TY - JOUR
T1 - Cell cycle oscillators underlying orderly proteolysis of E2F8
AU - Wasserman, Danit
AU - Nachum, Sapir
AU - Cohen, Meital
AU - Enrico, Taylor P.
AU - Noach-Hirsh, Meirav
AU - Parasol, Jasmin
AU - Zomer-Polak, Sarit
AU - Auerbach, Naomi
AU - Sheinberger-Chorni, Evelin
AU - Nevenzal, Hadas
AU - Levi-Dadon, Nofar
AU - Wang, Xianxi
AU - Lahmi, Roxane
AU - Michaely, Efrat
AU - Gerber, Doron
AU - Emanuele, Michael J.
AU - Tzura, Amit
N1 - Publisher Copyright: © 2020 Wasserman et al.
PY - 2020/4/1
Y1 - 2020/4/1
N2 - E2F8 is a transcriptional repressor that antagonizes E2F1 at the crossroads of the cell cycle, apoptosis, and cancer. Previously, we discovered that E2F8 is a direct target of the APC/C ubiquitin ligase. Nevertheless, it remains unknown how E2F8 is dynamically controlled throughout the entirety of the cell cycle. Here, using newly developed human cell-free systems that recapitulate distinct inter-mitotic and G1 phases and a continuous transition from prometaphase to G1, we reveal an interlocking dephosphorylation switch coordinating E2F8 degradation with mitotic exit and the activation of APC/CCdh1. Further, we uncover differential proteolysis rates for E2F8 at different points within G1 phase, accounting for its accumulation in late G1 while APC/CCdh1 is still active. Finally, we demonstrate that the F-box protein Cyclin F regulates E2F8 in G2-phase. Altogether, our data define E2F8 regulation throughout the cell cycle, illuminating an extensive coordination between phosphorylation, ubiquitination and transcription in mammalian cell cycle.
AB - E2F8 is a transcriptional repressor that antagonizes E2F1 at the crossroads of the cell cycle, apoptosis, and cancer. Previously, we discovered that E2F8 is a direct target of the APC/C ubiquitin ligase. Nevertheless, it remains unknown how E2F8 is dynamically controlled throughout the entirety of the cell cycle. Here, using newly developed human cell-free systems that recapitulate distinct inter-mitotic and G1 phases and a continuous transition from prometaphase to G1, we reveal an interlocking dephosphorylation switch coordinating E2F8 degradation with mitotic exit and the activation of APC/CCdh1. Further, we uncover differential proteolysis rates for E2F8 at different points within G1 phase, accounting for its accumulation in late G1 while APC/CCdh1 is still active. Finally, we demonstrate that the F-box protein Cyclin F regulates E2F8 in G2-phase. Altogether, our data define E2F8 regulation throughout the cell cycle, illuminating an extensive coordination between phosphorylation, ubiquitination and transcription in mammalian cell cycle.
UR - http://www.scopus.com/inward/record.url?scp=85082792810&partnerID=8YFLogxK
U2 - 10.1091/MBC.E19-12-0725
DO - 10.1091/MBC.E19-12-0725
M3 - مقالة
C2 - 31995441
SN - 1059-1524
VL - 31
SP - 725
EP - 740
JO - Molecular Biology of the Cell
JF - Molecular Biology of the Cell
IS - 8
ER -