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Role of the Exocyst Complex Component Sec6/8 in Genomic Stability.
- Source :
-
Molecular and cellular biology [Mol Cell Biol] 2015 Nov; Vol. 35 (21), pp. 3633-45. Date of Electronic Publication: 2015 Aug 17. - Publication Year :
- 2015
-
Abstract
- The exocyst is a heterooctomeric complex well appreciated for its role in the dynamic assembly of specialized membrane domains. Accumulating evidence indicates that this macromolecular machine also serves as a physical platform that coordinates regulatory cascades supporting biological systems such as host defense signaling, cell fate, and energy homeostasis. The isolation of multiple components of the DNA damage response (DDR) as exocyst-interacting proteins, together with the identification of Sec8 as a suppressor of the p53 response, suggested functional interactions between the exocyst and the DDR. We found that exocyst perturbation resulted in resistance to ionizing radiation (IR) and accelerated resolution of DNA damage. This occurred at the expense of genomic integrity, as enhanced recombination frequencies correlated with the accumulation of aberrant chromatid exchanges. Sec8 perturbation resulted in the accumulation of ATF2 and RNF20 and the promiscuous accumulation of DDR-associated chromatin marks and Rad51 repairosomes. Thus, the exocyst supports DNA repair fidelity by limiting the formation of repair chromatin in the absence of DNA damage.<br /> (Copyright © 2015, American Society for Microbiology. All Rights Reserved.)
- Subjects :
- Activating Transcription Factor 2 analysis
Activating Transcription Factor 2 metabolism
Apoptosis Regulatory Proteins analysis
Apoptosis Regulatory Proteins metabolism
Autophagy
Beclin-1
Cell Line, Tumor
Exocytosis
Gene Deletion
Humans
Intracellular Signaling Peptides and Proteins genetics
Membrane Proteins analysis
Membrane Proteins metabolism
Tumor Suppressor p53-Binding Protein 1
Ubiquitin-Protein Ligases analysis
Ubiquitin-Protein Ligases metabolism
Vesicular Transport Proteins analysis
DNA Repair
Genomic Instability
Vesicular Transport Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1098-5549
- Volume :
- 35
- Issue :
- 21
- Database :
- MEDLINE
- Journal :
- Molecular and cellular biology
- Publication Type :
- Academic Journal
- Accession number :
- 26283729
- Full Text :
- https://doi.org/10.1128/MCB.00768-15