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Asperpyridone A represents an unusual class of pyridone alkaloids with demonstrated potential for hypoglycemic activity, primarily by promoting glucose consumption in HepG2 cells. Trichodin A, initially isolated from the marine fungus Trichoderma sp. strain MF106, exhibits notable antibiotic activities against <i>Staphylococcus epidermidis</i>. Despite their pharmacological significance, the regulatory mechanisms governing their biosynthesis have remained elusive. In this investigation, we initiated the activation of a latent gene cluster, denoted as “<i>top</i>”, through the overexpression of the Zn₂Cys₆ transcription factor TopC in <i>Tolypocladium ophioglossoides</i>. The activation of the <i>top</i> cluster led to the biosynthesis of asperpyridone A, pyridoxatin, and trichodin A. Our study also elucidated that the regulator TopC exerts precise control over the biosynthesis of asperpyridone A and trichodin A through the detection of protein–nucleic acid interactions. Moreover, by complementing these findings with gene deletions involving <i>topA</i> and <i>topH</i>, we proposed a comprehensive biosynthesis pathway for asperpyridone A and trichodin A in <i>T. ophioglossoides</i>.