Activation of the gamma E-crystallin pseudogene in the human hereditary Coppock-like cataract

Hum Mol Genet. 1994 Feb;3(2):279-83. doi: 10.1093/hmg/3.2.279.

Abstract

The locus for the hereditary human Coppock-like cataract (CCL) is closely linked to a particular combination of polymorphic TaqI sites within the human gamma-crystallin gene cluster. Mapping of these sites shows that they define a 15 kb region encompassing the gamma D and psi gamma E gene. The gamma D and the psi gamma E gene were cloned from the CCL chromosome and characterized. The gamma D gene was functionally equivalent to its allele cloned from a wild-type chromosome. The CCL psi gamma E gene contains a cluster of sequence changes within and around its TATA box. Together these cause a ten-fold increase in the activity of the psi gamma E promoter, raising the level of expression of this gene to 30% of that of the gamma D gene. The predicted protein product of the psi gamma E gene is a 6 kD N-terminal gamma-crystallin fragment. Reactivation of the psi gamma E gene and concomitant overexpression of the gamma-crystallin fragment could be the cause of the Coppock-like cataract.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cataract / genetics*
  • Crystallins / genetics*
  • Gene Expression Regulation
  • Haplotypes / genetics
  • Humans
  • Molecular Sequence Data
  • Polymorphism, Genetic
  • Pseudogenes*
  • Sequence Alignment
  • Sequence Homology, Nucleic Acid
  • TATA Box

Substances

  • Crystallins

Associated data

  • GENBANK/S72943