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LRK-1, a C. elegans PARK8-Related Kinase, Regulates Axonal-Dendritic Polarity of SV Proteins
Neurons are polarized cells that contain distinct sets of proteins in their axons and dendrites. Synaptic vesicles (SV) and many SV proteins are exclusively localized in the presynaptic regions but not in dendrites. Despite their fundamental importance, the mechanisms underlying the polarized locali...
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Published in: | Current biology 2007-04, Vol.17 (7), p.592-598 |
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description | Neurons are polarized cells that contain distinct sets of proteins in their axons and dendrites. Synaptic vesicles (SV) and many SV proteins are exclusively localized in the presynaptic regions but not in dendrites. Despite their fundamental importance, the mechanisms underlying the polarized localization of SV proteins remain unclear. The transparent nematode
Caenorhabditis elegans can be used to examine sorting and transport of SV proteins in vivo. Here, we identify a novel protein kinase LRK-1, a
C. elegans homolog of the familial Parkinsonism gene
PARK8/
LRRK2 that is required for polarized localization of SV proteins. In
lrk-1 deletion mutants, SV proteins are localized to both presynaptic and dendritic endings in neurons. This aberrant localization of SV proteins in the dendrites is dependent on the AP-1 μ1 clathrin adaptor UNC-101, which is involved in polarized dendritic transport, but not on UNC-104 kinesin, which is required for the transport of SV to presynaptic regions. The LRK-1 proteins are localized in the Golgi apparatus. These results suggest that the LRK-1 protein kinase determines polarized sorting of SV proteins to the axons by excluding SV proteins from the dendrite-specific transport machinery in the Golgi. |
doi_str_mv | 10.1016/j.cub.2007.01.074 |
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Caenorhabditis elegans can be used to examine sorting and transport of SV proteins in vivo. Here, we identify a novel protein kinase LRK-1, a
C. elegans homolog of the familial Parkinsonism gene
PARK8/
LRRK2 that is required for polarized localization of SV proteins. In
lrk-1 deletion mutants, SV proteins are localized to both presynaptic and dendritic endings in neurons. This aberrant localization of SV proteins in the dendrites is dependent on the AP-1 μ1 clathrin adaptor UNC-101, which is involved in polarized dendritic transport, but not on UNC-104 kinesin, which is required for the transport of SV to presynaptic regions. The LRK-1 proteins are localized in the Golgi apparatus. These results suggest that the LRK-1 protein kinase determines polarized sorting of SV proteins to the axons by excluding SV proteins from the dendrite-specific transport machinery in the Golgi.</description><identifier>ISSN: 0960-9822</identifier><identifier>EISSN: 1879-0445</identifier><identifier>DOI: 10.1016/j.cub.2007.01.074</identifier><identifier>PMID: 17346966</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Animals ; Axons - metabolism ; Caenorhabditis elegans ; Caenorhabditis elegans - genetics ; Caenorhabditis elegans - metabolism ; Caenorhabditis elegans Proteins - genetics ; Caenorhabditis elegans Proteins - metabolism ; Cell Polarity ; CELLBIO ; Dendrites - metabolism ; Golgi Apparatus - metabolism ; Humans ; Intracellular Signaling Peptides and Proteins ; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 ; Nematoda ; Nerve Tissue Proteins - genetics ; Neurons - chemistry ; Neurons - cytology ; Neurons - metabolism ; Protein Serine-Threonine Kinases - chemistry ; Protein Serine-Threonine Kinases - genetics ; Protein Serine-Threonine Kinases - metabolism ; Synaptic Vesicles - chemistry ; Synaptic Vesicles - metabolism</subject><ispartof>Current biology, 2007-04, Vol.17 (7), p.592-598</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-1391de3b70572426f29fec2adf24da1b5f1f743bb6c5052d19e911287b245d2a3</citedby><cites>FETCH-LOGICAL-c491t-1391de3b70572426f29fec2adf24da1b5f1f743bb6c5052d19e911287b245d2a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17346966$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sakaguchi-Nakashima, Aisa</creatorcontrib><creatorcontrib>Meir, James Y.</creatorcontrib><creatorcontrib>Jin, Yishi</creatorcontrib><creatorcontrib>Matsumoto, Kunihiro</creatorcontrib><creatorcontrib>Hisamoto, Naoki</creatorcontrib><title>LRK-1, a C. elegans PARK8-Related Kinase, Regulates Axonal-Dendritic Polarity of SV Proteins</title><title>Current biology</title><addtitle>Curr Biol</addtitle><description>Neurons are polarized cells that contain distinct sets of proteins in their axons and dendrites. Synaptic vesicles (SV) and many SV proteins are exclusively localized in the presynaptic regions but not in dendrites. Despite their fundamental importance, the mechanisms underlying the polarized localization of SV proteins remain unclear. The transparent nematode
Caenorhabditis elegans can be used to examine sorting and transport of SV proteins in vivo. Here, we identify a novel protein kinase LRK-1, a
C. elegans homolog of the familial Parkinsonism gene
PARK8/
LRRK2 that is required for polarized localization of SV proteins. In
lrk-1 deletion mutants, SV proteins are localized to both presynaptic and dendritic endings in neurons. This aberrant localization of SV proteins in the dendrites is dependent on the AP-1 μ1 clathrin adaptor UNC-101, which is involved in polarized dendritic transport, but not on UNC-104 kinesin, which is required for the transport of SV to presynaptic regions. The LRK-1 proteins are localized in the Golgi apparatus. These results suggest that the LRK-1 protein kinase determines polarized sorting of SV proteins to the axons by excluding SV proteins from the dendrite-specific transport machinery in the Golgi.</description><subject>Animals</subject><subject>Axons - metabolism</subject><subject>Caenorhabditis elegans</subject><subject>Caenorhabditis elegans - genetics</subject><subject>Caenorhabditis elegans - metabolism</subject><subject>Caenorhabditis elegans Proteins - genetics</subject><subject>Caenorhabditis elegans Proteins - metabolism</subject><subject>Cell Polarity</subject><subject>CELLBIO</subject><subject>Dendrites - metabolism</subject><subject>Golgi Apparatus - metabolism</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins</subject><subject>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2</subject><subject>Nematoda</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Neurons - chemistry</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Protein Serine-Threonine Kinases - chemistry</subject><subject>Protein Serine-Threonine Kinases - genetics</subject><subject>Protein Serine-Threonine Kinases - metabolism</subject><subject>Synaptic Vesicles - chemistry</subject><subject>Synaptic Vesicles - metabolism</subject><issn>0960-9822</issn><issn>1879-0445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkE1rGzEQhkVISdw0P6CXoFNO2a1Gq5UscjJO2gQbapyPU0Bopdkgs95NpN3S_PuusaG39jTD8LwvzEPIV2A5MJDfNrkbqpwzpnIGOVPiiExgqnTGhCiPyYRpyTI95fyUfE5pwxjwqZYn5BRUIaSWckJelutFBlfU0nlOscFX2ya6mq0X02yNje3R00VobcIrusbXYXdJdPa7a22T3WDrY-iDo6uuseP2QbuaPjzTVex6DG36Qj7Vtkl4fphn5On77eP8Llv-_HE_ny0zJzT0GRQaPBaVYqXigsua6xodt77mwluoyhpqJYqqkq5kJfegUcP4iqq4KD23xRm53Pe-xe59wNSbbUgOm8a22A3JKFaIgnP5XxC0FErBDoQ96GKXUsTavMWwtfHDADM792ZjRvdm594wMKP7MXNxKB-qLfq_iYPsEbjeAzi6-BUwmuQCtg59iOh647vwj_o_OrORkg</recordid><startdate>20070403</startdate><enddate>20070403</enddate><creator>Sakaguchi-Nakashima, Aisa</creator><creator>Meir, James Y.</creator><creator>Jin, Yishi</creator><creator>Matsumoto, Kunihiro</creator><creator>Hisamoto, Naoki</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20070403</creationdate><title>LRK-1, a C. elegans PARK8-Related Kinase, Regulates Axonal-Dendritic Polarity of SV Proteins</title><author>Sakaguchi-Nakashima, Aisa ; 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Synaptic vesicles (SV) and many SV proteins are exclusively localized in the presynaptic regions but not in dendrites. Despite their fundamental importance, the mechanisms underlying the polarized localization of SV proteins remain unclear. The transparent nematode
Caenorhabditis elegans can be used to examine sorting and transport of SV proteins in vivo. Here, we identify a novel protein kinase LRK-1, a
C. elegans homolog of the familial Parkinsonism gene
PARK8/
LRRK2 that is required for polarized localization of SV proteins. In
lrk-1 deletion mutants, SV proteins are localized to both presynaptic and dendritic endings in neurons. This aberrant localization of SV proteins in the dendrites is dependent on the AP-1 μ1 clathrin adaptor UNC-101, which is involved in polarized dendritic transport, but not on UNC-104 kinesin, which is required for the transport of SV to presynaptic regions. The LRK-1 proteins are localized in the Golgi apparatus. These results suggest that the LRK-1 protein kinase determines polarized sorting of SV proteins to the axons by excluding SV proteins from the dendrite-specific transport machinery in the Golgi.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>17346966</pmid><doi>10.1016/j.cub.2007.01.074</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Axons - metabolism Caenorhabditis elegans Caenorhabditis elegans - genetics Caenorhabditis elegans - metabolism Caenorhabditis elegans Proteins - genetics Caenorhabditis elegans Proteins - metabolism Cell Polarity CELLBIO Dendrites - metabolism Golgi Apparatus - metabolism Humans Intracellular Signaling Peptides and Proteins Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 Nematoda Nerve Tissue Proteins - genetics Neurons - chemistry Neurons - cytology Neurons - metabolism Protein Serine-Threonine Kinases - chemistry Protein Serine-Threonine Kinases - genetics Protein Serine-Threonine Kinases - metabolism Synaptic Vesicles - chemistry Synaptic Vesicles - metabolism |
title | LRK-1, a C. elegans PARK8-Related Kinase, Regulates Axonal-Dendritic Polarity of SV Proteins |
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