcXvkG2LjqTSy_psgzqCANuZuGupLngP7ZNSVKhrnwEn9Ensd4OHA7nLH5-PoSuKVnTRZs4HteU8VycoITyIk855U-nKCFVQdIyo-wcXYRwJISWvMgSpGrcT12Ez_cP5To3-c1_ldbCAHHGvfQvxuNgIo4Ov0KYZAdvBo_PLiyGwQWIoA3W8yB7UAHDgGvsZQvajQHCJTqzsgvm6i9X6HB3e9ju0v3j_cO23qeqzERqVCkIs5XNWy04M7oQjKiKSWKoKcuKKlkw2bZcKpOpZWq15pUgRMhKCsr5Ct38nlXeheCNbUYPy_NzQ0nzDadZ4DQ_cPgXUKtcZw</recordid><startdate>201401</startdate><enddate>201401</enddate><creator>Simon, Mathilde Laetitia Audrey</creator><creator>Platre, Matthieu Pierre</creator><creator>Assil, Sonia</creator><creator>van Wijk, Ringo</creator><creator>Chen, William Yawei</creator><creator>Chory, Joanne</creator><creator>Dreux, Marlène</creator><creator>Munnik, Teun</creator><creator>Jaillais, Yvon</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201401</creationdate><title>A multi‐colour/multi‐affinity marker set to visualize phosphoinositide dynamics in A rabidopsis</title><author>Simon, Mathilde Laetitia Audrey ; Platre, Matthieu Pierre ; Assil, Sonia ; van Wijk, Ringo ; Chen, William Yawei ; Chory, Joanne ; Dreux, Marlène ; Munnik, Teun ; Jaillais, Yvon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c748-ec7802f9f5bd832ed6820c92a0e1e7791ca62abb3ace4c1e7bdd398008a9a8133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Simon, Mathilde Laetitia Audrey</creatorcontrib><creatorcontrib>Platre, Matthieu Pierre</creatorcontrib><creatorcontrib>Assil, Sonia</creatorcontrib><creatorcontrib>van Wijk, Ringo</creatorcontrib><creatorcontrib>Chen, William Yawei</creatorcontrib><creatorcontrib>Chory, Joanne</creatorcontrib><creatorcontrib>Dreux, Marlène</creatorcontrib><creatorcontrib>Munnik, Teun</creatorcontrib><creatorcontrib>Jaillais, Yvon</creatorcontrib><collection>CrossRef</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Simon, Mathilde Laetitia Audrey</au><au>Platre, Matthieu Pierre</au><au>Assil, Sonia</au><au>van Wijk, Ringo</au><au>Chen, William Yawei</au><au>Chory, Joanne</au><au>Dreux, Marlène</au><au>Munnik, Teun</au><au>Jaillais, Yvon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A multi‐colour/multi‐affinity marker set to visualize phosphoinositide dynamics in A rabidopsis</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><date>2014-01</date><risdate>2014</risdate><volume>77</volume><issue>2</issue><spage>322</spage><epage>337</epage><pages>322-337</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Phosphatidylinositolphosphates (
PIP
s) are phospholipids that contain a phosphorylated inositol head group.
PIP
s represent a minor fraction of total phospholipids, but are involved in many regulatory processes, such as cell signalling and intracellular trafficking. Membrane compartments are enriched or depleted in specific
PIP
s, providing a unique composition for these compartments and contributing to their identity. The precise subcellular localization and dynamics of most
PIP
species is not fully understood in plants. Here, we designed genetically encoded biosensors with distinct relative affinities and expressed them stably in
A
rabidopsis thaliana
. Analysis of this multi‐affinity ‘
PIP
line’ marker set revealed previously unrecognized localization of various
PIP
s in root epidermis. Notably, we found that
PI
(4,5)P
2
is able to localize
PIP
2
‐interacting protein domains to the plasma membrane in non‐stressed root epidermal cells. Our analysis further revealed that there is a gradient of
PI
4P, with the highest concentration at the plasma membrane, intermediate concentration in post‐Golgi/endosomal compartments, and the lowest concentration in the Golgi. Finally, we also found a similar gradient of
PI
3P from high in late endosomes to low in the tonoplast. Our library extends the range of available
PIP
biosensors, and will allow rapid progress in our understanding of
PIP
dynamics in plants.</abstract><doi>10.1111/tpj.12358</doi><tpages>16</tpages></addata></record> |
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language | eng |
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title | A multi‐colour/multi‐affinity marker set to visualize phosphoinositide dynamics in A rabidopsis |
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