The proteasome controls ESCRT-III–mediated cell division in an archaeon
Authors:
- Gabriel Tarrason RisaGRGabriel Tarrason Risa
- Fredrik HurtigFHFredrik Hurtig
- Sian BraySBSian Bray
- Anne E. HafnerAHAnne E. Hafner
- Lena Harker-KirschneckLHLena Harker-Kirschneck
- Peter FaullPFPeter Faull
- Colin DavisCDColin Davis
- Dimitra PapatziamouDPDimitra Papatziamou
- Delyan R. MutavchievDMDelyan R. Mutavchiev
- Catherine FanCFCatherine Fan
- Leticia MeneguelloLMLeticia Meneguello
- Andre Arashiro PulschenAPAndre Arashiro Pulschen
- 7 August 2020
- journal article
- research article
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 369 (6504) , 642-+
Abstract
Proteasomal control of division in Archaea: In eukaryotes, proteasome-mediated degradation of cell cycle factors triggers mitotic exit, DNA segregation, and cytokinesis, a process that culminates in abscission dependent on the protein ESCRT-III. By studying cell division in an archaeal relative of eukaryotes, Tarrason Risa et al. identified a role for the proteasome in triggering cytokinesis by an archaeal ESCRT-III homolog. Cell division in this archaeon was driven by stepwise remodeling of a composite ESCRT-III–based division ring, where rapid proteasome-mediated degradation of one ESCRT-III subunit triggered the constriction of the remaining ESCRT-III–based copolymer. These data strengthen the case for the eukaryotic cell division machinery having its origins in Archaea. Science , this issue p. eaaz2532Keywords
Funding Information
- Wellcome (203276/Z/16/Z)
- Francis Crick Institute (FC001999)
- Medical Research Council (MC_EX_G0800785)
- Cancer Research UK (C33246/A20147)
- Human Frontier Science Program (LT001027/2019)
- Vetenskapsrådet (621-2013-4685)
- BBSRC (BB/K009001/1)
- MRC (MC_CF12266)
- BBSRC Doctoral Training Grant (RG53842)
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