BMB Rep. 2016; 49(8): 443-448  
Ablation of Arg-tRNA-protein transferases results in defective neural tube development
Eunkyoung Kim1,2, Seonmu Kim1, Jung Hoon Lee1,2, Yong Tae Kwon2 & Min Jae Lee1,2,3,*
1Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, 2Department of Biomedical Sciences, Seoul National University Graduate School, 3Neuroscience Research Institute, Seoul National University College of Medicine, Seoul 03080, Korea
Correspondence to: Tel: +82-2-740-8254; Fax: +82-2-744-4534; E-mail: minjlee@snu.ac.kr
Published online: August 31, 2016.
© Korean Society for Biochemistry and Molecular Biology. All rights reserved.

Abstract
The arginylation branch of the N-end rule pathway is a ubiquitin-mediated proteolytic system in which post-translational conjugation of Arg by ATE1-encoded Arg-tRNA-proteintransferase to N-terminal Asp, Glu, or oxidized Cys residues generates essential degradation signals. Here, we characterized the ATE1?/? mice and identified the essential role of N-terminal arginylation in neural tube development. ATE1-null mice showed severe intracerebral hemorrhages and cystic space near the neural tubes. Expression of ATE1 was prominent in the developing brain and spinal cord, and this pattern overlapped with the migration path of neural stem cells. The ATE1?/? brain showed defective G-protein signaling. Finally, we observed reduced mitosis in ATE1?/? neuroepithelium and a significantly higher nitric oxide concentration in the ATE1?/? brain. Our results strongly suggest that the crucial role of ATE1 in neural tube development is directly related to proper turn-over of the RGS4 protein, which participate in the oxygen-sensing mechanism in the cells.
Keywords: Arginylation, ATE1, G protein signaling, N-end rule, Neural tube


This Article

e-submission

Archives