A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systems

Am J Hum Genet. 2009 Feb;84(2):134-47. doi: 10.1016/j.ajhg.2008.12.017. Epub 2009 Jan 29.

Abstract

Six infants in an Old Order Amish pedigree were observed to be affected with endocrine-cerebro-osteodysplasia (ECO). ECO is a previously unidentified neonatal lethal recessive disorder with multiple anomalies involving the endocrine, cerebral, and skeletal systems. Autozygosity mapping and sequencing identified a previously unknown missense mutation, R272Q, in ICK, encoding intestinal cell kinase (ICK). Our results established that R272 is conserved across species and among ethnicities, and three-dimensional analysis of the protein structure suggests protein instability due to the R272Q mutation. We also demonstrate that the R272Q mutant fails to localize at the nucleus and has diminished kinase activity. These findings suggest that ICK plays a key role in the development of multiple organ systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autopsy
  • Bone Diseases / blood
  • Bone Diseases / genetics*
  • Bone Diseases / pathology
  • Brain / enzymology
  • Central Nervous System Diseases / genetics*
  • Central Nervous System Diseases / pathology
  • Conserved Sequence
  • Endocrine System Diseases / blood
  • Endocrine System Diseases / genetics*
  • Endocrine System Diseases / pathology
  • Ethnicity / genetics*
  • Exons
  • Female
  • Genes, Recessive
  • Humans
  • Kidney / enzymology
  • Liver / enzymology
  • Male
  • Mutation*
  • Pedigree
  • Protein Serine-Threonine Kinases / blood
  • Protein Serine-Threonine Kinases / genetics*
  • Siblings
  • Species Specificity
  • Syndrome

Substances

  • CILK1 protein, human
  • Protein Serine-Threonine Kinases