胰岛素
ADP核糖基化
化学
内科学
细胞生物学
医学
生物
生物化学
酶
NAD+激酶
作者
Soumyadeep Sarkar,Fangjia Li,Youngki You,Emily C. Elliott,Kevin Zemaitis,Hyeyoon Kim,Lye Meng Markillie,Jeremiah Traeger,Samantha Powell,Mireia Ramos-Rodríguez,Xiaoyan Yi,Jacob R. Enriquez,Marina Gritsenko,Hugh Mitchell,Décio L. Eizirik,Anthony K. L. Leung,Lorenzo Pasquali,Lori Sussel,Thomas Metz,Raghavendra G. Mirmira
出处
期刊:Research Square - Research Square
日期:2025-05-21
标识
DOI:10.21203/rs.3.rs-6473437/v1
摘要
ADP-ribosylation is a common modification that occurs in proteins and nucleic acids, regulating many cellular processes ranging from DNA repair to inflammatory signaling. ADP-ribosylation plays an important role in cancer biology, infectious diseases, and obesity, but its role in the development of type 1 diabetes is not well understood. Here, we studied the role of ADP-ribosyltransferase PARP12 in type 1 diabetes development. PARP12 expression is highly induced in human islets treated with pro-inflammatory cytokines or β cells from diabetic donors. Proteomics analysis of MIN6 insulin-producing cells identified that the RNA machinery is regulated by PARP12 during inflammation. PARP12 also ADP-ribosylates 150 mRNAs, including the insulin mRNA. This mRNA ADP-ribosylation in turn modifies transcript localization and halts translation. Overall, our data identified a role for PARP12 in ADP-ribosylation and translation halting of mRNAs, which may affect insulin production during insulitis.
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