The first level of DNA organization in eukaryotes resides in the nucleosome, which consists of approximately 200 bp of DNA wrapped around the histone octamer. The nucleosome is regarded as the most fundamental element of chromosomal structure. Incorporation of other proteins into oligonucleosomal arrays gives rise to specific chromatin structures capable of specific nuclear functions such as transcriptional activity. The general goals of the proposed research are to identify and characterize the structural and functional states of nucleosomal arrays and to understand the role of histones, linker histones, and transcription factors in directing and maintaining higher order chromatin structures brought about by nucleosome array folding and self- association. Three specific tasks are proposed to address the hypothesis that the intrinsic conformational dynamics of nucleosomal arrays contribute to formation of the 30 nm chromatin fiber and higher chromosomal domains, and that folding provides a barrier to RNA polymerases that can be modified by other proteins such as H1 to achieve specific states of transcriptional activity. These studies are expected to provide the baseline necessary to attain the goal of assembling transcriptionally active and repressed chromatin states in vitro from pure components.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM045916-08
Application #
2701546
Study Section
Molecular and Cellular Biophysics Study Section (BBCA)
Project Start
1991-05-01
Project End
2000-04-30
Budget Start
1998-05-01
Budget End
1999-04-30
Support Year
8
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Texas Health Science Center San Antonio
Department
Biochemistry
Type
Schools of Medicine
DUNS #
800772162
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Kalashnikova, Anna A; Rogge, Ryan A; Hansen, Jeffrey C (2016) Linker histone H1 and protein-protein interactions. Biochim Biophys Acta 1859:455-61
Maeshima, Kazuhiro; Rogge, Ryan; Tamura, Sachiko et al. (2016) Nucleosomal arrays self-assemble into supramolecular globular structures lacking 30-nm fibers. EMBO J 35:1115-32
Szerlong, Heather J; Herman, Jacob A; Krause, Christine M et al. (2015) Proteomic characterization of the nucleolar linker histone H1 interaction network. J Mol Biol 427:2056-71
Kalashnikova, Anna A; Porter-Goff, Mary E; Muthurajan, Uma M et al. (2013) The role of the nucleosome acidic patch in modulating higher order chromatin structure. J R Soc Interface 10:20121022
Rogge, Ryan A; Kalashnikova, Anna A; Muthurajan, Uma M et al. (2013) Assembly of nucleosomal arrays from recombinant core histones and nucleosome positioning DNA. J Vis Exp :
Kalashnikova, Anna A; Winkler, Duane D; McBryant, Steven J et al. (2013) Linker histone H1.0 interacts with an extensive network of proteins found in the nucleolus. Nucleic Acids Res 41:4026-35
Szerlong, Heather J; Hansen, Jeffrey C (2012) Activator-dependent acetylation of chromatin model systems. Methods Mol Biol 833:289-310
McBryant, Steven J; Hansen, Jeffrey C (2012) Dynamic fuzziness during linker histone action. Adv Exp Med Biol 725:15-26
Panchenko, Tanya; Sorensen, Troy C; Woodcock, Christopher L et al. (2011) Replacement of histone H3 with CENP-A directs global nucleosome array condensation and loosening of nucleosome superhelical termini. Proc Natl Acad Sci U S A 108:16588-93
Muthurajan, Uma M; McBryant, Steven J; Lu, Xu et al. (2011) The linker region of macroH2A promotes self-association of nucleosomal arrays. J Biol Chem 286:23852-64

Showing the most recent 10 out of 18 publications