Literature DB >> 19270705

Segmental copy number variation shapes tissue transcriptomes.

Charlotte N Henrichsen1, Nicolas Vinckenbosch, Sebastian Zöllner, Evelyne Chaignat, Sylvain Pradervand, Frédéric Schütz, Manuel Ruedi, Henrik Kaessmann, Alexandre Reymond.   

Abstract

Copy number variation (CNV) is a key source of genetic diversity, but a comprehensive understanding of its phenotypic effect is only beginning to emerge. We have generated a CNV map in wild mice and classical inbred strains. Genome-wide expression data from six major organs show not only that expression of genes within CNVs tend to correlate with copy number changes, but also that CNVs influence the expression of genes in their vicinity, an effect that extends up to half a megabase. Genes within CNVs show lower expression and more specific spatial expression patterns than genes mapping elsewhere. Our analyses reveal differential constraint on copy number changes of genes expressed in different tissues. Dosage alterations of brain-expressed genes are less frequent than those of other genes and are buffered by tighter transcriptional regulation. Our study provides initial evidence that CNVs shape tissue transcriptomes on a global scale.

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Year:  2009        PMID: 19270705     DOI: 10.1038/ng.345

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  36 in total

1.  Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect.

Authors:  Jennifer A Lee; Ricardo E Madrid; Karen Sperle; Carolyn M Ritterson; Grace M Hobson; James Garbern; James R Lupski; Ken Inoue
Journal:  Ann Neurol       Date:  2006-02       Impact factor: 10.422

Review 2.  Side effects of genome structural changes.

Authors:  Alexandre Reymond; Charlotte N Henrichsen; Louise Harewood; Giuseppe Merla
Journal:  Curr Opin Genet Dev       Date:  2007-10-24       Impact factor: 5.578

3.  Completing the map of human genetic variation.

Authors:  Evan E Eichler; Deborah A Nickerson; David Altshuler; Anne M Bowcock; Lisa D Brooks; Nigel P Carter; Deanna M Church; Adam Felsenfeld; Mark Guyer; Charles Lee; James R Lupski; James C Mullikin; Jonathan K Pritchard; Jonathan Sebat; Stephen T Sherry; Douglas Smith; David Valle; Robert H Waterston
Journal:  Nature       Date:  2007-05-10       Impact factor: 49.962

4.  Significant gene content variation characterizes the genomes of inbred mouse strains.

Authors:  Gene Cutler; Lisa A Marshall; Ni Chin; Helene Baribault; Paul D Kassner
Journal:  Genome Res       Date:  2007-11-07       Impact factor: 9.043

5.  Genomic segmental polymorphisms in inbred mouse strains.

Authors:  Jiangzhen Li; Tao Jiang; Jian-Hua Mao; Allan Balmain; Leif Peterson; Charles Harris; Pulivarthi H Rao; Paul Havlak; Richard Gibbs; Wei-Wen Cai
Journal:  Nat Genet       Date:  2004-08-22       Impact factor: 38.330

6.  Diet and the evolution of human amylase gene copy number variation.

Authors:  George H Perry; Nathaniel J Dominy; Katrina G Claw; Arthur S Lee; Heike Fiegler; Richard Redon; John Werner; Fernando A Villanea; Joanna L Mountain; Rajeev Misra; Nigel P Carter; Charles Lee; Anne C Stone
Journal:  Nat Genet       Date:  2007-09-09       Impact factor: 38.330

Review 7.  Nuclear organization of the genome and the potential for gene regulation.

Authors:  Peter Fraser; Wendy Bickmore
Journal:  Nature       Date:  2007-05-24       Impact factor: 49.962

Review 8.  Position effect in human genetic disease.

Authors:  D J Kleinjan; V van Heyningen
Journal:  Hum Mol Genet       Date:  1998       Impact factor: 6.150

Review 9.  Long-range control of gene expression: emerging mechanisms and disruption in disease.

Authors:  Dirk A Kleinjan; Veronica van Heyningen
Journal:  Am J Hum Genet       Date:  2004-11-17       Impact factor: 11.025

10.  Mapping and sequencing of structural variation from eight human genomes.

Authors:  Jeffrey M Kidd; Gregory M Cooper; William F Donahue; Hillary S Hayden; Nick Sampas; Tina Graves; Nancy Hansen; Brian Teague; Can Alkan; Francesca Antonacci; Eric Haugen; Troy Zerr; N Alice Yamada; Peter Tsang; Tera L Newman; Eray Tüzün; Ze Cheng; Heather M Ebling; Nadeem Tusneem; Robert David; Will Gillett; Karen A Phelps; Molly Weaver; David Saranga; Adrianne Brand; Wei Tao; Erik Gustafson; Kevin McKernan; Lin Chen; Maika Malig; Joshua D Smith; Joshua M Korn; Steven A McCarroll; David A Altshuler; Daniel A Peiffer; Michael Dorschner; John Stamatoyannopoulos; David Schwartz; Deborah A Nickerson; James C Mullikin; Richard K Wilson; Laurakay Bruhn; Maynard V Olson; Rajinder Kaul; Douglas R Smith; Evan E Eichler
Journal:  Nature       Date:  2008-05-01       Impact factor: 49.962

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  158 in total

1.  Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

Authors:  Rui Luo; Stephan J Sanders; Yuan Tian; Irina Voineagu; Ni Huang; Su H Chu; Lambertus Klei; Chaochao Cai; Jing Ou; Jennifer K Lowe; Matthew E Hurles; Bernie Devlin; Matthew W State; Daniel H Geschwind
Journal:  Am J Hum Genet       Date:  2012-06-21       Impact factor: 11.025

Review 2.  Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

Authors:  Anne S Bassett; Stephen W Scherer; Linda M Brzustowicz
Journal:  Am J Psychiatry       Date:  2010-05-03       Impact factor: 18.112

Review 3.  Genome-wide approaches to schizophrenia.

Authors:  Jubao Duan; Alan R Sanders; Pablo V Gejman
Journal:  Brain Res Bull       Date:  2010-04-28       Impact factor: 4.077

4.  Copy number variation modifies expression time courses.

Authors:  Evelyne Chaignat; Emilie Aït Yahya-Graison; Charlotte N Henrichsen; Jacqueline Chrast; Frédéric Schütz; Sylvain Pradervand; Alexandre Reymond
Journal:  Genome Res       Date:  2010-11-17       Impact factor: 9.043

5.  CopyMap: localization and calling of copy number variation by joint analysis of hybridization data from multiple individuals.

Authors:  Sebastian Zöllner
Journal:  Bioinformatics       Date:  2010-10-05       Impact factor: 6.937

6.  Construction and phenotypic analysis of mice carrying a duplication of the major histocompatibility class I (MHC-I) locus.

Authors:  Olga Ermakova; Ekaterina Salimova; Lukasz Piszczek; Cornelius Gross
Journal:  Mamm Genome       Date:  2012-07-07       Impact factor: 2.957

7.  Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency.

Authors:  Janine Meienberg; Marianne Rohrbach; Stefan Neuenschwander; Katharina Spanaus; Cecilia Giunta; Sira Alonso; Eliane Arnold; Caroline Henggeler; Stephan Regenass; Andrea Patrignani; Silvia Azzarello-Burri; Bernhard Steiner; Anders O H Nygren; Thierry Carrel; Beat Steinmann; Gábor Mátyás
Journal:  Eur J Hum Genet       Date:  2010-07-21       Impact factor: 4.246

Review 8.  Evolutionary impact of transposable elements on genomic diversity and lineage-specific innovation in vertebrates.

Authors:  Ian A Warren; Magali Naville; Domitille Chalopin; Perrine Levin; Chloé Suzanne Berger; Delphine Galiana; Jean-Nicolas Volff
Journal:  Chromosome Res       Date:  2015-09       Impact factor: 5.239

9.  The Mouse Universal Genotyping Array: From Substrains to Subspecies.

Authors:  Andrew P Morgan; Chen-Ping Fu; Chia-Yu Kao; Catherine E Welsh; John P Didion; Liran Yadgary; Leeanna Hyacinth; Martin T Ferris; Timothy A Bell; Darla R Miller; Paola Giusti-Rodriguez; Randal J Nonneman; Kevin D Cook; Jason K Whitmire; Lisa E Gralinski; Mark Keller; Alan D Attie; Gary A Churchill; Petko Petkov; Patrick F Sullivan; Jennifer R Brennan; Leonard McMillan; Fernando Pardo-Manuel de Villena
Journal:  G3 (Bethesda)       Date:  2015-12-18       Impact factor: 3.154

10.  Loss of GSTM1, a NRF2 target, is associated with accelerated progression of hypertensive kidney disease in the African American Study of Kidney Disease (AASK).

Authors:  Jamison Chang; Jennie Z Ma; Qing Zeng; Sylvia Cechova; Adam Gantz; Caroline Nievergelt; Daniel O'Connor; Michael Lipkowitz; Thu H Le
Journal:  Am J Physiol Renal Physiol       Date:  2012-12-05
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