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Lack of Pwcr1/MBII-85 snoRNA is Critical for Neonatal Lethality in Prader–Willi Syndrome Mouse Models
Mammalian Genome (2005)
  • Feng Ding
  • Yelena Prints
  • Madhu S Dhar, University of Tennessee, Knoxville
  • Dabney K. Johnson
  • Carmen Garnacho-Montero
  • Robert D. Nicholls
  • Uta Francke
Abstract
Prader–Willi syndrome (PWS) is a neurobehavioral disorder caused by the lack of paternal expression of imprinted genes in the human chromosome region 15q11–13. Recent studies of rare human translocation patients narrowed the PWS critical genes to a 121-kb region containing PWCR1/HBII-85 and HBII-438 snoRNA genes. The existing mouse models of PWS that lack the expression of multiple genes, including Snrpn, Ube3a, and many intronic snoRNA genes, are characterized by 80%–100% neonatal lethality. To define the candidate region for PWS-like phenotypes in mice, we analyzed the expression of several genetic elements in mice carrying the large radiation-induced p30PUb deletion that includes the p locus. Mice having inherited this deletion from either parent develop normally into adulthood. By Northern blot and RT-PCR assays of brain tissue, we found that Pwcr1/MBII-85 snoRNAs are expressed normally, while MBII-52 snoRNAs are not expressed when the deletion is paternally inherited. Mapping of the distal deletion breakpoint indicated that the p30PUb deletion includes the entire MBII-52 snoRNA gene cluster and three previously unmapped EST sequences. The lack of expression of these elements in mice with a paternal p30PUb deletion indicates that they are not critical for the neonatal lethality observed in PWS mouse models. In addition, we identified MBII-436, the mouse homolog of the HBII-436 snoRNA, confirmed its imprinting status, and mapped it outside of the p30PUb deletion. Taking together all available data, we conclude that the lack of Pwcr1/MBII-85 snoRNA expression is the most likely cause for the neonatal lethality in PWS model mice.
Publication Date
June, 2005
Citation Information
Feng Ding, Yelena Prints, Madhu S Dhar, Dabney K. Johnson, et al.. "Lack of Pwcr1/MBII-85 snoRNA is Critical for Neonatal Lethality in Prader–Willi Syndrome Mouse Models" Mammalian Genome Vol. 16 Iss. 6 (2005)
Available at: http://works.bepress.com/madhu_dhar/11/