Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region

Genome Res. 1996 Aug;6(8):742-6. doi: 10.1101/gr.6.8.742.

Abstract

Small nuclear ribonucleoprotein-associated polypeptide N (snRPN) and an anonymous transcript, PAR-5, are two of the paternally expressed transcripts mapped to the Prader-Willi syndrome critical region. Using long-range PCR, we have isolated the genomic interval between snRPN and PAR-5, identified a novel transcript in this region, and termed it PAR-SN. Northern analysis demonstrates that PAR-SN is expressed in brain, skeletal muscle, and heart. Like snRPN and PAR-5, PAR-SN is expressed exclusively from the paternal homolog in cultured lymphoblasts. Sequence analysis of the transcript revealed no significant open reading frame but did include a polymorphic dinucleotide repeat (CA)17.

MeSH terms

  • Chromosome Mapping
  • DNA, Complementary / genetics*
  • DNA, Complementary / isolation & purification
  • Genome, Human*
  • Humans
  • Molecular Sequence Data
  • Prader-Willi Syndrome / genetics*
  • Ribonucleoproteins, Small Nuclear / genetics*
  • Transcription, Genetic

Substances

  • DNA, Complementary
  • Ribonucleoproteins, Small Nuclear

Associated data

  • GENBANK/U55937