Sequence-dependent and independent inhibition specific for mutant ataxin-3 by small interfering RNA

Ann Neurol. 2004 Jul;56(1):124-9. doi: 10.1002/ana.20141.

Abstract

In Machado-Joseph disease (MJD) gene, there is a C/G polymorphism immediately after the CAG repeat; the expanded CAG repeat tract is exclusively followed by C, whereas about half of wild-type alleles are followed by G. Using this C/G polymorphism, we have engineered the small interfering RNA (siRNA) which decreased the expression of mutant ataxin-3, Q79C, by 96.0%, whereas there was minimal reduction on that of the wild type, Q22G (5.9%). Furthermore, unexpectedly, the expression of another wild-type allele, Q22C, was also much less suppressed (22.5%) by this siRNA possibly due to difference of the secondary structure of the target RNA. This is the first report of sequence-independent discrimination of mutant and wild-type alleles by siRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ataxin-3
  • Base Sequence
  • Cells, Cultured
  • Humans
  • Machado-Joseph Disease / genetics
  • Molecular Sequence Data
  • Mutation*
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Nuclear Proteins
  • Polymorphism, Genetic
  • RNA / metabolism
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism*
  • Repressor Proteins
  • Trinucleotide Repeats

Substances

  • Nerve Tissue Proteins
  • Nuclear Proteins
  • RNA, Small Interfering
  • Repressor Proteins
  • RNA
  • ATXN3 protein, human
  • Ataxin-3