PLK-1 promotes the merger of the parental genome into a single nucleus by triggering lamina disassembly

Author:

Velez-Aguilera Griselda1ORCID,Nkombo Nkoula Sylvia1,Ossareh-Nazari Batool1,Link Jana2,Paouneskou Dimitra2,Van Hove Lucie1,Joly Nicolas1,Tavernier Nicolas1,Verbavatz Jean-Marc3,Jantsch Verena2ORCID,Pintard Lionel1ORCID

Affiliation:

1. Programme Equipe Labéllisée Ligue Contre le Cancer - Team Cell Cycle & Development - Université de Paris, CNRS, Institut Jacques Monod, Paris, France

2. Department of Chromosome Biology, Max Perutz Laboratories, University of Vienna, Vienna Biocenter, Vienna, Austria

3. Université de Paris, CNRS, Institut Jacques Monod, Paris, France

Abstract

Life of sexually reproducing organisms starts with the fusion of the haploid egg and sperm gametes to form the genome of a new diploid organism. Using the newly fertilizedCaenorhabditis eleganszygote, we show that the mitotic Polo-like kinase PLK-1 phosphorylates the lamin LMN-1 to promote timely lamina disassembly and subsequent merging of the parental genomes into a single nucleus after mitosis. Expression of non-phosphorylatable versions of LMN-1, which affect lamina depolymerization during mitosis, is sufficient to prevent the mixing of the parental chromosomes into a single nucleus in daughter cells. Finally, we recapitulate lamina depolymerization by PLK-1 in vitro demonstrating that LMN-1 is a direct PLK-1 target. Our findings indicate that the timely removal of lamin is essential for the merging of parental chromosomes at the beginning of life inC. elegansand possibly also in humans, where a defect in this process might be fatal for embryo development.

Funder

Agence Nationale de la Recherche

Ligue Contre le Cancer

Consejo Nacional de Ciencia y Tecnología

Austrian Science Fund

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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