17
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      WDR62 is associated with the spindle pole and is mutated in human microcephaly.

      Nature genetics
      Animals, Brain, anatomy & histology, Chromosome Mapping, Exons, genetics, Family, Female, Frameshift Mutation, Genes, Recessive, HeLa Cells, cytology, Homozygote, Humans, Male, Mice, Microcephaly, Mutation, Missense, Nerve Tissue Proteins, Oligonucleotide Array Sequence Analysis, methods, Spindle Apparatus

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Autosomal recessive primary microcephaly (MCPH) is a disorder of neurodevelopment resulting in a small brain. We identified WDR62 as the second most common cause of MCPH after finding homozygous missense and frame-shifting mutations in seven MCPH families. In human cell lines, we found that WDR62 is a spindle pole protein, as are ASPM and STIL, the MCPH7 and MCHP7 proteins. Mutant WDR62 proteins failed to localize to the mitotic spindle pole. In human and mouse embryonic brain, we found that WDR62 expression was restricted to neural precursors undergoing mitosis. These data lend support to the hypothesis that the exquisite control of the cleavage furrow orientation in mammalian neural precursor cell mitosis, controlled in great part by the centrosomes and spindle poles, is critical both in causing MCPH when perturbed and, when modulated, generating the evolutionarily enlarged human brain.

          Related collections

          Author and article information

          Comments

          Comment on this article