RT Journal Article SR Electronic T1 Both Doublecortin and Doublecortin-Like Kinase Play a Role in Cortical Interneuron Migration JF The Journal of Neuroscience JO J. Neurosci. FD Society for Neuroscience SP 3875 OP 3883 DO 10.1523/JNEUROSCI.4530-06.2007 VO 27 IS 14 A1 Gaëlle Friocourt A1 Judy S. Liu A1 Mary Antypa A1 Sonja Rakić A1 Christopher A. Walsh A1 John G. Parnavelas YR 2007 UL http://www.jneurosci.org/content/27/14/3875.abstract AB Type I lissencephaly, a genetic disease characterized by disorganized cortical layers and gyral abnormalities, is associated with severe cognitive impairment and epilepsy. Two genes, LIS1 and doublecortin (DCX), have been shown to be responsible for a large proportion of cases of type I lissencephaly. Both genes encode microtubule-associated proteins that have been shown to be important for radial migration of cortical pyramidal neurons. To investigate whether DCX also plays a role in cortical interneuron migration, we inactivated DCX in the ganglionic eminence of rat embryonic day 17 brain slices using short hairpin RNA. We found that, when DCX expression was blocked, the migration of interneurons from the ganglionic eminence to the cerebral cortex was slowed but not absent, similar to what had previously been reported for radial neuronal migration. In addition, the processes of DCX-deficient migrating interneurons were more branched than their counterparts in control experiments. These effects were rescued by DCX overexpression, confirming the specificity to DCX inactivation. A similar delay in interneuron migration was observed when Doublecortin-like kinase (DCLK), a microtubule-associated protein related to DCX, was inactivated, although the morphology of the cells was not affected. The importance of these genes in interneuron migration was confirmed by our finding that the cortices of Dcx, Dclk, and Dcx/Dclk mutant mice contained a reduced number of such cells in the cortex and their distribution was different compared with wild-type controls. However, the defect was different for each group of mutant animals, suggesting that DCX and DCLK have distinct roles in cortical interneuron migration.