Activators of p54/nrb can be delineated into two broad categories based on their mode of action: those that affect gene expression, leading to upregulated transcription of RNA processing components, and those that influence the post-translational modifications and protein-protein interactions of factors involved in RNA metabolism. For p54/nrb, an RNA-binding protein associated with nuclear domains and implicated in pre-mRNA splicing and other aspects of RNA processing, activators are not direct in their action but rather act through enhancement of transcriptional outputs or through signaling pathways that ultimately necessitate increased RNA processing capacity.
The upstream transcriptional activators, such as Retinoic Acid and Sodium Butyrate, initiate a cascade of gene expression that can increase the cellular concentration of RNA substrates and splicing factors, necessitating greater p54/nrb activity. On the other hand, compounds like PEP-005 and Forskolin trigger signaling pathways leading to the activation of protein kinases that can phosphorylate substrates and influence the transcription of genes, indirectly necessitating heightened p54/nrb function. The enhanced cellular demand for RNA processing brought on by such chemicals may manifest as an increase in the activity of p54/nrb, thus serving as indirect activators of its function. While not activators in the traditional sense, these chemicals enable conditions conducive to the functional enhancement of p54/nrb.
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