The Drosophila Genomics Resource Center (DGRC) supports the international community of scientists utilizing Drosophila melanogaster for biomedical research. The mission of the DGRC is to 1) provide broad access to genomics resources by acquiring, archiving, curating, and distributing genomics resources including clones, vectors, and cell lines; 2) facilitate effective use of these genomics resources by providing guidance and support; and 3) improve the genomics resources and protocols available for Drosophila research. By preserving vital research materials and distributing them efficiently, the DGRC assures economical access and enhances scientific rigor and reproducibility.
The first aim of this proposal is to continue and strengthen the successful DGRC programs for acquiring, distributing genomics resources and facilitating their effective use. This will include augmenting and updating data management systems, the web interface and user support, as well as continuing the effective cost recovery program. The goal is to maximize the long-term viability of the DGRC and its benefits to users and the NIH.
The second aim i s to increase the utility of Drosophila as a model system by generating new resources through four projects: 1) surveying the transfection and CRISPR/Cas9 efficiency of gene tagging across modENCODE cell lines, 2) generating a universal CRISPR/Cas9 based transfection toolkit for the insertion of constructs and the subsequent ability to generate stable transformants in any Drosophila cell line, 3) establishing a neuroblast cell line as a model for stem cell biology, and 4) creating new metabolic sensors for characterizing physiological processes in cell lines and Drosophila tissues.

Project Start
Project End
Budget Start
2018-04-20
Budget End
2019-03-31
Support Year
15
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Indiana University Bloomington
Department
Type
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401
Song, Wan; Zsindely, Nóra; Faragó, Anikó et al. (2018) Systematic genetic interaction studies identify histone demethylase Utx as potential target for ameliorating Huntington's disease. Hum Mol Genet 27:649-666
Bell, Jason C; Jukam, David; Teran, Nicole A et al. (2018) Chromatin-associated RNA sequencing (ChAR-seq) maps genome-wide RNA-to-DNA contacts. Elife 7:
Wood, Jason G; Schwer, Bjoern; Wickremesinghe, Priyan C et al. (2018) Sirt4 is a mitochondrial regulator of metabolism and lifespan in Drosophila melanogaster. Proc Natl Acad Sci U S A 115:1564-1569
White, Katharine A; Grillo-Hill, Bree K; Esquivel, Mario et al. (2018) ?-Catenin is a pH sensor with decreased stability at higher intracellular pH. J Cell Biol 217:3965-3976
Romé, Pierre; Ohkura, Hiroyuki (2018) A novel microtubule nucleation pathway for meiotic spindle assembly in oocytes. J Cell Biol 217:3431-3445
Lee, Nayoung; Park, Jina; Bae, Yong Chul et al. (2018) Time-Lapse Live-Cell Imaging Reveals Dual Function of Oseg4, Drosophila WDR35, in Ciliary Protein Trafficking. Mol Cells 41:676-683
Hassan, Abeer; Timerman, Yael; Hamdan, Rana et al. (2018) An RNAi Screen Identifies New Genes Required for Normal Morphogenesis of Larval Chordotonal Organs. G3 (Bethesda) 8:1871-1884
Harris, Kathryn P; Littleton, J Troy; Stewart, Bryan A (2018) Postsynaptic Syntaxin 4 negatively regulates the efficiency of neurotransmitter release. J Neurogenet 32:221-229
Sun, Qifei; Wu, Yipin; Jonusaite, Sima et al. (2018) Intracellular Chloride and Scaffold Protein Mo25 Cooperatively Regulate Transepithelial Ion Transport through WNK Signaling in the Malpighian Tubule. J Am Soc Nephrol 29:1449-1461
Gyoergy, Attila; Roblek, Marko; Ratheesh, Aparna et al. (2018) Tools Allowing Independent Visualization and Genetic Manipulation of Drosophila melanogaster Macrophages and Surrounding Tissues. G3 (Bethesda) 8:845-857

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