The HSP molecular chaperones are primordial proteins involved in cytoprotection during stress in all cellular organism. HSP gene expression is regulated by heat shock transcription factor 1 (HSF1). Maintaining the correct regulation of HSF1 is essential, as elevated HSF1 activity is involved in cancer cell survival and tumor progression while decreased HSF1 activity is involved in neuronal degeneration, aging and sensitivity to stress. We have in the preceding years of this grant characterized a number of regulatory phosphorylation sites HSF1 regulation and determined novel mechanisms for HSF1 regulation. In the current grant proposal we aim to determine: (1) the role of phosphorylation in HSF1 regulation in the cytoplasm. HSF1 is constitutively repressed by a mechanism involving phosphorylation at a key site (serine 121) that regulates HSP90 binding.
We aim to determine how phosphorylation at this site couples the activity of protein kinases to HSF1 regulation though modulating HSF1 interaction with molecular chaperone complexes. (2) Role of HSF1 phosphorylation in association with hsp promoters, transcriptional regulation and histone modification the nucleus. We have found that transcription of HSF1 is regulated by at least 4 phosphorylation sites at serines 195, 303, 307 and threonine 142. In this aim we will determine how phosphorylation regulates HSF1 occupation of hsp promoters and transcriptional activity in vivo and alters interaction with chromatin acetylates, deacetylases and chromatin remodeling proteins.
Our aim will to be to determine how upstream signal transduction networks regulate hsp genes. Understanding the basic pathways of HSF1 regulation will permit us to probe the mechanisms of HSP dysregulation in disease and to modify these pathways. ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA047407-19
Application #
7256335
Study Section
Radiation Therapeutics and Biology Study Section (RTB)
Program Officer
Wong, Rosemary S
Project Start
1988-05-01
Project End
2010-04-30
Budget Start
2007-05-04
Budget End
2008-04-30
Support Year
19
Fiscal Year
2007
Total Cost
$274,025
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02215
Murshid, Ayesha; Prince, Thomas L; Lang, Ben et al. (2018) Role of Heat Shock Factors in Stress-Induced Transcription. Methods Mol Biol 1709:23-34
Murshid, Ayesha; Theriault, Jimmy; Gong, Jianlin et al. (2018) Molecular Chaperone Receptors. Methods Mol Biol 1709:331-344
Eguchi, Takanori; Calderwood, Stuart K; Takigawa, Masaharu et al. (2017) Intracellular MMP3 Promotes HSP Gene Expression in Collaboration With Chromobox Proteins. J Cell Biochem 118:43-51
Calderwood, Stuart K; Gong, Jianlin (2016) Heat Shock Proteins Promote Cancer: It's a Protection Racket. Trends Biochem Sci 41:311-323
Calderwood, Stuart K; Neckers, Len (2016) Hsp90 in Cancer: Transcriptional Roles in the Nucleus. Adv Cancer Res 129:89-106
Eguchi, Taka; Prince, Thomas; Wegiel, Barbara et al. (2015) Role and Regulation of Myeloid Zinc Finger Protein 1 in Cancer. J Cell Biochem 116:2146-54
Bunch, Heeyoun; Calderwood, Stuart K (2015) TRIM28 as a novel transcriptional elongation factor. BMC Mol Biol 16:14
Calderwood, Stuart K (2015) Cdc37 as a co-chaperone to Hsp90. Subcell Biochem 78:103-12
Murshid, Ayesha; Borges, Thiago J; Calderwood, Stuart K (2015) Emerging roles for scavenger receptor SREC-I in immunity. Cytokine 75:256-60
Chou, Shiuh-Dih; Murshid, Ayesha; Eguchi, Takanori et al. (2015) HSF1 regulation of ?-catenin in mammary cancer cells through control of HuR/elavL1 expression. Oncogene 34:2178-2188

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