Novel myocilin mutation in a Chinese family with juvenile-onset open-angle glaucoma

Arch Ophthalmol. 2006 Jan;124(1):102-6. doi: 10.1001/archopht.124.1.102.

Abstract

Objective: To search for the genetic cause of juvenile-onset open-angle glaucoma (JOAG) in a Chinese family.

Methods: In a 3-generation glaucoma family affected with JOAG or ocular hypertension, we screened myocilin (MYOC) and optineurin (OPTN) for mutations and investigated apolipoprotein E (APOE) polymorphisms in 6 family members, 2 of them patients with JOAG, 2 patients with ocular hypertension, and 2 patients who were asymptomatic. Normal controls included 200 unrelated Chinese subjects. The COS-7 cell line was transfected with expression vectors encoding wild-type or mutated MYOC complementary DNA. Cellular and secreted MYOC proteins were characterized by Western blotting.

Results: One missense MYOC mutation, 734G>A: Cys245Tyr, was identified. It occurred in all 4 family members afflicted with JOAG or ocular hypertension but not in asymptomatic family members. No OPTN variations were observed. APOE polymorphism frequencies were similar to those for controls. The Cys245Tyr MYOC mutation cosegregated with the disorder within the family. It was absent in the 200 control subjects. The Cys245Tyr mutant MYOC protein formed homomultimeric complexes that migrated at molecular weights larger than their wild-type counterparts. These mutant complexes remained sequestered intracellularly in COS-7 cells.

Conclusions: The Cys245Tyr MYOC mutation was the genetic cause of JOAG in this Chinese family. This mutation may alter covalent bonds that formed between MYOC cysteines. Clinical Relevance Genetic tests of MYOC mutations may be beneficial to predict new cases of the disease in families with JOAG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Animals
  • Apolipoproteins E / genetics
  • Asians
  • COS Cells / metabolism
  • Cell Cycle Proteins
  • Chlorocebus aethiops
  • Cytoskeletal Proteins / genetics*
  • Cytoskeletal Proteins / metabolism
  • DNA Mutational Analysis
  • Eye Proteins / genetics*
  • Eye Proteins / metabolism
  • Female
  • Genetic Testing
  • Genetic Vectors
  • Glaucoma, Open-Angle / ethnology
  • Glaucoma, Open-Angle / genetics*
  • Glycoproteins / genetics*
  • Glycoproteins / metabolism
  • Humans
  • Intraocular Pressure
  • Male
  • Membrane Transport Proteins
  • Middle Aged
  • Mutation, Missense*
  • Ocular Hypertension / ethnology
  • Ocular Hypertension / genetics
  • Pedigree
  • Polymorphism, Genetic
  • Transcription Factor TFIIIA / genetics
  • Transfection

Substances

  • Apolipoproteins E
  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • Eye Proteins
  • Glycoproteins
  • Membrane Transport Proteins
  • OPTN protein, human
  • Transcription Factor TFIIIA
  • trabecular meshwork-induced glucocorticoid response protein