ClpS modulates but is not essential for bacterial N-end rule degradation

被引:59
作者
Wang, Kevin H.
Sauer, Robert T.
Baker, Tania A.
机构
[1] MIT, Dept Biol, Cambridge, MA 02139 USA
[2] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
关键词
targeted proteolysis; degradation motif; PheS; SUMO;
D O I
10.1101/gad.1511907
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In eubacteria, the ClpS adaptor has been proposed to be essential for degradation of N-end rule substrates by the AAA(+) protease ClpAP. To test this model, we assayed degradation of substrates bearing N-end rule sequences isolated in a genetic screen for efficient degradation tags. ClpS was not vital for degradation in vivo but rather stimulated turnover in a sequence-specific manner. Although ClpS substantially enhanced degradation of N-end substrates at low substrate concentrations in vitro, it suppressed the degradation rate when substrate was saturating. Thus, we conclude that ClpAP recognizes N-end rule substrates directly, whereas ClpS modulates this degradation pathway.
引用
收藏
页码:403 / 408
页数:6
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