The MACF1 puzzle: when a cytoskeletal giant causes multiple brain disorders

Connections. Spectraplakins sit at the interface of architecture and motion inside a cell. They do not merely hold structures together but coordinate how the cytoskeleton rearranges itself when neurons migrate, polarize, and extend processes. One of the central spectraplakins is encoded by MACF1, a microtubule–actin crosslinking factor that couples microtubules to actin filaments and helps steer growing microtubules. This job requires multiple binding domains, flexibility, and scale. Spectraplakins are therefore large proteins encoded by enormous genes. A recent study examined how variants in MACF1 translate into human brain disease, and why seemingly similar variants may lead to surprisingly different neurodevelopmental outcomes. Here is why interpreting MACF1 variants is so complex.

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SHANK3, epilepsy, and the excitatory/inhibitory imbalance

Postsynaptic. SHANK proteins are elements of the postsynaptic density, linking synaptic transmission with the cytoskeleton. Deletions in SHANK2 and SHANK3 are known genetic risk factors for a broad range of neurodevelopmental disorders. The role of the reciprocal duplications, however, has remained unclear. In recent paper in Nature, a novel mouse model expressing a SHANK3 transgene is investigated. The results of a mere 1.5 fold overexpression of the protein are dramatic, hinting at unanticipated mechanisms that regulate the balance between excitation and inhibition.  Continue reading