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Yap, Ee-Lynn

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Yap

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Ee-Lynn

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Yap, Ee-Lynn

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Author's Publications: search.filters.isAuthorOfPublication.d19e7a81-a2aa-4418-b8f8-29efbd1bf020

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    Bidirectional Perisomatic Inhibitory Plasticity of a Fos Neuronal Network
    (Springer Science and Business Media LLC, 2020-12-09) Yap, Ee-Lynn; Pettit, Noah L.; Davis, Christopher; Nagy, M. Aurel; Harmin, David; Golden, Emily; Dagliyan, Onur; Lin, Cindy; Rudolph, Stephanie; Sharma, Nikhil; Griffith, Eric C.; Harvey, Christopher D.; Greenberg, Michael
    Behavioral experiences activate the Fos transcription factor (TF) in sparse populations of neurons that are critical for encoding and recalling specific events1-3. However, there is limited understanding of the mechanisms by which experience drives circuit reorganization to establish a network of Fos-activated cells. It is also unknown if Fos is required in this process beyond serving as a marker of recent neural activity and, if so, which of its many gene targets underlie circuit reorganization. Here we demonstrate that when mice engage in spatial exploration of novel environments, perisomatic inhibition of Fos-expressing hippocampal CA1 pyramidal neurons by parvalbumin (PV)-interneurons (INs) is enhanced, while perisomatic inhibition by cholecystokinin (CCK)-INs is weakened. This bidirectional modulation of inhibition is abolished when the function of the Fos TF complex is disrupted. Single-cell RNA-sequencing, ribosome-associated mRNA profiling, and chromatin analyses, combined with electrophysiology, reveal that Fos activates the transcription of Scg2 (secretogranin II), a gene that encodes multiple distinct neuropeptides, to coordinate these changes in inhibition. As PV- and CCK-INs mediate distinct features of pyramidal cell activity4-6, the Scg2-dependent reorganization of inhibitory synaptic input might be predicted to affect network function in vivo. Consistent with this prediction, hippocampal gamma rhythms and pyramidal cell coupling to CA1 theta are significantly altered with loss of Scg2. These findings reveal an instructive role for Fos and Scg2 in establishing a network of Fos-activated neurons via the rewiring of local inhibition to form a selectively modulated state. The opposing plasticity mechanisms on distinct inhibitory pathways may support the consolidation of memories over time.