Identification of Estrogen Receptor-Related Receptor Gamma as a Direct Transcriptional Target of Angiogenin

Nuclear translocation of angiogenin (ANG) is essential for the proliferation of its target cells. ANG promotes rRNA synthesis, while whether it regulates mRNA transcription remains unknown. Using the chromatin immunoprecipitation method, we have identified 12 ANG-binding sequences. One of these sequences lies in the estrogen receptor-related receptor gamma (ERRc) gene which we designated as ANG-Binding Sequence within ERRc (ABSE). ABSE exhibited ANG-dependent repressor activity in the luciferase reporter system. Down-regulation of ANG increased ERRc expression, and active gene marker level at the ABSE region. The expression levels of ERRc targets genes, p21WAF/CIP and p27KIP1, and the occupation of ERRc on their promoter regions were increased in ANG-deficient cells accordingly. Furthermore, knockdown of ERRc promoted the proliferation rate in ANG-deficient breast cancer cells. Finally, immunohistochemistry staining showed negative correlation between ANG and ERRc in breast cancer tissue. Altogether, our study provides evidence that nuclear ANG directly binds to the ABSE of ERRc gene and inhibits ERRc transcription to promote breast cancer cell proliferation