This proposal focuses on the study of the transcription of selected Drosophila heat shock genes that are coordinately activated by heat shock yet differentially activated by normal developmental signals. We plan to further define cis-acting DNA sequence elements responsible for the heat shock and developmental activation of these genes by assaying the activity of in vitro-altered genes in germline transformants. This includes investigation of the spatial relationships and interdependence of the individual components of the heat shock and developmental regulatory responses. Such information will guide the formulation of testable mechanisms of transcriptional regulation. These studies of cis-acting regulatory elements of heat shock genes will be correlated with studies of the chromosomal configuration and chromatin structure of heat shock loci. We propose to determine the extent of the chromosomal region or domain that participates in gene activation by studies at the cytological level using a high resolution method of in situ hybridization to polytene chromosomes, and at the chromatin level by defining the region of enhanced nuclease sensitivity. At still higher resolution, we will use our newly-developed protein-DNA crosslinking method to examine in vivo interactions of specific proteins and DNA sequences and the changes in these protein-DNA associations that accompany gene activation by heat shock.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM025232-09
Application #
3272841
Study Section
Genetics Study Section (GEN)
Project Start
1978-04-01
Project End
1991-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
9
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Cornell University
Department
Type
Schools of Arts and Sciences
DUNS #
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Booth, Gregory T; Parua, Pabitra K; Sansó, Miriam et al. (2018) Cdk9 regulates a promoter-proximal checkpoint to modulate RNA polymerase II elongation rate in fission yeast. Nat Commun 9:543
Tome, Jacob M; Tippens, Nathaniel D; Lis, John T (2018) Single-molecule nascent RNA sequencing identifies regulatory domain architecture at promoters and enhancers. Nat Genet 50:1533-1541
Chu, Tinyi; Rice, Edward J; Booth, Gregory T et al. (2018) Chromatin run-on and sequencing maps the transcriptional regulatory landscape of glioblastoma multiforme. Nat Genet 50:1553-1564
Vihervaara, Anniina; Duarte, Fabiana M; Lis, John T (2018) Molecular mechanisms driving transcriptional stress responses. Nat Rev Genet 19:385-397
Parua, Pabitra K; Booth, Gregory T; Sansó, Miriam et al. (2018) A Cdk9-PP1 switch regulates the elongation-termination transition of RNA polymerase II. Nature 558:460-464
Mahat, Dig B; Lis, John T (2017) Use of conditioned media is critical for studies of regulation in response to rapid heat shock. Cell Stress Chaperones 22:155-162
Boija, Ann; Mahat, Dig Bijay; Zare, Aman et al. (2017) CBP Regulates Recruitment and Release of Promoter-Proximal RNA Polymerase II. Mol Cell 68:491-503.e5
Vihervaara, Anniina; Mahat, Dig Bijay; Guertin, Michael J et al. (2017) Transcriptional response to stress is pre-wired by promoter and enhancer architecture. Nat Commun 8:255
Watters, Kyle E; Strobel, Eric J; Yu, Angela M et al. (2016) Cotranscriptional folding of a riboswitch at nucleotide resolution. Nat Struct Mol Biol 23:1124-1131
Booth, Gregory T; Wang, Isabel X; Cheung, Vivian G et al. (2016) Divergence of a conserved elongation factor and transcription regulation in budding and fission yeast. Genome Res 26:799-811

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