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PML nuclear body biogenesis and oligomerization-driven leukemogenesis

PML nuclear bodies (NBs), which are increasingly recognized as the central hub of many cellular signaling events, are superassembled spherical complexes with diameters of 0.1–2 μm. Recent studies reveal that RING tetramerization and B1-box polymerization are key factors to the overall PML NBs assemb...

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Detalles Bibliográficos
Autores principales: Li, Yuwen, Ma, Xiaodan, Meng, Guoyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975047/
https://www.ncbi.nlm.nih.gov/pubmed/35399865
http://dx.doi.org/10.1097/BS9.0000000000000034
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author Li, Yuwen
Ma, Xiaodan
Meng, Guoyu
author_facet Li, Yuwen
Ma, Xiaodan
Meng, Guoyu
author_sort Li, Yuwen
collection PubMed
description PML nuclear bodies (NBs), which are increasingly recognized as the central hub of many cellular signaling events, are superassembled spherical complexes with diameters of 0.1–2 μm. Recent studies reveal that RING tetramerization and B1-box polymerization are key factors to the overall PML NBs assembly. The productive RBCC oligomerization allows subsequent PML biogenesis steps, including the PML auto-sumoylation and partners recruitment via SUMO–SIM interactions. In promyelocytic leukemia, the oncoprotein PML/RARα (P/R) inhibits PML NBs assembly and leads to a full-fledged leukemogenesis. In this review, we review the recent progress in PML and acute promyelocytic leukemia fields, highlighting the protein oligomerization as an important direction of future targeted therapy.
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spelling pubmed-89750472022-04-07 PML nuclear body biogenesis and oligomerization-driven leukemogenesis Li, Yuwen Ma, Xiaodan Meng, Guoyu Blood Sci Review Article PML nuclear bodies (NBs), which are increasingly recognized as the central hub of many cellular signaling events, are superassembled spherical complexes with diameters of 0.1–2 μm. Recent studies reveal that RING tetramerization and B1-box polymerization are key factors to the overall PML NBs assembly. The productive RBCC oligomerization allows subsequent PML biogenesis steps, including the PML auto-sumoylation and partners recruitment via SUMO–SIM interactions. In promyelocytic leukemia, the oncoprotein PML/RARα (P/R) inhibits PML NBs assembly and leads to a full-fledged leukemogenesis. In this review, we review the recent progress in PML and acute promyelocytic leukemia fields, highlighting the protein oligomerization as an important direction of future targeted therapy. Wolters Kluwer Health 2020-01-16 /pmc/articles/PMC8975047/ /pubmed/35399865 http://dx.doi.org/10.1097/BS9.0000000000000034 Text en Copyright © 2020 The Authors. Published by Wolters Kluwer Health Inc., on behalf of the Chinese Association for Blood Sciences. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review Article
Li, Yuwen
Ma, Xiaodan
Meng, Guoyu
PML nuclear body biogenesis and oligomerization-driven leukemogenesis
title PML nuclear body biogenesis and oligomerization-driven leukemogenesis
title_full PML nuclear body biogenesis and oligomerization-driven leukemogenesis
title_fullStr PML nuclear body biogenesis and oligomerization-driven leukemogenesis
title_full_unstemmed PML nuclear body biogenesis and oligomerization-driven leukemogenesis
title_short PML nuclear body biogenesis and oligomerization-driven leukemogenesis
title_sort pml nuclear body biogenesis and oligomerization-driven leukemogenesis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8975047/
https://www.ncbi.nlm.nih.gov/pubmed/35399865
http://dx.doi.org/10.1097/BS9.0000000000000034
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