Genome-wide prediction of imprinted murine genes

  1. Philippe P. Luedi1,
  2. Alexander J. Hartemink1,2, and
  3. Randy L. Jirtle3,4
  1. 1 Center for Bioinformatics and Computational Biology, Duke University, Durham, North Carolina 27708, USA
  2. 2 Department of Computer Science, Duke University, Durham, North Carolina 27708, USA
  3. 3 Department of Radiation Oncology, University Program in Genetics and Genomics, Duke University Medical Center, Durham, North Carolina 27710, USA

Abstract

Imprinted genes are epigenetically modified genes whose expression is determined according to their parent of origin. They are involved in embryonic development, and imprinting dysregulation is linked to cancer, obesity, diabetes, and behavioral disorders such as autism and bipolar disease. Herein, we train a statistical model based on DNA sequence characteristics that not only identifies potentially imprinted genes, but also predicts the parental allele from which they are expressed. Of 23,788 annotated autosomal mouse genes, our model identifies 600 (2.5%) to be potentially imprinted, 64% of which are predicted to exhibit maternal expression. These predictions allowed for the identification of putative candidate genes for complex conditions where parent-of-origin effects are involved, including Alzheimer disease, autism, bipolar disorder, diabetes, male sexual orientation, obesity, and schizophrenia. We observe that the number, type, and relative orientation of repeated elements flanking a gene are particularly important in predicting whether a gene is imprinted.

Footnotes

  • [Supplemental material is available online at www.genome.org.]

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.3303505.

  • 4 Corresponding author. E-mail jirtle{at}radonc.duke.edu; fax (919) 684-5584.

    • Accepted March 22, 2005.
    • Received September 30, 2004.
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