Nuclear Actin and Protein 4.1: Essential Interactions during Nuclear Assembly in vitro

• Published in: Proceedings of the National Academy of Sciences - PNAS 2003-09, Vol.100 (19), p.10752-10757
• Main Authors: Krauss, Sharon Wald, Chen, Cynthia, Penman, Sheldon, Heald, Rebecca
• Format: Article
• Language: English
• Subjects: Actins; Actins - metabolism; Animals; Antibodies; Biological Sciences; Cell Line; Cell nucleus; Cell Nucleus - metabolism; Cell Nucleus - ultrastructure; Cellular biology; Chromatin; Cytoskeletal Proteins; Cytoskeleton; Diploidy; DNA; DNA Replication; Epitopes; Humans; Membrane Proteins - metabolism; Microscopy, Fluorescence; Microscopy, Immunoelectron; Neuropeptides; Nuclear matrix; Nuclear structure; Ova; Protein Binding; Proteins; Xenopus
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1934680100

Structural protein 4.1, which has crucial interactions within the spectrin-actin lattice of the human red cell membrane skeleton, also is widely distributed at diverse intracellular sites in nucleated cells. We previously showed that 4.1 is essential for assembly of functional nuclei in vitro and that the capacity of 4.1 to bind actin is required. Here we report that 4.1 and actin colocalize in mammalian cell nuclei using fluorescence microscopy and, by higher-resolution detergent-extracted cell whole-mount electron microscopy, are associated on nuclear filaments. We also devised a cell-free assay using Xenopus egg extract containing fluorescent actin to follow actin during nuclear assembly. By directly imaging actin under nonperturbing conditions, the total nuclear actin population is retained and visualized in situ relative to intact chromatin. We detected actin initially when chromatin and nuclear pores began assembling. As nuclear lamina assembled, but preceding DNA synthesis, actin distributed in a reticulated pattern throughout the nucleus. Protein 4.1 epitopes also were detected when actin began to accumulate in nuclei, producing a diffuse coincident pattern. As nuclei matured, actin was detected both coincident with and also independent of 4.1 epitopes. To test whether acquisition of nuclear actin is required for nuclear assembly, the actin inhibitor latrunculin A was added to Xenopus egg extracts during nuclear assembly. Latrunculin A strongly perturbed nuclear assembly and produced distorted nuclear structures containing neither actin nor protein 4.1. Our results suggest that actin as well as 4.1 is necessary for nuclear assembly and that 4.1-actin interactions may be critical.