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Mouse PML protein isoforms and their role in Mouse Polyomavirus infection

abstract in conference proceedings
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Author
Anderová, Karolína
Ryabchenko, BorisORCiD Profile - 0000-0001-7076-256XWoS Profile - U-8964-2017Scopus Profile - 36142246600
Šroller, VojtěchORCiD Profile - 0000-0003-1534-6007WoS Profile - Q-1098-2017Scopus Profile - 23135496600
Horníková, LenkaORCiD Profile - 0000-0003-1539-8413WoS Profile - L-7348-2017Scopus Profile - 13105604900
Forstová, JitkaORCiD Profile - 0000-0003-0219-506XWoS Profile - L-7328-2017Scopus Profile - 6701385419
Huerfano Meneses, SandraORCiD Profile - 0000-0001-5221-3014WoS Profile - G-8469-2013Scopus Profile - 6506988916
Institute of Molecular Genetics of the Czech Academy of Sciences (IMG AS CR) a Micron z.s.

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Publication date
2023
Published in
WBW 2023 Book of Abstracts
Publisher / Publication place
(Praha)
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  • Faculty of Science
Abstract
Promyelocytic leukaemia nuclear bodies (PML NBs) are dynamic, spherical, membrane-less structures composed of the main scaffold PML protein and a variety of stable or transient partner proteins. Apart from many endogenous functions, PML NBs play an important role in antiviral defence, both as direct restriction factors and regulators of the interferon responses. Hence, many viruses developed effective mechanisms to counteract this restriction. This project uses Mouse polyomavirus (MPyV) as a model for studying interactions of PML and viral components. The mouse PML (mPML) protein occurs in three confirmed (mPML1-3) and six predicted (mPMLX1-X6) isoforms. Individual isoforms may affect the composition and functions of PML NBs and mediate antiviral effects.
Keywords
polyomavirus, isoforms, mPML NBs
Permanent link
https://hdl.handle.net/20.500.14178/1980
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Full text of this result is licensed under: Creative Commons Uveďte původ 4.0 International

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