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ADP核糖基转移酶与基本细胞信号通路之间的相互作用控制着细胞反应。

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

作者信息

Boehi Flurina, Manetsch Patrick, Hottiger Michael O

机构信息

Department of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.

Cancer Biology PhD Program of the Life Science Zurich Graduate School, University of Zurich, Zurich, Switzerland.

出版信息

Cell Discov. 2021 Nov 2;7(1):104. doi: 10.1038/s41421-021-00323-9.

Abstract

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-κB, JAK/STAT, Wnt-β-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.

摘要

信号级联提供了整合和交互的框架,使细胞能够对来自其周围环境和/或细胞自身内部的信号做出反应。哺乳动物细胞信号通路的动态调节通常由蛋白质翻译后修饰(PTM)级联来调控。ADP-核糖基化是一种由ADP-核糖基转移酶催化的PTM,根据向蛋白质底物添加一个或多个ADP-核糖单位,表现为单(单ADP-核糖基化)或多(多ADP-核糖基化)ADP-核糖基化。最近,ADP-核糖基化已成为一种重要的细胞调节剂,影响众多细胞过程,包括许多细胞内信号事件。在这里,我们概述了细胞内白喉毒素样ADP-核糖基转移酶(ARTD)家族成员与五个选定的信号通路(包括NF-κB、JAK/STAT、Wnt-β-连环蛋白、MAPK、PI3K/AKT)之间的相互作用,这些信号通路经常被描述为受ADP-核糖基转移酶控制或控制ADP-核糖基转移酶,以及这些相互作用如何影响细胞反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f69e/8560908/c70a0422074d/41421_2021_323_Fig1_HTML.jpg

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