Relative gene frequency among Prochlorococcus and Pelagibacter populations in the oligotrophic North Pacific (HOT) and North Atlantic (BATS) subtropical ocean gyres. (A) Detection of each Prochlorococcus gene at HOT and BATS, measured as the number of pyrosequencing reads. For each gene, the number of reads detected is proportional to the product of gene length and gene multiplicity per cell. Thus, assuming similar gene lengths at both sites, genes that fall along the diagonal trend have the same relative frequency at both sites, whereas those that fall above or below the diagonal are enriched at one site compared with the other. Squares represent significantly different frequencies between sites (G test; P < 0.01); circles represent nonsignificant differences. Colored squares represent genes whose chromosomal positions are depicted in B. (B) Genome comparison of two cultured isolates of Prochlorococcus (MED4 and MIT9301), with gray lines connecting homologous genes. Genes represented by corresponding colored squares in A are clustered together in a few distinct regions of the chromosome, including hypervariable genomic islands, in these isolates. Genes marked with an asterisk are up-regulated in response to P starvation (ref. 22 and Fig. S2). MED4 and MIT9301, isolated from the Mediterranean and the North Atlantic, respectively, are depicted because they carry the largest complements of phosphorus uptake genes among Prochlorococcus isolates (22). (C) Relative frequency of each Pelagibacter gene at HOT and BATS, as in A. (D) Genome comparison of two Pelagibacter strains, HTCC7211 and HTCC1062, as in B.