Purification, crystallization and preliminary X-ray diffraction analysis of the histone chaperone cia1 from fission yeast

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2005 Nov 1;61(Pt 11):971-3. doi: 10.1107/S1744309105030927. Epub 2005 Oct 20.

Abstract

In fission yeast, cia1+ is an essential gene that encodes a histone chaperone, a homologue of human CIA (CCG1-interacting factor A) and budding yeast Asf1p (anti-silencing function-1), which both facilitate nucleosome assembly by interacting with the core histones H3/H4. The conserved domain (residues 1-161) of the cia1+-encoded protein was expressed in Escherichia coli, purified to near-homogeneity and crystallized by the sitting-drop vapour-diffusion method. The protein was crystallized in the monoclinic space group C2, with unit-cell parameters a = 79.16, b = 40.53, c = 69.79 A, beta = 115.93 degrees and one molecule per asymmetric unit. The crystal diffracted to beyond 2.10 A resolution using synchrotron radiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Proteins / chemistry*
  • Crystallography, X-Ray
  • DNA, Complementary / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Escherichia coli / metabolism
  • Gene Silencing
  • Genetic Vectors
  • Histones / chemistry
  • Models, Statistical
  • Nucleosomes / chemistry
  • Saccharomyces cerevisiae Proteins / chemistry*
  • Schizosaccharomyces
  • Temperature
  • Transcription, Genetic
  • X-Ray Diffraction

Substances

  • Cell Cycle Proteins
  • Cia1p protein, S cerevisiae
  • DNA, Complementary
  • Histones
  • Nucleosomes
  • Saccharomyces cerevisiae Proteins