| Literature DB >> 24857730 |
Cyril Bernis1, Douglass J Forbes1.
Abstract
The large and complex eukaryotic nucleus is the arbiter of DNA replication, RNA transcription, splicing, and ribosome assembly. With the advent of in vitro nuclear reconstitution extracts derived from Xenopus eggs in the 1980s, it became possible to assemble multiple nuclei in vitro around added DNA or chromatin substrates. Such reconstituted nuclei contain a nuclear lamina, double nuclear membranes, nuclear pores, and are competent for DNA replication and nuclear import. In vitro nuclear reconstitution has allowed the assembly of "wild-type" and "biochemically mutant" nuclei in which the impact of individual components can be assessed. Here, we describe protocols for preparation of the nuclear reconstitution extract, nuclear reconstitution in vitro, assessment of nuclear membrane integrity, and a more specialized assay for nuclear pore assembly into preformed pore-free nuclear intermediates.Entities:
Keywords: 70kDa rhodamine dextran; BAPTA; Membrane integrity; Nuclear envelope; Nuclear membrane assembly; Nuclear pore complex; Nuclear pore complex assembly; Nuclear pore-free intermediates; Nuclear reconstitution assay; Vesicle–vesicle fusion; Xenopus egg extract; mAb414
Mesh:
Substances:
Year: 2014 PMID: 24857730 PMCID: PMC4454467 DOI: 10.1016/B978-0-12-417160-2.00008-4
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441