Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome

Science. 2008 Aug 8;321(5890):839-43. doi: 10.1126/science.1156121. Epub 2008 Jul 24.

Abstract

Duane's retraction syndrome (DRS) is a complex congenital eye movement disorder caused by aberrant innervation of the extraocular muscles by axons of brainstem motor neurons. Studying families with a variant form of the disorder (DURS2-DRS), we have identified causative heterozygous missense mutations in CHN1, a gene on chromosome 2q31 that encodes alpha2-chimaerin, a Rac guanosine triphosphatase-activating protein (RacGAP) signaling protein previously implicated in the pathfinding of corticospinal axons in mice. We found that these are gain-of-function mutations that increase alpha2-chimaerin RacGAP activity in vitro. Several of the mutations appeared to enhance alpha2-chimaerin translocation to the cell membrane or enhance its ability to self-associate. Expression of mutant alpha2-chimaerin constructs in chick embryos resulted in failure of oculomotor axons to innervate their target extraocular muscles. We conclude that alpha2-chimaerin has a critical developmental function in ocular motor axon pathfinding.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abducens Nerve / abnormalities
  • Amino Acid Sequence
  • Animals
  • Axons / physiology
  • Cell Line
  • Cell Membrane / metabolism
  • Chick Embryo
  • Chimerin 1 / chemistry
  • Chimerin 1 / genetics*
  • Chimerin 1 / metabolism*
  • Duane Retraction Syndrome / genetics*
  • Female
  • Gene Expression Profiling
  • Heterozygote
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation, Missense*
  • Oculomotor Muscles / embryology
  • Oculomotor Muscles / innervation
  • Oculomotor Muscles / metabolism
  • Oculomotor Nerve / abnormalities
  • Oculomotor Nerve / embryology
  • Pedigree

Substances

  • Chimerin 1

Associated data

  • PDB/1XA6
  • RefSeq/NM_001012952
  • RefSeq/NM_001113246
  • RefSeq/NM_001822
  • RefSeq/NP_001813