TANK2, a New TRF1-associated Poly(ADP-ribose) Polymerase, Causes Rapid Induction of Cell Death upon Overexpression
Tankyrase (TANK1) is a human telomere-associated poly(ADP-ribose) polymerase (PARP) that binds the telomere-binding protein TRF1 and increases telomere length when overexpressed. Here we report characterization of a second human tankyrase, tankyrase 2 (TANK2), which can also interact with TRF1 but h...
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description | Tankyrase (TANK1) is a human telomere-associated poly(ADP-ribose) polymerase (PARP) that binds the telomere-binding protein TRF1 and increases telomere length when overexpressed. Here we report characterization of a second human tankyrase, tankyrase 2 (TANK2), which can also interact with TRF1 but has properties distinct from those of TANK1. TANK2 is encoded by a 66-kilobase pair gene (TNKS2) containing 28 exons, which express a 6.7-kilobase pair mRNA and a 1166-amino acid protein. The protein shares 85% amino acid identity with TANK1 in the ankyrin repeat, sterile α-motif, and PARP catalytic domains but has a unique N-terminal domain, which is conserved in the murine TNKS2 gene. TANK2 interacted with TRF1 in yeast and in vitro and localized predominantly to a perinuclear region, similar to the properties of TANK1. In contrast to TANK1, however, TANK2 caused rapid cell death when highly overexpressed. TANK2-induced death featured loss of mitochondrial membrane potential, but not PARP1 cleavage, suggesting that TANK2 kills cells by necrosis. The cell death was prevented by the PARP inhibitor 3-aminobenzamide. In vivo, TANK2 may differ from TANK1 in its intrinsic or regulated PARP activity or its substrate specificity. |
doi_str_mv | 10.1074/jbc.M105968200 |
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Here we report characterization of a second human tankyrase, tankyrase 2 (TANK2), which can also interact with TRF1 but has properties distinct from those of TANK1. TANK2 is encoded by a 66-kilobase pair gene (TNKS2) containing 28 exons, which express a 6.7-kilobase pair mRNA and a 1166-amino acid protein. The protein shares 85% amino acid identity with TANK1 in the ankyrin repeat, sterile α-motif, and PARP catalytic domains but has a unique N-terminal domain, which is conserved in the murine TNKS2 gene. TANK2 interacted with TRF1 in yeast and in vitro and localized predominantly to a perinuclear region, similar to the properties of TANK1. In contrast to TANK1, however, TANK2 caused rapid cell death when highly overexpressed. TANK2-induced death featured loss of mitochondrial membrane potential, but not PARP1 cleavage, suggesting that TANK2 kills cells by necrosis. The cell death was prevented by the PARP inhibitor 3-aminobenzamide. In vivo, TANK2 may differ from TANK1 in its intrinsic or regulated PARP activity or its substrate specificity.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M105968200</identifier><identifier>PMID: 11454873</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>3-aminobenzamide ; Amino Acid Sequence ; Animals ; Base Sequence ; Cell Death - physiology ; Chromosome Mapping ; Cloning, Molecular ; DNA, Complementary ; DNA-Binding Proteins - metabolism ; Mice ; Molecular Sequence Data ; Open Reading Frames ; poly(ADP-ribose) polymerase ; Poly(ADP-ribose) Polymerases - chemistry ; Poly(ADP-ribose) Polymerases - genetics ; Poly(ADP-ribose) Polymerases - metabolism ; Poly(ADP-ribose) Polymerases - physiology ; RNA, Messenger - genetics ; TANK2 gene ; tankyrase ; Tankyrases ; telomere-binding protein ; Telomeric Repeat Binding Protein 1 ; TNKS2 gene ; TRF1 protein</subject><ispartof>The Journal of biological chemistry, 2001-09, Vol.276 (38), p.35891-35899</ispartof><rights>2001 © 2001 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-c506t-a9f2067a75679a9c148655b930b2cfbc5639a9fd5849744ea2718ca4af3dd0773</citedby><cites>FETCH-LOGICAL-c506t-a9f2067a75679a9c148655b930b2cfbc5639a9fd5849744ea2718ca4af3dd0773</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/11454873$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaminker, Patrick G.</creatorcontrib><creatorcontrib>Kim, Sahn-Ho</creatorcontrib><creatorcontrib>Taylor, Rebecca D.</creatorcontrib><creatorcontrib>Zebarjadian, Yeganeh</creatorcontrib><creatorcontrib>Funk, Walter D.</creatorcontrib><creatorcontrib>Morin, Gregg B.</creatorcontrib><creatorcontrib>Yaswen, Paul</creatorcontrib><creatorcontrib>Campisi, Judith</creatorcontrib><title>TANK2, a New TRF1-associated Poly(ADP-ribose) Polymerase, Causes Rapid Induction of Cell Death upon Overexpression</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Tankyrase (TANK1) is a human telomere-associated poly(ADP-ribose) polymerase (PARP) that binds the telomere-binding protein TRF1 and increases telomere length when overexpressed. Here we report characterization of a second human tankyrase, tankyrase 2 (TANK2), which can also interact with TRF1 but has properties distinct from those of TANK1. TANK2 is encoded by a 66-kilobase pair gene (TNKS2) containing 28 exons, which express a 6.7-kilobase pair mRNA and a 1166-amino acid protein. The protein shares 85% amino acid identity with TANK1 in the ankyrin repeat, sterile α-motif, and PARP catalytic domains but has a unique N-terminal domain, which is conserved in the murine TNKS2 gene. TANK2 interacted with TRF1 in yeast and in vitro and localized predominantly to a perinuclear region, similar to the properties of TANK1. In contrast to TANK1, however, TANK2 caused rapid cell death when highly overexpressed. TANK2-induced death featured loss of mitochondrial membrane potential, but not PARP1 cleavage, suggesting that TANK2 kills cells by necrosis. The cell death was prevented by the PARP inhibitor 3-aminobenzamide. In vivo, TANK2 may differ from TANK1 in its intrinsic or regulated PARP activity or its substrate specificity.</description><subject>3-aminobenzamide</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Cell Death - physiology</subject><subject>Chromosome Mapping</subject><subject>Cloning, Molecular</subject><subject>DNA, Complementary</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Open Reading Frames</subject><subject>poly(ADP-ribose) polymerase</subject><subject>Poly(ADP-ribose) Polymerases - chemistry</subject><subject>Poly(ADP-ribose) Polymerases - genetics</subject><subject>Poly(ADP-ribose) Polymerases - metabolism</subject><subject>Poly(ADP-ribose) Polymerases - physiology</subject><subject>RNA, Messenger - genetics</subject><subject>TANK2 gene</subject><subject>tankyrase</subject><subject>Tankyrases</subject><subject>telomere-binding protein</subject><subject>Telomeric Repeat Binding Protein 1</subject><subject>TNKS2 gene</subject><subject>TRF1 protein</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd1rFDEUxYModq2--ih5ELHQWfM5SR6XrdVibUtZwbeQydxxU3Y202SmH_-90V3ok3hfLhx-93C4B6G3lMwpUeLTTePn3ymRptaMkGdoRonmFZf053M0I4TRyjCpD9CrnG9IGWHoS3RAqZBCKz5DabW4-MaOscMXcI9X16e0cjlHH9wILb6Km8ePi5OrKoUmZjj6K_SQXIZjvHRThoyv3RBafLZtJz-GuMWxw0vYbPAJuHGNp6FIl3eQ4GFIkHMhXqMXndtkeLPfh-jH6efV8mt1fvnlbLk4r7wk9Vg50zFSK6dkrYwzngpdS9kYThrmu8bLmhe5a6UWRgkBjimqvROu421LlOKH6MPOd0jxdoI82j5kX6K5LcQpW0WpEqqW_wWp0kYzxgs434E-xZwTdHZIoXfp0VJi_9RhSx32qY5y8G7vPDU9tE_4_v8FeL8D1uHX-j4ksE2Ifg29Zaq2XFsutaEF0zsMyr_uAiSbfYCth7ac-NG2Mfwrwm9uS6K0</recordid><startdate>20010921</startdate><enddate>20010921</enddate><creator>Kaminker, Patrick G.</creator><creator>Kim, Sahn-Ho</creator><creator>Taylor, Rebecca D.</creator><creator>Zebarjadian, Yeganeh</creator><creator>Funk, Walter D.</creator><creator>Morin, Gregg B.</creator><creator>Yaswen, Paul</creator><creator>Campisi, Judith</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>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20010921</creationdate><title>TANK2, a New TRF1-associated Poly(ADP-ribose) Polymerase, Causes Rapid Induction of Cell Death upon Overexpression</title><author>Kaminker, Patrick G. ; Kim, Sahn-Ho ; Taylor, Rebecca D. ; Zebarjadian, Yeganeh ; Funk, Walter D. ; Morin, Gregg B. ; Yaswen, Paul ; Campisi, Judith</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-a9f2067a75679a9c148655b930b2cfbc5639a9fd5849744ea2718ca4af3dd0773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>3-aminobenzamide</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Cell Death - physiology</topic><topic>Chromosome Mapping</topic><topic>Cloning, Molecular</topic><topic>DNA, Complementary</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Open Reading Frames</topic><topic>poly(ADP-ribose) polymerase</topic><topic>Poly(ADP-ribose) Polymerases - chemistry</topic><topic>Poly(ADP-ribose) Polymerases - genetics</topic><topic>Poly(ADP-ribose) Polymerases - metabolism</topic><topic>Poly(ADP-ribose) Polymerases - physiology</topic><topic>RNA, Messenger - genetics</topic><topic>TANK2 gene</topic><topic>tankyrase</topic><topic>Tankyrases</topic><topic>telomere-binding protein</topic><topic>Telomeric Repeat Binding Protein 1</topic><topic>TNKS2 gene</topic><topic>TRF1 protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaminker, Patrick G.</creatorcontrib><creatorcontrib>Kim, Sahn-Ho</creatorcontrib><creatorcontrib>Taylor, Rebecca D.</creatorcontrib><creatorcontrib>Zebarjadian, Yeganeh</creatorcontrib><creatorcontrib>Funk, Walter D.</creatorcontrib><creatorcontrib>Morin, Gregg B.</creatorcontrib><creatorcontrib>Yaswen, Paul</creatorcontrib><creatorcontrib>Campisi, Judith</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>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</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>Kaminker, Patrick G.</au><au>Kim, Sahn-Ho</au><au>Taylor, Rebecca D.</au><au>Zebarjadian, Yeganeh</au><au>Funk, Walter D.</au><au>Morin, Gregg B.</au><au>Yaswen, Paul</au><au>Campisi, Judith</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TANK2, a New TRF1-associated Poly(ADP-ribose) Polymerase, Causes Rapid Induction of Cell Death upon Overexpression</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2001-09-21</date><risdate>2001</risdate><volume>276</volume><issue>38</issue><spage>35891</spage><epage>35899</epage><pages>35891-35899</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Tankyrase (TANK1) is a human telomere-associated poly(ADP-ribose) polymerase (PARP) that binds the telomere-binding protein TRF1 and increases telomere length when overexpressed. Here we report characterization of a second human tankyrase, tankyrase 2 (TANK2), which can also interact with TRF1 but has properties distinct from those of TANK1. TANK2 is encoded by a 66-kilobase pair gene (TNKS2) containing 28 exons, which express a 6.7-kilobase pair mRNA and a 1166-amino acid protein. The protein shares 85% amino acid identity with TANK1 in the ankyrin repeat, sterile α-motif, and PARP catalytic domains but has a unique N-terminal domain, which is conserved in the murine TNKS2 gene. TANK2 interacted with TRF1 in yeast and in vitro and localized predominantly to a perinuclear region, similar to the properties of TANK1. In contrast to TANK1, however, TANK2 caused rapid cell death when highly overexpressed. TANK2-induced death featured loss of mitochondrial membrane potential, but not PARP1 cleavage, suggesting that TANK2 kills cells by necrosis. The cell death was prevented by the PARP inhibitor 3-aminobenzamide. In vivo, TANK2 may differ from TANK1 in its intrinsic or regulated PARP activity or its substrate specificity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11454873</pmid><doi>10.1074/jbc.M105968200</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3-aminobenzamide Amino Acid Sequence Animals Base Sequence Cell Death - physiology Chromosome Mapping Cloning, Molecular DNA, Complementary DNA-Binding Proteins - metabolism Mice Molecular Sequence Data Open Reading Frames poly(ADP-ribose) polymerase Poly(ADP-ribose) Polymerases - chemistry Poly(ADP-ribose) Polymerases - genetics Poly(ADP-ribose) Polymerases - metabolism Poly(ADP-ribose) Polymerases - physiology RNA, Messenger - genetics TANK2 gene tankyrase Tankyrases telomere-binding protein Telomeric Repeat Binding Protein 1 TNKS2 gene TRF1 protein |
title | TANK2, a New TRF1-associated Poly(ADP-ribose) Polymerase, Causes Rapid Induction of Cell Death upon Overexpression |
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