Meiotic viral attenuation through an ancestral apoptotic pathway
The programmed release of apoptogenic proteins from mitochondria is a core event of apoptosis, although ancestral roles of this phenomenon are not known. In mammals, one such apoptogenic protein is Endonuclease G (EndoG), a conserved mitochondrial nuclease that fragments the DNA of dying cells. In t...
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Published in: | Proceedings of the National Academy of Sciences - PNAS Vol. 116; no. 33; pp. 16454 - 16462 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
National Academy of Sciences
13-08-2019
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Series: | From the Cover |
Subjects: | |
Online Access: | Get full text |
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Summary: | The programmed release of apoptogenic proteins from mitochondria is a core event of apoptosis, although ancestral roles of this phenomenon are not known. In mammals, one such apoptogenic protein is Endonuclease G (EndoG), a conserved mitochondrial nuclease that fragments the DNA of dying cells. In this work, we show that budding yeast executes meiotically programmed mitochondrial release of an EndoG homolog, Nuc1, during sporulation. In contrast to EndoG’s ostensible pro-death function during apoptosis, Nuc1 mitochondrial release is pro-survival, attenuating the cytosolic L-A and Killer double-stranded RNA mycoviruses and protecting meiotic progeny from the catastrophic consequences of their derepression. The protective viral attenuation role of this pathway illuminates a primordial role for mitochondrial release of EndoG, and perhaps of apoptosis itself. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by Reed B. Wickner, National Institutes of Health, Bethesda, MD, and approved June 14, 2019 (received for review January 16, 2019) Author contributions: J.G., S.C., F.C., T.Z., S.H., and M.D.M. designed research; J.G., S.C., F.C., T.Z., S.H., and M.D.M. performed research; G.A.M. contributed new reagents/analytic tools; J.G., S.C., F.C., T.Z., S.H., G.A.M., and M.D.M. analyzed data; and J.G. and M.D.M. wrote the paper. |
ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.1900751116 |