Hook3 interacts with PCM1 to regulate pericentriolar material assembly and the timing of neurogenesis
Centrosome functions are important in many brain developmental processes. Proper functioning of the centrosome relies on assembly of protein components into the pericentriolar material. This dynamic assembly is mediated by the trafficking of pericentriolar satellites, which are comprised of centr...
Main Authors: | , , , |
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Other Authors: | |
Format: | Article |
Language: | en_US |
Published: |
Elsevier
2010
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Online Access: | http://hdl.handle.net/1721.1/50868 https://orcid.org/0000-0003-1262-0592 |
Summary: | Centrosome functions are important in many brain developmental processes. Proper
functioning of the centrosome relies on assembly of protein components into the pericentriolar
material. This dynamic assembly is mediated by the trafficking of pericentriolar satellites, which are
comprised of centrosomal proteins. Here we demonstrate that trafficking of pericentriolar satellites
requires the interaction between Hook3 and Pericentriolar Material 1 (PCM1). Hook3, previously
shown to link the centrosome and the nucleus in C. elegans, is recruited to pericentriolar satellites
through interaction with PCM1, a protein associated with schizophrenia. Knocking down of Hook3 or
PCM1, or disrupting the Hook3-PCM1 interaction in vivo impairs interkinetic nuclear migration, a
featured behavior of embryonic neural progenitors. This in turn leads to overproduction of neurons
and premature depletion of the neural progenitor pool in the developing neocortex. These results
underscore the importance of centrosomal assembly in neurogenesis, and provide potential insights
into the etiology of brain developmental diseases related to centrosome dysfunction. |
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