RT Journal Article SR Electronic T1 Rbm8a Haploinsufficiency Disrupts Embryonic Cortical Development Resulting in Microcephaly JF The Journal of Neuroscience JO J. Neurosci. FD Society for Neuroscience SP 7003 OP 7018 DO 10.1523/JNEUROSCI.0018-15.2015 VO 35 IS 18 A1 Hanqian Mao A1 Louis-Jan Pilaz A1 John J. McMahon A1 Christelle Golzio A1 Danwei Wu A1 Lei Shi A1 Nicholas Katsanis A1 Debra L. Silver YR 2015 UL http://www.jneurosci.org/content/35/18/7003.abstract AB The cerebral cortex is built during embryonic neurogenesis, a period when excitatory neurons are generated from progenitors. Defects in neurogenesis can cause acute neurodevelopmental disorders, such as microcephaly (reduced brain size). Altered dosage of the 1q21.1 locus has been implicated in the etiology of neurodevelopmental phenotypes; however, the role of 1q21.1 genes in neurogenesis has remained elusive. Here, we show that haploinsufficiency for Rbm8a, an exon junction complex (EJC) component within 1q21.1, causes severe microcephaly and defective neurogenesis in the mouse. At the onset of neurogenesis, Rbm8a regulates radial glia proliferation and prevents premature neuronal differentiation. Reduced Rbm8a levels result in subsequent apoptosis of neurons, and to a lesser extent, radial glia. Hence, compared to control, Rbm8a-haploinsufficient brains have fewer progenitors and neurons, resulting in defective cortical lamination. To determine whether reciprocal dosage change of Rbm8a alters embryonic neurogenesis, we overexpressed human RBM8A in two animal models. Using in utero electroporation of mouse neocortices as well as zebrafish models, we find RBM8A overexpression does not significantly perturb progenitor number or head size. Our findings demonstrate that Rbm8a is an essential neurogenesis regulator, and add to a growing literature highlighting roles for EJC components in cortical development and neurodevelopmental pathology. Our results indicate that disruption of RBM8A may contribute to neurodevelopmental phenotypes associated with proximal 1q21.1 microdeletions.