Structure of the ArgRS–GlnRS–AIMP1 complex and its implications for mammalian translation

• Published in: Proceedings of the National Academy of Sciences - PNAS 2014-10, Vol.111 (42), p.15084-15089
• Main Authors: Fu, Yaoyao, Kim, Youngran, Jin, Kyeong Sik, Kim, Hyun Sook, Kim, Jong Hyun, Wang, DongMing, Park, Minyoung, Jo, Chang Hwa, Kwon, Nam Hoon, Kim, Doyeun, Kim, Myung Hee, Jeon, Young Ho, Hwang, Kwang Yeon, Kim, Sunghoon, Cho, Yunje
• Format: Article
• Language: English
• Subjects: Active sites; Amino acids; Amino Acyl-tRNA Synthetases - chemistry; Arginine-tRNA Ligase - chemistry; Binding Sites; Biochemistry; Biological Sciences; Catalytic activity; Cell growth; Chromatography, Gel; Circular Dichroism; Crystal structure; Crystallography, X-Ray; Cytokines - chemistry; Escherichia coli - metabolism; Eukaryotes; Glutathione Transferase - chemistry; Humans; Mammals; Models, Molecular; Molecular structure; Multiprotein Complexes; Mutagenesis; Mutation; Neoplasm Proteins - chemistry; Protein Biosynthesis; Protein Structure, Secondary; Protein Structure, Tertiary; Protein synthesis; Proteins; RNA-Binding Proteins - chemistry; Scattering, Radiation; Transfer RNA
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1408836111

Significance In higher eukaryotes, aminoacyl-tRNA synthetases (ARSs) are assembled to form a multisynthetase complex (MSC), which plays critical roles in translation and nontranslation functions essential for cell growth and survival of organisms. The MSC complex is comprised of nine different ARSs and three accessary proteins. The crystal structure of the arginyl-tRNA synthetase (ArgRS)–glutaminyl-tRNA synthase–aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 (AIMP1) subcomplex reveals that the N-terminal domains of ArgRS and AIMP1 form an extended coiled-coil structure, which provides a central depot for the assembly of a ternary complex. The stability of the N-terminal helix of ArgRS is critical for its ARS activity and noncanonical function of the subcomplex, explaining the significance of the MSC structure in translation and cellular functions. In higher eukaryotes, one of the two arginyl-tRNA synthetases (ArgRSs) has evolved to have an extended N-terminal domain that plays a crucial role in protein synthesis and cell growth and in integration into the multisynthetase complex (MSC). Here, we report a crystal structure of the MSC subcomplex comprising ArgRS, glutaminyl-tRNA synthetase (GlnRS), and the auxiliary factor aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 (AIMP1)/p43. In this complex, the N-terminal domain of ArgRS forms a long coiled-coil structure with the N-terminal helix of AIMP1 and anchors the C-terminal core of GlnRS, thereby playing a central role in assembly of the three components. Mutation of AIMP1 destabilized the N-terminal helix of ArgRS and abrogated its catalytic activity. Mutation of the N-terminal helix of ArgRS liberated GlnRS, which is known to control cell death. This ternary complex was further anchored to AIMP2/p38 through interaction with AIMP1. These findings demonstrate the importance of interactions between the N-terminal domains of ArgRS and AIMP1 for the catalytic and noncatalytic activities of ArgRS and for the assembly of the higher-order MSC protein complex.