Mitochondrial dysfunction induces SESN2 gene expression through Activating Transcription Factor 4

Garaeva, A.A.; Kovaleva, I.E.; Chumakov, P.M.; Evstafieva, A.G.

Авторы: Garaeva A.A., Kovaleva I.E., Chumakov P.M., Evstafieva A.G.
Журнал: Cell Cycle
Том: 15
Номер: 1
Год издания: 2016
Издательство: Landes Bioscience
Местоположение издательства: United States
Первая страница: 64
Последняя страница: 71
DOI: 10.1080/15384101.2015.1120929
Аннотация: We found that inhibitors of mitochondrial respiratory chain complexes III (myxothiazol) and I (piericidine) in some epithelial carcinoma cell lines induce transcription of the p53-responsive SESN2 gene that plays an important role in stress response and homeostatic regulation. However, the effect did not depend on p53 because i) there was no induction of p53 after the treatment with piericidine; ii) after the treatment with myxothiazol the peak of SESN2 gene upregulation occurred as early as 5h, before the onset of p53 activation (13h); iii) a supplementation with uridine that abolishes the p53 activation in response to myxothiazol did not abrogate the induction of SESN2 transcripts; iv) in the p53 negative HCT116 p53 -/- cells SESN2 transcription could be also induced by myxothiazol. In response to the respiratory chain inhibitors we observed an induction of ATF4, the key transcription factor of the integrated stress response (ISR). We found that the induction of SESN2 transcripts could be prevented by the ISR inhibitory small molecule ISRIB. Also, by inhibiting or overexpressing ATF4 with specific shRNA or ATF4-expressing constructs, respectively, we have confirmed the role of ATF4 in the SESN2 gene upregulation induced by mitochondrial dysfunction. At a distance of 228 bp upstream from the SESN2 transcription start site we found a candidate sequence for the ATF4 binding site and confirmed its requirement for the induction of SESN2 in luciferase reporter experiments. We suggest that the upregulation of SESN2 by mitochondrial dysfunction provides a homeostatic feedback that attenuates biosynthetic processes during temporal losses of energy supply from mitochondria thereby assisting better adaptation and viability of cells in hostile environments.
Добавил в систему: Евстафьева Александра Георгиевна

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Mitochondrial dysfunction induces SESN2 gene expression through Activating Transcription Factor 4статья

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