A simple and versatile system for the ATP-dependent assembly of chromatin

J Biol Chem. 2017 Nov 24;292(47):19478-19490. doi: 10.1074/jbc.M117.815365. Epub 2017 Oct 5.

Abstract

Chromatin is the natural form of DNA in the eukaryotic nucleus and is the substrate for diverse biological phenomena. The functional analysis of these processes ideally would be carried out with nucleosomal templates that are assembled with customized core histones, DNA sequences, and chromosomal proteins. Here we report a simple, reliable, and versatile method for the ATP-dependent assembly of evenly spaced nucleosome arrays. This minimal chromatin assembly system comprises the Drosophila nucleoplasmin-like protein (dNLP) histone chaperone, the imitation switch (ISWI) ATP-driven motor protein, core histones, template DNA, and ATP. The dNLP and ISWI components were synthesized in bacteria, and each protein could be purified in a single step by affinity chromatography. We show that the dNLP-ISWI system can be used with different DNA sequences, linear or circular DNA, bulk genomic DNA, recombinant or native Drosophila core histones, native human histones, the linker histone H1, the non-histone chromosomal protein HMGN2, and the core histone variants H3.3 and H2A.V. The dNLP-ISWI system should be accessible to a wide range of researchers and enable the assembly of customized chromatin with specifically desired DNA sequences, core histones, and other chromosomal proteins.

Keywords: chromatin; chromatin structure; histone; histone chaperone; nucleosome.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Adenosine Triphosphate / metabolism*
  • Animals
  • Chromatin / metabolism*
  • Chromatin Assembly and Disassembly*
  • DNA / metabolism
  • Drosophila melanogaster / metabolism*
  • Histones / metabolism*
  • Humans
  • Nucleoplasmins / metabolism*
  • Nucleosome Assembly Protein 1 / metabolism
  • Nucleosomes / metabolism
  • Transcription Factors / metabolism*

Substances

  • Chromatin
  • Histones
  • ISWI protein
  • Nucleoplasmins
  • Nucleosome Assembly Protein 1
  • Nucleosomes
  • Transcription Factors
  • Adenosine Triphosphate
  • DNA
  • Adenosine Triphosphatases