Laser-induced crosslinking of histones to DNA in chromatin and core particles: implications in studying histone-DNA interactions
- 11 December 1989
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 17 (23) , 10069-10081
- https://doi.org/10.1093/nar/17.23.10069
Abstract
UV laser irradiation has been used to covalently crosslink histones to DNA in nuclei, chromatin and core particles and the presence of the different histone species in the covalently linked material was detected immunochemically. When nuclei were irradiated and then trypsinized to cleave the N- and C- terminal histone tails, no histones have been found covalently linked to DNA. This finding shows that UV laser-induced crosslinking of histories to DNA is accomplished via the non-structured domains only. This unexpected way of crosslinking operated in chromatin, H1-depleted chromatin and core particles, i.e. independently of the chromatin structure. The efficiency of crosslinking, however, showed such a dependence: whilst the yield of crosslinks was similar in total and H1-depleted chromatin, in core particles the efficiency was 3–4 times lower for H2A, H2B and H4 and 10–12 times lower for H3. The decreased crosslinking efficiency, especially dramatic in the case of 1–43, is attributed to a reduced number of binding sites, and, respectively, is considered as a direct evidence for interaction of nonstructered tails of core histones with linker DNA.Keywords
This publication has 22 references indexed in Scilit:
- A highly basic histone H4 domain bound to the sharply bent region of nucleosomal DNANature, 1988
- Accessibility of the globular domain of histones H1 and H5 to antibodies upon folding of chromatinEuropean Journal of Biochemistry, 1987
- Histone hyperacetylation: its effects on nucleosome conformation and stabilityBiochemistry, 1986
- Differential dissociation of histone tails from core chromatinBiochemistry, 1984
- The role of histone H1 and non-structured domains of core histones in maintaining the orientation of nucleosomes within the chromatin fiberBiochemical and Biophysical Research Communications, 1984
- Salt‐Induced Conformational Transitions in ChromatinEuropean Journal of Biochemistry, 1983
- Nucleosomal Particles Open as the Histone Core Becomes HyperacetylatedEuropean Journal of Biochemistry, 1983
- Orientation of the nucleosome within the higher order structure of chromatinCell, 1980
- Nucleosome—nucleosome interaction in chromatinFEBS Letters, 1979
- High‐Resolution Proton‐Magnetic‐Resonance Studies of Chromatin Core ParticlesEuropean Journal of Biochemistry, 1978