Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response

The Kruppel-associated box (KRAB)-associated co-repressor KAP1 is an essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional factors. Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activat...

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Veröffentlicht in:The Journal of biological chemistry 2012-06, Vol.287 (23), p.18937-18952
Hauptverfasser: Hu, Chen, Zhang, Shengping, Gao, Xuan, Gao, Xiaojing, Xu, Xiaohong, Lv, Ya, Zhang, Yan, Zhu, Zhenhong, Zhang, Changqing, Li, Qiao, Wong, Jiemin, Cui, Yongping, Zhang, Wen, Ma, Lin, Wang, Chuangui
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container_end_page 18952
container_issue 23
container_start_page 18937
container_title The Journal of biological chemistry
container_volume 287
creator Hu, Chen
Zhang, Shengping
Gao, Xuan
Gao, Xiaojing
Xu, Xiaohong
Lv, Ya
Zhang, Yan
Zhu, Zhenhong
Zhang, Changqing
Li, Qiao
Wong, Jiemin
Cui, Yongping
Zhang, Wen
Ma, Lin
Wang, Chuangui
description The Kruppel-associated box (KRAB)-associated co-repressor KAP1 is an essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional factors. Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activated in response to DNA damage. A growing body of evidence suggests that ATM and ATR phosphorylate KAP1 at Ser-824 in response to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression. Here, we show that, depending on the type of DNA damage that occurs, KAP1 Ser-473 can be phosphorylated by ATM-Chk2 or ATR-Chk1 kinases. Phosphorylation of KAP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes. Moreover, KAP1 Ser-473 phosphorylation induced by DNA damage stimulated KAP1-E2F1 binding. Overexpression of heterochromatin protein 1 significantly inhibited E2F1-KAP1 binding. Elimination of KAP1 Ser-473 phosphorylation increased E2F1-targeted proapoptotic gene expression and E2F1-induced apoptosis in response to DNA damage. Furthermore, loss of phosphorylation of KAP1 Ser-473 led to less BRCA1 focus formation and slower kinetics of loss of γH2AX foci after DNA damage. KAP1 Ser-473 phosphorylation was required for efficient DNA repair and cell survival in response to DNA damage. Our studies reveal novel functions of KAP1 Ser-473 phosphorylation under stress. KAP1 is important for epigenetic modifications and the DNA damage response. Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis. KAP1 S473p is required for efficient DNA repair and cell survival under stress. Our studies reveal functions for KAP1 S473p under stress.
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Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activated in response to DNA damage. A growing body of evidence suggests that ATM and ATR phosphorylate KAP1 at Ser-824 in response to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression. Here, we show that, depending on the type of DNA damage that occurs, KAP1 Ser-473 can be phosphorylated by ATM-Chk2 or ATR-Chk1 kinases. Phosphorylation of KAP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes. Moreover, KAP1 Ser-473 phosphorylation induced by DNA damage stimulated KAP1-E2F1 binding. Overexpression of heterochromatin protein 1 significantly inhibited E2F1-KAP1 binding. Elimination of KAP1 Ser-473 phosphorylation increased E2F1-targeted proapoptotic gene expression and E2F1-induced apoptosis in response to DNA damage. Furthermore, loss of phosphorylation of KAP1 Ser-473 led to less BRCA1 focus formation and slower kinetics of loss of γH2AX foci after DNA damage. KAP1 Ser-473 phosphorylation was required for efficient DNA repair and cell survival in response to DNA damage. Our studies reveal novel functions of KAP1 Ser-473 phosphorylation under stress. KAP1 is important for epigenetic modifications and the DNA damage response. Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis. KAP1 S473p is required for efficient DNA repair and cell survival under stress. 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Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activated in response to DNA damage. A growing body of evidence suggests that ATM and ATR phosphorylate KAP1 at Ser-824 in response to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression. Here, we show that, depending on the type of DNA damage that occurs, KAP1 Ser-473 can be phosphorylated by ATM-Chk2 or ATR-Chk1 kinases. Phosphorylation of KAP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes. Moreover, KAP1 Ser-473 phosphorylation induced by DNA damage stimulated KAP1-E2F1 binding. Overexpression of heterochromatin protein 1 significantly inhibited E2F1-KAP1 binding. Elimination of KAP1 Ser-473 phosphorylation increased E2F1-targeted proapoptotic gene expression and E2F1-induced apoptosis in response to DNA damage. Furthermore, loss of phosphorylation of KAP1 Ser-473 led to less BRCA1 focus formation and slower kinetics of loss of γH2AX foci after DNA damage. KAP1 Ser-473 phosphorylation was required for efficient DNA repair and cell survival in response to DNA damage. Our studies reveal novel functions of KAP1 Ser-473 phosphorylation under stress. KAP1 is important for epigenetic modifications and the DNA damage response. Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis. KAP1 S473p is required for efficient DNA repair and cell survival under stress. 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Zhang, Shengping ; Gao, Xuan ; Gao, Xiaojing ; Xu, Xiaohong ; Lv, Ya ; Zhang, Yan ; Zhu, Zhenhong ; Zhang, Changqing ; Li, Qiao ; Wong, Jiemin ; Cui, Yongping ; Zhang, Wen ; Ma, Lin ; Wang, Chuangui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-e44c49f62aa88814092ab908bfbd5e0e508e61fb7017e7bd32790e2cd477933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Apoptosis</topic><topic>Apoptosis - physiology</topic><topic>Ataxia Telangiectasia Mutated Proteins</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Checkpoint Kinase 1</topic><topic>Checkpoint Kinase 2</topic><topic>Chk2</topic><topic>Chromatin Assembly and Disassembly</topic><topic>Co-repressor Transcription</topic><topic>DNA Damage</topic><topic>DNA Damage Response</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>E2F Transcription Factor</topic><topic>E2F1</topic><topic>E2F1 Transcription Factor - genetics</topic><topic>E2F1 Transcription Factor - metabolism</topic><topic>HEK293 Cells</topic><topic>HeLa Cells</topic><topic>HP1</topic><topic>Humans</topic><topic>KAP1</topic><topic>KRAB-ZNFs</topic><topic>Phosphorylation - genetics</topic><topic>Protein Kinases - genetics</topic><topic>Protein Kinases - metabolism</topic><topic>Protein Phosphorylation</topic><topic>Protein-Serine-Threonine Kinases - genetics</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><topic>Serine - genetics</topic><topic>Serine - metabolism</topic><topic>Signal Transduction</topic><topic>Tripartite Motif-Containing Protein 28</topic><topic>Tumor Suppressor Proteins - genetics</topic><topic>Tumor Suppressor Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Chen</creatorcontrib><creatorcontrib>Zhang, Shengping</creatorcontrib><creatorcontrib>Gao, Xuan</creatorcontrib><creatorcontrib>Gao, Xiaojing</creatorcontrib><creatorcontrib>Xu, Xiaohong</creatorcontrib><creatorcontrib>Lv, Ya</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Zhu, Zhenhong</creatorcontrib><creatorcontrib>Zhang, Changqing</creatorcontrib><creatorcontrib>Li, Qiao</creatorcontrib><creatorcontrib>Wong, Jiemin</creatorcontrib><creatorcontrib>Cui, Yongping</creatorcontrib><creatorcontrib>Zhang, Wen</creatorcontrib><creatorcontrib>Ma, Lin</creatorcontrib><creatorcontrib>Wang, Chuangui</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Chen</au><au>Zhang, Shengping</au><au>Gao, Xuan</au><au>Gao, Xiaojing</au><au>Xu, Xiaohong</au><au>Lv, Ya</au><au>Zhang, Yan</au><au>Zhu, Zhenhong</au><au>Zhang, Changqing</au><au>Li, Qiao</au><au>Wong, Jiemin</au><au>Cui, Yongping</au><au>Zhang, Wen</au><au>Ma, Lin</au><au>Wang, Chuangui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>287</volume><issue>23</issue><spage>18937</spage><epage>18952</epage><pages>18937-18952</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The Kruppel-associated box (KRAB)-associated co-repressor KAP1 is an essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional factors. Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activated in response to DNA damage. A growing body of evidence suggests that ATM and ATR phosphorylate KAP1 at Ser-824 in response to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression. Here, we show that, depending on the type of DNA damage that occurs, KAP1 Ser-473 can be phosphorylated by ATM-Chk2 or ATR-Chk1 kinases. Phosphorylation of KAP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes. Moreover, KAP1 Ser-473 phosphorylation induced by DNA damage stimulated KAP1-E2F1 binding. Overexpression of heterochromatin protein 1 significantly inhibited E2F1-KAP1 binding. Elimination of KAP1 Ser-473 phosphorylation increased E2F1-targeted proapoptotic gene expression and E2F1-induced apoptosis in response to DNA damage. Furthermore, loss of phosphorylation of KAP1 Ser-473 led to less BRCA1 focus formation and slower kinetics of loss of γH2AX foci after DNA damage. KAP1 Ser-473 phosphorylation was required for efficient DNA repair and cell survival in response to DNA damage. Our studies reveal novel functions of KAP1 Ser-473 phosphorylation under stress. KAP1 is important for epigenetic modifications and the DNA damage response. Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis. KAP1 S473p is required for efficient DNA repair and cell survival under stress. Our studies reveal functions for KAP1 S473p under stress.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22496453</pmid><doi>10.1074/jbc.M111.313262</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
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subjects Apoptosis
Apoptosis - physiology
Ataxia Telangiectasia Mutated Proteins
Cell Cycle Proteins - genetics
Cell Cycle Proteins - metabolism
Checkpoint Kinase 1
Checkpoint Kinase 2
Chk2
Chromatin Assembly and Disassembly
Co-repressor Transcription
DNA Damage
DNA Damage Response
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
E2F Transcription Factor
E2F1
E2F1 Transcription Factor - genetics
E2F1 Transcription Factor - metabolism
HEK293 Cells
HeLa Cells
HP1
Humans
KAP1
KRAB-ZNFs
Phosphorylation - genetics
Protein Kinases - genetics
Protein Kinases - metabolism
Protein Phosphorylation
Protein-Serine-Threonine Kinases - genetics
Protein-Serine-Threonine Kinases - metabolism
Repressor Proteins - genetics
Repressor Proteins - metabolism
Serine - genetics
Serine - metabolism
Signal Transduction
Tripartite Motif-Containing Protein 28
Tumor Suppressor Proteins - genetics
Tumor Suppressor Proteins - metabolism
title Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response
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