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Southern Illinois University

SWI/SNF-NUCLEOSOME INTERACTIONS AND DISASSEMBLY OF NUCLEOSOMES: NOVEL METHODOLOGIES FOR MAPPING PROTEIN-PROTEIN AND PROTEIN-DNA INTERACTION

Abstract

dc:description.abstract

AN ABSTRACT OF THE DISSERTATION OF MEKONNEN LEMMA DECHASSA, for the Doctor of Philosophy degree in MOLECULAR BIOLOGY, MICROBIOLOGY, AND BIOCHEMISTRY, presented on December 18, 2008, at Southern Illinois University Carbondale. TITLE: SWI/SNF-NUCLEOSOME INTERACTIONS AND DISASSEMBLY OF NUCLEOSOMES: NOVEL METHODOLOGIES FOR MAPPING PROTEIN-PROTEIN AND PROTEIN-DNA INTERACTION MAJOR PROFESSOR: Dr. Blaine Bartholomew The SWI/SNF complex disrupts and mobilizes chromatin in an ATP-dependent manner. A site-directed photoaffinity crosslinking approach in which photoreactive moieties attached at specific sites within histone octamer was developed and used to map the interactions of SWI/SNF with the histone octamer face of the nucleosome. We identified the subunits that contact the nucleosomal histone proteins. The catalytic Swi2/Snf2 and Snf5 subunit were found to interact with a large surface of nucleosomal histone proteins. Affinity proteolysis, using FeEDTA that is attached to DNA or the histone octamer as a probe, was applied to identify the domains and motifs of SWI/SNF subunits that interact with DNA and nucleosome. It was found that motifs in the N-terminal lobe of ATPase/helicase domain of Sw2/Snf2 are in close contact with both DNA and histone octamer. Crosslinking and peptide mapping by chemical proteolysis revealed that the region in the C-terminal lobe of ATPase/helicase domain of Swi2/Snf2 is bound to the internal nucleosome region that is two helical turns from the dyad axis. The impact on nucleosome remodeling by adjacent nucleosomes and the recruitment of SWI/SNF by transcriptional activator was examined using a high resolution histone-DNA contact mapping and a single molecule MAP-IT technique. The data shows that the presence of adjacent nucleosomes promotes nucleosome eviction and the recruitment of SWI/SNF by Gal4-VP16 to dinucleosomes restricted the nucleosome mobilization in one direction. Finally, based on the data from this study and previous reports, the mechanism how recruitment and neighboring nucleosomes alter the outcome of SWI/SNF remodeling is discussed.

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy
Level thesis:degree_level
Campus Only Dissertation
Discipline thesis:degree_discipline
Molecular Biology, Microbiology and Biochemistry
Year
2008

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Lemma Dechassa, Mekonnen
Contributors dc:contributor
  • Bartholomew, Blaine

Identifiers

dc:identifier.*
Repository record dc:identifier
https://opensiuc.lib.siu.edu/dissertations/267
OAI identifier oai:identifier
oai:opensiuc.lib.siu.edu:dissertations-1267

Chain of custody

source
Harvested from
Southern Illinois University
Base URL
opensiuc.lib.siu.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Lemma Dechassa, Mekonnen. SWI/SNF-NUCLEOSOME INTERACTIONS AND DISASSEMBLY OF NUCLEOSOMES: NOVEL METHODOLOGIES FOR MAPPING PROTEIN-PROTEIN AND PROTEIN-DNA INTERACTION. Campus Only Dissertation thesis, 2008. https://opensiuc.lib.siu.edu/dissertations/267