期刊
SCIENCE
卷 348, 期 6238, 页码 1027-1030出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.aaa6986
关键词
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资金
- Wellcome Trust [084812/Z/08/Z, 100140]
- Daiichi Sankyo Foundation of Life Science
- Japan Society for the Promotion of Science
- Wellcome Trust [084812/Z/08/Z] Funding Source: Wellcome Trust
The integrated stress response (ISR) modulates messenger RNA translation to regulate the mammalian unfolded protein response (UPR), immunity, and memory formation. A chemical ISR inhibitor, ISRIB, enhances cognitive function and modulates the UPR in vivo. To explore mechanisms involved in ISRIB action, we screened cultured mammalian cells for somatic mutations that reversed its effect on the ISR. Clustered missense mutations were found at the amino-terminal portion of the delta subunit of guanine nucleotide exchange factor (GEF) eIF2B. When reintroduced by CRISPR-Cas9 gene editing of wild-type cells, these mutations reversed both ISRIB-mediated inhibition of the ISR and its stimulatory effect on eIF2B GEF activity toward its substrate, the translation initiation factor eIF2, in vitro. Thus, ISRIB targets an interaction between eIF2 and eIF2B that lies at the core of the ISR.
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