Our long-term goal is to decipher the mechanisms that control differential gene expression in metazoan systems. Differential gene expression is a major determinant in development, and misregulation of transcription can lead to numerous diseases. Although vast amounts of gene expression data are available, little is known about the mechanisms that regulate gene expression at a systems level. The expression of each gene is a balance between transcription activation and repression, governed by multiple transcription factors (TFs). Between 5-10% of metazoan genes encode TFs. Each TF regulates the expression of multiple target genes by binding both to protein partners and to target gene DMA. The multiple interactions TFs engage in, and the concerted action of multiple TFs per gene suggests that differential gene expression is the result of intricate transcription regulatory networks (TRNs) in which many TFs are functionally connected. The general aim of this proposal is to map TRNs that control intestinal development in the nematode Caenhorhabditis elegans. C. elegans intestinal development is an excellent system to understand differential gene expression because genome-wide intestinal expression data are available and because transcription regulation plays a pivotal role in this tissue. We will identify intestinal TRNs by mapping protein-DNA and protein-protein interactions involving intestinal promoters and TFs using high-throughput yeast one -and two-hybrid systems. We will generate a database for data tracking, data analysis and to make the data publicly available. To validate interactions, we will manually and computationally integrate protein interactions with available gene expression and phenotypic data. In addition, we will initiate the validation of protein interactions by experimental methods. The mapping of intestinal TRNs will reveal transcriptional mechanisms that underlie differential gene expression in intestinal development. Since this is a conserved biological program, these TRNs may provide insights into mammalian differential gene expression as well.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
3R01DK068429-05S1
Application #
7865571
Study Section
Special Emphasis Panel (ZRG1-GGG-D (90))
Program Officer
Karp, Robert W
Project Start
2009-07-20
Project End
2011-05-31
Budget Start
2009-07-20
Budget End
2011-05-31
Support Year
5
Fiscal Year
2009
Total Cost
$43,362
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Genetics
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
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Fuxman Bass, Juan I; Reece-Hoyes, John S; Walhout, Albertha J M (2016) Gene-Centered Yeast One-Hybrid Assays. Cold Spring Harb Protoc 2016:pdb.top077669
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Fuxman Bass, Juan I; Reece-Hoyes, John S; Walhout, Albertha J M (2016) Colony Lift Colorimetric Assay for ?-Galactosidase Activity. Cold Spring Harb Protoc 2016:pdb.prot088963
Fuxman Bass, Juan I; Reece-Hoyes, John S; Walhout, Albertha J M (2016) Zymolyase-Treatment and Polymerase Chain Reaction Amplification from Genomic and Plasmid Templates from Yeast. Cold Spring Harb Protoc 2016:pdb.prot088971

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