LOK Is a Novel Mouse STE20-like Protein Kinase That Is Expressed Predominantly in Lymphocytes
We have identified a new gene, designatedlok (lymphocyte-oriented kinase), that encodes a 966-amino acid protein kinase whose catalytic domain at the N terminus shows homology to that of the STE20 family members involved in mitogen-activated protein (MAP) kinase cascades. The non-catalytic domain of...
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Veröffentlicht in: | The Journal of biological chemistry 1997-09, Vol.272 (36), p.22679-22684 |
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creator | Kuramochi, Satomi Moriguchi, Tetsuo Kuida, Keisuke Endo, Junji Semba, Kentaro Nishida, Eisuke Karasuyama, Hajime |
description | We have identified a new gene, designatedlok (lymphocyte-oriented kinase), that encodes a 966-amino acid protein kinase whose catalytic domain at the N terminus shows homology to that of the STE20 family members involved in mitogen-activated protein (MAP) kinase cascades. The non-catalytic domain of LOK does not have any similarity to that of other known members of the family. There is a proline-rich motif with Src homology region 3 binding potential, followed by a long coiled-coil structure at the C terminus. LOK is expressed as a 130-kDa protein, which was detected predominantly in lymphoid organs such as spleen, thymus, and bone marrow, in contrast to other mammalian members of the STE20 family. LOK phosphorylated itself as well as substrates such as myelin basic protein and histone IIA on serine and threonine residues but not on tyrosine residues, establishing LOK as a novel serine/threonine kinase. When coexpressed in COS7 cells with the known MAP kinase isoforms (ERK, JNK, and p38), LOK activated none of them in contrast to PAK- and GCK-related kinases. These results suggest that LOK could be involved in a novel signaling pathway in lymphocytes, which is distinct from the known MAP kinase cascades. |
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The non-catalytic domain of LOK does not have any similarity to that of other known members of the family. There is a proline-rich motif with Src homology region 3 binding potential, followed by a long coiled-coil structure at the C terminus. LOK is expressed as a 130-kDa protein, which was detected predominantly in lymphoid organs such as spleen, thymus, and bone marrow, in contrast to other mammalian members of the STE20 family. LOK phosphorylated itself as well as substrates such as myelin basic protein and histone IIA on serine and threonine residues but not on tyrosine residues, establishing LOK as a novel serine/threonine kinase. When coexpressed in COS7 cells with the known MAP kinase isoforms (ERK, JNK, and p38), LOK activated none of them in contrast to PAK- and GCK-related kinases. These results suggest that LOK could be involved in a novel signaling pathway in lymphocytes, which is distinct from the known MAP kinase cascades.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.272.36.22679</identifier><identifier>PMID: 9278426</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amino Acid Sequence ; Animals ; Base Sequence ; Calcium-Calmodulin-Dependent Protein Kinases - metabolism ; Catalysis ; Cloning, Molecular ; COS Cells ; Enzyme Activation ; Gene Expression Regulation, Enzymologic ; Humans ; Intracellular Signaling Peptides and Proteins ; Lymphocytes - enzymology ; MAP Kinase Kinase Kinases ; Mice ; Molecular Sequence Data ; Protein-Serine-Threonine Kinases - genetics ; Protein-Serine-Threonine Kinases - metabolism ; Saccharomyces cerevisiae Proteins ; Sequence Homology, Amino Acid</subject><ispartof>The Journal of biological chemistry, 1997-09, Vol.272 (36), p.22679-22684</ispartof><rights>1997 © 1997 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c447t-c7ef42debc85eff8bb651055a5f71bab4df33e2b439d1a01a583877c79e5480c3</citedby><cites>FETCH-LOGICAL-c447t-c7ef42debc85eff8bb651055a5f71bab4df33e2b439d1a01a583877c79e5480c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9278426$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuramochi, Satomi</creatorcontrib><creatorcontrib>Moriguchi, Tetsuo</creatorcontrib><creatorcontrib>Kuida, Keisuke</creatorcontrib><creatorcontrib>Endo, Junji</creatorcontrib><creatorcontrib>Semba, Kentaro</creatorcontrib><creatorcontrib>Nishida, Eisuke</creatorcontrib><creatorcontrib>Karasuyama, Hajime</creatorcontrib><title>LOK Is a Novel Mouse STE20-like Protein Kinase That Is Expressed Predominantly in Lymphocytes</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>We have identified a new gene, designatedlok (lymphocyte-oriented kinase), that encodes a 966-amino acid protein kinase whose catalytic domain at the N terminus shows homology to that of the STE20 family members involved in mitogen-activated protein (MAP) kinase cascades. The non-catalytic domain of LOK does not have any similarity to that of other known members of the family. There is a proline-rich motif with Src homology region 3 binding potential, followed by a long coiled-coil structure at the C terminus. LOK is expressed as a 130-kDa protein, which was detected predominantly in lymphoid organs such as spleen, thymus, and bone marrow, in contrast to other mammalian members of the STE20 family. LOK phosphorylated itself as well as substrates such as myelin basic protein and histone IIA on serine and threonine residues but not on tyrosine residues, establishing LOK as a novel serine/threonine kinase. When coexpressed in COS7 cells with the known MAP kinase isoforms (ERK, JNK, and p38), LOK activated none of them in contrast to PAK- and GCK-related kinases. These results suggest that LOK could be involved in a novel signaling pathway in lymphocytes, which is distinct from the known MAP kinase cascades.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Calcium-Calmodulin-Dependent Protein Kinases - metabolism</subject><subject>Catalysis</subject><subject>Cloning, Molecular</subject><subject>COS Cells</subject><subject>Enzyme Activation</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Humans</subject><subject>Intracellular Signaling Peptides and Proteins</subject><subject>Lymphocytes - enzymology</subject><subject>MAP Kinase Kinase Kinases</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Protein-Serine-Threonine Kinases - genetics</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Saccharomyces cerevisiae Proteins</subject><subject>Sequence Homology, Amino Acid</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM9v0zAYhq0JNLqxOxekHBC3FP-MY25oKtu0wpAoEhdk2c6XxSOJOzvd6H8_b612QEL44sP7vK_sB6E3BM8JlvzDjXVzKumcVXNKK6kO0IzgmpVMkJ8v0AxjSkpFRf0KHaV0g_PhihyiQ0VlzWk1Q7-WV5fFRSpM8TXcQV98CZsExffVguKy97-h-BbDBH4sLv1ocrLqzPTIL_6sI6QETQagCUNOx6nfFplcbod1F9x2gvQavWxNn-Bkfx-jH58Xq9Pzcnl1dnH6aVk6zuVUOgktpw1YVwto29raShAshBGtJNZY3rSMAbWcqYYYTIyoWS2lkwoEr7Fjx-j9bncdw-0G0qQHnxz0vRkhf0jL7IBSJf8LkgrLCiuVQbwDXQwpRWj1OvrBxK0mWD-q11m9zuo1q_ST-lx5u9_e2AGa58Ledc7f7fLOX3f3PoK2PrgOhr9nPu4wyMLuPESdnIfRQZMrbtJN8P9-wwPh253s</recordid><startdate>19970905</startdate><enddate>19970905</enddate><creator>Kuramochi, Satomi</creator><creator>Moriguchi, Tetsuo</creator><creator>Kuida, Keisuke</creator><creator>Endo, Junji</creator><creator>Semba, Kentaro</creator><creator>Nishida, Eisuke</creator><creator>Karasuyama, Hajime</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</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>7T5</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19970905</creationdate><title>LOK Is a Novel Mouse STE20-like Protein Kinase That Is Expressed Predominantly in Lymphocytes</title><author>Kuramochi, Satomi ; Moriguchi, Tetsuo ; Kuida, Keisuke ; Endo, Junji ; Semba, Kentaro ; Nishida, Eisuke ; Karasuyama, Hajime</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-c7ef42debc85eff8bb651055a5f71bab4df33e2b439d1a01a583877c79e5480c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Calcium-Calmodulin-Dependent Protein Kinases - metabolism</topic><topic>Catalysis</topic><topic>Cloning, Molecular</topic><topic>COS Cells</topic><topic>Enzyme Activation</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Humans</topic><topic>Intracellular Signaling Peptides and Proteins</topic><topic>Lymphocytes - enzymology</topic><topic>MAP Kinase Kinase Kinases</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Protein-Serine-Threonine Kinases - genetics</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Saccharomyces cerevisiae Proteins</topic><topic>Sequence Homology, Amino Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuramochi, Satomi</creatorcontrib><creatorcontrib>Moriguchi, Tetsuo</creatorcontrib><creatorcontrib>Kuida, Keisuke</creatorcontrib><creatorcontrib>Endo, Junji</creatorcontrib><creatorcontrib>Semba, Kentaro</creatorcontrib><creatorcontrib>Nishida, Eisuke</creatorcontrib><creatorcontrib>Karasuyama, Hajime</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuramochi, Satomi</au><au>Moriguchi, Tetsuo</au><au>Kuida, Keisuke</au><au>Endo, Junji</au><au>Semba, Kentaro</au><au>Nishida, Eisuke</au><au>Karasuyama, Hajime</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LOK Is a Novel Mouse STE20-like Protein Kinase That Is Expressed Predominantly in Lymphocytes</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1997-09-05</date><risdate>1997</risdate><volume>272</volume><issue>36</issue><spage>22679</spage><epage>22684</epage><pages>22679-22684</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>We have identified a new gene, designatedlok (lymphocyte-oriented kinase), that encodes a 966-amino acid protein kinase whose catalytic domain at the N terminus shows homology to that of the STE20 family members involved in mitogen-activated protein (MAP) kinase cascades. The non-catalytic domain of LOK does not have any similarity to that of other known members of the family. There is a proline-rich motif with Src homology region 3 binding potential, followed by a long coiled-coil structure at the C terminus. LOK is expressed as a 130-kDa protein, which was detected predominantly in lymphoid organs such as spleen, thymus, and bone marrow, in contrast to other mammalian members of the STE20 family. LOK phosphorylated itself as well as substrates such as myelin basic protein and histone IIA on serine and threonine residues but not on tyrosine residues, establishing LOK as a novel serine/threonine kinase. When coexpressed in COS7 cells with the known MAP kinase isoforms (ERK, JNK, and p38), LOK activated none of them in contrast to PAK- and GCK-related kinases. 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subjects | Amino Acid Sequence Animals Base Sequence Calcium-Calmodulin-Dependent Protein Kinases - metabolism Catalysis Cloning, Molecular COS Cells Enzyme Activation Gene Expression Regulation, Enzymologic Humans Intracellular Signaling Peptides and Proteins Lymphocytes - enzymology MAP Kinase Kinase Kinases Mice Molecular Sequence Data Protein-Serine-Threonine Kinases - genetics Protein-Serine-Threonine Kinases - metabolism Saccharomyces cerevisiae Proteins Sequence Homology, Amino Acid |
title | LOK Is a Novel Mouse STE20-like Protein Kinase That Is Expressed Predominantly in Lymphocytes |
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