Literature DB >> 20829226

Effects of cis-regulatory variation differ across regions of the adult human brain.

Federica Buonocore1, Matthew J Hill, Colin D Campbell, Paul B Oladimeji, Aaron R Jeffries, Claire Troakes, Tibor Hortobagyi, Brenda P Williams, Jonathan D Cooper, Nicholas J Bray.   

Abstract

Cis-regulatory variation is considered to be an important determinant of human phenotypic variability, including susceptibility to complex disease. Recent studies have shown that the effects of cis-regulatory polymorphism on gene expression can differ widely between tissues. In the present study, we tested whether the effects of cis-regulatory variation can also differ between regions of the adult human brain. We used relative allelic expression to measure cis-effects on the RNA expression of five candidate genes for neuropsychiatric illness (ZNF804A, NOS1, RGS4, AKT1 and TCF4) across multiple discrete brain regions within individual subjects. For all five genes, we observed significant differences in allelic expression between brain regions in several individual subjects, suggesting regional differences in the effects of cis-regulatory polymorphism to be a common phenomenon. As well as highlighting an important caveat for studies of regulatory polymorphism in the brain, our findings indicate that it is possible to delineate brain areas in which cis-regulatory variants are active. This may provide important insights into the fundamental biology of neuropsychiatric phenotypes with which such variants are associated.

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Year:  2010        PMID: 20829226      PMCID: PMC3298852          DOI: 10.1093/hmg/ddq380

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  25 in total

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Authors:  Nicholas J Bray; Paul R Buckland; Michael J Owen; Michael C O'Donovan
Journal:  Hum Genet       Date:  2003-05-01       Impact factor: 4.132

2.  Allelic variation in gene expression is common in the human genome.

Authors:  H Shuen Lo; Zhining Wang; Ying Hu; Howard H Yang; Sheryl Gere; Kenneth H Buetow; Maxwell P Lee
Journal:  Genome Res       Date:  2003-08       Impact factor: 9.043

3.  Extreme context specificity in differential allelic expression.

Authors:  James M Wilkins; Lorraine Southam; Andrew J Price; Zehra Mustafa; Andrew Carr; John Loughlin
Journal:  Hum Mol Genet       Date:  2007-01-12       Impact factor: 6.150

4.  Widespread monoallelic expression on human autosomes.

Authors:  Alexander Gimelbrant; John N Hutchinson; Benjamin R Thompson; Andrew Chess
Journal:  Science       Date:  2007-11-16       Impact factor: 47.728

5.  Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction.

Authors:  Jeanne Amiel; Marlene Rio; Loic de Pontual; Richard Redon; Valerie Malan; Nathalie Boddaert; Perrine Plouin; Nigel P Carter; Stanislas Lyonnet; Arnold Munnich; Laurence Colleaux
Journal:  Am J Hum Genet       Date:  2007-03-23       Impact factor: 11.025

6.  Low mRNA levels of RGS4 splice variants in Alzheimer's disease: association between a rare haplotype and decreased mRNA expression.

Authors:  L Emilsson; P Saetre; E Jazin
Journal:  Synapse       Date:  2006-03-01       Impact factor: 2.562

7.  Context-specific functional effects of IFNGR1 promoter polymorphism.

Authors:  Oliver Koch; Dominic P Kwiatkowski; Irina A Udalova
Journal:  Hum Mol Genet       Date:  2006-04-06       Impact factor: 6.150

8.  Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.

Authors:  Nicholas J Bray; Anna Preece; Nigel M Williams; Valentina Moskvina; Paul R Buckland; Michael J Owen; Michael C O'Donovan
Journal:  Hum Mol Genet       Date:  2005-05-25       Impact factor: 6.150

9.  Severe mental retardation with breathing abnormalities (Pitt-Hopkins syndrome) is caused by haploinsufficiency of the neuronal bHLH transcription factor TCF4.

Authors:  Antje Brockschmidt; Unda Todt; Soojin Ryu; Alexander Hoischen; Christina Landwehr; Stefanie Birnbaum; Wilhelm Frenck; Bernhard Radlwimmer; Peter Lichter; Hartmut Engels; Wolfgang Driever; Christian Kubisch; Ruthild G Weber
Journal:  Hum Mol Genet       Date:  2007-05-03       Impact factor: 6.150

10.  Genetics of gene expression and its effect on disease.

Authors:  Valur Emilsson; Gudmar Thorleifsson; Bin Zhang; Amy S Leonardson; Florian Zink; Jun Zhu; Sonia Carlson; Agnar Helgason; G Bragi Walters; Steinunn Gunnarsdottir; Magali Mouy; Valgerdur Steinthorsdottir; Gudrun H Eiriksdottir; Gyda Bjornsdottir; Inga Reynisdottir; Daniel Gudbjartsson; Anna Helgadottir; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Unnur Styrkarsdottir; Solveig Gretarsdottir; Kristinn P Magnusson; Hreinn Stefansson; Ragnheidur Fossdal; Kristleifur Kristjansson; Hjortur G Gislason; Tryggvi Stefansson; Bjorn G Leifsson; Unnur Thorsteinsdottir; John R Lamb; Jeffrey R Gulcher; Marc L Reitman; Augustine Kong; Eric E Schadt; Kari Stefansson
Journal:  Nature       Date:  2008-03-16       Impact factor: 49.962

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  21 in total

1.  Identification of miR-423 and miR-499 polymorphisms on affecting the risk of hepatocellular carcinoma in a large-scale population.

Authors:  Yanyun Ma; Rui Wang; Jun Zhang; Wenshuai Li; Chunfang Gao; Jie Liu; Jiucun Wang
Journal:  Genet Test Mol Biomarkers       Date:  2014-05-22

2.  The impact of cis-acting polymorphisms on the human phenotype.

Authors:  Bryony L Jones; Dallas M Swallow
Journal:  Hugo J       Date:  2011-07-20

3.  Allelic differences in nuclear protein binding at a genome-wide significant risk variant for schizophrenia in ZNF804A.

Authors:  M J Hill; N J Bray
Journal:  Mol Psychiatry       Date:  2011-03-01       Impact factor: 15.992

Review 4.  An integrative functional genomics approach for discovering biomarkers in schizophrenia.

Authors:  Marquis P Vawter; Firoza Mamdani; Fabio Macciardi
Journal:  Brief Funct Genomics       Date:  2011-12-08       Impact factor: 4.241

5.  Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex.

Authors:  Ilaria Guella; Adolfo Sequeira; Brandi Rollins; Ling Morgan; Richard M Myers; Stanley J Watson; Huda Akil; William E Bunney; Lynn E Delisi; William Byerley; Marquis P Vawter
Journal:  Schizophr Res       Date:  2013-12-07       Impact factor: 4.939

6.  Postnatal neurodevelopmental expression and glutamate-dependent regulation of the ZNF804A rodent homologue.

Authors:  Eric H Chang; Anne Kirtley; Toni-Shay S Chandon; Philip Borger; Sehba Husain-Krautter; Valerie Vingtdeux; Anil K Malhotra
Journal:  Schizophr Res       Date:  2015-07-08       Impact factor: 4.939

7.  Allelic imbalance associated with the schizophrenia risk SNP rs1344706 indicates a cis-acting variant in ZNF804A.

Authors:  Ilaria Guella; Marquis P Vawter
Journal:  Schizophr Res       Date:  2014-01-23       Impact factor: 4.939

Review 8.  SNPing cancer in the bud: microRNA and microRNA-target site polymorphisms as diagnostic and prognostic biomarkers in cancer.

Authors:  David W Salzman; Joanne B Weidhaas
Journal:  Pharmacol Ther       Date:  2012-09-03       Impact factor: 12.310

9.  Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain.

Authors:  Hywel J Williams; Valentina Moskvina; Rhodri L Smith; Sarah Dwyer; Giancarlo Russo; Michael J Owen; Michael C O'Donovan
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2011-08-02       Impact factor: 3.568

10.  Translating Genetic Risk Loci Into Molecular Risk Mechanisms for Schizophrenia.

Authors:  Nicholas J Bray; Matthew J Hill
Journal:  Schizophr Bull       Date:  2015-11-04       Impact factor: 9.306

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