Many studies have used "reverse" genetics to produce "knock-out" and transg
enic mice to explore the roles of various molecules in long-term potentiati
on LTP) and spatial memory. The existence of a variety of inbred strains of
mice provides an additional way of exploring the genetic bases of learning
and memory. We examined behavioral memory and LTP expression in area CA1 o
f hippocampal slices prepared from four different inbred strains of mice: C
57BL/6J, CBA/J, DBA/2J, and 129/SvEms-+(Ter?)/J. We found that LTP induced
by four 100-Hz trains of stimulation was robust and long-lasting in C57BL/6
J and DBA/2J mice but decayed in CBA/J and 129/SvEms-+(Ter?)/J mice. LTP in
duced by one 100-Hz train was significantly smaller after I hr in the 129/S
vEms-+(Ter?)/J mice than in the other three strains. Theta-burst LTP was sh
orter lasting in CBA/J, DBA/2J, and 129/SvEms-+(Ter?)/J mice than in C57BL/
6J mice. We also observed specific memory deficits, among particular mouse
strains, in spatial and nonspatial tests of hippocampus-dependent memory. C
BA/J mice showed defective learning in the Morris water maze, and both DBA/
2J and CBA/J strains displayed deficient long-term memory in contextual and
cued fear conditioning tests. Our findings provide strong support for a ge
netic basis for some forms of synaptic plasticity that are linked to behavi
oral long-term memory and suggest that genetic background can influence the
electrophysiological and behavioral phenotypes observed in genetically mod
ified mice generated fur elucidating the molecular bases of learning, memor
y, and LTP.