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The autophagy protein Ambra1 regulates gene expression by supporting novel transcriptional complexes

Authors :
Alexander Loftus
Alex von Kriegsheim
Jimi Wills
Alison F. Munro
Billie Georgina Cooper Griffith
Adam Byron
Christina Schoenherr
Margaret C. Frame
Source :
J Biol Chem, Schoenherr, C, Byron, A, Griffith, B, Loftus, A, Wills, J C, Munro, A F, Von Kriegsheim, A & Frame, M C 2020, ' The autophagy protein Ambra1 regulates gene expression by supporting novel transcriptional complexes ', Journal of Biological Chemistry, pp. jbc.RA120.012565 . https://doi.org/10.1074/jbc.RA120.012565, Schoenherr, C, Byron, A, Griffith, B G C, Loftus, A E P, Wills, J C, Munro, A F, von Kriegsheim, A & Frame, M C 2020, ' The autophagy protein Ambra1 regulates gene expression by supporting novel transcriptional complexes ', Journal of Biological Chemistry, vol. 295, no. 34, pp. 12045-12057 . https://doi.org/10.1074/jbc.RA120.012565
Publication Year :
2020

Abstract

Ambra1 is considered an autophagy and trafficking protein with roles in neurogenesis and cancer cell invasion. Here, we report that Ambra1 also localizes to the nucleus of cancer cells, where it has a novel nuclear scaffolding function that controls gene expression. Using biochemical fractionation and proteomics, we found that Ambra1 binds to multiple classes of proteins in the nucleus, including nuclear pore proteins, adaptor proteins such as FAK and Akap8, chromatin-modifying proteins, and transcriptional regulators like Brg1 and Atf2. We identified biologically important genes, such as Angpt1, Tgfb2, Tgfb3, Itga8, and Itgb7, whose transcription is regulated by Ambra1-scaffolded complexes, likely by altering histone modifications and Atf2 activity. Therefore, in addition to its recognized roles in autophagy and trafficking, Ambra1 scaffolds protein complexes at chromatin, regulating transcriptional signaling in the nucleus. This novel function for Ambra1, and the specific genes impacted, may help to explain the wider role of Ambra1 in cancer cell biology.

Details

ISSN :
1083351X
Volume :
295
Issue :
34
Database :
OpenAIRE
Journal :
The Journal of biological chemistry
Accession number :
edsair.doi.dedup.....e78bd97cfd53fdd8c2edaef1ab5c3889
Full Text :
https://doi.org/10.1074/jbc.RA120.012565