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The deubiquitinase USP15 antagonizes Parkin-mediated mitochondrial ubiquitination and mitophagy
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Knockdown of USP15 and USP30 increased the rate of mitophagy but had no discernible effect on parkin recruitment.
“knockdown of these DUBs increased the rate of mitophagy but had no discernible effect on parkin recruitment.”
From USP8 regulates mitophagy by removing K6‐linked ubiquitin conjugates from parkin (2014) · cites this paper as Cornelissen et al, 2014
The 'Knockdown of USP15 enhances mitophagy' section reports increased Parkin-dependent mitophagy after USP15 knockdown. The 'USP15 antagonizes Parkin-mediated mitochondrial ubiquitination' section reports no effect on Parkin translocation, but that experiment tested USP15 overexpression, not knockdown. The copy does not report the claimed mitophagy or recruitment effects for USP30 knockdown. (LLM, conf=0.88)
Experimental — accuracy not yet measuredTwo recent studies identified a role for USP15 and USP30 in parkin-mediated mitophagy.
“two recent studies identified a role for USP15 and the mitochondrial DUB USP30 in parkin-mediated mitophagy”
From USP8 regulates mitophagy by removing K6‐linked ubiquitin conjugates from parkin (2014) · cites this paper as Cornelissen et al, 2014
Overexpression of USP15 and USP30 leads to deubiquitination of parkin substrates on mitochondria, which slows mitochondrial clearance by autophagy.
“overexpression of these DUBs leads to deubiquitination of parkin substrates on mitochondria, which in turn slowed the rate of mitochondrial clearance by autophagy.”
From USP8 regulates mitophagy by removing K6‐linked ubiquitin conjugates from parkin (2014) · cites this paper as Cornelissen et al, 2014
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Citations
Cites
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
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PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1
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Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin
Clark, I. E., Dodson, M. W., Jiang, C., Cao, J. H., Huh, J. R., Seol, J. H., Yoo, S. J., Hay, B. A., & Guo, M. (2006) · Nature · doi:10.1038/nature04779 · Cited by 1,788
Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin
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Mitochondrial pathology and apoptotic muscle degeneration in Drosophila parkin mutants
Greene, J. C., Whitworth, A. J., Kuo, I., Andrews, L. A., Feany, M. B., & Pallanck, L. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0737556100 · Cited by 1,203
Parkin is activated by PINK1-dependent phosphorylation of ubiquitin at Ser65
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p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria
Okatsu, K., Saisho, K., Shimanuki, M., Nakada, K., Shitara, H., Sou, Y., Kimura, M., Sato, S., Hattori, N., Komatsu, M., et al. (2010) · Genes to Cells · doi:10.1111/j.1365-2443.2010.01426.x · Cited by 397
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“Immunostaining of cultured cells was performed as described (17).”
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Metadata
- Authors
- Cornelissen, T., Haddad, D., Wauters, F., Van Humbeeck, C., Mandemakers, W., Koentjoro, B., Sue, C., Gevaert, K., De Strooper, B., Verstreken, P., & Vandenberghe, W.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2014-05-22
- Volume
- 23
- Issue
- 19
- Pages
- 5227-5242
- ISSN
- 0964-6906
- 1460-2083
- Cited by
- 327
- References
- 9
- Language
- en
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