RAIDD mutations underlie the pathogenesis of thin lissencephaly (TLIS).

PLoS One

College of Pharmacy, Chung-Ang University, Seoul, South Korea.

Published: March 2019

Abnormal regulation of caspase-2-mediated neuronal cell death causes neurodegenerative diseases and defective brain development. PIDDosome is caspase-2 activating complex composed of PIDD, RAIDD, and caspase-2. Recent whole-exome sequencing study showed that the RAIDD mutations in the death domain (DD), including G128R, F164C, R170C, and R170H mutations, cause thin lissencephaly (TLIS) by reducing caspase-2-mediated neuronal apoptosis. Given that the molecular structure of the RAIDD DD:PIDD DD complex is available, in this study, we analyzed the molecular mechanisms underlying TLIS caused by the RAIDD TLIS variants by performing mutagenesis and biochemical assays.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6169973PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0205042PLOS

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