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Endogenous polyamines (putrescine, spermidine, and spermine) occupy distinct binding sites along genomic DNA via mainly electrostatic interactions. Their site-specific occupancy influences local secondary structure transitions (B-A-Z forms), stabilizes unusual conformations under certain conditions, alters hydration shells within grooves, exhibits some sequence preference based on base composition/motif context—and ultimately regulates access for other nuclear proteins involved in gene regulation processes. This dynamic equilibrium is crucial for maintaining genome integrity and cellular homeostasis.
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