RT Journal Article
SR Electronic
T1 A Cyclin A – Myb-MuvB – Aurora B network regulates the choice between mitotic cycles and polyploid endoreplication cycles
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 449983
DO 10.1101/449983
A1 Michael D. Rotelli
A1 Robert A. Policastro
A1 Anna M. Bolling
A1 Andrew W. Killion
A1 Abraham J. Weinberg
A1 Michael J. Dixon
A1 Gabriel E. Zentner
A1 Claire E. Walczak
A1 Mary A. Lilly
A1 Brian R. Calvi
YR 2018
UL http://biorxiv.org/content/early/2018/11/15/449983.abstract
AB Cells switch to polyploid endoreplication cycles during development, wound healing, and cancer. We used integrated approaches in Drosophila to determine how mitotic cycles are remodeled into endoreplication cycles, and how similar this remodeling is between developmental and induced endoreplicating cells (devECs and iECs). We found that while only devECs had a dampened E2F1 transcriptome, repression of a Cyclin A - Myb-MuvB - Aurora B mitotic network promoted endoreplication in both devECs and iECs. Cyclin A associated with and activated Myb-MuvB to induce transcription of mitotic genes, with expression of one, Aurora B, being key for mitotic commitment. Knockdown of Cyclin A, Myb, Aurora B, or downstream cytokinetic proteins induced distinct types of endoreplication, suggesting that repression of different mitotic network steps may explain the known diversity of polyploid cycles. These findings reveal how remodeling of a mitotic network promotes polyploid cycles that contribute to development, wound healing, and cancer.