HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.

Abstract
The Angelman/Prader-Willi syndrome (AS/PWS) domain contains at least 8 imprinted genes regulated by a bipartite imprinting center (IC) associated with the SNRPN gene. One component of the IC, the PWS-IC, governs the paternal epigenotype and expression of paternal genes. The mechanisms by which imprinting and expression of paternal genes within the AS/PWS domain - such as MKRN3 and NDN - are regulated by the PWS-IC are unclear. The syntenic region in the mouse is organized and imprinted similarly to the human domain with the murine PWS-IC defined by a 6 kb interval within the Snrpn locus that includes the promoter. To identify regulatory elements that may mediate PWS-IC function, we mapped the location and allele-specificity of DNase I hypersensitive (DH) sites within the PWS-IC in brain cells, then identified transcription factor binding sites within a subset of these DH sites. Six major paternal-specific DH sites were detected in the Snrpn gene, five of which map within the 6 kb PWS-IC. We postulate these five DH sites represent functional components of the murine PWS-IC. Analysis of transcription factor binding within multiple DH sites detected nuclear respiratory factors (NRF's) and YY1 specifically on the paternal allele. NRF's and YY1 were also detected in the paternal promoter region of the murine Mrkn3 and Ndn genes. These results suggest that NRF's and YY1 may facilitate PWS-IC function and coordinately regulate expression of paternal genes. The presence of NRF's also suggests a link between transcriptional regulation within the AS/PWS domain and regulation of respiration. 3C analyses indicated Mkrn3 lies in close proximity to the PWS-IC on the paternal chromosome, evidence that the PWS-IC functions by allele-specific interaction with its distal target genes. This could occur by allele-specific co-localization of the PWS-IC and its target genes to transcription factories containing NRF's and YY1.
AuthorsSara Rodriguez-Jato, Jixiu Shan, Jyoti Khadake, Arnold D Heggestad, Xiaojie Ma, Karen A Johnstone, James L Resnick, Thomas P Yang
JournalPloS one (PLoS One) Vol. 8 Issue 2 Pg. e52390 ( 2013) ISSN: 1932-6203 [Electronic] United States
PMID23390487 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Nuclear Respiratory Factors
  • YY1 Transcription Factor
  • Yy1 protein, mouse
  • snRNP Core Proteins
  • Deoxyribonuclease I
Topics
  • Alleles
  • Angelman Syndrome (genetics, metabolism, pathology)
  • Animals
  • Base Sequence
  • Binding Sites
  • Deoxyribonuclease I (metabolism)
  • Gene Expression Regulation
  • Genetic Loci
  • Genomic Imprinting
  • Humans
  • Mice
  • Mice, Transgenic
  • Molecular Sequence Data
  • Nuclear Respiratory Factors (genetics, metabolism)
  • Prader-Willi Syndrome (genetics, metabolism, pathology)
  • Protein Binding
  • Regulatory Elements, Transcriptional
  • Synteny
  • Transcription, Genetic
  • YY1 Transcription Factor (genetics, metabolism)
  • snRNP Core Proteins (genetics, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: