| Literature DB >> 30184494 |
Ying Cheng1, Peipei Liu1, Qian Zheng1, Ge Gao1, Jiapei Yuan1, Pengfeng Wang2, Jinliang Huang1, Leiming Xie1, Xinping Lu1, Tanjun Tong3, Jun Chen3, Zhi Lu1, Jisong Guan1, Geng Wang4.
Abstract
Mitochondrial dysfunctions play major roles in many diseases. However, how mitochondrial stresses are relayed to downstream responses remains unclear. Here we show that the RNA component of mammalian telomerase TERC is imported into mitochondria, processed to a shorter form TERC-53, and then exported back to the cytosol. We found that the import is regulated by PNPASE, and the processing is controlled by mitochondrion-localized RNASET2. Cytosolic TERC-53 levels respond to changes in mitochondrial functions but have no direct effect on these functions. These findings uncover a mitochondrial RNA trafficking pathway and provide a potential mechanism for mitochondria to relay their functional states to other cellular compartments.Entities:
Keywords: RNA; RNASET2; TERC; export; import; mitochondria; mitochondrial dysfunction; processing; retrograde signaling; telomerase
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Year: 2018 PMID: 30184494 DOI: 10.1016/j.celrep.2018.08.003
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423