Uba1 functions in Atg7- and Atg3-independent autophagy

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Uba1 functions in Atg7- and Atg3-independent autophagy

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Title: Uba1 functions in Atg7- and Atg3-independent autophagy
Author: Chang, Tsun-Kai; Shravage, Bhupendra V.; Hayes, Sebastian D.; Powers, Christine M.; Simin, Rachel T.; Harper, J. Wade; Baehrecke, Eric H.

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Citation: Chang, Tsun-Kai, Bhupendra V. Shravage, Sebastian D. Hayes, Christine M. Powers, Rachel T. Simin, J. Wade Harper, and Eric H. Baehrecke. 2013. “Uba1 functions in Atg7- and Atg3-independent autophagy.” Nature cell biology 15 (9): 1067-1078. doi:10.1038/ncb2804. http://dx.doi.org/10.1038/ncb2804.
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Abstract: Autophagy is a conserved process that delivers components of the cytoplasm to lysosomes for degradation. The E1 and E2 enzymes encoded by Atg7 and Atg3 are thought to be essential for autophagy involving the ubiquitin-like protein Atg8. Here, we describe an Atg7- and Atg3-independent autophagy pathway that facilitates programmed reduction of cell size during intestine cell death. Although multiple components of the core autophagy pathways, including Atg8, are required for autophagy and cells to shrink in the midgut of the intestine, loss of either Atg7 or Atg3 function does not influence these cellular processes. Rather, Uba1, the E1 used in ubiquitination, is required for autophagy and reduction of cell size. Our data reveal that distinct autophagy programs are used by different cells within an animal, and disclose an unappreciated role for ubiquitin activation in autophagy.
Published Version: doi:10.1038/ncb2804
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762904/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12064440
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