The Single Nuclear Lamin of Caenorhabditis elegans Forms In Vitro Stable Intermediate Filaments and Paracrystals with a Reduced Axial Periodicity

• Published in: Journal of molecular biology 2003-01, Vol.325 (2), p.241-247
• Main Authors: Karabinos, Anton, Schünemann, Jürgen, Meyer, Michael, Aebi, Ueli, Weber, Klaus
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Caenorhabditis elegans; Caenorhabditis elegans - metabolism; Caenorhabditis elegans Proteins - chemistry; Caenorhabditis elegans Proteins - metabolism; Chickens - metabolism; Ciona intestinalis; Ciona intestinalis - metabolism; Crystallization; Dimerization; intermediate filament; Intermediate Filaments - metabolism; lamin; Lamins - chemistry; Lamins - genetics; Lamins - metabolism; Lamins - ultrastructure; Molecular Sequence Data; Nuclear Lamina - chemistry; Nuclear Lamina - metabolism; paracrystals; Periodicity; Recombinant Proteins - chemistry; Recombinant Proteins - genetics; Recombinant Proteins - metabolism; Sequence Alignment
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1016/S0022-2836(02)01240-8

The lamins of the tunicate Ciona intestinalis and the nematode Caenorhabditis elegans show unusual sequence features when compared to the more than 35 metazoan lamin sequences currently known. We therefore analyzed the in vitro assembly of these two lamins by electron microscopy using chicken lamin B2 as a control. While lamin dimers usually appear as a rod carrying two globules at one end, these globules are absent from Ciona lamin, which lacks the central 105-residue region of the tail domain. The deletion of 14 residues or two heptads from the coiled coil rod domain of the single C. elegans lamin results in a 1.5-nm shortening of the dimer rod. Similarly, the paracrystals assembled from the C. elegans lamin exhibit a 3.1-nm reduction of the true axial repeat compared to that of chicken lamin B2 paracrystals. We speculate that the banding pattern in the C. elegans lamin paracrystals arises from a relative stagger between dimers and/or a positioning of the globular tail domain relative to the central rod that is distinct from that observed in chicken lamin B2 paracrystals. Here we show that a nuclear lamin can assemble in vitro into 10-nm intermediate filaments (IFs). C. elegans lamin in low ionic strength Tris-buffers at a pH of 7.2–7.4 provides a stable population of lamin IFs. Some implications of this filament formation are discussed.