Literature DB >> 18055845

Computational and experimental identification of novel human imprinted genes.

Philippe P Luedi1, Fred S Dietrich, Jennifer R Weidman, Jason M Bosko, Randy L Jirtle, Alexander J Hartemink.   

Abstract

Imprinted genes are essential in embryonic development, and imprinting dysregulation contributes to human disease. We report two new human imprinted genes: KCNK9 is predominantly expressed in the brain, is a known oncogene, and may be involved in bipolar disorder and epilepsy, while DLGAP2 is a candidate bladder cancer tumor suppressor. Both genes lie on chromosome 8, not previously suspected to contain imprinted genes. We identified these genes, along with 154 others, based on the predictions of multiple classification algorithms using DNA sequence characteristics as features. Our findings demonstrate that DNA sequence characteristics, including recombination hot spots, are sufficient to accurately predict the imprinting status of individual genes in the human genome.

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Year:  2007        PMID: 18055845      PMCID: PMC2099581          DOI: 10.1101/gr.6584707

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  58 in total

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Journal:  Mol Cell Biol       Date:  1995-05       Impact factor: 4.272

5.  Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome.

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Journal:  Nat Genet       Date:  2004-12-19       Impact factor: 38.330

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Review 7.  Cytosine methylation and the ecology of intragenomic parasites.

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Journal:  Trends Genet       Date:  1997-08       Impact factor: 11.639

Review 8.  Cellular memory and dynamic regulation of polycomb group proteins.

Authors:  Frédéric Bantignies; Giacomo Cavalli
Journal:  Curr Opin Cell Biol       Date:  2006-05-02       Impact factor: 8.382

9.  The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus.

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Journal:  Nature       Date:  1991-01-03       Impact factor: 49.962

10.  Sp1 elements protect a CpG island from de novo methylation.

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Journal:  Nature       Date:  1994-09-29       Impact factor: 49.962

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  151 in total

1.  Genetic variation in imprinted genes is associated with risk of late-onset Alzheimer's disease.

Authors:  Mamoonah Chaudhry; Xingbin Wang; Mikhil N Bamne; Shahida Hasnain; F Yesim Demirci; Oscar L Lopez; M Ilyas Kamboh
Journal:  J Alzheimers Dis       Date:  2015       Impact factor: 4.472

Review 2.  Pathogenesis and consequences of uniparental disomy in cancer.

Authors:  Hideki Makishima; Jaroslaw P Maciejewski
Journal:  Clin Cancer Res       Date:  2011-04-25       Impact factor: 12.531

3.  Genomic landscape of human allele-specific DNA methylation.

Authors:  Fang Fang; Emily Hodges; Antoine Molaro; Matthew Dean; Gregory J Hannon; Andrew D Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2012-04-20       Impact factor: 11.205

4.  Identification and resolution of artifacts in the interpretation of imprinted gene expression.

Authors:  Charlotte Proudhon; Déborah Bourc'his
Journal:  Brief Funct Genomics       Date:  2010-09-08       Impact factor: 4.241

Review 5.  Allele-specific methylation in the human genome: implications for genetic studies of complex disease.

Authors:  Emma L Meaburn; Leonard C Schalkwyk; Jonathan Mill
Journal:  Epigenetics       Date:  2010-10-01       Impact factor: 4.528

6.  Chediak-Higashi syndrome with early developmental delay resulting from paternal heterodisomy of chromosome 1.

Authors:  Irini Manoli; Gretchen Golas; Wendy Westbroek; Thierry Vilboux; Thomas C Markello; Wendy Introne; Dawn Maynard; Ben Pederson; Ekaterini Tsilou; Michael B Jordan; P Suzanne Hart; James G White; William A Gahl; Marjan Huizing
Journal:  Am J Med Genet A       Date:  2010-06       Impact factor: 2.802

7.  Genomic imprinting in diabetes.

Authors:  Braxton D Mitchell; Toni I Pollin
Journal:  Genome Med       Date:  2010-08-23       Impact factor: 11.117

8.  Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder.

Authors:  Przemyslaw Szafranski; Avinash V Dharmadhikari; Erwin Brosens; Priyatansh Gurha; Katarzyna E Kolodziejska; Ou Zhishuo; Piotr Dittwald; Tadeusz Majewski; K Naga Mohan; Bo Chen; Richard E Person; Dick Tibboel; Annelies de Klein; Jason Pinner; Maya Chopra; Girvan Malcolm; Gregory Peters; Susan Arbuckle; Sixto F Guiang; Virginia A Hustead; Jose Jessurun; Russel Hirsch; David P Witte; Isabelle Maystadt; Neil Sebire; Richard Fisher; Claire Langston; Partha Sen; Paweł Stankiewicz
Journal:  Genome Res       Date:  2012-10-03       Impact factor: 9.043

Review 9.  Epigenetics and obesity.

Authors:  Reinhard Stöger
Journal:  Pharmacogenomics       Date:  2008-12       Impact factor: 2.533

10.  Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP).

Authors:  Thilo Herzfeld; Nicole Wolf; Pia Winter; Holger Hackstein; Daniel Vater; Ulrich Müller
Journal:  Neurogenetics       Date:  2008-09-23       Impact factor: 2.660

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