Comprehensive analysis of CpG islands in human chromosomes 21 and 22

<jats:p> CpG islands are useful markers for genes in organisms containing 5-methylcytosine in their genomes. In addition, CpG islands located in the promoter regions of genes can play important roles in gene silencing during processes such as X-chromosome inactivation, imprinting, and silencing of intragenomic parasites. The generally accepted definition of what constitutes a CpG island was proposed in 1987 by Gardiner-Garden and Frommer [Gardiner-Garden, M. & Frommer, M. (1987) <jats:italic>J. Mol. Biol.</jats:italic> 196, 261–282] as being a 200-bp stretch of DNA with a C+G content of 50% and an observed CpG/expected CpG in excess of 0.6. Any definition of a CpG island is somewhat arbitrary, and this one, which was derived before the sequencing of mammalian genomes, will include many sequences that are not necessarily associated with controlling regions of genes but rather are associated with intragenomic parasites. We have therefore used the complete genomic sequences of human chromosomes 21 and 22 to examine the properties of CpG islands in different sequence classes by using a search algorithm that we have developed. Regions of DNA of greater than 500 bp with a G+C equal to or greater than 55% and observed CpG/expected CpG of 0.65 were more likely to be associated with the 5′ regions of genes and this definition excluded most <jats:italic>Alu</jats:italic> -repetitive elements. We also used genome sequences to show strong CpG suppression in the human genome and slight suppression in <jats:italic>Drosophila melanogaster</jats:italic> and <jats:italic>Saccharomyces cerevisiae</jats:italic> . This finding is compatible with the recent detection of 5-methylcytosine in <jats:italic>Drosophila</jats:italic> , and might suggest that <jats:italic>S. cerevisiae</jats:italic> has, or once had, CpG methylation. </jats:p>