Date published: 2025-9-15

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Yotiao Activators

Yotiao, formally known as the A-kinase anchor protein 9 (AKAP9), plays a critical role in the molecular orchestration of various signaling pathways within the cell. As a scaffolding protein, it facilitates the precise localization of protein kinase A (PKA) to specific cellular compartments, thereby ensuring that phosphorylation events occur with spatial and temporal accuracy. The expression of Yotiao is a finely tuned process, integral to the maintenance of cellular homeostasis, and has been shown to be susceptible to modulation by various intracellular signals and external compounds. Understanding the regulation of Yotiao is not only crucial for comprehending its role in cellular physiology but also for appreciating the complexity of intracellular signaling networks.

Several biochemical agents are known to potentially induce the expression of Yotiao, each acting through distinct molecular mechanisms. Forskolin, for example, is a diterpene that directly activates adenylate cyclase, thereby increasing the levels of cyclic AMP (cAMP) within the cell, a secondary messenger that is instrumental in the activation of PKA. The activation of PKA can then lead to the phosphorylation of transcription factors, which may enhance the transcription of the AKAP9 gene. Retinoic acid, another agent, engages with its nuclear receptors to promote the transcription of genes, including those involved in the scaffolding of signaling molecules such as Yotiao. Similarly, the cAMP analog, dibutyryl cAMP, is capable of permeating the cellular membrane and mimicking the action of endogenous cAMP, thus potentially upregulating AKAP9 transcription through the activation of cAMP-dependent pathways. Phorbol esters like Phorbol 12-myristate 13-acetate (PMA) activate protein kinase C (PKC), which is another pathway that may lead to the stimulation of transcription factors and subsequent increase in AKAP9 gene expression. Lithium chloride indirectly stimulates the expression of several genes by inhibiting glycogen synthase kinase 3 (GSK-3), a negative regulator of gene transcription. In a more epigenetic context, compounds such as Trichostatin A (TSA) and sodium butyrate, both histone deacetylase inhibitors, can lead to a more relaxed chromatin state, making the gene promoter regions, including that of AKAP9, more accessible for transcriptional machinery, hence potentially enhancing Yotiao expression. These compounds illustrate the diversity of molecules that can sway the expression of pivotal cellular components like Yotiao, highlighting the complexity of cellular regulation and the intricate web of intracellular communication.

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