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MATERNAL IMPRINTING OF HUMAN SNRPN, A GENE DELETED IN PRADER-WILLI-SYNDROME
Author(s): REED ML, LEFF SE
Source: NATURE GENETICS    Volume: 6    Issue: 2    Pages: 163-167    Published: FEB 1994  
Times Cited: 120     References: 32     
Abstract: Prader-Willi syndrome (PWS), a human neuroendocrine disorder, is associated with deficiencies of paternal chromosome 15q12. Small nuclear ribonucleoprotein polypeptide N (SNRPN) is the first expressed gene identified in the PWS critically deleted region. Following our demonstration that the murine homologue of SNRPN is imprinted, we have characterized a sequence polymorphism within expressed portions of human SNRPN and show that human SNRPN is monoallelically expressed in fetal brain and heart and in adult brain. Analysis of maternal DNA and SNRPN cDNA confirmed that the maternal allele of SNRPN is not expressed in fetal brain and heart. Maternal imprinting of SNRPN supports the hypothesis that paternal absence of SNRPN is responsible for the PWS phenotype.
Document Type: Article
Language: English
Addresses:
1. STANFORD UNIV, SCH MED, DEPT MOLEC PHARMACOL, STANFORD, CA 94305 USA
Publisher: NATURE PUBLISHING CO, 345 PARK AVE SOUTH, NEW YORK, NY 10010-1707
Subject Category: Genetics & Heredity
IDS Number: MU763
ISSN: 1061-4036
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