BRCA1 Forms a Functional Complex with γ-H2AX as a Late Response to Genotoxic Stress
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Updated: Jun 8, 2026

Visualization of DNA Repair Proteins Interaction by Immunofluorescence
Published on: June 26, 2020
Susan A Krum1, Esther de la Rosa Dalugdugan, Gustavo A Miranda-Carboni
1Molecular Biology Institute, Jonsson Comprehensive Cancer Center, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
Abstract:
Following genotoxic stress, the histone H2AX becomes phosphorylated at serine 139 by the ATM/ATR family of kinases. The tumor suppressor BRCA1, also phosphorylated by ATM/ATR kinases, is one of several proteins that colocalize with phospho-H2AX (γ-H2AX) at sites of active DNA repair. Both the precise mechanism and the purpose of BRCA1 recruitment to sites of DNA damage are unknown. Here we show that BRCA1 and γ-H2AX form an acid-stable biochemical complex on chromatin after DNA damage. Maximal association of BRCA1 with γ-H2AX correlates with reduced global γ-H2AX levels on chromatin late in the repair process. Since BRCA1 is known to have E3 ubiquitin ligase activity in vitro, we examined H2AX for evidence of ubiquitination. We found that H2AX is ubiquitinated at lysines 119 and 119 in vivo and that blockage of 26S proteasome function stabilizes γ-H2AX levels within cells. When BRCA1 levels were reduced, ubiquitination of H2AX was also reduced, and the cells retained higher levels of phosphorylated H2AX. These results indicate that BRCA1 is recruited into stable complexes with γ-H2AX and that the complex is involved in attenuation of the γ-H2AX repair signal after DNA damage.
Insights
BRCA1 forms a complex with phosphorylated H2AX (γ-H2AX) at DNA damage sites. This complex helps reduce the DNA repair signal by ubiquitylating H2AX, indicating BRCA1
Area of Science:
- DNA repair mechanisms
- Cellular response to genotoxic stress
- Biochemistry of DNA damage signaling
Background:
- Genotoxic stress triggers histone H2AX phosphorylation to form γ-H2AX.
- BRCA1, a tumor suppressor, is recruited to DNA damage sites and co-localizes with γ-H2AX.
- The exact role of BRCA1 recruitment and its interaction with γ-H2AX remain unclear.
Purpose of the Study:
- To investigate the biochemical interaction between BRCA1 and γ-H2AX after DNA damage.
- To elucidate the functional significance of BRCA1-γ-H2AX complex formation in DNA repair signaling.
Main Methods:
- Formation and characterization of an acid-stable BRCA1-γ-H2AX chromatin complex.
- Assessment of H2AX ubiquitination in vivo and its dependence on BRCA1.
- Analysis of γ-H2AX levels upon inhibition of proteasome function and BRCA1 depletion.
Main Results:
- BRCA1 and γ-H2AX form a stable biochemical complex on chromatin post-DNA damage.
- BRCA1-γ-H2AX complex formation correlates with decreased γ-H2AX levels during late-stage repair.
- H2AX ubiquitination at Lys119/120 was observed in vivo, and proteasome inhibition stabilized γ-H2AX.
- Reduced BRCA1 levels diminished H2AX ubiquitination and increased persistent γ-H2AX.
Conclusions:
- BRCA1 is recruited to form stable complexes with γ-H2AX at DNA damage sites.
- The BRCA1-γ-H2AX complex plays a role in attenuating the γ-H2AX DNA repair signal.
- BRCA1-mediated ubiquitination of H2AX contributes to the resolution of the DNA damage response.
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