D3Ertd751e, situated on Chromosome 3, emerges as a pivotal player in transcriptional regulation with a multifaceted role predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific, and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. The gene's involvement in the intricate orchestration of transcription by RNA polymerase II underscores its significance in cellular processes, particularly in the nuanced control of gene expression. Further strengthening its biological relevance, D3Ertd751e exhibits orthology with human ZNF267 and ZNF519, highlighting evolutionary conservation and potential functional parallels across species.
The activation of D3Ertd751e is a finely tuned process influenced by various molecular players. Epigenetic modifiers, such as histone deacetylase inhibitors like Valproic Acid and Trichostatin A, exert their impact by altering chromatin structure through histone acetylation. This epigenetic modification creates a more permissive environment for D3Ertd751e transcription, facilitating its up-regulation and consequent engagement in cellular processes. Signaling pathway modulators, exemplified by SB431542, indirectly affect D3Ertd751e activation by impinging on the TGF-β signaling pathway, showcasing the intricate cross-talk that regulates the gene's expression. Additionally, small molecules like Forskolin and Ionomycin act as indirect activators by influencing cellular signaling cascades, leading to the modulation of transcription factors associated with D3Ertd751e expression. Collectively, these diverse mechanisms underscore the sophisticated regulatory network governing the activation of D3Ertd751e, contributing to its pivotal role in transcriptional control and cellular differentiation.
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