Literature DB >> 23205161

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

Bryony L Jones1, Dallas M Swallow.   

Abstract

Cis-acting polymorphisms that affect gene expression are now known to be frequent, although the extent and mechanisms by which such variation affects the human phenotype are, as yet, only poorly understood. Key signatures of cis-acting variation are differences in gene expression that are tightly associated with regulatory SNPs or expression Quantitative Trait Loci (eQTL) and an imbalance of allelic expression (AEI) in heterozygous samples. Such cis-acting sequence differences appear often to have been under selection within and between populations and are also thought to be important in speciation. Here we describe the example of lactase persistence. In medical research, variants that affect regulation in cis have been implicated in both monogenic and polygenic disorders, and in the metabolism of drugs. In this review we suggest that by further understanding common regulatory variations and how they interact with other genetic and environmental variables it will be possible to gain insight into important mechanisms behind complex disease, with the potential to lead to new methods of diagnosis and treatments.

Entities:  

Keywords:  Allelic expression; Cis-acting polymorphism; Gene expression; Phenotypic variability; Regulation; Soft selective sweeps

Year:  2011        PMID: 23205161      PMCID: PMC3238023          DOI: 10.1007/s11568-011-9155-4

Source DB:  PubMed          Journal:  Hugo J        ISSN: 1877-6558


  106 in total

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Authors:  G D Stormo
Journal:  Bioinformatics       Date:  2000-01       Impact factor: 6.937

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Authors:  Gregory A Wray
Journal:  Nat Rev Genet       Date:  2007-03       Impact factor: 53.242

Review 3.  Regulatory polymorphisms and their contribution to interindividual differences in the expression of enzymes influencing drug and toxicant disposition.

Authors:  Ronald N Hines; Sevasti B Koukouritaki; Mark T Poch; Michael C Stephens
Journal:  Drug Metab Rev       Date:  2008       Impact factor: 4.518

4.  T-13910 DNA variant associated with lactase persistence interacts with Oct-1 and stimulates lactase promoter activity in vitro.

Authors:  Rikke H Lewinsky; Tine G K Jensen; Jette Møller; Allan Stensballe; Jørgen Olsen; Jesper T Troelsen
Journal:  Hum Mol Genet       Date:  2005-11-21       Impact factor: 6.150

5.  Cooperative influence of genetic polymorphisms on interleukin 6 transcriptional regulation.

Authors:  C F Terry; V Loukaci; F R Green
Journal:  J Biol Chem       Date:  2000-06-16       Impact factor: 5.157

6.  The hitch-hiking effect of a favourable gene.

Authors:  J M Smith; J Haigh
Journal:  Genet Res       Date:  1974-02       Impact factor: 1.588

7.  Chance caught on the wing: cis-regulatory evolution and the origin of pigment patterns in Drosophila.

Authors:  Nicolas Gompel; Benjamin Prud'homme; Patricia J Wittkopp; Victoria A Kassner; Sean B Carroll
Journal:  Nature       Date:  2005-02-03       Impact factor: 49.962

8.  The lactase persistence/non-persistence polymorphism is controlled by a cis-acting element.

Authors:  Y Wang; C B Harvey; W S Pratt; V R Sams; M Sarner; M Rossi; S Auricchio; D M Swallow
Journal:  Hum Mol Genet       Date:  1995-04       Impact factor: 6.150

9.  The T allele of a single-nucleotide polymorphism 13.9 kb upstream of the lactase gene (LCT) (C-13.9kbT) does not predict or cause the lactase-persistence phenotype in Africans.

Authors:  Charlotte A Mulcare; Michael E Weale; Abigail L Jones; Bruce Connell; David Zeitlyn; Ayele Tarekegn; Dallas M Swallow; Neil Bradman; Mark G Thomas
Journal:  Am J Hum Genet       Date:  2004-04-20       Impact factor: 11.025

Review 10.  RNA-Seq: a revolutionary tool for transcriptomics.

Authors:  Zhong Wang; Mark Gerstein; Michael Snyder
Journal:  Nat Rev Genet       Date:  2009-01       Impact factor: 53.242

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  10 in total

1.  Diversity of lactase persistence alleles in Ethiopia: signature of a soft selective sweep.

Authors:  Bryony L Jones; Tamiru O Raga; Anke Liebert; Pawel Zmarz; Endashaw Bekele; E Thomas Danielsen; Anders Krüger Olsen; Neil Bradman; Jesper T Troelsen; Dallas M Swallow
Journal:  Am J Hum Genet       Date:  2013-08-29       Impact factor: 11.025

2.  Refinement in localization and identification of gene regions associated with Crohn disease.

Authors:  Heather Elding; Winston Lau; Dallas M Swallow; Nikolas Maniatis
Journal:  Am J Hum Genet       Date:  2012-12-13       Impact factor: 11.025

3.  Cervical cancer-associated promoter polymorphism affects akna expression levels.

Authors:  G A Martínez-Nava; K Torres-Poveda; A Lagunas-Martínez; M Bahena-Román; M A Zurita-Díaz; E Ortíz-Flores; A García-Carrancá; V Madrid-Marina; A I Burguete-García
Journal:  Genes Immun       Date:  2014-11-06       Impact factor: 2.676

4.  Heterozygosity for the common perforin mutation, p.A91V, impairs the cytotoxicity of primary natural killer cells from healthy individuals.

Authors:  Imran G House; Kevin Thia; Amelia J Brennan; Richard Tothill; Alexander Dobrovic; Wei Z Yeh; Richard Saffery; Zac Chatterton; Joseph A Trapani; Ilia Voskoboinik
Journal:  Immunol Cell Biol       Date:  2015-03-17       Impact factor: 5.126

5.  A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.

Authors:  Damian Smedley; Max Schubach; Julius O B Jacobsen; Sebastian Köhler; Tomasz Zemojtel; Malte Spielmann; Marten Jäger; Harry Hochheiser; Nicole L Washington; Julie A McMurry; Melissa A Haendel; Christopher J Mungall; Suzanna E Lewis; Tudor Groza; Giorgio Valentini; Peter N Robinson
Journal:  Am J Hum Genet       Date:  2016-08-25       Impact factor: 11.025

6.  Latitude, sunshine, and human lactase phenotype distributions may contribute to geographic patterns of modern disease: the inflammatory bowel disease model.

Authors:  Andrew Szilagyi; Henry Leighton; Barry Burstein; Xiaoqing Xue
Journal:  Clin Epidemiol       Date:  2014-05-27       Impact factor: 4.790

7.  The Importance of Lactose in the Human Diet: Outcomes of a Mexican Consensus Meeting.

Authors:  Enrique Romero-Velarde; Dagoberto Delgado-Franco; Mariana García-Gutiérrez; Carmen Gurrola-Díaz; Alfredo Larrosa-Haro; Ericka Montijo-Barrios; Frits A J Muskiet; Belinda Vargas-Guerrero; Jan Geurts
Journal:  Nutrients       Date:  2019-11-12       Impact factor: 5.717

8.  Mapping the genetic architecture of gene regulation in whole blood.

Authors:  Katharina Schramm; Carola Marzi; Claudia Schurmann; Maren Carstensen; Eva Reinmaa; Reiner Biffar; Gertrud Eckstein; Christian Gieger; Hans-Jörgen Grabe; Georg Homuth; Gabriele Kastenmüller; Reedik Mägi; Andres Metspalu; Evelin Mihailov; Annette Peters; Astrid Petersmann; Michael Roden; Konstantin Strauch; Karsten Suhre; Alexander Teumer; Uwe Völker; Henry Völzke; Rui Wang-Sattler; Melanie Waldenberger; Thomas Meitinger; Thomas Illig; Christian Herder; Harald Grallert; Holger Prokisch
Journal:  PLoS One       Date:  2014-04-16       Impact factor: 3.240

9.  An intronic PICALM polymorphism, rs588076, is associated with allelic expression of a PICALM isoform.

Authors:  Ishita Parikh; Christopher Medway; Steven Younkin; David W Fardo; Steven Estus
Journal:  Mol Neurodegener       Date:  2014-08-29       Impact factor: 18.879

10.  The polymorphism rs6918289 located in the downstream region of the TREM2 gene is associated with TNF-α levels and IMT-F.

Authors:  Vesna Gorenjak; Alex-Ander Aldasoro Arguinano; Sébastien Dadé; Maria G Stathopoulou; Dwaine R Vance; Christine Masson; Sophie Visvikis-Siest
Journal:  Sci Rep       Date:  2018-05-08       Impact factor: 4.379

  10 in total

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