
Cortical inhibition has critical roles in not only stabilization of neural circuit activity but also delicate control of frequency and timing of neuronal spiking, which underlie proper cortical processing. Therefore, a malfunction of inhibitory circuits could lead to severe brain disorders such as epilepsy, autism and schizophrenia. In the cortex, inhibition is mediated through local GABAergic interneurons, which comprise approximately 20% of the cortical neuronal population. Although numerically minor, GABAergic neurons display a large degree of heterogeneity regarding morphology, physiology, and connectivity. This striking feature has been thought to confer a rich repertory of inhibitory controls on neural circuitry and enable various types of neuronal computations. Thus, studying development, connectivity and function in each subtype of GABA neurons should tell us a blueprint of brain circuits, a principle of local circuit formation and ultimately hints for how the brain works. We have generated and characterized over 20 Cre and inducible CreER knockin lines, which reliably target major subtypes of GABAergic interneurons. Taking full advantage of this genetic resource we will ask following questions: