The broad, long-term goal of the proposed study is to determine, at the molecular level, the mechanisms by which chromatin structure is regulated. We believe this study is important, since chromatin structure plays critical roles in many essential biological processes that rely on protein-DNA interactions, such as transcription, DNA replication, DNA repair and recombination. Consistent with the important roles of chromatin in cells, mutations and mis-regulation of chromatin remodeling factors, proteins that regulate chromatin structure, are frequently found in malignant human diseases, such as leukemia and solid tumors. Therefore, uncovering the mechanisms of chromatin regulation will not only advance our knowledge of essential biological processes, but also the underlying mechanisms of human diseases. To this end, we propose a series of experiments to identify the functions and the mechanisms of action of Isw1 and Isw2 chromatin remodeling complexes using the budding yeast, Saccharomyces cerevisiae, as a model organism. Both Isw1 and Isw2 belong to a group of chromatin remodeling complexes that are highly conserved from yeast to humans. Therefore, what we learn in this system will have general implications. We will take advantage of powerful molecular genetic and biochemical tools available in this organism to accomplish our goal. Specifically, we will: (1) Determine the mechanisms of Isw2 complex-dependent chromatin remodeling by using a conditional allele of the ISW2 gene. (2) Determine how Isw2 complex is targeted and regulated in cells. (3) Identify additional functions of Isw2 complex. (4) Identify functions of Isw1 complex in cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM058465-07
Application #
6848308
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Carter, Anthony D
Project Start
1999-02-01
Project End
2008-01-31
Budget Start
2005-02-01
Budget End
2006-01-31
Support Year
7
Fiscal Year
2005
Total Cost
$426,723
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
Cutler, Sam; Lee, Laura J; Tsukiyama, Toshio (2018) Chromatin Remodeling Factors Isw2 and Ino80 Regulate Chromatin, Replication, and Copy Number of the Saccharomyces cerevisiae Ribosomal DNA Locus. Genetics 210:1543-1556
Alcid, Eric A; Tsukiyama, Toshio (2016) Expansion of antisense lncRNA transcriptomes in budding yeast species since the loss of RNAi. Nat Struct Mol Biol 23:450-5
Alcid, Eric A; Tsukiyama, Toshio (2016) Systematic approaches to identify functional lncRNAs. Curr Opin Genet Dev 37:46-50
McKnight, Jeffrey N; Tsukiyama, Toshio; Bowman, Gregory D (2016) Sequence-targeted nucleosome sliding in vivo by a hybrid Chd1 chromatin remodeler. Genome Res 26:693-704
Lee, Laura; Rodriguez, Jairo; Tsukiyama, Toshio (2015) Chromatin remodeling factors Isw2 and Ino80 regulate checkpoint activity and chromatin structure in S phase. Genetics 199:1077-91
Rodriguez, Jairo; McKnight, Jeffrey N; Tsukiyama, Toshio (2014) Genome-Wide Analysis of Nucleosome Positions, Occupancy, and Accessibility in Yeast: Nucleosome Mapping, High-Resolution Histone ChIP, and NCAM. Curr Protoc Mol Biol 108:21.28.1-16
Alcid, Eric A; Tsukiyama, Toshio (2014) ATP-dependent chromatin remodeling shapes the long noncoding RNA landscape. Genes Dev 28:2348-60
Rodriguez, Jairo; Tsukiyama, Toshio (2013) ATR-like kinase Mec1 facilitates both chromatin accessibility at DNA replication forks and replication fork progression during replication stress. Genes Dev 27:74-86
Yadon, Adam N; Singh, Badri Nath; Hampsey, Michael et al. (2013) DNA looping facilitates targeting of a chromatin remodeling enzyme. Mol Cell 50:93-103
Yadon, Adam N; Tsukiyama, Toshio (2013) DNA looping-dependent targeting of a chromatin remodeling factor. Cell Cycle 12:1809-10

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