Abstract
Nuclear lamins are nucleus-specific intermediate filaments (IF) found at the inner nuclear membrane (INM) of the nuclear envelope (NE). Together with nuclear envelope transmembrane proteins, they form the nuclear lamina and are crucial for gene regulation and mechanical robustness of the nucleus and the whole cell. Recently, we characterized Dictyostelium NE81 as an evolutionarily conserved lamin-like protein, both on the sequence and functional level. Here, we show on the structural level that the Dictyostelium NE81 is also capable of assembling into filaments, just as metazoan lamin filament assemblies. Using field-emission scanning electron microscopy, we show that NE81 expressed in Xenopous oocytes forms filamentous structures with an overall appearance highly reminiscent of Xenopus lamin B2. The in vitro assembly properties of recombinant His-tagged NE81 purified from Dictyostelium extracts are very similar to those of metazoan lamins. Super-resolution stimulated emission depletion (STED) and expansion microscopy (ExM), as well as transmission electron microscopy of negatively stained purified NE81, demonstrated its capability of forming filamentous structures under low-ionic-strength conditions. These results recommend Dictyostelium as a non-mammalian model organism with a well-characterized nuclear envelope involving all relevant protein components known in animal cells.
Highlights
In all eukaryotes, the nuclear envelope consists of an outer and inner membrane
We showed that the nuclear lamina of the model organism Dictyostelium discoideum contains a protein, NE81, that is evolutionarily related to lamins, and performs major lamin functions [12,13]
We opted for expression of tagged NE81 in Dictyostelium cells followed by affinity purification and in vitro assembly
Summary
The nuclear envelope consists of an outer and inner membrane. The outer nuclear membrane (ONM) is directly connected both to the endoplasmic reticulum and, at the nuclear pore complexes (NPCs), to the inner nuclear membrane (INM). The perinuclear space separates the INM and ONM and is continuous with the lumen of the endoplasmic reticulum (ER). At the INM, transmembrane proteins and associated filamentous proteins within the nuclear matrix form a fibrous nuclear lamina. While higher plants (Archaeplastida) and some unicellular Excavata such as Trypanosoma employ specialized filamentous proteins to form fibrous protein assemblies at the INM, the major components of the nuclear lamina in metazoans are specialized intermediate filament (IF) proteins called lamins [1,2]. Through so-called linker of nucleoskeleton and cytoskeleton (LINC)
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