application): An understanding of the mechanism of eukaryotic gene regulation is indispensable in trying to cure cancer. The difference between a normal cell and a transformed or malignant cell is largely due to alterations in the transcription of specific genes. Recently it has become apparent that one very important aspect of gene regulation is the manner in which the DNA is packaged into chromatin & how the chromatin can be remodeled so that DNA is accessible to the transcriptional machinery. Current studies have demonstrated the existence of large protein complexes that remodel chromatin with the subsequent effect of gene activation. The structures of these protein complexes and their mechanism of chromatin remodeling are not known and in only a few cases have the proteins involved been identified. The work in this application proposes to use positioned nucleosomes, protein-protein crosslinking, and site-directed DNA-protein photocrosslinking to study the structure of the yeast SWI/SNF complexes and the underlying mechanism whereby they remodel chromatin in an ATP-dependent fashion. Data clearly indicate that SWI/SNF plays a pivotal role in gene expression. First is the extensive literature showing that SWI/SNF acts as a transcriptional activator. Second, biochemical and genetic data demonstrate that SWI/SNF functions as a chromatin remodeling machine. And third, SWI/SNF appears to be important enough that it may be carried around with the Pol II holoenzyme in approximately stoichiometric amounts. Finally, there is even evidence that links some cancers with defective SWI/SNF complexes or to altered interactions with SWI/SNF. The questions addressed by this proposal are the following. First, what happens to the histones as the nucleosome is remodeled by different chromatin remodeling factors such as the yeast SWI/SNF and RSC complexes? Are the nucleosomes displaced from DNA, or is the structure of the nucleosome altered to make the DNA more accessible and if so, how is it altered? Second, what are the mechanistic steps involved in the remodeling of chromatin? What is the basis of the ATP-driven chromatin remodeling activity of SWI/SNF? How does the chromatin remodeling factor contact the nucleosomal DNA and alter/disrupt the contacts of hstones with DNA? What are the structural and functional differences of the different chromatin remodeling factors present in yeast? Third, how does a chromatin remodeling factor get recruited to a particular site on DNA? Are there direct interactions between SWI/SNF complexes and transcriptional activators, or are there adaptor factors that are required for the selective association of the chromatin remodeling factor?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM048413-07
Application #
2857164
Study Section
Molecular Biology Study Section (MBY)
Project Start
1993-01-01
Project End
2001-12-31
Budget Start
1999-01-01
Budget End
1999-12-31
Support Year
7
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Southern Illinois University Carbondale
Department
Biochemistry
Type
Schools of Medicine
DUNS #
939007555
City
Carbondale
State
IL
Country
United States
Zip Code
62901
Sen, Payel; Luo, Jie; Hada, Arjan et al. (2017) Loss of Snf5 Induces Formation of an Aberrant SWI/SNF Complex. Cell Rep 18:2135-2147
Prasad, Rashmi; D'Arcy, Sheena; Hada, Arjan et al. (2016) Coordinated Action of Nap1 and RSC in Disassembly of Tandem Nucleosomes. Mol Cell Biol 36:2262-71
Harada, Bryan T; Hwang, William L; Deindl, Sebastian et al. (2016) Stepwise nucleosome translocation by RSC remodeling complexes. Elife 5:
Kim, Sang-Ah; Chatterjee, Nilanjana; Jennings, Matthew J et al. (2015) Extranucleosomal DNA enhances the activity of the LSD1/CoREST histone demethylase complex. Nucleic Acids Res 43:4868-80
Li, Ming; Hada, Arjan; Sen, Payel et al. (2015) Dynamic regulation of transcription factors by nucleosome remodeling. Elife 4:
Chatterjee, Nilanjana; North, Justin A; Dechassa, Mekonnen Lemma et al. (2015) Histone Acetylation near the Nucleosome Dyad Axis Enhances Nucleosome Disassembly by RSC and SWI/SNF. Mol Cell Biol 35:4083-92
Kapoor, Prabodh; Bao, Yunhe; Xiao, Jing et al. (2015) Regulation of Mec1 kinase activity by the SWI/SNF chromatin remodeling complex. Genes Dev 29:591-602
Bartholomew, Blaine (2014) Regulating the chromatin landscape: structural and mechanistic perspectives. Annu Rev Biochem 83:671-96
Sen, Payel; Vivas, Paula; Dechassa, Mekonnen Lemma et al. (2013) The SnAC domain of SWI/SNF is a histone anchor required for remodeling. Mol Cell Biol 33:360-70
Hota, Swetansu K; Bhardwaj, Saurabh K; Deindl, Sebastian et al. (2013) Nucleosome mobilization by ISW2 requires the concerted action of the ATPase and SLIDE domains. Nat Struct Mol Biol 20:222-9

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