Transgenic and knockout mice have played a very important role in biomedical research for the development of animal models for human diseases and for addressing many different biological questions. The transgenic mouse core facility of the NYU School of Medicine combines the services and resources of the Skirball Institute and the Cancer Institute. The TgESCF currently provides four basic services: production of transgenic mice by zygote injection, production of ES cell chimeras by blastocyst injection or morula aggregation, rederivation of mouse strains, and sperm cryopreservation. Over the next 5 years, the transgenic facility will continue to provide these services, but will also provide new services such as the generation and genotyping of knockout ES cell lines, embryo cyropreservation, the purification of DMA constructs, and assisted reproduction techniques. In the past year, transgenic mice have been produced using inbred FVB/N and C57BL/6 mice, and ES cell chimeras have been produced by injection of ES cells into C57BL/6 blastocysts. To enable investigators to house pathogen-free animals in the Skirball animal facility, rederivation of mouse strains has continued to be important, especially as new staff are recruited who work with mice. Over the past 10 years the .transgenic facility has generated -3,600 transgenic founders from ~670 DMA constructs (including BAC-based constructs), generated ES cell chimeras from -370 ES cell knockout lines and rederived -460 mutant lines. During the period of the current Cancer Center Support Grant (2002-2006), 251 DNA constructs were injected and 877 founders were obtained, chimeras were made from 143 targeted ES cell clones, and 261 mouse strains were rederived. We also froze sperm from 17 mutant mouse strains. In addition to these services, the core director and coordinator provided researchers with support related to work with transgenic and knockout mice, such as training in mouse husbandry and consultation in transgenic and ES cell approaches.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016087-31
Application #
8232201
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2011-03-01
Budget End
2012-02-29
Support Year
31
Fiscal Year
2011
Total Cost
$117,908
Indirect Cost
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Pelzek, Adam J; Shopsin, Bo; Radke, Emily E et al. (2018) Human Memory B Cells Targeting Staphylococcus aureus Exotoxins Are Prevalent with Skin and Soft Tissue Infection. MBio 9:
Chiou, Kenneth L; Bergey, Christina M (2018) Methylation-based enrichment facilitates low-cost, noninvasive genomic scale sequencing of populations from feces. Sci Rep 8:1975
Jose, Cynthia C; Jagannathan, Lakshmanan; Tanwar, Vinay S et al. (2018) Nickel exposure induces persistent mesenchymal phenotype in human lung epithelial cells through epigenetic activation of ZEB1. Mol Carcinog 57:794-806
Kourtis, Nikos; Lazaris, Charalampos; Hockemeyer, Kathryn et al. (2018) Oncogenic hijacking of the stress response machinery in T cell acute lymphoblastic leukemia. Nat Med 24:1157-1166
Formenti, Silvia C; Lee, Percy; Adams, Sylvia et al. (2018) Focal Irradiation and Systemic TGF? Blockade in Metastatic Breast Cancer. Clin Cancer Res 24:2493-2504
Snuderl, Matija; Kannan, Kasthuri; Pfaff, Elke et al. (2018) Recurrent homozygous deletion of DROSHA and microduplication of PDE4DIP in pineoblastoma. Nat Commun 9:2868
Stafford, James M; Lee, Chul-Hwan; Voigt, Philipp et al. (2018) Multiple modes of PRC2 inhibition elicit global chromatin alterations in H3K27M pediatric glioma. Sci Adv 4:eaau5935
Lee, Chul-Hwan; Yu, Jia-Ray; Kumar, Sunil et al. (2018) Allosteric Activation Dictates PRC2 Activity Independent of Its Recruitment to Chromatin. Mol Cell 70:422-434.e6
Aiello, Nicole M; Maddipati, Ravikanth; Norgard, Robert J et al. (2018) EMT Subtype Influences Epithelial Plasticity and Mode of Cell Migration. Dev Cell 45:681-695.e4
Jung, Heekyung; Baek, Myungin; D'Elia, Kristen P et al. (2018) The Ancient Origins of Neural Substrates for Land Walking. Cell 172:667-682.e15

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