Stabilization of RNT-1 Protein, Runt-related Transcription Factor (RUNX) Protein Homolog of Caenorhabditis elegans, by Oxidative Stress through Mitogen-activated Protein Kinase Pathway

被引:13
作者
Lee, Kiho [1 ]
Shim, Jiwon [1 ]
Bae, Jaebum [2 ]
Kim, Young-Joon [2 ]
Lee, Junho [1 ]
机构
[1] Seoul Natl Univ, Dept Biol Sci, WCU Dept Biophys & Chem Biol, Res Ctr Cellul, Seoul 151742, South Korea
[2] Yonsei Univ, Dept Biochem, Coll Life Sci & Technol, Seoul 120749, South Korea
关键词
C-ELEGANS; DEPENDENT PHOSPHORYLATION; MEDIATED DEGRADATION; CELL-PROLIFERATION; MAPK PHOSPHATASE; OSTEOCALCIN GENE; EXPRESSION; METHYLATION; RECEPTOR; CANCER;
D O I
10.1074/jbc.M111.314146
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RUNX proteins are evolutionarily conserved transcription factors known to be involved in various developmental processes. Here we report a new role for a RUNX protein: a role in stress response. We show that RNT-1, the Caenorhabditis elegans RUNX homolog, is constantly produced and degraded by the ubiquitination-proteasome pathway in the intestine of the nematode. RNT-1 was rapidly stabilized by oxidative stress, and the rnt-1-mutant animals were more sensitive to oxidative stress, indicating that rapid RNT-1 stabilization is a defense response against the oxidative stress. The MAP kinase pathway is required for RNT-1 stabilization, and RNT-1 was phosphorylated by SEK-1/PMK-1 in vitro. ChIP-sequencing analysis revealed a feedback loop mechanism of the MAP kinase pathway by the VHP-1 phosphatase in the RNT-1-mediated oxidative stress response. We propose that rnt-1 is regulated at the protein level for its role in the immediate response to environmental challenges in the intestine.
引用
收藏
页码:10444 / 10452
页数:9
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