RAD54L2 inhibitors are a class of chemical compounds designed to target and inhibit the activity of RAD54L2, a protein involved in the homologous recombination (HR) DNA repair pathway. RAD54L2, a member of the SWI/SNF family of DNA-dependent ATPases, plays a crucial role in facilitating the repair of DNA double-strand breaks (DSBs) by promoting the remodeling of chromatin structures and the stabilization of the RAD51 nucleoprotein filament. This filament is essential for the search and pairing of homologous DNA sequences during HR. RAD54L2 is thought to assist in this process by stimulating the dissociation of RAD51 from DNA after strand invasion, enabling the subsequent repair steps to occur. Inhibiting RAD54L2 can disrupt this process, leading to compromised HR activity and a reduced ability to repair DSBs efficiently.
In research, RAD54L2 inhibitors are valuable tools for studying the mechanisms of DNA repair and understanding the specific functions of RAD54L2 in the homologous recombination pathway. By blocking RAD54L2's activity, researchers can investigate how cells respond to DNA damage in the absence of a fully functional HR pathway. This allows for a deeper exploration of how different repair pathways, such as non-homologous end joining (NHEJ), are activated when HR is impaired. Additionally, RAD54L2 inhibitors provide insight into the role of chromatin remodeling in DNA repair processes, as well as how cells maintain genomic stability under conditions of replication stress and DNA damage. These studies help elucidate the intricate balance between DNA repair, cell cycle regulation, and genome integrity, offering a better understanding of cellular responses to genotoxic stress.
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