A functional proteomics approach links the ubiquitin-related modifier Urm1 to a tRNA modification pathway

被引:92
作者
Schlieker, Christian D. [1 ]
Van der Veen, Annemarthe G. [1 ]
Damon, Jadyn R. [1 ]
Spooner, Eric [1 ]
Ploegh, Hidde L. [1 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
关键词
cytokinesis; thiolation; urmylation; wobble nucleoside; MOCS3;
D O I
10.1073/pnas.0808756105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Urm1 is a highly conserved ubiquitin-related modifier of unknown function. A reduction of cellular Urm1 levels causes severe cytokinesis defects in HeLa cells, resulting in the accumulation of enlarged multinucleated cells. To understand the underlying mechanism, we applied a functional proteomics approach and discovered an enzymatic activity that links Urm1 to a tRNA modification pathway. Unlike ubiquitin (Ub) and many Ub-like modifiers, which are commonly conjugated to proteinaceous targets, Urm1 is activated by an unusual mechanism to yield a thiocarboxylate intermediate that serves as sulfur donor in tRNA thiolation reactions. This mechanism is reminiscent of that used by prokaryotic sulfur carriers and thus defines the evolutionary link between ancient Ub progenitors and the eukaryotic Ub/Ub-like modification systems.
引用
收藏
页码:18255 / 18260
页数:6
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