Deletion analysis of AGD1 reveals domains crucial for plasma membrane recruitment and function in root hair polarity
AGD1, a plant ACAP-type ADP-ribosylation factor-GTPase activating protein (ARF-GAP), functions in specifying root hair polarity in To better understand how AGD1 modulates root hair growth, we generated full-length and domain-deleted AGD1-green fluorescent protein (GFP) constructs, and followed their...
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Veröffentlicht in: | Journal of cell science 2018-01, Vol.131 (2), p.jcs203828-jcs203828 |
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container_title | Journal of cell science |
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creator | Yoo, Cheol-Min Naramoto, Satoshi Sparks, J Alan Khan, Bibi Rafeiza Nakashima, Jin Fukuda, Hiroo Blancaflor, Elison B |
description | AGD1, a plant ACAP-type ADP-ribosylation factor-GTPase activating protein (ARF-GAP), functions in specifying root hair polarity in
To better understand how AGD1 modulates root hair growth, we generated full-length and domain-deleted AGD1-green fluorescent protein (GFP) constructs, and followed their localization during root hair development. AGD1-GFP localized to the cytoplasm and was recruited to specific regions of the root hair plasma membrane (PM). Distinct PM AGD1-GFP signal was first detected along the site of root hair bulge formation. The construct continued to mark the PM at the root hair apical dome, but only during periods of reduced growth. During rapid tip growth, AGD1-GFP labeled the PM of the lateral flanks and dissipated from the apical-most PM. Deletion analysis and a single domain GFP fusion revealed that the pleckstrin homology (PH) domain is the minimal unit required for recruitment of AGD1 to the PM. Our results indicate that differential recruitment of AGD1 to specific PM domains is an essential component of the membrane trafficking machinery that facilitates root hair developmental phase transitions and responses to changes in the root microenvironment. |
doi_str_mv | 10.1242/jcs.203828 |
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To better understand how AGD1 modulates root hair growth, we generated full-length and domain-deleted AGD1-green fluorescent protein (GFP) constructs, and followed their localization during root hair development. AGD1-GFP localized to the cytoplasm and was recruited to specific regions of the root hair plasma membrane (PM). Distinct PM AGD1-GFP signal was first detected along the site of root hair bulge formation. The construct continued to mark the PM at the root hair apical dome, but only during periods of reduced growth. During rapid tip growth, AGD1-GFP labeled the PM of the lateral flanks and dissipated from the apical-most PM. Deletion analysis and a single domain GFP fusion revealed that the pleckstrin homology (PH) domain is the minimal unit required for recruitment of AGD1 to the PM. Our results indicate that differential recruitment of AGD1 to specific PM domains is an essential component of the membrane trafficking machinery that facilitates root hair developmental phase transitions and responses to changes in the root microenvironment.</description><identifier>ISSN: 0021-9533</identifier><identifier>EISSN: 1477-9137</identifier><identifier>DOI: 10.1242/jcs.203828</identifier><identifier>PMID: 28646092</identifier><language>eng</language><publisher>England: The Company of Biologists Ltd</publisher><subject>Adenosine diphosphate ; ADP-ribosylation factor ; Clonal deletion ; Cytoplasm ; Fluorescence ; Green fluorescent protein ; Guanosine triphosphatases ; Hair cells ; Homology ; Localization ; Machinery and equipment ; Membrane trafficking ; Phase transitions ; Pleckstrin ; Polarity ; Recruitment</subject><ispartof>Journal of cell science, 2018-01, Vol.131 (2), p.jcs203828-jcs203828</ispartof><rights>2018. Published by The Company of Biologists Ltd.</rights><rights>Copyright The Company of Biologists Ltd Jan 15, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-7cfa5a7bc2b2a1a67cc7a05d63234e53abaa48f1038e4f488b1d447d27bf14573</citedby><cites>FETCH-LOGICAL-c381t-7cfa5a7bc2b2a1a67cc7a05d63234e53abaa48f1038e4f488b1d447d27bf14573</cites><orcidid>0000-0001-6115-9670 ; 0000-0002-7824-9266 ; 0000-0002-3373-6343</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3665,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28646092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoo, Cheol-Min</creatorcontrib><creatorcontrib>Naramoto, Satoshi</creatorcontrib><creatorcontrib>Sparks, J Alan</creatorcontrib><creatorcontrib>Khan, Bibi Rafeiza</creatorcontrib><creatorcontrib>Nakashima, Jin</creatorcontrib><creatorcontrib>Fukuda, Hiroo</creatorcontrib><creatorcontrib>Blancaflor, Elison B</creatorcontrib><title>Deletion analysis of AGD1 reveals domains crucial for plasma membrane recruitment and function in root hair polarity</title><title>Journal of cell science</title><addtitle>J Cell Sci</addtitle><description>AGD1, a plant ACAP-type ADP-ribosylation factor-GTPase activating protein (ARF-GAP), functions in specifying root hair polarity in
To better understand how AGD1 modulates root hair growth, we generated full-length and domain-deleted AGD1-green fluorescent protein (GFP) constructs, and followed their localization during root hair development. AGD1-GFP localized to the cytoplasm and was recruited to specific regions of the root hair plasma membrane (PM). Distinct PM AGD1-GFP signal was first detected along the site of root hair bulge formation. The construct continued to mark the PM at the root hair apical dome, but only during periods of reduced growth. During rapid tip growth, AGD1-GFP labeled the PM of the lateral flanks and dissipated from the apical-most PM. Deletion analysis and a single domain GFP fusion revealed that the pleckstrin homology (PH) domain is the minimal unit required for recruitment of AGD1 to the PM. Our results indicate that differential recruitment of AGD1 to specific PM domains is an essential component of the membrane trafficking machinery that facilitates root hair developmental phase transitions and responses to changes in the root microenvironment.</description><subject>Adenosine diphosphate</subject><subject>ADP-ribosylation factor</subject><subject>Clonal deletion</subject><subject>Cytoplasm</subject><subject>Fluorescence</subject><subject>Green fluorescent protein</subject><subject>Guanosine triphosphatases</subject><subject>Hair cells</subject><subject>Homology</subject><subject>Localization</subject><subject>Machinery and equipment</subject><subject>Membrane trafficking</subject><subject>Phase transitions</subject><subject>Pleckstrin</subject><subject>Polarity</subject><subject>Recruitment</subject><issn>0021-9533</issn><issn>1477-9137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkU9LwzAYh4Mobk4vfgAJeBGhM__atEfZdAoDL3oub9MEM9pmJqmwb29004OnHN7nfXjz-yF0ScmcMsHuNirMGeElK4_QlAops4pyeYymhDCaVTnnE3QWwoYQIlklT9GElYUoSMWmKC51p6N1A4YBul2wATuD71dLir3-1NAF3Loe7BCw8qOy0GHjPN52EHrAve4bD4NObJra2OshJlGLzTioH6sdsHcu4newact14G3cnaMTk8z64vDO0Nvjw-viKVu_rJ4X9-tM8ZLGTCoDOchGsYYBhUIqJYHkbcEZFzrn0ACI0tD0dS2MKMuGtkLIlsnGUJFLPkM3e-_Wu49Rh1j3NijddelkN4aappx4VQhCE3r9D9240adIQs0IKcqqknmeqNs9pbwLwWtTb73twe9qSurvLurURb3vIsFXB-XY9Lr9Q3_D51_A8YVJ</recordid><startdate>20180115</startdate><enddate>20180115</enddate><creator>Yoo, Cheol-Min</creator><creator>Naramoto, Satoshi</creator><creator>Sparks, J Alan</creator><creator>Khan, Bibi Rafeiza</creator><creator>Nakashima, Jin</creator><creator>Fukuda, Hiroo</creator><creator>Blancaflor, Elison B</creator><general>The Company of Biologists Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6115-9670</orcidid><orcidid>https://orcid.org/0000-0002-7824-9266</orcidid><orcidid>https://orcid.org/0000-0002-3373-6343</orcidid></search><sort><creationdate>20180115</creationdate><title>Deletion analysis of AGD1 reveals domains crucial for plasma membrane recruitment and function in root hair polarity</title><author>Yoo, Cheol-Min ; 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subjects | Adenosine diphosphate ADP-ribosylation factor Clonal deletion Cytoplasm Fluorescence Green fluorescent protein Guanosine triphosphatases Hair cells Homology Localization Machinery and equipment Membrane trafficking Phase transitions Pleckstrin Polarity Recruitment |
title | Deletion analysis of AGD1 reveals domains crucial for plasma membrane recruitment and function in root hair polarity |
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