The Janus kinases (Jaks)
The Janus kinase (Jak) family is one of ten recognized families of non-receptor tyrosine kinases. Mammals have four members of this family, Jak1, Jak2, Jak3 and Tyrosine kinase 2 (Tyk2). Birds, fish and insects also have Jaks. Each protein has a kinase domain and a catalytically inactive pseudo-kina...
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Veröffentlicht in: | Genome Biology (Online Edition) 2004-01, Vol.5 (12), p.253-253, Article 253 |
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description | The Janus kinase (Jak) family is one of ten recognized families of non-receptor tyrosine kinases. Mammals have four members of this family, Jak1, Jak2, Jak3 and Tyrosine kinase 2 (Tyk2). Birds, fish and insects also have Jaks. Each protein has a kinase domain and a catalytically inactive pseudo-kinase domain, and they each bind cytokine receptors through amino-terminal FERM (Band-4.1, ezrin, radixin, moesin) domains. Upon binding of cytokines to their receptors, Jaks are activated and phosphorylate the receptors, creating docking sites for signaling molecules, especially members of the signal transducer and activator of transcription (Stat) family. Mutations of the Drosophila Jak (Hopscotch) have revealed developmental defects, and constitutive activation of Jaks in flies and humans is associated with leukemia-like syndromes. Through the generation of Jak-deficient cell lines and gene-targeted mice, the essential, nonredundant functions of Jaks in cytokine signaling have been established. Importantly, deficiency of Jak3 is the basis of human autosomal recessive severe combined immunodeficiency (SCID); accordingly, a selective Jak3 inhibitor has been developed, forming a new class of immunosuppressive drugs. |
doi_str_mv | 10.1186/gb-2004-5-12-253 |
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Mammals have four members of this family, Jak1, Jak2, Jak3 and Tyrosine kinase 2 (Tyk2). Birds, fish and insects also have Jaks. Each protein has a kinase domain and a catalytically inactive pseudo-kinase domain, and they each bind cytokine receptors through amino-terminal FERM (Band-4.1, ezrin, radixin, moesin) domains. Upon binding of cytokines to their receptors, Jaks are activated and phosphorylate the receptors, creating docking sites for signaling molecules, especially members of the signal transducer and activator of transcription (Stat) family. Mutations of the Drosophila Jak (Hopscotch) have revealed developmental defects, and constitutive activation of Jaks in flies and humans is associated with leukemia-like syndromes. Through the generation of Jak-deficient cell lines and gene-targeted mice, the essential, nonredundant functions of Jaks in cytokine signaling have been established. Importantly, deficiency of Jak3 is the basis of human autosomal recessive severe combined immunodeficiency (SCID); accordingly, a selective Jak3 inhibitor has been developed, forming a new class of immunosuppressive drugs.</description><identifier>ISSN: 1474-760X</identifier><identifier>ISSN: 1465-6906</identifier><identifier>EISSN: 1474-760X</identifier><identifier>EISSN: 1465-6914</identifier><identifier>DOI: 10.1186/gb-2004-5-12-253</identifier><identifier>PMID: 15575979</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Amino acids ; Animals ; Biological Evolution ; Cytokines ; Drosophila ; Epidermal growth factors ; Genes ; Humans ; Immunodeficiency ; Insects ; Leukemia ; Mutual fund industry ; Phenols (Class of compounds) ; Protein Conformation ; Protein Family Review ; Protein-Tyrosine Kinases - chemistry ; Protein-Tyrosine Kinases - genetics ; Protein-Tyrosine Kinases - metabolism ; Severe combined immunodeficiency ; Tyrosine</subject><ispartof>Genome Biology (Online Edition), 2004-01, Vol.5 (12), p.253-253, Article 253</ispartof><rights>COPYRIGHT 2004 BioMed Central Ltd.</rights><rights>Copyright © 2004 BioMed Central Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b560t-c4b00fddca50b4dd2588113993e7afc695a849d3cfcb3d31ae0e1376d56d535b3</citedby><cites>FETCH-LOGICAL-b560t-c4b00fddca50b4dd2588113993e7afc695a849d3cfcb3d31ae0e1376d56d535b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC545791/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC545791/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15575979$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamaoka, Kunihiro</creatorcontrib><creatorcontrib>Saharinen, Pipsa</creatorcontrib><creatorcontrib>Pesu, Marko</creatorcontrib><creatorcontrib>Holt, 3rd, Vance E T</creatorcontrib><creatorcontrib>Silvennoinen, Olli</creatorcontrib><creatorcontrib>O'Shea, John J</creatorcontrib><title>The Janus kinases (Jaks)</title><title>Genome Biology (Online Edition)</title><addtitle>Genome Biol</addtitle><description>The Janus kinase (Jak) family is one of ten recognized families of non-receptor tyrosine kinases. Mammals have four members of this family, Jak1, Jak2, Jak3 and Tyrosine kinase 2 (Tyk2). Birds, fish and insects also have Jaks. Each protein has a kinase domain and a catalytically inactive pseudo-kinase domain, and they each bind cytokine receptors through amino-terminal FERM (Band-4.1, ezrin, radixin, moesin) domains. Upon binding of cytokines to their receptors, Jaks are activated and phosphorylate the receptors, creating docking sites for signaling molecules, especially members of the signal transducer and activator of transcription (Stat) family. Mutations of the Drosophila Jak (Hopscotch) have revealed developmental defects, and constitutive activation of Jaks in flies and humans is associated with leukemia-like syndromes. Through the generation of Jak-deficient cell lines and gene-targeted mice, the essential, nonredundant functions of Jaks in cytokine signaling have been established. Importantly, deficiency of Jak3 is the basis of human autosomal recessive severe combined immunodeficiency (SCID); accordingly, a selective Jak3 inhibitor has been developed, forming a new class of immunosuppressive drugs.</description><subject>Amino acids</subject><subject>Animals</subject><subject>Biological Evolution</subject><subject>Cytokines</subject><subject>Drosophila</subject><subject>Epidermal growth factors</subject><subject>Genes</subject><subject>Humans</subject><subject>Immunodeficiency</subject><subject>Insects</subject><subject>Leukemia</subject><subject>Mutual fund industry</subject><subject>Phenols (Class of compounds)</subject><subject>Protein Conformation</subject><subject>Protein Family Review</subject><subject>Protein-Tyrosine Kinases - chemistry</subject><subject>Protein-Tyrosine Kinases - genetics</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Severe combined immunodeficiency</subject><subject>Tyrosine</subject><issn>1474-760X</issn><issn>1465-6906</issn><issn>1474-760X</issn><issn>1465-6914</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>KPI</sourceid><recordid>eNp1kctLxDAQxoMorq-7J9mTuIdq0jzaHjwsi49dBT0oeAt5tcZtG21a0f_elC7qgpJAhsz3m0y-AeAQwVOEUnZWyCiGkEQ0QnEUU7wBdhBJSJQw-LT5Kx6BXe9fIEQZidk2GCFKE5ol2Q44fHg244WoOz9e2lp448cnC7H0k32wlYvSm4PVuQceLy8eZtfR7d3VfDa9jSRlsI0UkRDmWitBoSRaxzRNEcJZhk0icsUyKlKSaaxyJbHGSBhoEE6YpmFjKvEeOB_qvnayMlqZum1EyV8bW4nmkzth-Xqmts-8cO-cEppkKPCzgZfW_cOvZ5SreCF57xunHMU8-BaqHK-6aNxbZ3zLK-uVKUtRG9d5zhLEEEz7504HYSFKw22du1BUhaVNZZWrTW7D_ZRBHFwgrAcma0DQtOajLUTnPb-5n69r4aBVjfO-Mfn3NxDk_cD_avzot30_wGrC-AtY76Wr</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Yamaoka, Kunihiro</creator><creator>Saharinen, Pipsa</creator><creator>Pesu, Marko</creator><creator>Holt, 3rd, Vance E T</creator><creator>Silvennoinen, Olli</creator><creator>O'Shea, John J</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>KPI</scope><scope>IAO</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20040101</creationdate><title>The Janus kinases (Jaks)</title><author>Yamaoka, Kunihiro ; Saharinen, Pipsa ; Pesu, Marko ; Holt, 3rd, Vance E T ; Silvennoinen, Olli ; O'Shea, John J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b560t-c4b00fddca50b4dd2588113993e7afc695a849d3cfcb3d31ae0e1376d56d535b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino acids</topic><topic>Animals</topic><topic>Biological Evolution</topic><topic>Cytokines</topic><topic>Drosophila</topic><topic>Epidermal growth factors</topic><topic>Genes</topic><topic>Humans</topic><topic>Immunodeficiency</topic><topic>Insects</topic><topic>Leukemia</topic><topic>Mutual fund industry</topic><topic>Phenols (Class of compounds)</topic><topic>Protein Conformation</topic><topic>Protein Family Review</topic><topic>Protein-Tyrosine Kinases - chemistry</topic><topic>Protein-Tyrosine Kinases - genetics</topic><topic>Protein-Tyrosine Kinases - metabolism</topic><topic>Severe combined immunodeficiency</topic><topic>Tyrosine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamaoka, Kunihiro</creatorcontrib><creatorcontrib>Saharinen, Pipsa</creatorcontrib><creatorcontrib>Pesu, Marko</creatorcontrib><creatorcontrib>Holt, 3rd, Vance E T</creatorcontrib><creatorcontrib>Silvennoinen, Olli</creatorcontrib><creatorcontrib>O'Shea, John J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Global Issues</collection><collection>Gale Academic OneFile</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genome Biology (Online Edition)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamaoka, Kunihiro</au><au>Saharinen, Pipsa</au><au>Pesu, Marko</au><au>Holt, 3rd, Vance E T</au><au>Silvennoinen, Olli</au><au>O'Shea, John J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Janus kinases (Jaks)</atitle><jtitle>Genome Biology (Online Edition)</jtitle><addtitle>Genome Biol</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>5</volume><issue>12</issue><spage>253</spage><epage>253</epage><pages>253-253</pages><artnum>253</artnum><issn>1474-760X</issn><issn>1465-6906</issn><eissn>1474-760X</eissn><eissn>1465-6914</eissn><abstract>The Janus kinase (Jak) family is one of ten recognized families of non-receptor tyrosine kinases. Mammals have four members of this family, Jak1, Jak2, Jak3 and Tyrosine kinase 2 (Tyk2). Birds, fish and insects also have Jaks. Each protein has a kinase domain and a catalytically inactive pseudo-kinase domain, and they each bind cytokine receptors through amino-terminal FERM (Band-4.1, ezrin, radixin, moesin) domains. Upon binding of cytokines to their receptors, Jaks are activated and phosphorylate the receptors, creating docking sites for signaling molecules, especially members of the signal transducer and activator of transcription (Stat) family. Mutations of the Drosophila Jak (Hopscotch) have revealed developmental defects, and constitutive activation of Jaks in flies and humans is associated with leukemia-like syndromes. Through the generation of Jak-deficient cell lines and gene-targeted mice, the essential, nonredundant functions of Jaks in cytokine signaling have been established. 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subjects | Amino acids Animals Biological Evolution Cytokines Drosophila Epidermal growth factors Genes Humans Immunodeficiency Insects Leukemia Mutual fund industry Phenols (Class of compounds) Protein Conformation Protein Family Review Protein-Tyrosine Kinases - chemistry Protein-Tyrosine Kinases - genetics Protein-Tyrosine Kinases - metabolism Severe combined immunodeficiency Tyrosine |
title | The Janus kinases (Jaks) |
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