Affinity Purification of Specific Chromatin Segments from Chromosomal Loci in Yeast
Author:
Affiliation:
1. Department of Structural Biology, Stanford University School of Medicine, Stanford, California 94305
Abstract
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Link
https://journals.asm.org/doi/pdf/10.1128/MCB.23.24.9275-9282.2003
Reference17 articles.
1. Almer, A., H. Rudolph, A. Hinnen, and W. Horz. 1986. Removal of positioned nucleosomes from the yeast PHO5 promoter upon PHO5 induction releases additional upstream activating DNA elements.EMBO J. 5 : 2689-2696.
2. Ansari, A., T. H. Cheng, and M. R. Gartenberg. 1999 . Isolation of selected chromatin fragments from yeast by site-specific recombination in vivo. Methods 17 : 104-111.
3. Boeger, H., J. Griesenbeck, J. S. Strattan, and R. D. Kornberg. 2003. Nucleosomes unfold completely at a transcriptionally active promoter. Mol. Cell. 11 : 1587-1598.
4. Brazas, R. M., and D. J. Stillman. 1993. The Swi5 zinc-finger and Grf10 homeodomain proteins bind DNA cooperatively at the yeast HO promoter. Proc. Natl. Acad. Sci. USA 90 : 11237-11241.
5. Godde, J. S., and A. P. Wolffe. 1995. Disruption of reconstituted nucleosomes. The effect of particle concentration, MgCl2 and KCl concentration, the histone tails, and temperature. J. Biol. Chem. 270 : 27399-27402.
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