The experiments described in this proposal are designed to further our understanding of the biology of transposable elements and the molecular bases underlying their interaction with the genome of the host. In particular, we propose to study the gypsy retrotransposon and the mechanisms by which ifs insertion into various genes results in phenotypes that can be suppressed or enhanced by second site mutations at various modifier loci. Two of these loci, su(Hw) and mod(mdg4), appear to have parallel or complementary roles in the generation of these phenotypes. In addition to their effect on gypsy, the proteins encoded by these two genes may play important roles in general aspects of the control of gene expression in Drosophila. The role of the su(Hw) product will be investigated by examining domains of the protein involved in various aspects of its function both in the generation of gypsy-induced phenotypes and in normal development. In addition, putative genes whose expression is affected by this protein win be identified and analyzed. Other factors acting in conjunction with su (Hw) will be isolated by genetic and biochemical means, and further characterized. One of these putative factors might be encoded by the mod(mdg4) locus, which appears to belong to a family of structurally related proteins. The mod(mdg4) gene as well as other members of the family will be cloned and characterized. The analysis of the structure of the proteins encoded by these genes and their putative interactions with su(Hw), will increase our understanding of their mechanism of action and the basis of their effect on the phenotype of gypsy-induced mutations. These experiments may allow the characterization of a network of proteins that play general and fundamental roles in the expression of cellular genes and for which biochemical assays are unavailable. Finally, experiments will be carried out to determine the molecular bases of the control of retrotransposon mobilization in the Drosophila genome by examining various aspects of gypsy expression at which this control could be exerted.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM035463-06
Application #
3288264
Study Section
Genetics Study Section (GEN)
Project Start
1986-04-01
Project End
1995-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
6
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Arts and Sciences
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Rowley, M Jordan; Corces, Victor G (2018) Organizational principles of 3D genome architecture. Nat Rev Genet 19:789-800
Nichols, Michael H; Corces, Victor G (2018) A tethered-inchworm model of SMC DNA translocation. Nat Struct Mol Biol 25:906-910
Xu, Chenhuan; Corces, Victor G (2018) Genome-Wide Mapping of Protein-DNA Interactions on Nascent Chromatin. Methods Mol Biol 1766:231-238
Lyu, Xiaowen; Rowley, M Jordan; Corces, Victor G (2018) Architectural Proteins and Pluripotency Factors Cooperate to Orchestrate the Transcriptional Response of hESCs to Temperature Stress. Mol Cell 71:940-955.e7
Ando-Kuri, Masami; Rivera, I Sarahi M; Rowley, M Jordan et al. (2018) Analysis of Chromatin Interactions Mediated by Specific Architectural Proteins in Drosophila Cells. Methods Mol Biol 1766:239-256
Arzate-Mejía, Rodrigo G; Recillas-Targa, Félix; Corces, Victor G (2018) Developing in 3D: the role of CTCF in cell differentiation. Development 145:
Rowley, M Jordan; Nichols, Michael H; Lyu, Xiaowen et al. (2017) Evolutionarily Conserved Principles Predict 3D Chromatin Organization. Mol Cell 67:837-852.e7
Hashimoto, Hideharu; Wang, Dongxue; Horton, John R et al. (2017) Structural Basis for the Versatile and Methylation-Dependent Binding of CTCF to DNA. Mol Cell 66:711-720.e3
Jung, Yoon Hee; Sauria, Michael E G; Lyu, Xiaowen et al. (2017) Chromatin States in Mouse Sperm Correlate with Embryonic and Adult Regulatory Landscapes. Cell Rep 18:1366-1382
Gómez-Díaz, Elena; Yerbanga, Rakiswendé S; Lefèvre, Thierry et al. (2017) Epigenetic regulation of Plasmodium falciparum clonally variant gene expression during development in Anopheles gambiae. Sci Rep 7:40655

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