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Publication : An essential role of N-terminal arginylation in cardiovascular development.

First Author  Kwon YT Year  2002
Journal  Science Volume  297
Issue  5578 Pages  96-9
PubMed ID  12098698 Mgi Jnum  J:77750
Mgi Id  MGI:2182515 Doi  10.1126/science.1069531
Citation  Kwon YT, et al. (2002) An essential role of N-terminal arginylation in cardiovascular development. Science 297(5578):96-9
abstractText  The enzymatic conjugation of arginine to the N-termini of proteins is a part of the ubiquitin-dependent N-end rule pathway of protein degradation. In mammals, three N-terminal residues-aspartate, glutamate, and cysteine-are substrates for arginylation. The mouse ATE1 gene encodes a family of Arg-tRNA-protein transferases (R-transferases) that mediate N-terminal arginylation. We constructed ATE1-lacking mouse strains and found that ATE1-/- embryos die with defects in heart development and in angiogenic remodeling of the early vascular plexus. Through biochemical analyses, we show that N-terminal cysteine, in contrast to N-terminal aspartate and glutamate, is oxidized before its arginylation by R-transferase, suggesting that the arginylation branch of the N-end rule pathway functions as an oxygen sensor.
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