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Published on: August 12, 2015
SUMO1 negatively regulates BRCA1-mediated transcription, via modulation of promoter occupancy
Mi Ae Park1, Yeong-Jae Seok, Gajin Jeong
1Department of Biological Sciences & Department of Molecular Science and Technology Ajou University, Suwon, Korea.
Abstract:
BRCA1, a tumor suppressor gene, is implicated in the repression and activation of transcription via interactions with a diverse range of proteins. The mechanisms regulating the action of BRCA1 are not fully understood. Here, we use the promoters of Gadd45alpha, p27(KIP1) and p21(WAF1/CIP1) to demonstrate that SUMO1 represses transactivation potential of BRCA1 by causing BRCA1 to be released from the promoters and augmenting histone deacetylation via recruitment of histone deacetylase (HDAC) activity. Consistently, silencing of SUMO1 led to recruitment of BRCA1 and release of HDAC1 at the BRCA1 target promoters, and subsequent transcriptional activation of the BRCA1 target genes. Furthermore, a sumoylation-incompetent mutant missing the sumoylation donor site suppressed BRCA1-induced activation of transcription, whereas E2 UBC9 or the dominant-negative mutant UBC9 had no effect, implying that repression of BRCA1-mediated activation of transcription by SUMO1 is independent of sumoylation. Repression of BRCA1-mediated activation of transcription by SUMO1 was reversed by DNA damage by inducing the release of SUMO1 from the Gadd45alpha promoter and the recruitment of BRCA1, along with increased histone acetylation, to enhance activation of transcription. Together, our data provide evidence that SUMO1 plays a role in the activation-repression switch of BRCA1-mediated transcription via modulation of promoter occupancy.
Insights
Small Ubiquitin-like Modifier 1 (SUMO1) represses BRCA1
Area of Science:
- Molecular Biology
- Gene Regulation
- Cancer Research
Background:
- BRCA1 is a tumor suppressor involved in gene transcription.
- Mechanisms controlling BRCA1 activity are not fully understood.
Purpose of the Study:
- To investigate the role of SUMO1 in regulating BRCA1's transcriptional activity.
- To elucidate the mechanisms by which SUMO1 influences BRCA1 function.
Main Methods:
- Utilized promoters of Gadd45alpha, p27(KIP1), and p21(WAF1/CIP1).
- Investigated protein interactions and promoter occupancy.
- Employed gene silencing and mutant protein analyses.
- Assessed histone acetylation and deacetylation levels.
Main Results:
- SUMO1 represses BRCA1 transactivation by promoting BRCA1 release from promoters and increasing histone deacetylation.
- SUMO1 silencing enhances BRCA1 recruitment and gene activation.
- SUMO1's repressive effect is independent of sumoylation.
- DNA damage reverses SUMO1-mediated repression, increasing BRCA1 recruitment and histone acetylation.
Conclusions:
- SUMO1 acts as a key regulator in the activation-repression switch of BRCA1-mediated transcription.
- SUMO1 modulates BRCA1's promoter occupancy to control gene expression.
- Understanding this interplay is crucial for cancer research and therapeutic strategies.
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