Controlling the mitochondrial antisense - role of the SUV3-PNPase complex and its co-factor GRSF1 in mitochondrial RNA surveillance
Transcription of the human mitochondrial genome produces a vast amount of non-coding antisense RNAs. These RNA species can form G-quadraplexes (G4), which affect their decay. We found that the mitochondrial degradosome, a complex of RNA helicase SUPV3L1 (best known as SUV3) and the ribonuclease PNPT...
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Published in: | Molecular & cellular oncology Vol. 5; no. 6; p. e1516452 |
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Abstract | Transcription of the human mitochondrial genome produces a vast amount of non-coding antisense RNAs. These RNA species can form G-quadraplexes (G4), which affect their decay. We found that the mitochondrial degradosome, a complex of RNA helicase SUPV3L1 (best known as SUV3) and the ribonuclease PNPT1 (also known as PNPase), together with G4-melting protein GRSF1, is a key player in restricting antisense mtRNAs. |
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AbstractList | Transcription of the human mitochondrial genome produces a vast amount of non-coding antisense RNAs. These RNA species can form G-quadraplexes (G4), which affect their decay. We found that the mitochondrial degradosome, a complex of RNA helicase SUPV3L1 (best known as SUV3) and the ribonuclease PNPT1 (also known as PNPase), together with G4-melting protein GRSF1, is a key player in restricting antisense mtRNAs. |
Author | Stepien, Piotr P. Kulinski, Tomasz M. Pietras, Zbigniew Borowski, Lukasz S. Cysewski, Dominik Szczesny, Roman J. Dziembowski, Andrzej Wojcik, Magdalena A. Szewczyk, Maciej |
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Cites_doi | 10.1093/nar/gkp903 10.1093/nar/gks1130 10.1038/nsmb.1814 10.1016/j.celrep.2015.01.030 10.1038/s41467-018-05007-9 10.1016/j.cmet.2013.02.006 10.1093/nar/gkx380 10.1126/science.aaf5371 10.1038/s41586-018-0363-0 10.1093/nar/gkf647 |
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Snippet | Transcription of the human mitochondrial genome produces a vast amount of non-coding antisense RNAs. These RNA species can form G-quadraplexes (G4), which... |
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Title | Controlling the mitochondrial antisense - role of the SUV3-PNPase complex and its co-factor GRSF1 in mitochondrial RNA surveillance |
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