Approaches:
![]() |
![]() CA1 and Dentate Gyrus Cre Lines
Molecular Genetics
Our laboratory generates mice with specific genetic changes to test the involvement of certain molecular components in learning and memory. We also use other molecular strategies to manipulate brain function, including viral vectors and pharmacological manipulations. For example, we have derived genetic mutations that affect learning in mice, and others that only affect memory. We are using information from these studies to develop treatments for genetic disorders that affect learning and memory in humans. For example, we are currently testing treatments of Neurofibromatosis type I and TSC that derived from our mouse studies of this disorder.
|
Inducible, and region restricted mutations
One of the goals of our molecular genetic studies is to develop strategies that allow us to manipulate gene function at specific times and in defined brain regions. For example, we have recently used a strategy that takes advantage of the ligand binding domain of the estrogen receptor. This strategy allows us to regulate the function of a transgenic mutant transcription factor (CREB). We were able to fully induce the function of this mutant protein in 6 hr. and to completely shut it down in 24 hr. The pictures above show Cre-mediated gene deletions directed specifically to the dentate gyrus or the CA1 region of the hippocampus. These regional-specific genetic deletions will be critical to dissect the function of hippocampal networks
|
|
Viral vectors
With viral vectors (in collaboration with Rachael Neve), we have been able to introduce exogenous CREB into the amygdala (a brain structure key to emotions) of adult CREB mutant mice. After restoring CREB in the amygdala, the mutant mice regained the ability to form certain types of emotional memory, indicating that CREB in the amygdala is required for the establishment of emotional memories. With viral vectors, we also showed that CREB can determine where memories are stored in networks (click here for the PDF)
|
|
Molecular Genetics · PRISM · Electrophysiology · Neuroanatomy · in vivo Imaging · Behavioral Analyses · Bridging Mice and Men
|
|