SNRPN upstream reading frame protein explained

SNRPN upstream reading frame protein is a protein that in humans is encoded by the SNURF gene.[1] [2]

Function

This gene encodes a highly basic protein localized to the nucleus. The evolutionarily constrained open reading frame is found on a bicistronic transcript which has a downstream ORF encoding the small nuclear ribonucleoprotein polypeptide N. The upstream coding region utilizes the first three exons of the transcript, a region that has been identified as an imprinting center. Multiple transcription initiation sites have been identified and extensive alternative splicing occurs in the 5' untranslated region but the full-length nature of these transcripts has not been determined. An alternate exon has been identified that substitutes for exon 4 and leads to a truncated, monocistronic transcript. Alternative splicing or deletion caused by a translocation event in the 5' untranslated region or coding region of this gene leads to Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure. The function of this protein is not yet known.

Further reading

Notes and References

  1. Gray TA, Saitoh S, Nicholls RD . An imprinted, mammalian bicistronic transcript encodes two independent proteins . Proceedings of the National Academy of Sciences of the United States of America . 96 . 10 . 5616–21 . May 1999 . 10318933 . 21909 . 10.1073/pnas.96.10.5616 . 1999PNAS...96.5616G . free .
  2. Web site: Entrez Gene: SNURF SNRPN upstream reading frame.