AMBRA1, a Novel BH3-Like Protein: New Insights Into the AMBRA1-BCL2-Family Proteins Relationship
- PMID: 28215535
- DOI: 10.1016/bs.ircmb.2016.09.002
AMBRA1, a Novel BH3-Like Protein: New Insights Into the AMBRA1-BCL2-Family Proteins Relationship
Abstract
Cellular homeostasis swings like a pendulum backward and forward between life and death. Two of the main processes, which regulate this equilibrium, are autophagy and apoptosis. While autophagy is a highly conserved self-digestion mechanism that mediates degradation of damaged or surplus components, apoptosis is a programmed cell suicide in which typical death signals induce the elimination of undesired cells. Both these processes are highly regulated by complex molecular machineries, including some common proteins whose "dual role" favors one process or the other. Among these proteins, the well-known antiapoptotic factor BCL2 downregulates autophagy through interactions with the essential autophagic effectors, BECN1/BECLIN 1 and AMBRA1. Recently, we have demonstrated that the proautophagic protein AMBRA1 contains a BH3 domain necessary for AMBRA1 binding with the antiapoptotic factor BCL2. We found that the AMBRA1-BCL2 couple have a "dual role" in autophagy and apoptosis: the mitochondrial pool of BCL2 is able to inhibit AMBRA1-dependent autophagy, whereas in cell death conditions, the cleaved form of AMBRA1 (AMBRA1CT), resulting from CASP/CASPASES-cleavage, abrogates the prosurvival activity of BCL2 and promotes a proapoptotic amplification loop. The CASP-cleaved form of AMBRA1 bound other antiapoptotic members of the BCL2 family proteins such as MCL1 and BCL2L1/BCL-X; by contrast, no binding could be detected with the proapoptotic-BCL2 factors such as BAK1/BAK and BAX. These findings underline an intricate interplay between autophagy and cell death in which the proautophagic protein AMBRA1 and the antiapoptotic BCL2 family members are the major players. Here, we give an overview of the AMBRA1-BCL2 family proteins interactome and its involvement in controlling life and cell death. We discuss a putative therapeutic target which offers the novel BH3 motif identified in the C-terminal part of AMBRA1.
Keywords: AMBRA1; Apoptosis; Autophagy; BCL2 family proteins; BH3 motif.
© 2017 Elsevier Inc. All rights reserved.
Similar articles
-
Prosurvival AMBRA1 turns into a proapoptotic BH3-like protein during mitochondrial apoptosis.Autophagy. 2016 Jun 2;12(6):963-75. doi: 10.1080/15548627.2016.1164359. Epub 2016 Apr 28. Autophagy. 2016. PMID: 27123694 Free PMC article.
-
BAX and BAK1 are dispensable for ABT-737-induced dissociation of the BCL2-BECN1 complex and autophagy.Autophagy. 2015;11(3):452-9. doi: 10.1080/15548627.2015.1017191. Autophagy. 2015. PMID: 25715028 Free PMC article.
-
Impaired autophagy and APP processing in Alzheimer's disease: The potential role of Beclin 1 interactome.Prog Neurobiol. 2013 Jul-Aug;106-107:33-54. doi: 10.1016/j.pneurobio.2013.06.002. Epub 2013 Jul 1. Prog Neurobiol. 2013. PMID: 23827971 Review.
-
Autophagy and apoptosis are regulated by stress on Bcl2 by AMBRA1 in the endoplasmic reticulum and mitochondria.Theor Biol Med Model. 2019 Oct 29;16(1):18. doi: 10.1186/s12976-019-0113-5. Theor Biol Med Model. 2019. PMID: 31665034 Free PMC article.
-
Bcl-2 family members: dual regulators of apoptosis and autophagy.Autophagy. 2008 Jul;4(5):600-6. doi: 10.4161/auto.6260. Epub 2008 May 12. Autophagy. 2008. PMID: 18497563 Free PMC article. Review.
Cited by
-
AMBRA1 p.Gln30Arg Mutation, Identified in a Cowden Syndrome Family, Exhibits Hyperproliferative Potential in hTERT-RPE1 Cells.Int J Mol Sci. 2022 Sep 22;23(19):11124. doi: 10.3390/ijms231911124. Int J Mol Sci. 2022. PMID: 36232425 Free PMC article.
-
Alterations of the interactome of Bcl-2 proteins in breast cancer at the transcriptional, mutational and structural level.PLoS Comput Biol. 2019 Dec 11;15(12):e1007485. doi: 10.1371/journal.pcbi.1007485. eCollection 2019 Dec. PLoS Comput Biol. 2019. PMID: 31825969 Free PMC article.
-
AMBRA1 phosphorylation by CDK1 and PLK1 regulates mitotic spindle orientation.Cell Mol Life Sci. 2023 Aug 16;80(9):251. doi: 10.1007/s00018-023-04878-6. Cell Mol Life Sci. 2023. PMID: 37584777 Free PMC article.
-
GSK3β‑mediated Ser156 phosphorylation modulates a BH3‑like domain in BCL2L12 during TMZ‑induced apoptosis and autophagy in glioma cells.Int J Mol Med. 2018 Aug;42(2):905-918. doi: 10.3892/ijmm.2018.3672. Epub 2018 May 11. Int J Mol Med. 2018. PMID: 29749471 Free PMC article.
-
HUWE1 E3 ligase promotes PINK1/PARKIN-independent mitophagy by regulating AMBRA1 activation via IKKα.Nat Commun. 2018 Sep 14;9(1):3755. doi: 10.1038/s41467-018-05722-3. Nat Commun. 2018. PMID: 30217973 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials