Changes in gene transcription are important in the progression of cancer, in most other human diseases, and in the aging process, as well as in the development of multicellular organisms at all stages. In recent years it has become clear that chromosome topology plays a vital role in gene regulation, as well as other nuclear processes. The major determinant of this topology involves regulatory DNA known as insulators. Tools available in Drosophila make it possible to study mechanisms of insulator action and interaction in detail, in a true in vivo context. This proposal is to study mechanisms of chromatin-based gene regulation involving insulators, including those recently discovered in the well-characterized Drosophila gene even skipped. These studies will address basic questions of how regulatory DNA that mediates chromosome topology carries out its function in 3 dimensions inside the nucleus. They will show how chromosome architecture interfaces with alternative transcriptional states by integrating the topology of insulator pairing with that of enhancer-promoter interactions. A unique contribution of these studies will be to identify an insulator pairing code that can be used to predict and design chromosome architecture and the consequence effects on gene expression. In mammals, insulators are known to be involved in cell-type specific gene regulation and in key developmental decisions, as well as in oncogenesis and inherited human disorders. Therefore, these studies will have direct applications to research on human diseases.
The Specific Aims are:
Aim 1. Define the molecular basis of insulator pairing specificity and its effects on chromosome architecture and gene expression.
Aim 2. Determine the topological and functional consequences of manipulating endogenous insulators within and surrounding the eve locus.
Aim 3. Test whether insulator pairing in cis competes with or facilitates insulator pairing in trans, and determine the resulting effects on gene expression.

Public Health Relevance

Changes in gene transcription are important in the development and progression of most human diseases, in inherited disorders and the aging process, and in embryonic development. A detailed understanding of how such changes are regulated is the basis for diagnostic tools and intervention strategies, and is the general subject of this proposal. Further advancement holds the promise of novel approaches, and of increasingly effective interventions, in the diagnosis, treatment and prevention of human disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM117458-03
Application #
9532876
Study Section
Nuclear and Cytoplasmic Structure/Function and Dynamics Study Section (NCSD)
Program Officer
Ainsztein, Alexandra M
Project Start
2016-09-08
Project End
2020-07-31
Budget Start
2018-08-01
Budget End
2019-07-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Thomas Jefferson University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Chen, Hongtao; Levo, Michal; Barinov, Lev et al. (2018) Dynamic interplay between enhancer-promoter topology and gene activity. Nat Genet 50:1296-1303
Chetverina, Darya; Fujioka, Miki; Erokhin, Maksim et al. (2017) Boundaries of loop domains (insulators): Determinants of chromosome form and function in multicellular eukaryotes. Bioessays 39:
Peacock, Jacob; Jaynes, James B (2017) Using competition assays to quantitatively model cooperative binding by transcription factors and other ligands. Biochim Biophys Acta Gen Subj 1861:2789-2801