Phospho-regulation and function of ULK1-ATG13 during the cell cycle.

Autophagy

High Magnetic Field Laboratory, Key Laboratory of High Magnetic Field and Ion Beam Physical Biology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, P. R. China.

Published: April 2021

Although it has been reported that some autophagy-related proteins could regulate the cell cycle, the function of ULK1-ATG13, the only protein kinase complex in macroautophagy/autophagy, remains unclear. We recently found that mitotic ULK1 and ATG13 are both substrates of the key cell cycle regulator CDK1-CCNB/cyclin B. CDK1-induced ULK1-ATG13 phosphorylation promotes mitotic autophagy and cell cycle progression. Moreover, and double-knockout significantly inhibits cell cycle progression and tumor cell proliferation and . These findings bridge the mutual regulation between autophagic and mitotic key kinases and provide a theoretical basis for autophagy- and cell division-related diseases based on combination therapy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8078760PMC
http://dx.doi.org/10.1080/15548627.2021.1898750DOI Listing

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