Volume 10 Supplement 2

Proceedings of the 1st French-Italian meeting on laminopathies and other nuclear envelope-related diseases

Open Access

Emerin oligomerisation properties, impact on lamin and actin recognition

  • Isaline Herrada1 and
  • Sophie Zinn-Justin1
Orphanet Journal of Rare Diseases201510(Suppl 2):O17

https://doi.org/10.1186/1750-1172-10-S2-O17

Published: 11 November 2015

Since a few years, several studies have revealed the essential role played by the nuclear envelope in the cell response to mechanical demands of their immediate surroundings. A systematic scaling between the concentration of lamins within the nucleoskeleton and tissue elasticity was observed. This tuning in the nuclear lamina composition was associated to changes in nuclear mechanical properties. In addition to the lamin expression level, the phosphorylation states of lamins A and C and of their partner emerin might contribute to the transmission of a mechanical signal. In particular, in response to a force applied on nesprin-1 in isolated nuclei, emerin is phosphorylated on tyrosine residues Tyr74 and Tyr95, and these phosphorylation events are essential to trigger a nuclear mechanical response to tension. We have evaluated the capacity of the nucleoplasmic region of emerin to oligomerize, in the wild-type case as well as in emerin with mutations causing EDMD. We report large structural differences between wild-type emerin and several mutants. The impact of these structural differences on lamin and actin recognition is currently being studied. The role of emerin phosphorylation on emerin structure and binding properties is also being characterized, in order to reveal defects due to mutations causing EDMD.

Authors’ Affiliations

(1)
Institut de Biologie Intégrative de la Cellule, CEA, CNRS, Université Paris Sud

Copyright

© Herrada and Zinn-Justin 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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