Browsing by Author "Li, Rong"

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    ASCB statement of commitment to diversity, equity, and inclusion
    Murray, Sandra A.; Holzbaur, Erika L. F.; Munson, Mary; Cimini, Daniela; Lane, Timothy F.; Alvania, Rebecca; Applewhite, Derek A.; Chang, Fred; Chen, Elizabeth H.; Earnshaw, William C.; Evans, Chantell S.; Li, Rong; Mierzwa, Beata E.; Oliver, Tiffany; Segarra, Veronica A.; Skop, Ahna R.; Weaver, Lesley N.; Asai, David J.; Boyce, Michael; Zavala, Maria Elena; Hammonds-Odie, Latanya; Vigoreaux, Jim (American Society for Cell Biology, 2024-07-22)
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    BRCA1 mutations attenuate super-enhancer function and chromatin looping in haploinsufficient human breast epithelial cells
    Zhang, Xiaowen; Wang, Yao; Chiang, Huai-Chin; Hsieh, Yuan-Pang; Lu, Chang; Park, Ben H.; Jatoi, Ismail; Jin, Victor X.; Hu, Yanfen; Li, Rong (2019-04-17)
    Background BRCA1-associated breast cancer originates from luminal progenitor cells. BRCA1 functions in multiple biological processes, including double-strand break repair, replication stress suppression, transcriptional regulation, and chromatin reorganization. While non-malignant cells carrying cancer-predisposing BRCA1 mutations exhibit increased genomic instability, it remains unclear whether BRCA1 haploinsufficiency affects transcription and chromatin dynamics in breast epithelial cells. Methods H3K27ac-associated super-enhancers were compared in primary breast epithelial cells from BRCA1 mutation carriers (BRCA1mut/+) and non-carriers (BRCA1+/+). Non-tumorigenic MCF10A breast epithelial cells with engineered BRCA1 haploinsufficiency were used to confirm the H3K27ac changes. The impact of BRCA1 mutations on enhancer function and enhancer-promoter looping was assessed in MCF10A cells. Results Here, we show that primary mammary epithelial cells from women with BRCA1 mutations display significant loss of H3K27ac-associated super-enhancers. These BRCA1-dependent super-enhancers are enriched with binding motifs for the GATA family. Non-tumorigenic BRCA1mut/+ MCF10A cells recapitulate the H3K27ac loss. Attenuated histone mark and enhancer activity in these BRCA1mut/+ MCF10A cells can be partially restored with wild-type BRCA1. Furthermore, chromatin conformation analysis demonstrates impaired enhancer-promoter looping in BRCA1mut/+ MCF10A cells. Conclusions H3K27ac-associated super-enhancer loss is a previously unappreciated functional deficiency in ostensibly normal BRCA1 mutation-carrying breast epithelium. Our findings offer new mechanistic insights into BRCA1 mutation-associated transcriptional and epigenetic abnormality in breast epithelial cells and tissue/cell lineage-specific tumorigenesis.