The Gene Targeting Shared Resource was established 10 years ago to assist Cancer Center members who use animal models in constructing and managing genetically altered mouse strains. Located in the Woodbury Animal Shared Resource, this Shared Resource provides services including the generation of transgenic mice by pronuclear injection of DNA, gene targeting in mouse embryonic stem (ES) cells, generation of ES cell chimeras with genetically altered ES cells, and cryopreservation services for both embryos and sperm. To expand on these services further, the facility has recently developed protocols for producing ES cell-derived mice by tetraploid blastocyst injections, a procedure that has greatly facilitated the rapid generation of cancer mouse models at CSHL. It also generated ES cell lines for gene targeting in C57BL/6J mice, which, when fully incorporated, will enable researchers to produce pure mouse strains rapidly in one of the most widely used genetic backgrounds. Finally the Gene Targeting Shared Resource has added karyotyping as a step in the production of chimeric mice;by identifying ES cells with a normal chromosome complement, the efficiency of germline transmission has been greatly enhanced. The rapid incorporation of new technologies within the Resource helps keep research in the Cancer Center at the cutting edge. In addition, its internal development efforts continue to provide Cancer Center investigators with new tools and method to speed up the production of mouse models while maintaining low costs.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA045508-26
Application #
8473674
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2013-08-01
Budget End
2014-07-31
Support Year
26
Fiscal Year
2013
Total Cost
$201,774
Indirect Cost
$127,993
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
065968786
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724
Cheng, Derek; Tuveson, David (2018) Kras in Organoids. Cold Spring Harb Perspect Med 8:
Albrengues, Jean; Shields, Mario A; Ng, David et al. (2018) Neutrophil extracellular traps produced during inflammation awaken dormant cancer cells in mice. Science 361:
Cook, Natalie; Basu, Bristi; Smith, Donna-Michelle et al. (2018) A phase I trial of the ?-secretase inhibitor MK-0752 in combination with gemcitabine in patients with pancreatic ductal adenocarcinoma. Br J Cancer 118:793-801
Melnikov, Sergey V; Rivera, Keith D; Ostapenko, Denis et al. (2018) Error-prone protein synthesis in parasites with the smallest eukaryotic genome. Proc Natl Acad Sci U S A 115:E6245-E6253
Krishnan, Navasona; Bonham, Christopher A; Rus, Ioana A et al. (2018) Harnessing insulin- and leptin-induced oxidation of PTP1B for therapeutic development. Nat Commun 9:283
Pommier, Arnaud; Anaparthy, Naishitha; Memos, Nicoletta et al. (2018) Unresolved endoplasmic reticulum stress engenders immune-resistant, latent pancreatic cancer metastases. Science 360:
Krishnan, Navasona; Felice, Christy; Rivera, Keith et al. (2018) DPM-1001 decreased copper levels and ameliorated deficits in a mouse model of Wilson's disease. Genes Dev 32:944-952
Tiriac, Herve; Bucobo, Juan Carlos; Tzimas, Demetrios et al. (2018) Successful creation of pancreatic cancer organoids by means of EUS-guided fine-needle biopsy sampling for personalized cancer treatment. Gastrointest Endosc 87:1474-1480
Nattestad, Maria; Goodwin, Sara; Ng, Karen et al. (2018) Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. Genome Res 28:1126-1135
Connell, Claire M; Raby, Sophie E M; Beh, Ian et al. (2018) Cancer Immunotherapy Trials Underutilize Immune Response Monitoring. Oncologist 23:116-117

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