Cited by 5,223Genomics and Chromatin DynamicsChromosomal and Genetic VariationsGenomics and Phylogenetic Studies

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

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The ENCODE Project Consortium·2007·Nature

Abstract

We report the generation and analysis of functional data from multiple, diverse experiments performed on a targeted 1% of the human genome as part of the pilot phase of the ENCODE Project. These data have been further integrated and augmented by a number of evolutionary and computational analyses. Together, our results advance the collective knowledge about human genome function in several major areas. First, our studies provide convincing evidence that the genome is pervasively transcribed, such that the majority of its bases can be found in primary transcripts, including non-protein-coding transcripts, and those that extensively overlap one another. Second, systematic examination of transcriptional regulation has yielded new understanding about transcription start sites, including their relationship to specific regulatory sequences and features of chromatin accessibility and histone modification. Third, a more sophisticated view of chromatin structure has emerged, including its inter-relationship with DNA replication and transcriptional regulation. Finally, integration of these new sources of information, in particular with respect to mammalian evolution based on inter- and intra-species sequence comparisons, has yielded new mechanistic and evolutionary insights concerning the functional landscape of the human genome. Together, these studies are defining a path for pursuit of a more comprehensive characterization of human genome function.

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  • Tet2-deficient HSPC exhibit similar characteristics to PU.1-deficient HSPC, namely the capacity to undergo accelerated expansion in the context of chronic inflammation, coupled with altered cell cycle activity.

    “Indeed, Tet2-deficient HSPC exhibit similar characteristics to PU.1-deficient HSPC, namely the capacity to undergo accelerated expansion in the context of chronic inflammation, coupled with altered cell cycle activity (Consortium et al., 2007; Caiado et al., 2022).”

    From PU.1 is required to restrain myelopoiesis during chronic inflammatory stress (2023) · cites this paper as Consortium et al., 2007

    The passages from “Regulation of transcription” concern genomic regulatory elements and transcription-factor binding, not Tet2- or PU.1-deficient HSPC. Searches for those cells, chronic inflammation, accelerated expansion, and altered cell-cycle activity found no passage addressing the claim. Page numbers were not available in our copy. (LLM, conf=0.76)

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References 202 · Cited by 5,223

Research works printed but not linked: 2

  1. UCSC Genome Browser Daryl J. Thomas 25,26 , Kate Rosenbloom 26 , Rachel A. Harte 26 , Angie S. Hinrichs 26 , Heather Trumbower 26 , Hiram Clawson 26 , Jennifer Hillman-Jackson 26 , Ann S. Zweig 26 , Kayla Smith 26 , Archana Thakkapallayil 26 , Galt Barber 26 , Robert M. Kuhn 26 , Donna Karolchik 26 , David Haussler 25,26,60 & W. James Kent 25,26 NATURE | Vol 447 | 14 June 2007 Nature ©2007 Publishing Group Variation Emmanouil T. Dermitzakis 12 , Lluis Armengol 76 , Christine P. Bird 12 , Taane G. Clark 38 , Gregory M. Cooper 33 {, Paul I. W. de Bakker 77 , Andrew D. Kern 26 , Nuria Lopez-Bigas 5 , Joel D. Martin 50,59 , Barbara E. Stranger 12 , Daryl J. Thomas 25,26 , Abigail Woodroffe 78 , Serafim Batzoglou 53 , Eugene Davydov 53 , Antigone Dimas 12 , Eduardo Eyras 5 , Ingileif B. Hallgrı ´msdo ´ttir 79 , Ross C. Hardison 50,59 , Julian Huppert 12 , Arend Sidow 33,62 , James Taylor 49,50 , Heather Trumbower 26 , Michael C. Zody 77 , Roderic Guigo ´4,5 , James C. Mullikin 7 , Gonc ¸alo R. Abecasis 78 , Xavier Estivill 76,80 & Ewan Birney 1 . *NISC Comparative Sequencing Program Gerard G. Bouffard 7,48 , Xiaobin Guan 48 , Nancy F. Hansen 48 , Jacquelyn R. Idol 7 , Valerie V.B. Maduro 7 , Baishali Maskeri 48 , Jennifer C. McDowell 48 , Morgan Park 48 , Pamela J. Thomas 48 , Alice C. Young 48 & Robert W. Blakesley 7,48 Baylor College of Medicine, Human Genome Sequencing Center Donna M. Muzny 63 , Erica Sodergren 63 , David A. Wheeler 63 , Kim C. Worley 63 , Huaiyang Jiang 63 , George M. Weinstock 63 & Richard A. Gibbs 63 ; Washington University Genome Sequencing Center Tina Graves 64 , Robert Fulton 64 , Elaine R. Mardis 64 & Richard K. Wilson 64 Broad Institute Michele Clamp 65 , James Cuff 65 , Sante Gnerre 65 , David B. Jaffe 65 , Jean L. Chang 65 , Kerstin Lindblad-Toh 65 & Eric S. Lander 65,66 Children's Hospital Oakland Research Institute Maxim Koriabine 67 , Mikhail Nefedov 67 , Kazutoyo Osoegawa 67 , Yuko Yoshinaga 67 , Baoli Zhu 67 & Pieter J. de Jong 67 Affiliations for participants: 1 EMBL-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD, UK. 2 Department of Genome Sciences, 1705 NE Pacific Street, Box 357730, University of Washington, Seattle, Washington 98195, USA.
  2. Charles Street, Cambridge, Massachusetts 02141, USA. 66 Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, Massachusetts 02142, USA.

Authors
The ENCODE Project Consortium
Venue
Nature
Published
2007-06
Volume
447
Issue
7146
Pages
799-816
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2102304447
Cited by
5,223
References
202
Citations by year
2026: 35 · 2025: 71 · 2024: 110 · 2023: 142 · 2022: 149 · 2021: 202 · 2020: 232 · 2019: 203 · 2018: 246 · 2017: 236 · 2016: 233 · 2015: 296 · 2014: 309 · 2013: 376 · 2012: 460
FWCI
191.07
Type
journal article
Language
en
Open access
Locations
  • Nature (publishedVersion)
  • PubMed (publishedVersion)
  • Research at the University of Copenhagen (University of Copenhagen) (publishedVersion)
  • Archive ouverte UNIGE (University of Geneva) (publishedVersion, other-oa)
  • PubMed Central (acceptedVersion)
  • Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
  • RECERCAT (Consorci de Serveis Universitaris de Catalunya) (acceptedVersion, other-oa)
  • CaltechAUTHORS (California Institute of Technology) (submittedVersion)
  • eScholarship@UMassChan (submittedVersion)
  • The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
  • UCL Discovery (University College London) (submittedVersion)
  • Publikationsdatenbank der Fraunhofer-Gesellschaft (Fraunhofer-Gesellschaft) (submittedVersion)
  • IRIS (submittedVersion)
  • Research Portal (King's College London) (submittedVersion)
  • ANU Open Research (Australian National University) (submittedVersion)
  • Fraunhofer-Publica (Fraunhofer-Gesellschaft) (submittedVersion)
  • Research Explorer (The University of Manchester) (submittedVersion)
  • LSHTM Research Online (London School of Hygiene and Tropical Medicine) (submittedVersion)
  • SERVAL (Université de Lausanne) (submittedVersion)
  • Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
Funders
  • National Science Foundation
  • Howard Hughes Medical Institute
  • Wellcome Trust (062023, 077198)
  • European Molecular Biology Laboratory
  • European Commission
  • Deutsche Forschungsgemeinschaft
  • Ministry of Education, Culture, Sports, Science and Technology
  • Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
  • Generalitat de Catalunya
  • Knut och Alice Wallenbergs Stiftelse
  • Vetenskapsrådet
  • Barcelona Supercomputing Center
  • National Institutes of Health
  • Biotechnology and Biological Sciences Research Council
  • RIKEN
  • National Human Genome Research Institute (R01HG003532, U01HG003157, U54HG003067, R01HG003110, U01HG003156, U54HG003079, R01HG003541, U54HG003273, U01HG002523, K22HG003169, U01HG003151, U01HG003162, R01HG003129, U01HG003147, P41HG002371, R01HG003521, U01HG003168, U01HG003150, U01HG003161, R01HG002238, R01HG003143)
  • National Cancer Institute (F32CA108313)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
Keywords
ENCODE, functional elements, pervasive transcription, transcription start sites, transcriptional regulation, chromatin accessibility, histone modifications, chromatin structure, DNA replication, mammalian evolution, sequence comparison
MeSH terms
Chromatin, DNA Replication, Exons, Heterozygote, Histones, Humans, Pilot Projects, Protein Binding, Regulatory Sequences, Nucleic Acid, RNA, Messenger, Transcription Factors, Transcription, Genetic, Genetic Variation, Genome, Human, Conserved Sequence, Evolution, Molecular, RNA, Untranslated, Genomics, Transcription Initiation Site, Chromatin Immunoprecipitation

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