Cell fate regulation by chromatin ADP-ribosylation

被引：21
作者：
Abplanalp, Jeannette [1 ]
Hottiger, Michael O. [1 ]
机构：
[1] Univ Zurich, Dept Mol Mech Dis, Winterthurerstr 190, CH-8057 Zurich, Switzerland
来源：
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY | 2017年 / 63卷
基金：
瑞士国家科学基金会;
关键词：
ARTD; PARP; Chromatin; Histone; ADP-ribosylation; Differentiation; Pluripotency; POLY(ADENOSINE DIPHOSPHATE RIBOSYLATION); AGGRESSIVE LYMPHOMA FAMILY; APOPTOSIS-INDUCING PROTEIN; POLY(ADP-RIBOSE) POLYMERASE-1; GENE-EXPRESSION; ADIPOCYTE DIFFERENTIATION; MOLECULAR-CLONING; CORE HISTONE; DNA; RIBOSE;
D O I：
10.1016/j.semcdb.2016.09.010
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
ADP-ribosylation is an evolutionarily conserved complex posttranslational modification that alters protein function and/or interaction. Intracellularly, it is mainly catalyzed by diphtheria toxin-like ADPribosyltransferases ( ARTDs), which attach one or several ADP-ribose residues onto target proteins. Several specific mono-and poly-ADP-ribosylation binding modules exist; hydrolases reverse the modification. The best-characterized ARTD family member, ARTD1, regulates various DNA-associated processes. Here, we focus on the role of ARTD1-mediated chromatin ADP-ribosylation in development, differentiation, and pluripotency, and the recent development of new methodologies that will enable more insight into these processes. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码：114 / 122
页数：9
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