This core consists of a central breeding and typing facility to coordinate the maintenance and distribution of mice used by investigators of the Center. The mice to be housed in this facility are explicitly defined. The maintenance of transgenic mice is critical to this Center, and the need for such a core is well justified with 5 of the 6 projects utilizing genetically modified mice. Therefore, it is appropriate to maintain a transgenic mouse Core within the Center. The level of mouse activity described in the application justifies the hiring of someone to manage the colonies and type offspring (particularly once new lines of mice are being generated). Unfortunately, with the information provided, it is difficult to estimate how many mice need to be genotyped over a given period, what services are already provided by the Comparative Medicine staff as part of their per diem charges (e.g. is colony management part of that charge?), or to what extent the hiring of such a position reduces per diem charges. Nevertheless, given that the Core is maintaining both single and double transgenic mice, the centralization of screening is a prudent move. This will ensure quality (validity of genotypes) and availability of mice to the members of the Center.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH058880-03
Application #
6507449
Study Section
Special Emphasis Panel (ZMH1)
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
3
Fiscal Year
2001
Total Cost
$165,355
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Redondo, Roger L; Kim, Joshua; Arons, Autumn L et al. (2014) Bidirectional switch of the valence associated with a hippocampal contextual memory engram. Nature 513:426-30
Kohara, Keigo; Pignatelli, Michele; Rivest, Alexander J et al. (2014) Cell type-specific genetic and optogenetic tools reveal hippocampal CA2 circuits. Nat Neurosci 17:269-79
Liu, Xu; Ramirez, Steve; Tonegawa, Susumu (2014) Inception of a false memory by optogenetic manipulation of a hippocampal memory engram. Philos Trans R Soc Lond B Biol Sci 369:20130142
Dragoi, George; Tonegawa, Susumu (2013) Development of schemas revealed by prior experience and NMDA receptor knock-out. Elife 2:e01326
Dragoi, George; Tonegawa, Susumu (2013) Distinct preplay of multiple novel spatial experiences in the rat. Proc Natl Acad Sci U S A 110:9100-5
Dolan, Bridget M; Duron, Sergio G; Campbell, David A et al. (2013) Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by the small-molecule PAK inhibitor FRAX486. Proc Natl Acad Sci U S A 110:5671-6
Suh, Junghyup; Foster, David J; Davoudi, Heydar et al. (2013) Impaired hippocampal ripple-associated replay in a mouse model of schizophrenia. Neuron 80:484-93
Buschman, Timothy J; Denovellis, Eric L; Diogo, Cinira et al. (2012) Synchronous oscillatory neural ensembles for rules in the prefrontal cortex. Neuron 76:838-846
Nakashiba, Toshiaki; Cushman, Jesse D; Pelkey, Kenneth A et al. (2012) Young dentate granule cells mediate pattern separation, whereas old granule cells facilitate pattern completion. Cell 149:188-201
Liu, Xu; Ramirez, Steve; Pang, Petti T et al. (2012) Optogenetic stimulation of a hippocampal engram activates fear memory recall. Nature 484:381-5

Showing the most recent 10 out of 32 publications