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Comparative Study
. 2001 Nov;11(11):1854-60.
doi: 10.1101/gr.174501.

Determinants of CpG islands: expression in early embryo and isochore structure

Affiliations
Comparative Study

Determinants of CpG islands: expression in early embryo and isochore structure

L Ponger et al. Genome Res. 2001 Nov.

Abstract

In an attempt to understand the origin of CpG islands (CGIs) in mammalian genomes, we have studied their location and structure according to the expression pattern of genes and to the G + C content of isochores in which they are embedded. We show that CGIs located over the transcription start site (named start CGIs) are very different structurally from the others (named no-start CGIs): (1) 61.6% of the no-start CGIs are due to repeated sequences (79 % are due to Alus), whereas only 5.6% of the start CGIs are due to such repeats; (2) start CGIs are longer and display a higher CpGo/e ratio and G + C level than no-start CGIs. The frequency of tissue-specific genes associated to a start CGI varies according to the genomic G + C content, from 25% in G + C-poor isochores to 64% in G + C-rich isochores. Conversely, the frequency of housekeeping genes associated to a start CGI (90%) is independent of the isochore context. Interestingly, the structure of start CGIs is very similar for tissue-specific and housekeeping genes. Moreover, 93% of genes expressed in early embryo are found to exhibit a CpG island over their transcription start point. These observations are consistent with the hypothesis that the occurrence of these CGIs is the consequence of gene expression at this stage, when the methylation pattern is installed.

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Figures

Figure 1
Figure 1
The length, the CpGo/e ratio, and the (G + C) frequency of start CGIs according to the tissue breadth of expression and the isochore classes of the associated genes. (○) 0–1 tissue; (▪) 2–5 tissues; (▴) 6–16 tissues; (♦) 17–24 tissues. Error bars, SE. n = 373.
Figure 2
Figure 2
The length, the CpGo/e ratio, and the (G + C) frequency of the different types of CGIs, start CGIs (n = 373), no-start CGIs (n = 565), and repeat-CGIs (n = 908). (○) Repeat CGIs; (▪) no-start CGIs; (▴); start CGIs. Error bars, SE.
Figure 3
Figure 3
Frequency of genes with a start CGI according to their tissue breadth of expression and the isochore G + C content. n = 864 genes. (○) 0–1 tissue; (▪) 2–5 tissues; (▴) 6–16 tissues; (♦) 17–24 tissues.

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References

    1. Aissani B, Bernardi G. CpG islands, genes and isochores in the genomes of vertebrates. Gene. 1991;106:185–195. - PubMed
    1. Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acids Res. 1997;25:3389–3402. - PMC - PubMed
    1. Antequera F, Bird A. Number of CpG islands and genes in human and mouse. Proc Natl Acad Sci. 1993;90:11995–11999. - PMC - PubMed
    1. ————— CpG islands as genomic footprints of promoters that are associated with replication origins. Curr Biol. 1999;9:661–667. - PubMed
    1. Antequera F, Boyes J, Bird A. High levels of de novo methylation and altered chromatin structure at CpG islands in cell lines. Cell. 1990;62:503–514. - PubMed

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