Nemo-like kinase is critical for p53 stabilization and function in response to DNA damage

被引:0
|
作者
H-H Zhang
S-Z Li
Z-Y Zhang
X-M Hu
P-N Hou
L Gao
R-L Du
X-D Zhang
机构
[1] College of Life Sciences,Department of Cell Biology
[2] Wuhan University,Department of Cardiology
[3] Institute of Cardiovascular Disease,undefined
[4] Union Hospital,undefined
[5] Tongji Medical College,undefined
[6] Hua Zhong University of Science and Technology,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The DNA damage response (DDR) acts as a protective mechanism for maintaining cell homeostasis. Nemo-like kinase (NLK) is a serine/threonine-protein kinase that has an important role in many pathways; however, its function in the DDR has not yet been defined. In our study, NLK-deficient HCT116 cells were found to be resistant to etoposide-induced cell death. We demonstrated that NLK is required for p53 activation in response to DNA damage. Remarkably, mechanistic studies revealed that NLK interacts with p53 and stabilizes p53 by blocking MDM2-mediated p53 ubiquitination and degradation. Furthermore, NLK enhances p53 activity and affects expression downstream of p53. Interestingly, these functions of NLK are not related to its kinase activity. Consistent with these results, NLK-deficient cells have a resistance effect on DNA damage. Therefore, these findings emphasize that NLK is a novel factor in DDR mechanisms.
引用
收藏
页码:1656 / 1663
页数:7
相关论文
共 50 条
  • [31] p53 partners with RNA in the DNA damage response
    Huarte, Maite
    NATURE GENETICS, 2016, 48 (11) : 1298 - 1299
  • [32] p53 partners with RNA in the DNA damage response
    Maite Huarte
    Nature Genetics, 2016, 48 : 1298 - 1299
  • [33] Nemo-like kinase (NLK) gene regulates apoptosis via the p53 signaling pathway in Litopenaeus vannamei under low-temperature stress
    Yin, Xiaoli
    Ren, Yinghao
    Luo, Weitao
    Liao, Meiqiu
    Huang, Lin
    Zhuang, Xueqi
    Liu, Yuan
    Wang, Weina
    DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY, 2022, 131
  • [34] Phosphorylation of Ser-20 mediates stabilization of human p53 in response to DNA damage
    Chehab, NH
    Malikzay, A
    Stavridi, ES
    Halazonetis, TD
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) : 13777 - 13782
  • [35] Induction of ASAP (MAP9) contributes to p53 stabilization in response to DNA damage
    Basbous, Jihane
    Knani, Dora
    Bonneaud, Nathalie
    Giorgi, Dominique
    Brondello, Jean-Marc
    Rouquier, Sylvie
    CELL CYCLE, 2012, 11 (12) : 2380 - 2390
  • [36] The Combination of Pulsatile and Switch-Like Behaviors of p53 in Response to DNA Damage
    Zhang, Xiao-Peng
    Liu, Feng
    Wang, Wei
    BIOPHYSICAL JOURNAL, 2011, 100 (03) : 33 - 33
  • [37] DNA-dependent protein kinase-independent activation of p53 in response to DNA damage
    Burma, S
    Kurimasa, A
    Xie, GF
    Taya, Y
    Araki, R
    Abe, M
    Crissman, HA
    Ouyang, H
    Li, GC
    Chen, DJ
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (24) : 17139 - 17143
  • [38] p53 N-terminus-targeted protein kinase activity is stimulated in response to wild type p53 and DNA damage
    Knippschild, U
    Milne, D
    Campbell, L
    Meek, D
    ONCOGENE, 1996, 13 (07) : 1387 - 1393
  • [39] Tau affects P53 function and cell fate during the DNA damage response
    Martina Sola
    Claudia Magrin
    Giona Pedrioli
    Sandra Pinton
    Agnese Salvadè
    Stéphanie Papin
    Paolo Paganetti
    Communications Biology, 3
  • [40] Tau affects P53 function and cell fate during the DNA damage response
    Sola, Martina
    Magrin, Claudia
    Pedrioli, Giona
    Pinton, Sandra
    Salvade, Agnese
    Papin, Stephanie
    Paganetti, Paolo
    COMMUNICATIONS BIOLOGY, 2020, 3 (01)