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        <dc:title>DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation</dc:title>
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        <bibo:abstract>The forebrain hemispheres are predominantly separated during embryogenesis by the interhemispheric fissure (IHF). Radial astroglia remodel the IHF to form a continuous substrate between the hemispheres for midline crossing of the corpus callosum (CC) and hippocampal commissure (HC). Deleted in colorectal carcinoma (DCC) and netrin 1 (NTN1) are molecules that have an evolutionarily conserved function in commissural axon guidance. The CC and HC are absent in &lt;jats:italic&gt;Dcc&lt;/jats:italic&gt; and &lt;jats:italic&gt;Ntn1&lt;/jats:italic&gt; knockout mice, while other commissures are only partially affected, suggesting an additional aetiology in forebrain commissure formation. Here, we find that these molecules play a critical role in regulating astroglial development and IHF remodelling during CC and HC formation. Human subjects with &lt;jats:italic&gt;DCC&lt;/jats:italic&gt; mutations display disrupted IHF remodelling associated with CC and HC malformations. Thus, axon guidance molecules such as DCC and NTN1 first regulate the formation of a midline substrate for dorsal commissures prior to their role in regulating axonal growth and guidance across it.</bibo:abstract>
        <bibo:volume>10</bibo:volume>
        <dc:publisher>eLife Sciences Publications</dc:publisher>
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