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Timing of APC/C substrate degradation is determined by fzy/fzr specificity of destruction boxes
Author(s) -
Zur Amit,
Brandeis Michael
Publication year - 2002
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/cdf452
Subject(s) - biology , microbiology and biotechnology , anaphase promoting complex , mitosis , cyclin b1 , degradation (telecommunications) , cyclin , cell cycle , biochemistry , cell , cyclin dependent kinase 1 , telecommunications , computer science
The a naphase p romoting c omplex/ c yclosome (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 .