Truttmann Matthias C, Cruz Victor E, Guo Xuanzong, Engert Christoph, Schwartz Thomas U, Ploegh Hidde L
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America.
Department of Biology, Massachusetts Institute of Technology (MIT), Cambridge, Massachusetts, United States of America.
PLoS Genet. 2016 May 3;12(5):e1006023. doi: 10.1371/journal.pgen.1006023. eCollection 2016 May.
Protein AMPylation by Fic domain-containing proteins (Fic proteins) is an ancient and conserved post-translational modification of mostly unexplored significance. Here we characterize the Caenorhabditis elegans Fic protein FIC-1 in vitro and in vivo. FIC-1 is an AMPylase that localizes to the nuclear surface and modifies core histones H2 and H3 as well as heat shock protein 70 family members and translation elongation factors. The three-dimensional structure of FIC-1 is similar to that of its human ortholog, HYPE, with 38% sequence identity. We identify a link between FIC-1-mediated AMPylation and susceptibility to the pathogen Pseudomonas aeruginosa, establishing a connection between AMPylation and innate immunity in C. elegans.
含Fic结构域的蛋白质(Fic蛋白)介导的蛋白质AMP化是一种古老且保守的翻译后修饰,其重要性大多尚未被探索。在此,我们在体外和体内对秀丽隐杆线虫Fic蛋白FIC-1进行了表征。FIC-1是一种定位于核表面的AMPylase,可修饰核心组蛋白H2和H3以及热休克蛋白70家族成员和翻译延伸因子。FIC-1的三维结构与其人类直系同源物HYPE相似,序列同一性为38%。我们确定了FIC-1介导的AMP化与对铜绿假单胞菌病原体易感性之间的联系,从而在秀丽隐杆线虫中建立了AMP化与先天免疫之间的联系。