Abstract
In 1980, Nishikai and Reichlin recognized a precipitating system by Ouchterlony immunodiffusion, labeled Jo-1 after the prototype patient, that was apparently specific for myositis [1]. In 1983, using 32P-labeled HeLa cells or mouse Friend erythroleukemia cells as a source of antigen, Rosa et al. recognized that a tRNAhis was immunoprecipitated by anti-Jo-1 -containing sera from myositis patients [2]. Shortly thereafter, Mathews and Bernstein showed that a protein of Mr 50,000 was immunoprecipitated from 35S-labeled HeLa cell extracts by anti-Jo-l-containing sera, and that the enzyme which joins histidine to tRNAhis, histidyl-tRNA synthetase (HRS), was inhibited by these sera [3].
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Abbreviations
- Jo-1 = HRS:
-
histidyl-tRNA synthetase
- PL-7 = TRS:
-
threonyl-tRNA synthetase
- PL-12 = ARS:
-
alanyl-tRNA synthetase
- EJ = GRS:
-
glycyl-tRNA synthetase
- OJ = IRS:
-
isoleucyl-tRNA synthetase
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© 1994 Springer Science+Business Media Dordrecht
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Plotz, P., Targoff, I. (1994). Myositis-associated antigens. Aminoacyl-tRNA synthetases Jo-1, PL-7, PL-12, EJ, and OJ. In: Van Venrooij, W.J., Maini, R.N. (eds) Manual of Biological Markers of Disease. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5444-4_17
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