Please use this identifier to cite or link to this item: http://lib.jncasr.ac.in:8080/jspui/handle/10572/593
Title: A K52Q substitution in the globular domain of histone H1t modulates its nucleosome binding properties
Authors: Ramesh, Sneha
Srinivas Bharath, M M
Chandra, Nagasuma R
Rao, M R S
Keywords: histone H1t
globular domain
nucleosome binding property
Ribosomal-Rna Gene
Linker Histone
Dna Condensation
C-Terminus
Chromatin
Identification
Spermiogenesis
Site
H5
Particle
Issue Date: 30-Oct-2006
Publisher: Elsevier Science BV
Citation: FEBS Letters 580(25), 5999–6006 (2006)
Abstract: A comparison of the globular domain sequences of the somatic H1d and testis-specific H1t revealed a single substitution of lysine 52 in H1d to glutamine 54 in H1t, which is one of the three crucial residues within the second DNA binding site. The globular domains of both histones were modeled using the crystal structure of chicken GH5 as a template and was also docked onto the nucleosome structure. The glutamine residue in histone H1t forms a hydrogen bond with main chain carbonyl of methionine-52 (in H1t) and is spatially oriented away from the nucleosome dyad axis. A consequence of this change was a lower affinity of recombinant histone H1t towards Four-way junction DNA and reconstituted 5S mononucleosomes. When Gin-54 in Histone H1t was mutated to lysine, its binding affinity towards DNA substrates was comparable to that of histone H1d. The differential binding of histones H1d and H1t towards reconstituted mononucleosomes was also reflected in the chromatosome-stop assay. 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Description: Restricted Access
URI: http://hdl.handle.net/10572/593
Other Identifiers: 0014-5793
Appears in Collections:Research Papers (M.R.S. Rao)

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