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Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competition

  • Karen M. Lower
  • , Jim R. Hughes
  • , Marco De Gobbi
  • , Shirley Henderson
  • , Vip Viprakasit
  • , Chris Fisher
  • , Anne Goriely
  • , Helena Ayyub
  • , Jackie Sloane-Stanley
  • , Douglas Vernimmen
  • , Cordelia Langford
  • , David Garrick
  • , Richard J. Gibbons
  • , Douglas R. Higgs
  • John Radcliffe Hospital
  • Oxford University Hospitals NHS Foundation Trust
  • Wellcome Trust Sanger Institute

Research output: Contribution to journalArticlepeer-review

80 Citations (Scopus)

Abstract

It is well established that all of the cis-acting sequences required for fully regulated human α-globin expression are contained within a region of ≈120 kb of conserved synteny. Here, we show that activation of this cluster in erythroid cells dramatically affects expression of apparently unrelated and noncontiguous genes in the 500 kb surrounding this domain, including a gene (NME4) located 300 kb from the α-globin cluster. Changes in NME4 expression are mediated by physical cis-interactions between this gene and the α-globin regulatory elements. Polymorphic structural variation within the globin cluster, altering the number of α-globin genes, affects the pattern of NME4 expression by altering the competition for the shared α-globin regulatory elements. These findings challenge the concept that the genome is organized into discrete, insulated regulatory domains. In addition, this work has important implications for our understanding of genome evolution, the interpretation of genome-wide expression, expression-quantitative trait loci, and copy number variant analyses.

Original languageEnglish
Pages (from-to)21771-21776
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume106
Issue number51
DOIs
Publication statusPublished - 22 Dec 2009

Keywords

  • 4C
  • Allele-specific expression
  • Chromosome looping
  • Copy number variants
  • Globin gene expression

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