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Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region.
Author(s) -
Yi Ning,
Anna V. Roschke,
Susan L. Christian,
J Lesser,
James S. Sutcliffe,
David H. Ledbetter
Publication year - 1996
Publication title -
genome research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.556
H-Index - 297
eISSN - 1549-5469
pISSN - 1088-9051
DOI - 10.1101/gr.6.8.742
Subject(s) - biology , dinucleotide repeat , genetics , open reading frame , genomic imprinting , microbiology and biotechnology , gene , gene mapping , gene expression , peptide sequence , chromosome , dna methylation
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.

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