LEM2 phase separation promotes ESCRT-mediated nuclear envelope reformation

Alexander Appen, Dollie LaJoie, Isabel E. Johnson, Michael J. Trnka, Sarah M. Pick, Alma L. Burlingame, Katharine S. Ullman () and Adam Frost ()
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Alexander Appen: University of California
Dollie LaJoie: University of Utah
Isabel E. Johnson: University of California
Michael J. Trnka: University of California, San Francisco
Sarah M. Pick: University of Freiburg
Alma L. Burlingame: University of California, San Francisco
Katharine S. Ullman: University of Utah
Adam Frost: University of California

Nature, 2020, vol. 582, issue 7810, 115-118

Abstract: Abstract During cell division, remodelling of the nuclear envelope enables chromosome segregation by the mitotic spindle1. The reformation of sealed nuclei requires ESCRTs (endosomal sorting complexes required for transport) and LEM2, a transmembrane ESCRT adaptor2–4. Here we show how the ability of LEM2 to condense on microtubules governs the activation of ESCRTs and coordinated spindle disassembly. The LEM motif of LEM2 binds BAF, conferring on LEM2 an affinity for chromatin5,6, while an adjacent low-complexity domain (LCD) promotes LEM2 phase separation. A proline–arginine-rich sequence within the LCD binds to microtubules and targets condensation of LEM2 to spindle microtubules that traverse the nascent nuclear envelope. Furthermore, the winged-helix domain of LEM2 activates the ESCRT-II/ESCRT-III hybrid protein CHMP7 to form co-oligomeric rings. Disruption of these events in human cells prevented the recruitment of downstream ESCRTs, compromised spindle disassembly, and led to defects in nuclear integrity and DNA damage. We propose that during nuclear reassembly LEM2 condenses into a liquid-like phase and coassembles with CHMP7 to form a macromolecular O-ring seal at the confluence between membranes, chromatin and the spindle. The properties of LEM2 described here, and the homologous architectures of related inner nuclear membrane proteins7,8, suggest that phase separation may contribute to other critical envelope functions, including interphase repair8–13 and chromatin organization14–17.

Date: 2020
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DOI: 10.1038/s41586-020-2232-x

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