The RNA binding protein RALY suppresses p53 activity and promotes lung tumorigenesis

The tumor suppressor p53 plays a pivotal role in tumor prevention. The activity of p53 is mainly restrained by the ubiquitin E3 ligase Mdm2. However, it is not well understood how the Mdm2-p53 pathway is intricately regulated. Here we report that the RNA binding protein RALY functions as an oncogenic factor in lung cancer. RALY simultaneously binds to Mdm2 and the deubiquitinating enzyme USP7. Via these interactions, RALY not only stabilizes Mdm2 by stimulating the deubiquitinating activity of USP7 toward Mdm2 but also increases the trans-E3 ligase activity of Mdm2 toward p53. Consequently, RALY enhances Mdm2-mediated ubiquitination and degradation of p53. Functionally, RALY promotes lung tumorigenesis, at least partially, via negative regu-lation of p53. These findings suggest that RALY destabilizes p53 by modulating the function of Mdm2 at mul-tiple levels. Our study also indicates a critical role for RALY in promoting lung tumorigenesis via p53 inhibition.

Automated summary

The RNA binding protein RALY functions as an oncogenic factor in lung cancer by stabilizing Mdm2 and enhancing its E3 ligase activity toward p53. This leads to increased ubiquitination and degradation of p53, promoting lung tumorigenesis.