1. PERK-mediated induction of microRNA-483 disrupts cellular ATP homeostasis during the unfolded protein response.
- Author
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Hiramatsu N, Chiang K, Aivati C, Rodvold JJ, Lee JM, Han J, Chea L, Zanetti M, Koo EH, and Lin JH
- Subjects
- Activating Transcription Factor 4 genetics, Activating Transcription Factor 4 metabolism, Apoptosis, Creatine Kinase, BB Form genetics, Creatine Kinase, BB Form metabolism, HEK293 Cells, HeLa Cells, Homeostasis, Humans, MicroRNAs genetics, eIF-2 Kinase genetics, Adenosine Triphosphate metabolism, MicroRNAs metabolism, Unfolded Protein Response, eIF-2 Kinase metabolism
- Abstract
Endoplasmic reticulum (ER) stress activates the unfolded protein response (UPR), which reduces levels of misfolded proteins. However, if ER homeostasis is not restored and the UPR remains chronically activated, cells undergo apoptosis. The UPR regulator, PKR-like endoplasmic reticulum kinase (PERK), plays an important role in promoting cell death when persistently activated; however, the underlying mechanisms are poorly understood. Here, we profiled the microRNA (miRNA) transcriptome in human cells exposed to ER stress and identified miRNAs that are selectively induced by PERK signaling. We found that expression of a PERK-induced miRNA, miR-483, promotes apoptosis in human cells. miR-483 induction was mediated by a transcription factor downstream of PERK, activating transcription factor 4 (ATF4), but not by the CHOP transcription factor. We identified the creatine kinase brain-type ( CKB ) gene, encoding an enzyme that maintains cellular ATP reserves through phosphocreatine production, as being repressed during the UPR and targeted by miR-483. We found that ER stress, selective PERK activation, and CKB knockdown all decrease cellular ATP levels, leading to increased vulnerability to ER stress-induced cell death. Our findings identify miR-483 as a downstream target of the PERK branch of the UPR. We propose that disruption of cellular ATP homeostasis through miR-483-mediated CKB silencing promotes ER stress-induced apoptosis.
- Published
- 2020
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