Interplay between ADP-ribosyltransferases and essential cell signaling pathways controls cellular responses

被引:24
作者
Boehi, Flurina [1 ,2 ]
Manetsch, Patrick [1 ,3 ]
Hottiger, Michael O. [1 ]
机构
[1] Univ Zurich, Dept Mol Mech Dis, Zurich, Switzerland
[2] Univ Zurich, Life Sci Zurich Grad Sch, Canc Biol PhD Program, Zurich, Switzerland
[3] Univ Zurich, Mol Life Sci PhD Program, Life Sci Zurich Grad Sch, Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
NF-KAPPA-B; POLY(ADP-RIBOSE) POLYMERASE-1; WNT/BETA-CATENIN; PARP-INHIBITOR; ENERGY HOMEOSTASIS; INDUCED APOPTOSIS; OXIDATIVE STRESS; GENE-EXPRESSION; BETA-CATENIN; DNA-REPAIR;
D O I
10.1038/s41421-021-00323-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Signaling cascades provide integrative and interactive frameworks that allow the cell to respond to signals from its environment and/or from within the cell itself. The dynamic regulation of mammalian cell signaling pathways is often modulated by cascades of protein post-translational modifications (PTMs). ADP-ribosylation is a PTM that is catalyzed by ADP-ribosyltransferases and manifests as mono- (MARylation) or poly- (PARylation) ADP-ribosylation depending on the addition of one or multiple ADP-ribose units to protein substrates. ADP-ribosylation has recently emerged as an important cell regulator that impacts a plethora of cellular processes, including many intracellular signaling events. Here, we provide an overview of the interplay between the intracellular diphtheria toxin-like ADP-ribosyltransferase (ARTD) family members and five selected signaling pathways (including NF-kappa B, JAK/STAT, Wnt-beta-catenin, MAPK, PI3K/AKT), which are frequently described to control or to be controlled by ADP-ribosyltransferases and how these interactions impact the cellular responses.
引用
收藏
页数:22
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