APAF-1-ALT, a novel alternative splicing form of APAF-1, potentially causes impeded ability of undergoing DNA damage-induced apoptosis in the LNCaP human prostate cancer cell line

We have found a novel alternative splicing product of the apoptotic Protease activating factor 1 (APAF-1), termed APAF-1-ALT, in the LNCaP human prostate Cancer cell line. APAF-1-ALT harbors the Caspase recruitment domain and an incomplete CED-4 like/ATPase domain, but lacks the WD-40 repeat units. The LNCaP cell expressed the full-length APAF-1 weakly and APAF-1-ALT rather abundantly, especially after mycoplasma Infection. LNCaP underwent a retarded DNA damage-induced Apoptosis, which was independent of Caspase 9 activity. APAF-1-ALT functioned less effectively in inducing Apoptosis than did APAF-1-XL, the full-length APAF-1, in transient transfection. Moreover, APAF-1-ALT interfered with APAF-1-XL's ability to induce Apoptosis in transient double transfection experiment. These results indicate that APAF-1-ALT is a molecule that is deficient and impeded for mediating Apoptosis and that it may contribute to the resistance to DNA damage-induced treatment observed in LNCaP.