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Extracellular potentials were recorded with stereotrodeor tetrode-configured bundles of 25-μm Formvar-coated nichrome wires carried by a miniature microdrive (79). Under ketamine (50 mg per kilogram of body weight) and xylazine (2 mg/kg) anesthesia, the electrode array was implanted at 1.7 mm posterior to bregma, and 1.7 mm right of the midline, just above the dorsal hippocampus. The electrode was lowered gradually each day, after which recordings were evaluated for spike unit activity. Recordings were passed through a unity gain preamplifier-headstage, amplified (10,000 times) and bandpass-filtered (0.3 to 0.6 kHz low cut, and 5 to 6 kHz high cut), and digitized at 32 kHz (Data Translation DT2821) with Enhanced Discovery software (DataWave Technologies). Animal position was tracked with a video camera system (DataWave Technologies) that followed an incandescent headstage lamp at 60 Hz. Single cells were isolated by waveform parameters (Autocut, Data-Wave Technologies), and cell isolations were considered stable when clusters remained within fixed boundaries throughout testing.
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6844227052
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Δ- mutant mice were from the F2 generation of a cross between strains 129 and C57BL/6. Data from WT littermates from both groups (n = 2 from each) were combined, because their genetic backgrounds were very similar and their results were statistically indistinguishable. Mice were housed individually and kept at 95% ad libitum body weight.
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6844225700
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2 (four pixels of 2.37 cm by 2.37 cm) where the average firing rate was at least two times the cell's overall firing rate. By these criteria a place cell could have multiple discontiguous place fields (see Fig. 1) that were considered separately in assessments of spatial selectivity.
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A place field was considered fixed or only rotated if all its pixels were within 15 cm (half of the arm's length) of the axial expanse of the original place field either in the same arm or the appropriate 90°-rotated arm, respectively. Fixed place fields were assumed to be under the control of unidentified stable environmental cues.
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In rats distal cues control the largest proportion of place cells (19), but in WT mice local cues predominate. However, when local cues were removed and replaced with identical smooth black arms in a separate analysis, most place cells remained spatially selective. This result indicates that although place cells in mice attend preferentially to local cues, they also respond to distal cues.
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Funded by grants from the Whitehall Foundation, Beckman Foundation, Klingenstein Foundation, McKnight Foundation, and NIH (AG 13622) to AJ.S., the Deutsche Forschungsgemeinschaft to K.P.G., NIH (MH51570) to H.E., and Human Frontier Science Program Fellowship to Y.H.C.
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