Role of Rap1 in DNA damage response: implications in stem cell homeostasis and cancer

被引:12
作者
Khattar, Ekta [1 ]
Tergaonkar, Vinay [2 ]
机构
[1] SVKMs NMIMS Deemed Be Univ, Sunandan Divatia Sch Sci, Vile Pk West, Mumbai 400056, Maharashtra, India
[2] ASTAR, Inst Mol & Cell Biol, Singapore, Singapore
关键词
TELOMERE PROTECTION; END; TRF2; TRANSLOCATIONS; IDENTIFICATION; RECOMBINATION; HETEROGENEITY; MECHANISMS; CHECKPOINT; DOMAINS;
D O I
10.1016/j.exphem.2020.08.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mammalian Rap1 is a part of the telomere binding complex named shelterin and is one of the most conserved telomeric proteins. With its essential requirement in lower species to its becoming necessary in higher species, it appears to have gained and lost several functions simultaneously evolving with telomeres. Mammalian Rap1 has been reported to play a role in inflammation, metabolism, and oxidative stress. Mammalian Rap1 has also been found to regulate DNA damage response from telomeres in senescent cells. Recently our group uncovered its novel role in stem cell maintenance, and modulation of the chemotherapeutic response. Mechanistically it was found to function as an adaptor via protein-protein interactions and to modulate the response to DNA damage. In the current review we highlight newly identified functions of Rap1 in regulating telomeric and general DNA damage response with its impact at the cellular and organismal levels. (C) 2020 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:12 / 17
页数:6
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