Literature DB >> 11454739

Species-specific organization of CpG island promoters at mammalian homologous genes.

M Cuadrado1, M Sacristán, F Antequera.   

Abstract

An essential issue derived from the sequencing of the human and other genomes is the identification of gene regulatory elements. Using in vivo footprinting and expression analysis, here we show that mouse and human CpG island promoters at homologous genes have a completely different organization in terms of size and binding of transcription factors. Despite these species-specific differences, a unifying picture emerges from the precise confinement of protein--DNA interactions between the 5' boundary of the CpG islands and the transcription initiation site. This finding allows direct localization of promoters on genomic sequences and reveals a very high rate of variation and evolutionary divergence of mammalian regulatory regions. Our results also show that CpG island promoters associated with tissue-specific genes, such as the human alpha-globin, are bound by ubiquitous factors that allow a constitutive low level of expression in many cell types.

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Year:  2001        PMID: 11454739      PMCID: PMC1083945          DOI: 10.1093/embo-reports/kve131

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  31 in total

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Authors:  F Antequera; A Bird
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Journal:  Nature       Date:  2000-02-03       Impact factor: 49.962

3.  Identification and analysis of eukaryotic promoters: recent computational approaches.

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Journal:  Nature       Date:  2001-02-15       Impact factor: 49.962

Review 5.  Endless forms: the evolution of gene regulation and morphological diversity.

Authors:  S B Carroll
Journal:  Cell       Date:  2000-06-09       Impact factor: 41.582

Review 6.  Evolution of transcriptional regulation.

Authors:  D Tautz
Journal:  Curr Opin Genet Dev       Date:  2000-10       Impact factor: 5.578

Review 7.  CpG-rich islands and the function of DNA methylation.

Authors:  A P Bird
Journal:  Nature       Date:  1986 May 15-21       Impact factor: 49.962

8.  In vivo structure of two divergent promoters at the human PCNA locus. Synthesis of antisense RNA and S phase-dependent binding of E2F complexes in intron 1.

Authors:  S Tommasi; G P Pfeifer
Journal:  J Biol Chem       Date:  1999-09-24       Impact factor: 5.157

9.  Human-mouse genome comparisons to locate regulatory sites.

Authors:  W W Wasserman; M Palumbo; W Thompson; J W Fickett; C E Lawrence
Journal:  Nat Genet       Date:  2000-10       Impact factor: 38.330

10.  The sequence of the human genome.

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Journal:  Science       Date:  2001-02-16       Impact factor: 47.728

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  13 in total

1.  CpG island chromatin: a platform for gene regulation.

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Review 2.  CpG islands and the regulation of transcription.

Authors:  Aimée M Deaton; Adrian Bird
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3.  Identification of a promoter for the human C1Q-tumor necrosis factor-related protein-5 gene associated with late-onset retinal degeneration.

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4.  Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes.

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5.  RNA interference rescue by bacterial artificial chromosome transgenesis in mammalian tissue culture cells.

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-02-03       Impact factor: 11.205

6.  Orphan CpG islands identify numerous conserved promoters in the mammalian genome.

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7.  Functional dissection of the mouse tyrosinase locus control region identifies a new putative boundary activity.

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8.  A downstream CpG island controls transcript initiation and elongation and the methylation state of the imprinted Airn macro ncRNA promoter.

Authors:  Martha V Koerner; Florian M Pauler; Quanah J Hudson; Federica Santoro; Anna Sawicka; Philipp M Guenzl; Stefan H Stricker; Yvonne M Schichl; Paulina A Latos; Ruth M Klement; Katarzyna E Warczok; Jacek Wojciechowski; Christian Seiser; Robert Kralovics; Denise P Barlow
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9.  DNA methylation immediately adjacent to active histone marking does not silence transcription.

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10.  Benchmarking tools for the alignment of functional noncoding DNA.

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