Transgenic and knockout mice have played a very important role in biomedical research for the developmentof animal models for human diseases and for addressing many different biological questions. The transgenicmouse core facility of the NYU School of Medicine combines the services and resources of the SkirballInstitute and the Cancer Institute. The TgESCF currently provides four basic services: production oftransgenic mice by zygote injection, production of ES cell chimeras by blastocyst injection or morulaaggregation, rederivation of mouse strains, and sperm cryopreservation. Over the next 5 years, thetransgenic facility will continue to provide these services, but will also provide new services such as thegeneration and genotyping of knockout ES cell lines, embryo cyropreservation, the purification of DMAconstructs, and assisted reproduction techniques. In the past year, transgenic mice have been producedusing inbred FVB/N and C57BL/6 mice, and ES cell chimeras have been produced by injection of ES cellsinto C57BL/6 blastocysts. To enable investigators to house pathogen-free animals in the Skirball animalfacility, rederivation of mouse strains has continued to be important, especially as new staff are recruitedwho work with mice. Over the past 10 years the .transgenic facility has generated -3,600 transgenic foundersfrom ~670 DMA constructs (including BAC-based constructs), generated ES cell chimeras from -370 ES cellknockout lines and rederived -460 mutant lines. During the period of the current Cancer Center SupportGrant (2002-2006), 251 DNA constructs were injected and 877 founders were obtained, chimeras weremade from 143 targeted ES cell clones, and 261 mouse strains were rederived. We also froze sperm from17 mutant mouse strains. In addition to these services, the core director and coordinator providedresearchers with support related to work with transgenic and knockout mice, such as training in mousehusbandry 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 #
2P30CA016087-28
Application #
7714238
Study Section
Subcommittee G - Education (NCI)
Project Start
2008-04-18
Project End
2013-02-28
Budget Start
2008-04-18
Budget End
2009-02-28
Support Year
28
Fiscal Year
2008
Total Cost
$73,224
Indirect Cost
Name
New York University
Department
Type
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Litwinoff, Evelyn M S; Gold, Merav Y; Singh, Karan et al. (2018) Myeloid ATG16L1 does not affect adipose tissue inflammation or body mass in mice fed high fat diet. Obes Res Clin Pract 12:174-186
Snetkova, Valentina; Skok, Jane A (2018) Enhancer talk. Epigenomics 10:483-498
Fan, Xiaozhou; Alekseyenko, Alexander V; Wu, Jing et al. (2018) Human oral microbiome and prospective risk for pancreatic cancer: a population-based nested case-control study. Gut 67:120-127
Gregory, Ann C; Sullivan, Matthew B; Segal, Leopoldo N et al. (2018) Smoking is associated with quantifiable differences in the human lung DNA virome and metabolome. Respir Res 19:174
Lee, Chul-Hwan; Holder, Marlene; Grau, Daniel et al. (2018) Distinct Stimulatory Mechanisms Regulate the Catalytic Activity of Polycomb Repressive Complex 2. Mol Cell 70:435-448.e5
Bertrand, Anne; Baron, Maria; Hoang, Dung M et al. (2018) In Vivo Evaluation of Neuronal Transport in Murine Models of Neurodegeneration Using Manganese-Enhanced MRI. Methods Mol Biol 1779:527-541
Taylor, Martin S; Altukhov, Ilya; Molloy, Kelly R et al. (2018) Dissection of affinity captured LINE-1 macromolecular complexes. Elife 7:
Wang, Sophia S; Carrington, Mary; Berndt, Sonja I et al. (2018) HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes. Cancer Res 78:4086-4096
Jung, Seungyoun; Allen, Naomi; Arslan, Alan A et al. (2018) Anti-Müllerian hormone and risk of ovarian cancer in nine cohorts. Int J Cancer 142:262-270
Gong, Yixiao; Lazaris, Charalampos; Sakellaropoulos, Theodore et al. (2018) Stratification of TAD boundaries reveals preferential insulation of super-enhancers by strong boundaries. Nat Commun 9:542

Showing the most recent 10 out of 1170 publications