A cooperative network at the nuclear envelope counteracts LINC-mediated forces during oogenesis in C. elegans

Author:

Liu Chenshu12ORCID,Rex Rachel3ORCID,Lung Zoe2,Wang John S.2ORCID,Wu Fan2,Kim Hyung Jun1ORCID,Zhang Liangyu12ORCID,Sohn Lydia L.3ORCID,Dernburg Abby F.124ORCID

Affiliation:

1. California Institute for Quantitative Biosciences (QB3) and Department of Molecular and Cell Biology, University of California Berkeley, Berkeley, CA 94720, USA.

2. Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.

3. Department of Mechanical Engineering, University of California Berkeley, Berkeley, CA 94720, USA.

4. Department of Biological Sciences and Engineering, Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Abstract

Oogenesis involves transduction of mechanical forces from the cytoskeleton to the nuclear envelope (NE). In Caenorhabditis elegans , oocyte nuclei lacking the single lamin protein LMN-1 are vulnerable to collapse under forces mediated through LINC (linker of nucleoskeleton and cytoskeleton) complexes. Here, we use cytological analysis and in vivo imaging to investigate the balance of forces that drive this collapse and protect oocyte nuclei. We also use a mechano-node-pore sensing device to directly measure the effect of genetic mutations on oocyte nuclear stiffness. We find that nuclear collapse is not a consequence of apoptosis. It is promoted by dynein, which induces polarization of a LINC complex composed of Sad1 and UNC-84 homology 1 (SUN-1) and ZYGote defective 12 (ZYG-12). Lamins contribute to oocyte nuclear stiffness and cooperate with other inner nuclear membrane proteins to distribute LINC complexes and protect nuclei from collapse. We speculate that a similar network may protect oocyte integrity during extended oocyte arrest in mammals.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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