RRC ID 36888
著者 Masuda K, Chiyoda T, Sugiyama N, Segura-Cabrera A, Kabe Y, Ueki A, Banno K, Suematsu M, Aoki D, Ishihama Y, Saya H, Kuninaka S.
タイトル LATS1 and LATS2 phosphorylate CDC26 to modulate assembly of the tetratricopeptide repeat subcomplex of APC/C.
ジャーナル PLoS One
Abstract In budding yeast, the Mitotic Exit Network (MEN) regulates anaphase promoting complex/cyclosome (APC/C) via the Dbf2-Cdc14 signaling cascade. Dbf2 kinase phosphorylates and activates Cdc14 phosphatase, which removes the inhibitory phosphorylation of the APC/C cofactor Cdh1. Although each component of the MEN was highly conserved during evolution, there is presently no evidence supporting direct phosphorylation of CDC14 by large tumor suppressor kinase 1 (LATS1), the human counterpart of Dbf2; hence, it is unclear how LATS1 regulates APC/C. Here, we demonstrate that LATS1 phosphorylates the Thr7 (T7) residue of the APC/C component CDC26 directly. Nocodazole-induced phosphorylation of T7 was reduced by knockdown of LATS1 and LATS2 in HeLa cells, indicating that both of these kinases contribute to the phosphorylation of CDC26 in vivo. The T7 residue of CDC26 is critical for its interaction with APC6, a tetratricopeptide repeat-containing subunit of APC/C, and mutation of this residue to Asp (T7D) reduced the interaction of CDC26 with APC6. Replacement of endogenous CDC26 in HeLa cells with exogenous phosphor-mimic T7D-mutated CDC26 increased the elution size of APC/C subunits in a gel filtration assay, implying a change in the APC/C assembly upon phosphorylation of CDC26. Furthermore, T7D-mutated CDC26 promoted the ubiquitination of polo-like kinase 1, a well-known substrate of APC/C. Overall, these results suggest that LATS1/2 are novel kinases involved in APC/C phosphorylation and indicate a direct regulatory link between LATS1/2 and APC/C.
巻・号 10(2)
ページ e0118662
公開日 2015-1-1
DOI 10.1371/journal.pone.0118662
PII PONE-D-14-47799
PMID 25723520
PMC PMC4344199
MeSH Amino Acid Sequence Anaphase-Promoting Complex-Cyclosome / chemistry Anaphase-Promoting Complex-Cyclosome / metabolism* HEK293 Cells HeLa Cells Humans Molecular Sequence Data Phosphorylation Protein Multimerization* Protein Processing, Post-Translational* Protein Serine-Threonine Kinases / metabolism* Protein Structure, Tertiary Tumor Suppressor Proteins / metabolism*
IF 2.74
引用数 8
WOS 分野 CELL BIOLOGY
リソース情報
ヒト・動物細胞 293T(RCB2202)