Defining functional DNA elements in the human genome.

Journal Article (Journal Article;Review)

With the completion of the human genome sequence, attention turned to identifying and annotating its functional DNA elements. As a complement to genetic and comparative genomics approaches, the Encyclopedia of DNA Elements Project was launched to contribute maps of RNA transcripts, transcriptional regulator binding sites, and chromatin states in many cell types. The resulting genome-wide data reveal sites of biochemical activity with high positional resolution and cell type specificity that facilitate studies of gene regulation and interpretation of noncoding variants associated with human disease. However, the biochemically active regions cover a much larger fraction of the genome than do evolutionarily conserved regions, raising the question of whether nonconserved but biochemically active regions are truly functional. Here, we review the strengths and limitations of biochemical, evolutionary, and genetic approaches for defining functional DNA segments, potential sources for the observed differences in estimated genomic coverage, and the biological implications of these discrepancies. We also analyze the relationship between signal intensity, genomic coverage, and evolutionary conservation. Our results reinforce the principle that each approach provides complementary information and that we need to use combinations of all three to elucidate genome function in human biology and disease.

Full Text

Duke Authors

Cited Authors

  • Kellis, M; Wold, B; Snyder, MP; Bernstein, BE; Kundaje, A; Marinov, GK; Ward, LD; Birney, E; Crawford, GE; Dekker, J; Dunham, I; Elnitski, LL; Farnham, PJ; Feingold, EA; Gerstein, M; Giddings, MC; Gilbert, DM; Gingeras, TR; Green, ED; Guigo, R; Hubbard, T; Kent, J; Lieb, JD; Myers, RM; Pazin, MJ; Ren, B; Stamatoyannopoulos, JA; Weng, Z; White, KP; Hardison, RC

Published Date

  • April 29, 2014

Published In

Volume / Issue

  • 111 / 17

Start / End Page

  • 6131 - 6138

PubMed ID

  • 24753594

Pubmed Central ID

  • PMC4035993

Electronic International Standard Serial Number (EISSN)

  • 1091-6490

Digital Object Identifier (DOI)

  • 10.1073/pnas.1318948111


  • eng

Conference Location

  • United States