Timing of APC/C substrate degradation is determined by fzy/fzr specificity of destruction boxes

被引:74
作者
Zur, A [1 ]
Brandeis, M [1 ]
机构
[1] Hebrew Univ Jerusalem, Alexander Silberman Inst Life Sci, Dept Genet, IL-91904 Jerusalem, Israel
关键词
APC; C; cyclosome; destruction box; fizzy; fizzy-related;
D O I
10.1093/emboj/cdf452
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The anaphase promoting complex/cyclosome (APC/C), activated by fzy and fzr, degrades cell cycle proteins that carry RXXL or KEN destruction boxes (d-boxes). APC/C substrates regulate sequential events and must be degraded in the correct order during mitosis and G(1). We studied how d-boxes determine APC/C-fzy/APC/C-fzr specificity and degradation timing. Cyclin B1 has an RXXL box and is degraded by both APC/C-fzy and APC/C-fzr; fzy has a KEN box and is degraded by APC/C-fzr only. We characterized the degradation of substrates with swapped d-boxes. Cyclin B1 with KEN was degraded by APC/C-fzr only. Fzy with RXXL could be degraded by APC/C-fzy and APC/C-fzr. Interestingly, APC/C-fzy- but not APC/C-fzr-specific degradation is highly dependent on the location of RXXL. We studied degradation of tagged substrates in real time and observed that APC/C-fzr is activated in early G(1). These observations demonstrate how d-box specificities of APC/C-fzy and APC/C-fzr, and the successive activation of APC/C by fzy and fzr, establish the temporal degradation pattern. Our observations can explain further why some endogenous RXXL substrates are degraded by APC/C-fzy, while others are restricted to APC/C-fzr.
引用
收藏
页码:4500 / 4510
页数:11
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