G to C transversion at a splice acceptor site causes exon skipping in the cystatin B gene

Mutat Res. 1997 Sep;382(1-2):67-74. doi: 10.1016/s1383-5726(97)00010-1.

Abstract

Several mutations have been described in the proteinase inhibitor cystatin B gene from individuals affected with progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1). One of these mutations, a 1925G-->C transition at the 3'-splice acceptor site of the intron 1, was postulated to lead to inappropriate splicing of a primary transcript of the cystatin B gene in EPM1 patients. In an effort to understand the expression of the 1925G-->C mutation, the sequence of cystatin B mRNA transcripts from lymphoblastoid cell lines of heterozygous patients carrying the mutation were analyzed. RT-PCR of total mRNA showed two main products: the apparently normal transcript and an aberrant, 102 bp shorter transcript. Direct PCR sequencing showed that the aberrant transcript is a consequence of exon 2 skipping.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Line
  • Cystatin B
  • Cystatins / genetics*
  • DNA Mutational Analysis
  • Epilepsies, Myoclonic / genetics*
  • Exons / genetics
  • Genes / genetics
  • Heterozygote
  • Humans
  • Lymphocytes
  • Point Mutation / genetics*
  • Polymerase Chain Reaction / methods
  • RNA Splicing / genetics*
  • RNA, Messenger / genetics*

Substances

  • CSTB protein, human
  • Cystatins
  • RNA, Messenger
  • Cystatin B