BRCA1-A and BRISC: multifunctional molecular machines for ubiquitin signaling
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The K63-linkage specific deubiquitinase BRCC36 forms the core of two multi-subunit deubiquitination complexes: BRCA1-A and BRISC. BRCA1-A is recruited to DNA repair foci, edits ubiquitin signals on chromatin, and sequesters BRCA1 away from the site of damage, suppressing homologous recombination by limiting resection. BRISC forms a complex with metabolic enzyme SHMT2 and regulates the immune response, mitosis, and hematopoiesis. Almost two decades of research have revealed how BRCA1-A and BRISC use the same core of subunits to perform very distinct biological tasks.
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SHMT2 has a novel function that contributes to immune regulation through the BRISC complex.
“Recent structural studies have identified a novel function of SHMT2 that contributes to immune regulation through the BRISC complex.”
From A review of small-molecule inhibitors of one-carbon enzymes: SHMT2 and MTHFD2 in the spotlight (2021) · cites this paper as [130]
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Phosphopeptide interactions with BRCA1 BRCT domains: More than just a motif
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The BRCA1-Interacting Protein Abraxas Is Required for Genomic Stability and Tumor Suppression
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High BRE expression in pediatric MLL-rearranged AML is associated with favorable outcome
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RAP80 Is Critical in Maintaining Genomic Stability and Suppressing Tumor Development
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Three-Dimensional Architecture of the Human BRCA1-A Histone Deubiquitinase Core Complex
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Periasamy, J., Kurdekar, V., Jasti, S., Nijaguna, M. B., Boggaram, S. S., Hurakadli, M. A., Raina, D., Kurup, L. M., Chintha, C., Manjunath, K., et al. (2018) · Cell chemical biology · doi:10.1016/j.chembiol.2018.02.012 · Cited by 23 · see citing works
Prokaryotic Ubiquitin-Like Protein and Its Ligase/Deligase Enyzmes
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Structural Basis for the BRCA1 BRCT Interaction with the Proteins ATRIP and BAAT1
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Expression of the BRCA1 complex member BRE predicts disease free survival in breast cancer
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Loss of BRCA1-A Complex Function in RAP80 Null Tumor Cells
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Molecular Basis for Impaired DNA Damage Response Function Associated with the RAP80 ΔE81 Defect
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Eukaryote specific folds: Part of the whole
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Structural and Functional Implication of RAP80 ΔGlu81 Mutation
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Role of MERIT40 in stabilization of BRCA1 complex: A protein–protein interaction study
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Preliminary crystallographic studies of BRCA1 BRCT–ABRAXAS complex
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BioE3 identifies specific substrates of ubiquitin E3 ligases
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A review of small-molecule inhibitors of one-carbon enzymes: SHMT2 and MTHFD2 in the spotlight
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Structural and Functional Basis of JAMM Deubiquitinating Enzymes in Disease
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BRCA1-A and LIG4 complexes mediate ecDNA biogenesis and cancer drug resistance
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Loss of Brcc3 in Zebrafish Embryos Increases Their Susceptibility to DNA Damage Stress
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Identification of BRCC3 and BRCA1 as Regulators of TAZ Stability and Activity
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- Authors
- Rabl, J.
- Affiliations
- ETH Zurich (CH)
- Corresponding author
- Rabl, Julius
- ORCID
- Rabl, Julius
- Venue
- Biomolecules
- Publisher
- MDPI AG
- Published
- 2020-10-31
- Volume
- 10
- Issue
- 11
- Pages
- 1503
- ISSN
- 2218-273X (ISSN-L)
- PMC
- PMC7692841
- OpenAlex
- W3095939912
- Cited by
- 31
- References
- 121
- Citations by year
- 2026: 7 · 2025: 7 · 2024: 5 · 2023: 4 · 2022: 2 · 2021: 6
- FWCI
- 0.29
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Biomolecules (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Repository for Publications and Research Data (ETH Zurich) (publishedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- ETH Zürich Research Collection (cc-by)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
- Keywords
- BRCC36, deubiquitination, K63-linked ubiquitin, ubiquitin signaling, DNA repair, homologous recombination, DNA resection, chromatin, SHMT2, immune response, mitosis, hematopoiesis, molecular machines
- MeSH terms
- Deubiquitinating Enzymes, Chromatin, DNA Repair, DNA-Binding Proteins, Hematopoiesis, Humans, Immunity, Mitosis, Glycine Hydroxymethyltransferase, BRCA1 Protein, Ubiquitin, SUMO-1 Protein, Histone Chaperones
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