MOLECULAR BIOLOGY CORE DEFINITION The purpose of the Molecular Biology core is to facilitate the application of the tools of molecular genetics to the study of gastrointestinal peptides and their physiological functions. In all aspects, the Molecular Biology Core functions to provide essential services and serves as an educational resource to all Center Investigators. Although basic molecular techniques are widely available to Center investigators through commercial sources, there remain specific services that are best provided by pooled resources and by highly trained personnel such as those that can be provided by a Center. During the prior funding period, three Core programs were provided: the Transgenic Animal Program, the Viral Vector Program and the Gene Expression Program. The Molecular Biology Core has added a Microarray Gene Chip Program and has essentially updated the Gene Expression Program to provide education and training in those techniques that can be performed in the investigators own laboratory after receiving some theoretical and practical training. Since investigator needs have likely moved beyond basic gene expression approaches to involve such techniques as chromatin structure and analysis, this primarily education program has been renamed the Molecular Techniques Training Program. Investigators needing assistance with basic molecular techniques, e.g., quantitative RT-PCR and more sophisticated techniques, e.g., chromatin immunoprecipitation assays (ChIP), can receive training from the Core Director (Dr. Merchant) and her associate (Dr. Bai). The specific objectives of the four Molecular Biology Core Programs are as follows: 1. The purpose of the Transgenic Rodent Program is to facilitate the generation of mouse and rat models to study regulatory peptides in a physiologic context. Transgenic and embryonic (ES) cell technology will be available to all Center members through a centralized core facility at the University of Michigan Medical Center. The Program's specific objectives are as follows: a. To serve as an educational resource for all aspects of transgenic and ES cell research, from the design of DNA constructs to animal husbandry and analysis of phenotypes. b. To prepare transgenic mice and rats from cloned DNA provided by Center investigators. c. To generate mouse ES cell clones with targeted gene mutations in collaboration with Center investigators. d. To prepare ES cell chimeric mice by microinjection of ES cells into blastocyts. e. To provide equipment and reagents for transgenic and ES cell production. f. To offer technologies to assist in rodent colony management, including mouse strain cryopreservation and recovery, conversion of mice to SPF status by embryo transfer, and in vitro fertilization (IVF). 2. The purpose of the Viral Vector Program is to facilitate the use of viral vectors for in vitro and in vivo gene transfer into mammalian cells, with emphasis on adenoviral vectors. The Vector Program's specific objectives are as follows: a. To serve as an educational resource for the use of viral vectors for gene transfer. b. To train Center investigators in how to construct and grow viral stocks to use in their research. c. To provide access to vectors and facilities to construct a variety of viral vectors with emphasis on adenoviral vectors. d. To provide reagent volume amounts of adenoviral vectors to Center investigators. 3. The purpose of the Microarray Gene Chip Program is to assist Center scientists in the use of highthroughput RNA profiling and genotyping methods towards delineating the role of gut hormones in health and disease. The Program comprises a separate component within the existing Affymetrix and cDNA Microarray Core, which serves all investigators affiliated with the University of Michigan Central Campus and Medical School Campus, as well as several NIH-funded Centers. As a component of the Core, the objectives of the Microarray Gene Chip Program are as follows: a. To actively assist Center investigators with the design, conduct and analysis of gene expression profiling experiments using oligonucleotide- and cDNA-based microarray technology. These services include probe preparation, labeling, hybridization, washing, and data acquisition for microarray and GeneChip experiments. b. To provide expertise and assistance for the statistical analysis of microarray-acquired data, for handling large data sets, and for data-mining large data sets; c. To provide the means for the validation of microarray-acquired data using quantitative polymerase chain reaction technology. d. To offer tools for genomic studies, including a SNP haplotyping service and Affymetrix HuSNP GeneChip services. 4. The purpose of the Molecular Techniques Training Program is to provide Center investigators with the theory behind and access to practical training in molecular techniques, e.g., RNA interference and chromatin immunoprecipitation assays (ChIP). The Program's specific objectives are as follows: a. To serve as an educational resource for the application of gene expression techniques, e.g., electrophoretic mobility shift assays (EMSAs, gel shifts), DNA footprinting, DNA methylation, transfections, promoter construction and analysis, quantitative PCR, reporter gene assays, RNA interference, ChIP analysis. b. To train investigators in specialized techniques, e.g., DNA binding and ChIP assays. c. To review applications to the Microarray Program. d. To provide and maintain the equipment to analyze reporter gene assays.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK034933-25
Application #
8001986
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2009-12-01
Budget End
2010-11-30
Support Year
25
Fiscal Year
2010
Total Cost
$157,827
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Tsai, Yu-Hwai; Czerwinski, Michael; Wu, Angeline et al. (2018) A Method for Cryogenic Preservation of Human Biopsy Specimens and Subsequent Organoid Culture. Cell Mol Gastroenterol Hepatol 6:218-222.e7
Morhardt, Tina L; Hayashi, Atsushi; Kao, John Y et al. (2018) Regional control of regulatory immune cells in the intestine. Curr Pathobiol Rep 6:29-34
Zhou, Shi-Yi; Gillilland 3rd, Merritt; Wu, Xiaoyin et al. (2018) FODMAP diet modulates visceral nociception by lipopolysaccharide-mediated intestinal inflammation and barrier dysfunction. J Clin Invest 128:267-280
Perry, Jeffrey W; Chen, Yanhua; Speliotes, Elizabeth et al. (2018) Functional Analysis of the Dengue Virus Genome Using an Insertional Mutagenesis Screen. J Virol 92:
Cruz-Acuña, Ricardo; Quirós, Miguel; Huang, Sha et al. (2018) Publisher Correction: PEG-4MAL hydrogels for human organoid generation, culture, and in vivo delivery. Nat Protoc :
Hannigan, Geoffrey D; Duhaime, Melissa B; Ruffin 4th, Mack T et al. (2018) Diagnostic Potential and Interactive Dynamics of the Colorectal Cancer Virome. MBio 9:
Cruz-Acuña, Ricardo; Quirós, Miguel; Huang, Sha et al. (2018) PEG-4MAL hydrogels for human organoid generation, culture, and in vivo delivery. Nat Protoc 13:2102-2119
Ye, Wei; Takabayashi, Hidehiko; Yang, Yitian et al. (2018) Regulation of Gastric Lgr5+ve Cell Homeostasis by Bone Morphogenetic Protein (BMP) Signaling and Inflammatory Stimuli. Cell Mol Gastroenterol Hepatol 5:523-538
Brady, Graham F; Kwan, Raymond; Bragazzi Cunha, Juliana et al. (2018) Lamins and Lamin-Associated Proteins in Gastrointestinal Health and Disease. Gastroenterology 154:1602-1619.e1
Hu, Yongjun; Song, Feifeng; Jiang, Huidi et al. (2018) SLC15A2 and SLC15A4 Mediate the Transport of Bacterially Derived Di/Tripeptides To Enhance the Nucleotide-Binding Oligomerization Domain-Dependent Immune Response in Mouse Bone Marrow-Derived Macrophages. J Immunol 201:652-662

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