Pum3, a member of the Pumilio and Fem-3 mRNA-binding factor family, possesses distinctive features, including tandem pumilio homolog domains and the ability to bind DNA and RNA without sequence specificity. Involved in diverse biological processes, Pum3 plays a crucial role in cellular functions, and its dysregulation is linked to testicular germ cell tumors in mice. Activation of Pum3 involves a complex interplay with various chemical activators targeting distinct cellular processes.
Chemicals like Actinomycin D and Tunicamycin directly activate Pum3 by inducing RNA transcription inhibition and endoplasmic reticulum stress, respectively. Indirect activators, such as Etoposide and 5-Fluorouracil, induce DNA damage and interfere with DNA/RNA synthesis, triggering stress responses that lead to Pum3 upregulation. Stimulators like AICAR and 2-Deoxyglucose activate Pum3 through AMPK, influencing cellular energy status. The involvement of Pum3 in stress response pathways, including DNA repair and unfolded protein response, is evident in its activation by various chemicals. In conclusion, the diverse activators of Pum3 highlight its intricate regulatory network and its role in cellular stress responses and DNA damage repair. Understanding the nuanced mechanisms of Pum3 activation provides insights into potential avenues for manipulating its function in various biological processes.
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