Human Molecular Genetics Advance Access published online on July 14, 2004
Human Molecular Genetics, doi:10.1093/hmg/ddh207
© 2004 by Oxford University Press
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Institute of Medical Genetics, Charité University Hospital, Humboldt University, Augustenburger Platz 1, 13353 Berlin, Germany
* To whom correspondence should be addressed. E-mail: peter.robinson{at}charite.de.
A key open question in the understanding of the biology of DNA methylation relates to the origin and function of CpG islands, stretches of GC-rich and relatively CpG rich DNA sequence that often colocalize with promoter regions. All housekeeping but also a substantial minority of tissue-specific genes are associated with CpG islands. Limited experimental evidence suggests that CpG islands are associated with promoters or replication origins active during early development. While this hypothesis is attractive for widely expressed genes, which would be expected to be expressed during early development, many tissue-specific genes also contain CpG islands. In this work we used a genome-wide Gene-Ontology (GO)-based approach to analyze associations between GO terms and the presence of 5' CpG islands in human RefSeq genes. We found that 19 of the 3849 GO terms with at least one annotated human sequence showed a highly significant association with the likelihood of 5' CpG islands being present in genes annotated to that term. In particular, the term development showed a highly significantly increased proportion of 5' CpG island genes. The overrepresentation of 5' CpG island genes was even more significant for tissue-specific RefSeqs annotated to development as well as many of its descendent terms. In addition, the proportion of ESTs from embryonic libraries amongst tissue-specific genes was twice as high for RefSeqs with 5' CpG islands as for those without CpG islands. These results provide strong support for previous speculations that early embryonic expression is associated with CpG islands.
Article
Gene-ontology analysis reveals association of tissue-specific 5' CpG-island genes with development and embryogenesis
2 Institute of Medical Genetics, Charité University Hospital, Augustenburger Platz 1, 13353 Berlin, Germany
3 EBI-Hinxton, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, United Kingdom
4 Institute of Medical Genetics, Charité University Hospital, Augustenburger Platz 1, 13353 Berlin, Germany; Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany
5 Institute of Medical Genetics, Charité University Hospital, Augustenburger Platz 1, 13353 Berlin, Germany; Gene Mapping Center and Department of Molecular Genetics, Max Delbrück Center, Robert-Rössle-Str. 10, 13092 Berlin-Buch, Germany
![]()
Abstract ![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
Y. Kotliarov, S. Kotliarova, N. Charong, A. Li, J. Walling, E. Aquilanti, S. Ahn, M. E. Steed, Q. Su, A. Center, et al. Correlation Analysis between Single-Nucleotide Polymorphism and Expression Arrays in Gliomas Identifies Potentially Relevant Target Genes Cancer Res., February 15, 2009; 69(4): 1596 - 1603. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Vardhanabhuti, J. Wang, and S. Hannenhalli Position and distance specificity are important determinants of cis-regulatory motifs in addition to evolutionary conservation Nucleic Acids Res., May 11, 2007; 35(10): 3203 - 3213. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Saxonov, P. Berg, and D. L. Brutlag A genome-wide analysis of CpG dinucleotides in the human genome distinguishes two distinct classes of promoters PNAS, January 31, 2006; 103(5): 1412 - 1417. [Abstract] [Full Text] [PDF] |
||||


