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Dynein pulling forces counteract lamin-mediated nuclear stability during nuclear envelope repair

Authors :
Hai-Yin Wu
Shirin Bahmanyar
Curtis Broberg
Brian Wysolmerski
Michael A. Q. Martinez
Reza Farhadifar
Lauren Penfield
Michael Mauro
Ronald Biggs
Daniel J. Needleman
Source :
Molecular Biology of the Cell
Publication Year :
2018

Abstract

Transient nuclear envelope (NE) ruptures in the Caenorhabditis elegans zygote are caused by a weakened nuclear lamina during nuclear positioning. Dynein-pulling forces enhance the severity of ruptures, while lamin restricts nucleocytoplasmic mixing and allows stable NE repair. This work is the first mechanistic analysis of NE rupture and repair in an organism.<br />Recent work done exclusively in tissue culture cells revealed that the nuclear envelope (NE) ruptures and repairs in interphase. The duration of NE ruptures depends on lamins; however, the underlying mechanisms and relevance to in vivo events are not known. Here, we use the Caenorhabditis elegans zygote to analyze lamin’s role in NE rupture and repair in vivo. Transient NE ruptures and subsequent NE collapse are induced by weaknesses in the nuclear lamina caused by expression of an engineered hypomorphic C. elegans lamin allele. Dynein-generated forces that position nuclei enhance the severity of transient NE ruptures and cause NE collapse. Reduction of dynein forces allows the weakened lamin network to restrict nucleo–cytoplasmic mixing and support stable NE recovery. Surprisingly, the high incidence of transient NE ruptures does not contribute to embryonic lethality, which is instead correlated with stochastic chromosome scattering resulting from premature NE collapse, suggesting that C. elegans tolerates transient losses of NE compartmentalization during early embryogenesis. In sum, we demonstrate that lamin counteracts dynein forces to promote stable NE repair and prevent catastrophic NE collapse, and thus provide the first mechanistic analysis of NE rupture and repair in an organismal context.

Details

ISSN :
19394586
Volume :
29
Issue :
7
Database :
OpenAIRE
Journal :
Molecular biology of the cell
Accession number :
edsair.doi.dedup.....74b7ad21dfe5c97116d91bcac70a5038