By: Edgar Bonte1
, Peter B. Becker1
, Peter B. Becker1| Abstract |
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A rigorous biochemical analysis of chromatin structure and function requires the assembly of chromatin in vitro. A useful
alternative to reconstituting nucleosomal arrays from pure or recombinant histones by salt gradient dialysis is the assembly
of more complex chromatin from assembly extracts under physiological conditions. Extracts from preblastoderm embryos have
proven to be particularly efficient, due to the presence of large stores of native complexes of histones, histone chaperones
and ATP-dependent nucleosome spacing factors. The resulting chromatin is an excellent approximation of physiological chromatin
in vivo. This chapter describes the preparation of chromatin assembly extracts and the chromatin assembly reaction.
Book Title: Chromatin Protocols: Second Edition
Series: Methods in Molecular Biology | Volume: 523 | Pub. Date: Dec-01-2008 | Page Range: 1-10 | DOI: 10.1007/978-1-59745-190-1_1
Subject: Cell Biology
Key Words: Nucleosome assembly - chromatin reconstitution - in vitro analysis - linker histone -
Drosophila
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