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Viral Bcl2s’ transmembrane domain interact with host Bcl2 proteins to control cellular apoptosis
Viral control of programmed cell death relies in part on the expression of viral analogs of the B-cell lymphoma 2 (Bcl2) protein known as viral Bcl2s (vBcl2s). vBcl2s control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. Here, we show that the carboxyl-termin...
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Published in: | Nature communications 2020-11, Vol.11 (1), p.6056-15, Article 6056 |
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description | Viral control of programmed cell death relies in part on the expression of viral analogs of the B-cell lymphoma 2 (Bcl2) protein known as viral Bcl2s (vBcl2s). vBcl2s control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. Here, we show that the carboxyl-terminal hydrophobic region of herpesviral and poxviral vBcl2s can operate as transmembrane domains (TMDs) and participate in their homo-oligomerization. Additionally, we show that the viral TMDs mediate interactions with cellular pro- and anti-apoptotic Bcl2 TMDs within the membrane. Furthermore, these intra-membrane interactions among viral and cellular proteins are necessary to control cell death upon an apoptotic stimulus. Therefore, their inhibition represents a new potential therapy against viral infections, which are characterized by short- and long-term deregulation of programmed cell death.
Viral analogs of B-cell lymphoma 2 (Bcl2), known as vBcl2s, control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. Here, García-Murria et al. report on transmembrane domains (TMDs) in the C-terminal hydrophobic region of herpes- and poxviral vBcl2s, which mediate homo-oligomerization and interactions with cellular Bcl2 TMDs to control apoptosis. |
doi_str_mv | 10.1038/s41467-020-19881-9 |
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Viral analogs of B-cell lymphoma 2 (Bcl2), known as vBcl2s, control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. Here, García-Murria et al. report on transmembrane domains (TMDs) in the C-terminal hydrophobic region of herpes- and poxviral vBcl2s, which mediate homo-oligomerization and interactions with cellular Bcl2 TMDs to control apoptosis.</description><identifier>ISSN: 2041-1723</identifier><identifier>EISSN: 2041-1723</identifier><identifier>DOI: 10.1038/s41467-020-19881-9</identifier><identifier>PMID: 33247105</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13 ; 14 ; 14/19 ; 631/326/596/2557 ; 631/45/612/1256 ; Amino Acid Sequence ; Analogs ; Apoptosis ; B-cell lymphoma ; Cell death ; Cell Line ; Cell Membrane - drug effects ; Cell Membrane - metabolism ; Deregulation ; Doxorubicin - pharmacology ; Fluorescence ; Humanities and Social Sciences ; Humans ; Hydrophobic and Hydrophilic Interactions ; Hydrophobicity ; Lymphocytes B ; Lymphoma ; Membranes ; Mortality ; multidisciplinary ; Oligomerization ; Protein Binding - drug effects ; Protein Domains ; Protein Multimerization - drug effects ; Proteins ; Proto-Oncogene Proteins c-bcl-2 - chemistry ; Proto-Oncogene Proteins c-bcl-2 - metabolism ; Science ; Science (multidisciplinary) ; Transmembrane domains ; Viral Proteins - chemistry ; Viral Proteins - metabolism</subject><ispartof>Nature communications, 2020-11, Vol.11 (1), p.6056-15, Article 6056</ispartof><rights>The Author(s) 2020. corrected publication 2021</rights><rights>The Author(s) 2020. corrected publication 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2020, corrected publication 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c568t-32f17d2bcd22c012ed3963b66b1440ac3d180efe41cc7456a92f9ebfca6c8b103</citedby><cites>FETCH-LOGICAL-c568t-32f17d2bcd22c012ed3963b66b1440ac3d180efe41cc7456a92f9ebfca6c8b103</cites><orcidid>0000-0002-9076-7760 ; 0000-0001-6365-4501 ; 0000-0002-1910-1229</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2509902722/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2509902722?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33247105$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García-Murria, Maria Jesús</creatorcontrib><creatorcontrib>Duart, Gerard</creatorcontrib><creatorcontrib>Grau, Brayan</creatorcontrib><creatorcontrib>Diaz-Beneitez, Elisabet</creatorcontrib><creatorcontrib>Rodríguez, Dolores</creatorcontrib><creatorcontrib>Mingarro, Ismael</creatorcontrib><creatorcontrib>Martínez-Gil, Luis</creatorcontrib><title>Viral Bcl2s’ transmembrane domain interact with host Bcl2 proteins to control cellular apoptosis</title><title>Nature communications</title><addtitle>Nat Commun</addtitle><addtitle>Nat Commun</addtitle><description>Viral control of programmed cell death relies in part on the expression of viral analogs of the B-cell lymphoma 2 (Bcl2) protein known as viral Bcl2s (vBcl2s). vBcl2s control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. Here, we show that the carboxyl-terminal hydrophobic region of herpesviral and poxviral vBcl2s can operate as transmembrane domains (TMDs) and participate in their homo-oligomerization. Additionally, we show that the viral TMDs mediate interactions with cellular pro- and anti-apoptotic Bcl2 TMDs within the membrane. Furthermore, these intra-membrane interactions among viral and cellular proteins are necessary to control cell death upon an apoptotic stimulus. Therefore, their inhibition represents a new potential therapy against viral infections, which are characterized by short- and long-term deregulation of programmed cell death.
Viral analogs of B-cell lymphoma 2 (Bcl2), known as vBcl2s, control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. 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Gerard</au><au>Grau, Brayan</au><au>Diaz-Beneitez, Elisabet</au><au>Rodríguez, Dolores</au><au>Mingarro, Ismael</au><au>Martínez-Gil, Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Viral Bcl2s’ transmembrane domain interact with host Bcl2 proteins to control cellular apoptosis</atitle><jtitle>Nature communications</jtitle><stitle>Nat Commun</stitle><addtitle>Nat Commun</addtitle><date>2020-11-27</date><risdate>2020</risdate><volume>11</volume><issue>1</issue><spage>6056</spage><epage>15</epage><pages>6056-15</pages><artnum>6056</artnum><issn>2041-1723</issn><eissn>2041-1723</eissn><abstract>Viral control of programmed cell death relies in part on the expression of viral analogs of the B-cell lymphoma 2 (Bcl2) protein known as viral Bcl2s (vBcl2s). vBcl2s control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. Here, we show that the carboxyl-terminal hydrophobic region of herpesviral and poxviral vBcl2s can operate as transmembrane domains (TMDs) and participate in their homo-oligomerization. Additionally, we show that the viral TMDs mediate interactions with cellular pro- and anti-apoptotic Bcl2 TMDs within the membrane. Furthermore, these intra-membrane interactions among viral and cellular proteins are necessary to control cell death upon an apoptotic stimulus. Therefore, their inhibition represents a new potential therapy against viral infections, which are characterized by short- and long-term deregulation of programmed cell death.
Viral analogs of B-cell lymphoma 2 (Bcl2), known as vBcl2s, control apoptosis by interacting with host pro- and anti-apoptotic members of the Bcl2 family. Here, García-Murria et al. report on transmembrane domains (TMDs) in the C-terminal hydrophobic region of herpes- and poxviral vBcl2s, which mediate homo-oligomerization and interactions with cellular Bcl2 TMDs to control apoptosis.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33247105</pmid><doi>10.1038/s41467-020-19881-9</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-9076-7760</orcidid><orcidid>https://orcid.org/0000-0001-6365-4501</orcidid><orcidid>https://orcid.org/0000-0002-1910-1229</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 13 14 14/19 631/326/596/2557 631/45/612/1256 Amino Acid Sequence Analogs Apoptosis B-cell lymphoma Cell death Cell Line Cell Membrane - drug effects Cell Membrane - metabolism Deregulation Doxorubicin - pharmacology Fluorescence Humanities and Social Sciences Humans Hydrophobic and Hydrophilic Interactions Hydrophobicity Lymphocytes B Lymphoma Membranes Mortality multidisciplinary Oligomerization Protein Binding - drug effects Protein Domains Protein Multimerization - drug effects Proteins Proto-Oncogene Proteins c-bcl-2 - chemistry Proto-Oncogene Proteins c-bcl-2 - metabolism Science Science (multidisciplinary) Transmembrane domains Viral Proteins - chemistry Viral Proteins - metabolism |
title | Viral Bcl2s’ transmembrane domain interact with host Bcl2 proteins to control cellular apoptosis |
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