Brd3os, an opposite strand counterpart to BRD3, is implicated in diverse biological processes through its involvement in transcriptional regulation. The identified activators modulate Brd3os expression and function, impacting its role in cellular processes. Chemical activators like JQ1, PFI-3, and I-BET151 directly activate Brd3os by inhibiting BET bromodomains, enhancing transcriptional activity. SAHA, Trichostatin A, and Panobinostat activate Brd3os through HDAC inhibition, promoting chromatin accessibility and facilitating transcriptional activation.
Curcumin and Quercetin indirectly activate Brd3os by modulating NF-κB signaling, influencing Brd3os expression in a context-dependent manner. 5-Aza-2'-deoxycytidine and Decitabine act indirectly by demethylating DNA, altering the epigenetic landscape and promoting transcriptional activation. Resveratrol modulates Brd3os through SIRT1, affecting expression and function. Romidepsin and other identified activators collectively offer a spectrum of mechanisms to modulate Brd3os, showcasing its versatility in cellular processes. In conclusion, understanding Brd3os activation provides insights into the intricate regulatory networks influencing its role in transcriptional regulation. The identified activators offer a foundation for exploring the dynamic interplay of Brd3os in diverse cellular contexts and its potential implications in cellular homeostasis.
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