K259-SUMOylation of DGCR8 promoted by p14ARF exerts a tumor-suppressive function

• 来源期刊: 分子细胞生物学报（英文版）
• 年，卷（期）: 2016,（5）
• 页码范围: 456-458
• 页数: 3页
• 语种: 中文
• DOI: 10.1093/jmcb/mjw030

摘要

Dear Editor, DGCR8 is essential for the miRNA biogenesis (Han et al.,2004,2006;QuickCleveland et al.,2014).We recently reported that at K707-SUMOylation of DGCR8 influences its affinity with primiRNAs and controls the direct functions of pri-miRNAs in gene silencing.However,the K707R mutation does not remove all SUM01 modifications of DGCR8 (Zhu et al.,2015),suggesting that DGCR8 bears other SUMOylation sites.Here,we identified K259 as an alternative site for DGCR8 SUMOylation that was directly promoted by p14ARF in the nucleus.We also demonstrated a notable role of K259-SUMOylation in preventing DGCR8 nuclear export that is required for its function in the processing of pri-miRNAs into pre-miRNAs and tumor suppression.