Evolution of motif variants and positional bias of the cyclic-AMP response element

  • Brandon Smith1Email author,

    Affiliated with

    • Hung Fang2,

      Affiliated with

      • Youlian Pan4,

        Affiliated with

        • P Roy Walker1,

          Affiliated with

          • A Fazel Famili4 and

            Affiliated with

            • Marianna Sikorska3

              Affiliated with

              BMC Evolutionary Biology20077(Suppl 1):S15

              DOI: 10.1186/1471-2148-7-S1-S15

              Published: 8 February 2007



              Transcription factors regulate gene expression by interacting with their specific DNA binding sites. Some transcription factors, particularly those involved in transcription initiation, always bind close to transcription start sites (TSS). Others have no such preference and are functional on sites even tens of thousands of base pairs (bp) away from the TSS.

              The Cyclic-AMP response element (CRE) binding protein (CREB) binds preferentially to a palindromic sequence (TGACGTCA), known as the canonical CRE, and also to other CRE variants. CREB can activate transcription at CREs thousands of bp away from the TSS, but in mammals CREs are found far more frequently within 1 to 150 bp upstream of the TSS than in any other region. This property is termed positional bias.

              The strength of CREB binding to DNA is dependent on the sequence of the CRE motif. The central CpG dinucleotide in the canonical CRE (TGA CG TCA) is critical for strong binding of CREB dimers. Methylation of the cytosine in the CpG can inhibit binding of CREB. Deamination of the methylated cytosines causes a C to T transition, resulting in a functional, but lower affinity CRE variant, TGA T GTCA.


              We performed genome-wide surveys of CREs in a number of species (from worm to human) and showed that only vertebrates exhibited a CRE positional bias. We performed pair-wise comparisons of human CREs with orthologous sequences in mouse, rat and dog genomes and found that canonical and TGA T GTCA variant CREs are highly conserved in mammals. However, when orthologous sequences differ, canonical CREs in human are most frequently TGA T GTCA in the other species and vice-versa. We have identified 207 human CREs showing such differences.


              Our data suggest that the positional bias of CREs likely evolved after the separation of urochordata and vertebrata. Although many canonical CREs are conserved among mammals, there are a number of orthologous genes that have canonical CREs in one species but the TGA T GTCA variant in another. These differences are likely due to deamination of the methylated cytosines in the CpG and may contribute to differential transcriptional regulation among orthologous genes.


              Identification of transcription factor binding sites is crucial to the understanding of gene regulation at the transcriptional level and for deciphering gene regulatory networks. In recent years, the power of bioinformatics and the emergence of complete genome sequences from a variety of species have made it possible to perform global in silico surveys for putative binding sites of individual transcription factors.

              The Cyclic-AMP response element binding protein (CREB) belongs to the bZip family of transcription factors that contain basic leucine zipper motifs. CREB activates target genes by binding to the cAMP-response element (CRE) most frequently located in the promoter region [1]. Examples of bZip proteins binding to CRE and CRE-like motifs have been described in eukaryotes from yeast to human [1, 2]. In mammals, CREB plays an important role in many biological processes [1] and can be activated through several signaling pathways (see reviews: [1, 3]). For instance, CREB has been implicated in multiple functions essential to the brain, including responses to emotional stimuli [4], learning and long-term memory formation [59]. Dysfunction in CREB-regulated transcription also contributes to neurodegeneration [1012]. The canonical CRE is a palindromic octamer, TGACGTCA. However, degenerate CREs and half-CREs (TGACG) are also found to be functional in many of the CREB targets identified so far [1], suggesting a tolerance of CREB for CREs in terms of sequence recognition and binding. More than 100 mammalian CREB target genes have been identified to date (reviewed in [1, 13]), and there are thousands of putative CREB binding sites that are likely to be functional [14, 15].

              It has been observed that, in mammalian genomes, the canonical CRE shows a positional bias [16] towards the proximal promoter region [15, 17], although it remains unclear how this feature has evolved. Mammalian genomes, as is typical of vertebrate genomes, are globally methylated [18] and contain many CpG islands [19, 20]. CpG islands are 200 bp or longer DNA regions with GC-content greater than 50% and a higher than expected number of CpG dinucleotides [21]. Approximately 60 percent of human genes (including most, if not all, house-keeping genes) have CpG islands in their promoters [22]. Most CpG dinucleotides in mammalian genomes contain 5-methylcytosine [22]. However, although CpG dinucleotides in CpG islands can be methylated, they are typically maintained in an unmethylated state [22]. CpGs are usually methylated on both complementary strands, but are sometimes maintained in a hemi-methylated state [23]. The central dinucleotide of the canonical CRE motif, CpG, is known to be methylated in some cases [14]. Such methylation inhibits CREB binding [14] and presumably also increases the rate of C to T transition due to spontaneous deamination of methyl-C. These transitions are often not corrected by DNA repair mechanisms and can be retained as single nucleotide polymorphisms that may cause altered gene expression and changes in phenotype. These transitions may persist through evolution, potentially resulting in differences in CRE function in orthologous genes. CREs with a central TpG (or CpA) have lower affinity for CREB binding compared to the canonical CRE [24, 25], but have been shown to be functional in some genes [2529]. Deamination of both complements of a fully methylated CpG dinucleotide results in a change from CpG to TpA. The TGA TA TCA motif is not known to function as a CRE.

              In this study, we performed genome-wide searches for the canonical CRE and a variant CRE motif (TGA T GTCA, called the TG-variant in this work) in promoter regions of human, mouse, rat, dog, chicken, fish, frog, fruit fly, sea squirt and worm, to determine if the positional bias of CREs is present in other genomes and to establish the point in evolutionary history that the positional bias of CREs started to appear. We also performed comparative genomics analyses to investigate the conservation of orthologous CRE motifs in human, mouse, rat and dog. We focused on differences in the central dinucleotide of the CRE motifs, which is critical for strong CREB binding. Since, in mammals, methylation of sites other than the CpG dinucleotides is rare, TG-variant CREs are not expected to be affected by methylation mechanisms. Using pairwise comparisons of human CREs with orthologous sequences in mouse, rat and dog, we identified known and putative CREs that show CpG to TpG transitions in the core of the CRE motif between orthologous genes. Such differences between CREs in the promoter regions of orthologous genes may cause significant differences in temporal or tissue specific expression in these orthologs.

              Results and Discussion

              Positional bias of CRE-like motifs

              We performed a search of the literature to obtain information on the sequence of CREs in known CREB target genes. A total of 110 CREs in 93 known CREB target genes were retrieved. Although in some cases sequences longer than the 8 bp core motif were reported, only the core motifs were considered in this study. A total of 46 distinct CRE variants were identified. We searched a set of genomic sequences containing more than 46,000 human sequences spanning -1,000 bp to +1,000 bp with respect to the TSS, defined as "TSS spanning regions" (TSS-SRs) (see methods). The searches were performed on both the forward and reverse strands with respect to the direction of transcription. Using these sequences we computed representation index (RI) values in 40 × 50 bp windows along the TSS-SRs (see methods) for the 46 reported CRE variants and a non-CRE motif TGA TA TCA (TA-motif). The canonical CRE motif was highly over-represented in 3 adjacent 50 bp windows over the -1 to -150 bp region (mean RI(-1 to -150) 8.7), but under-represented outside this region (mean RI(outside -1 to -150) 0.8). The difference between these two mean RI values was used as a measure of positional bias towards the region from -1 to -150 bp. Positional bias values of all 47 motifs were computed and motifs with positional bias values greater than 2.6 standard deviations from the mean (P < 0.01) were classified as significant. Figure 1 shows the representation index (RI) profiles of 5 CRE motifs with the highest positional bias values and the non-CRE TA-motif. The canonical CRE and the TG-variant (TGA TG TCA) showed the highest positional bias (values 7.9 and 3.8, respectively) and were the only motifs to have significant positional bias. When considered separately, TG-variant motifs on the forward and reverse strand (with respect to the direction of transcription) were found to have similar positional bias values (data not shown). We selected the canonical CRE and the TG-variant to investigate the evolution of positional bias of CREs.
              Figure 1

              Variation of representation index (RI) of CRE motifs over human TSS-SR regions. The representation index of each 50 bp window along the human TSS-SRs are plotted for the 5 CRE motifs showing the strongest positional bias in the 3 windows from -1 to -150 bp away from the TSS.

              Evolution of the positional bias of the canonical CRE

              Since CREs have been described in a broad range of eukaryotes, we performed bi-directional searches for canonical and TG-variant CREs in the genomes of 9 organisms to see if the CRE positional bias is conserved. We computed RI values in 50 bp windows in the TSS-SR regions. Plots of normalized RI values of the canonical CRE versus distance from the TSS revealed a strong positional bias toward the TSS in the genomes of human (H. Sapiens), mouse (M. musculus), rat (R. norvegicus), chicken (G. gallus), frog (X. tropicalis) and zebrafish (D. rerio) (Figure 2A,B) but not in the genomes of the sea squirt (C. intestinalis), fruit fly (D. melanogaster) and worm (C. elegans) (Figure 2C). Positional bias was also observed for the TG-variant in human, mouse, and rat (Figure 2D). Little or no positional bias was observed for the TG-variant in chicken, frog and zebrafish (Figure 2E) and no positional bias was seen in the sea squirt, fruit fly and worm (Figure 2F). The CRE positional bias likely evolved after the separation of urochordata and vertebrata.
              Figure 2

              Variation of representation index (RI) over the TSS-SR of 9 species. The normalised representation index of each 50 bp window along the TSS-SRs are plotted for the canonical (TGACGTCA) and TG-variant (TGATGTCA) CREs in mouse, rat and dog (A and D); chicken, frog and fish (B and E); and sea squirt, fly and worm (C and F), respectively. In order to be comparable on the same scale, we normalised the RI values in each 50 bp by dividing them by the sum of all RI values in the 40 windows over the TSS-SRs. The values presented are percentages.

              It would seem that selective conservation of canonical CREs located close to the TSS occurred during evolution. It is known that activated CREB is involved in the recruitment of other transcriptional co-activators, such as CREB binding protein, to promoter regions close to the TSS to facilitate transcription [30]. We postulate that this requirement for CREB to be in close proximity to the TSS might have imposed functional constraints on the location of the CRE and contributed to the evolution of CRE positional bias. We hypothesize that the positional bias of the TG-variant motif is a consequence of CpG to TpG transitions in canonical CREs due to cytosine methylation-deamination events. We explore this hypothesis in the following sections.

              Conservation of CREs in mammalian genomes

              Using pair-wise comparisons, putative CREs from our survey in the human genome were checked for conservation of the motif sequence in mouse, rat and dog using the "LiftOver" tool [31, 32]. Over 11,000 human CREs were mapped to orthologous sequences in mouse, rat or dog. The frequency of identical orthologous sequences found in mouse, rat or dog was used as a measure of conservation of the CRE motif variants. Table 1 shows the five most highly conserved CRE motifs between human and the other mammals. The canonical CRE had the highest motif conservation value (mean 57.0 ± 0.3%) and the TG-variant was the second most conserved (mean 33.5 ± 1.0%). Using the pair-wise comparisons of human canonical and TG-variant CREs with orthologous sequences in mouse, rat and dog, we investigated the frequency of occurrence of all possible octet motifs. Table 2 shows the five most frequently occurring motif pairs for human canonical and TG-variant CREs. We found that when human canonical CREs are not conserved in the other species they are most frequently the TG-variant (4.3 ± 0.3%) or its reverse complement, TGA CA TCA (CA-variant, 3.6 ± 0.8%) (Table 2). This is not surprising since, due to the high frequency of deamination of methylated cytosines in CpG dinucleotides to thymidine, CpG to TpG or CpA transitions are the most frequent DNA mutation in mammals [33]. Interestingly, the TA-motif, which can result from double-deamination of methylated CpG, was rare (0.2 ± 0.1%). Human TG-variants are most frequently found in the canonical form in the other mammals when they are not conserved (Table 2). Interestingly, for human TG-variant CREs, the third most frequent motif pair was the reverse complement, CA-variant CRE. Such differences may occur when the central CpG of an ancestral canonical CRE is methylated and deaminated on different strands during divergent evolution. In fact we identified 7 cases where canonical, TG-variant and CA-variant CREs are found in orthologous sequences in human, mouse, rat and dog. One of these was located 305 bp upstream of the TSS of human CALCA, a known CREB target gene. This CRE was canonical in human and rat, TG-variant in mouse and CA-variant in dog. The fourth most frequent motif pair in human TG-variant CREs was the non-functional TA-motif. These motif pairs could have been generated from an ancestral canonical CRE that was methyl-CpG deaminated on only one strand in human, but on both strands in the other species. Taken together these data show that both canonical and TG-variant CREs are highly conserved among mammals and that mutations involving CpG to TpG transitions are the most commonly occurring differences found in orthologous CREs.
              Table 1

              Conservation of human CREs in mouse, rat, and dog

              CRE Motif

              Percentage of sequences conserved






































              Table 2

              Frequency of orthologous sequences

              In human

              In mouse, rat or dog

              Number of occurrences

              Mean percentage of all occurrences
















              TGA T GTCA








              TGAC A TCA








              TGACG C CA








              TGACGTC G
















              TGA C GTCA








              TGA CA TCA








              TGAT A TCA








              T T A C GTCA







              Sites differing from the human sequence are highlighted in bold.

              CRE methylation and CpG islands

              Many mammalian promoters contain CpG islands, which are regions of high CpG density and hypomethylation. In order to investigate the frequency that CRE variants occur within CpG islands, we mapped the positions of human canonical and TG-variant CREs and the TA-motif onto the human CpG island track using the UCSC table browser data retrieval tool [34].

              We found that 62% of human canonical CREs, but only 7% of TG-variant CREs and 2% of TA-motifs, were found in CpG islands. We looked at a subset of the canonical and TG-variant CREs that are conserved in at least one other mammal (mouse, rat or dog) and found that 81% of canonical, but only 13% of TG-variant CREs are located in CpG islands in human. Therefore, the CREs within the CpG islands appear to be more conserved. Since CpG islands are less methylated than other genomic DNA regions, CpG dinucleotides in CpG islands are less prone to spontaneous methyl-C deamination. This in turn may reduce the rate of mutation of canonical CREs in CpG islands to the TG- or CA-variants, or to the TA-motif. CREs that are outside of CpG islands are not protected from methylation and many of these may have been subject to deamination during evolution. We also found that the positional bias was stronger for both canonical and TG-variant CREs in CpG islands versus those not in CpG islands (data not shown).

              To address the question of whether the rate of CpG to TpG transitions is different for CREs within or outside of the CpG islands, we analyzed the CpG island status of four subsets of human and mouse orthologous CREs: (1) CREs that were canonical in both human and mouse (CG:CG); (2) CREs that were TG-variants in both human and mouse (TG:TG); (3) CREs that were canonical in human, but TG-variants in mouse (CG:TG); and (4) CREs that were TG-variants in human, but canonical in mouse (TG:CG) (see Table 3). These sets were then partitioned according to whether the CRE pairs were or were not in a CpG island in human. We found that 80% of the CG:CG CRE pairs, but only 16% of TG:TG CRE pairs were in CpG islands in human. This is consistent with our findings above (see 'conservation of CREs in mammalian genomes'). Sixty percent of the CG:TG pairs and 32% of the TG:CG pairs were found in CpG islands. According to these results, when human canonical CREs are located outside a CpG island, they are twice as likely to be paired with TG-variants (CG:TG) than with canonical CREs (CG:CG) in mouse (40% and 20%, respectively). Similarly, the percentage of TG:CG pairs in human CpG islands is almost double the percentage of TG:TG pairs (32% and 17%, respectively). We also found that 80% of human canonical CREs that are conserved in mouse are in a CpG island in human versus only 57% of those not conserved in mouse. Taken together these data suggest that although CpG to TpG transitions within canonical CREs do occur in CpG island regions, the rates of transition are much higher when the CREs lie in non-CpG island regions.
              Table 3

              Canonical and TG-variant CREs in human CpG islands

              In human

              In mouse

              human:mouse pair

              Number of occurrences

              Percentage in CpG islands of all occurrences


              In CpG island



              TGA CG TCA

              TGA CG TCA






              TGA TG TCA





              TGA TG TCA

              TGA CG TCA






              TGA TG TCA





              Tissue specific methylation of canonical CREs has been shown to inhibit CREB binding [14] and methylation-dependant regulation of CREB activity has been demonstrated [3538]. Most variants of the canonical CRE contain the motif TGACG, which are considered to be half-site CREs [1], and can also be methylated at the CpG. Such regulation, however, is not likely to function on TG-variant CREs since they lack the CpG dinucleotide that is the usual target of DNA methyltransferases in mammals. It has been established that TG-variant CREs are functional in a number of mammalian genes including PLAT, Cga, RARA, RARB, NTS and CFTR [2529], but they may have lower specificity for CRE-binding proteins than canonical CREs [25]. Thus, a gene that is regulated by a canonical CRE in one species and a TG-variant in another species may show differences in basal, temporal or tissue specific gene expression. From the pair-wise comparisons of human CREs to orthologous sequences in other mammals we identified 99 human canonical CREs that were TG-variant CREs in at least one other species and 108 human TG-variant CREs that were canonical CREs in at least one other species (See Additional File 1). Further investigation is required to establish whether these putative CREs contribute to differences in gene expression that are relevant to human development or disease.

              The appearance of heavily methylated genomes and CpG islands both coincide with the evolution of vertebrates [18, 22]. CpG islands tend to associate with the 5'-end of genes, often spanning proximal promoter regions [22]. The urochordate, Ciona intestalis, has a fractionally methylated genome and shows examples of sequence resembling vertebrate CpG islands [39], which may hint at the beginning of the evolution of the CpG islands seen in vertebrates. We found that, unlike all the other chordates in our study, Ciona has no positional bias of the canonical CRE, suggesting that the positional bias of CREs evolved after the separation of vertebrates from the other chordates. Antequera [22] proposed a model for CpG island evolution in vertebrates that involves protection of CpG island regions from DNA methylation by the initial assembly of the replication machinery. Since vertebrate CpG islands are hypomethylated regions in a sea of CpG methylation, it follows that the evolution of this feature was dependent on the evolution of genome-wide methylation. Most of the canonical CREs identified in this study were found to be located within CpG islands. We propose that, in addition to the selective pressure for CREs to be in close proximity to the TSS, the evolution of positional bias of canonical CREs was also assisted by the maintenance of CpG islands in a hypomethylated state in vertebrates. CREs that lie outside of the boundaries of CpG islands are more likely to be methylated and are vulnerable to methyl-cytosine deamination to thymidine. Our finding that most TG-variant CREs, which can be formed by CpG to TpG transition in canonical CREs, were found outside CpG islands supports this hypothesis.

              We speculate that early vertebrates had many more canonical CRE motifs distributed throughout the genome than today's vertebrates and that genome-wide methylation and deamination of methyl-CpG has removed many of these motifs from vertebrate genomes. A whole genome survey showed that the human genome contains only 25% of the expected number of canonical CRE motifs (data not shown). CpG islands may have preserved CREs (especially canonical CREs) as functional transcription factor binding sites in regions close to the core promoter. The result of this process is the observed positional bias of the canonical CRE. CpG islands however are not necessarily stable over time. There is evidence to suggest that mouse CpG islands have eroded [40]. Evolutionary changes in the CpG island status of genes could leave canonical CREs exposed to methylation and trigger conversion to the TG-variant. Also, CpG islands are not devoid of methylation. Canonical CREs in CpG islands can still be methylated, in some cases in a tissue dependent or temporal manner. In fact, we found that 12 out of 26 canonical CREs recently identified as always methylated or differentially methylated [14] were located in CpG islands. We further speculate that the weaker positional bias observed in the TG-variant is simply a consequence of deamination of methyl-C in the core of the canonical CREs.


              In summary, our data suggest that a positional bias of canonical CREs towards the TSS evolved in vertebrates after the separation from urochordates. The weaker positional bias observed in the TG-variant is likely a consequence of deamination of methyl-C in the core of the canonical CREs. The canonical CRE is the most highly conserved CRE variant in mammals and shows the strongest positional bias toward the TSS. The most frequent mutations in canonical CREs are likely due to methyl-C deamination events. We observed that most canonical CREs lay within CpG islands where they are likely maintained in an un-methylated state, thus protecting them from methyl-C deamination. Conversely, TG-variant CREs were generally found in non-CpG island regions. Many of these TG-variant CREs may have been formed from canonical CREs through methyl-C deamination. Our discovery of orthologous CREs with different dynamic methylation potential amongst mammals may help to uncover important differences in the regulation of orthologous CREB target genes relevant to human development and disease. In future work we would like to extend our study to other transcription factors that show positional bias and bind to sites with methylation-sensitive CpG dinucleotides.


              Sources of the sequences

              The sequence spanning -1,000 bp to +1,000 bp with respect to the TSS, defined as "TSS spanning region" (TSS-SR), was chosen for analysis in this study. For the study of CpG → TpG transitions in orthologous genes a comprehensive search for CREs was first performed in human on both strands of the TSS-SRs. Since genes are frequently represented by multiple sequences with different TSSs, a database of human TSS-SRs was generated comprising all sequences with a defined TSS from H-inv [41], RefSeq [42] and the Mammalian Gene Collection (MGC, [43]). The sequences were obtained from the UCSC genome database by means of the table browser data retrieval tool [34] using UCSC genome version hg17. Only sequences with unique TSS positions that are different from the genomic positions of the start codon of corresponding genes were considered. In this dataset, many genes are represented by multiple TSS-SRs due to the presence of alternate TSSs in the source databases. The numbers of sequences obtained from each source and those in the final dataset are summarized in Table 4.
              Table 4

              Summary of human (hg17) TSS-SRs




              Sequences with unique genomic position w.r.t. the TSS





              RefSeq: Sequences from NCBIs RefSeq collection, MGC: Sequences from the Mammalian Genome Collection, hINV: Sequences from the human invitational clone database

              Sequences from 9 species, Homo sapiens, Mus musculus, Rattus norvegicus, Gallus gallus, Xenopus tropicalis, Danio rerio, Ciona intestinalis, Drosophila melanogaster and Caenorhabditis elegans, were obtained from the UCSC genome database in a similar manner. However, for each species only a single source was used and the sequences were not filtered for redundancies. Table 5 summarizes the source and the number of TSS-SRs for each species.
              Table 5

              Summary of TSS-SRs from 9 species


              UCSC Genome version

              UCSC Data Table

              Number of sequences

              Homo sapiens


              RefSeq Genes


              Mus musculus


              RefSeq Genes


              Rattus norvegicus


              RefSeq Genes


              Gallus gallus


              RefSeq Genes


              Xenopus tropicalis


              JGI genes


              Danio rerio


              RefSeq Genes


              Ciona intestinalis


              JGI genes


              Drosophila melanogaster


              RefSeq Genes


              Caenorhabditis elegans


              RefSeq Genes


              Measuring motif positional bias

              The representation index (RI) was used to measure representation of a motif in a set of sequences and was defined as the total number of occurrences of a motif (N) divided by the statistical expectation value (E) of the motif in a given set of sequences [44]. Motif expectation values were calculated using the following formula:

              E = p (Mf) × (Sequence Length - n +1) × (number of sequences)

              Where p (Mf) = ∏ p ( x i ) { i = 1, 2,......, n }, Mf is a motif; p (Mf) is the motif probability; p ( x i ) is the probability of each base in a motif calculated using the average contents of A, C, G, T respectively in each 50 bp window of the sequence set; x i is the base at position i; and n is the length of the motif. In this study, RI values were calculated for each of the 40 × 50 bp windows along the TSS-SR (-1,000 to +1,000 bp). Motif searches and RI value calculations were performed using BioMiner, a suite of data mining tools designed and built in house.

              Positional bias in the region from -1 to -150 bp with respect to the TSS was defined as the difference in mean RI values between the 3 × 50 bp windows from -1 to -150 bp and the other 37 × 50 bp windows. The positional bias of a motif was classified as significant if the value was greater than 2.6 standard deviations (p < 0.01) from the mean of the positional bias values of all motifs.

              Verification of CREs by cross-species sequence comparison

              LiftOver [31], a tool at UCSC for conversion of genome coordinates between assemblies either within a species or between species, was used to convert the genomic coordinates of all human CREs to mouse, rat and dog coordinates. Sequences at these coordinates were then interrogated for the presence of a CRE in each target species. The cross-referenced CREs are referred to as orthologous CREs in this study.



              The authors would like to thank members of the BioMine team from the NRC, Institute of Information Technology for their efforts in the development of the software used in this study. This study was funded by the National Research Council of Canada and was supported by the NRC Genomics and Health Initiative. This is National Research Council Canada's publication NRC 48739.

              This article has been published as part of BMC Evolutionary Biology Volume 7 Supplement 1, 2007: First International Conference on Phylogenomics. The full contents of the supplement are available online at http://​www.​biomedcentral.​com/​bmcevolbiol/​7?​issue=​S1.

              Authors’ Affiliations

              Neurogenomics Group, Institute for Biological Sciences, National Research Council of Canada
              Glycosyltransferases and Neuroglycomics Group, Institute for Biological Sciences, National Research Council of Canada
              Neurogenesis and Brain Repair Group, Institute for Biological Sciences, National Research Council of Canada
              Integrated Reasoning Group, Institute for Information Technology, National Research Council of Canada


              1. Mayr B, Montminy M: Transcriptional regulation by the phosphorylation–dependent factor CREB. Nat Rev Mol Cell Biol 2001, 2: 599–609.View ArticlePubMed
              2. Nehlin JO, Carlberg M, Ronne H: Yeast SKO1 gene encodes a bZIP protein that binds to the CRE motif and acts as a repressor of transcription. Nucleic Acids Res 1992, 20: 5271–5278.View ArticlePubMed
              3. Shaywitz AJ, Greenberg ME: CREB: a stimulus–induced transcription factor activated by a diverse array of extracellular signals. Annu Rev Biochem 1999, 68: 821–861.View ArticlePubMed
              4. Barrot M, Olivier JD, Perrotti LI, DiLeone RJ, Berton O, Eisch AJ, Impey S, Storm DR, Neve RL, Yin JC, Zachariou V, Nestler EJ: CREB activity in the nucleus accumbens shell controls gating of behavioral responses to emotional stimuli. Proc Natl Acad Sci 2002, 99: 11435–11440.View ArticlePubMed
              5. Yin JC, Tully T: CREB and the formation of long–term memory. Curr Opin Neurobiol 1996, 6: 264–268.View ArticlePubMed
              6. Huang EP, Stevens CF: The matter of mind: molecular control of memory. Essays Biochem 1998, 33: 165–178.PubMed
              7. Impey S, Smith DM, Obrietan K, Donahue R, Wade C, Storm DR: Stimulation of cAMP response element (CRE)–mediated transcription during contextual learning. Nat Neurosci 1998, 1: 595–601.View ArticlePubMed
              8. Mayford M, Kandel ER: Genetic approaches to memory storage. Trends Genet 1999, 15: 463–470.View ArticlePubMed
              9. Lamprecht R: CREB: a message to remember. Cell Mol Life Sci 1999, 55: 554–563.View ArticlePubMed
              10. Mantamadiotis T, Lemberger T, Bleckmann SC, Kern H, Kretz O, Martin Villalba A, Tronche F, Kellendonk C, Gau D, Kapfhammer J, Otto C, Schmid W, Schutz G: Disruption of CREB function in brain leads to neurodegeneration. Nat Genet 2002, 31: 47–54.View ArticlePubMed
              11. Dragunow M: CREB and neurodegeneration. Front Biosci 2004, 9: 100–103.View ArticlePubMed
              12. Beglopoulos V, Shen J: Regulation of CRE–dependent transcription by presenilins: prospects for therapy of Alzheimer's disease. Trends Pharmacol Sci 2006, 27: 33–40.View ArticlePubMed
              13. Lonze BE, Ginty DD: Function and regulation of CREB family transcription factors in the nervous system. Neuron 2002, 35: 605–623.View ArticlePubMed
              14. Zhang X, Odom DT, Koo SH, Conkright MD, Canettieri G, Best J, Chen H, Jenner R, Herbolsheimer E, Jacobsen E, Kadam S, Ecker JR, Emerson B, Hogenesch JB, Unterman T, Young RA, Montminy M: Genome–wide analysis of cAMP–response element binding protein occupancy, phosphorylation, and target gene activation in human tissues. Proc Natl Acad Sci 2005, 102: 4459–4464.View ArticlePubMed
              15. Conkright MD, Guzman E, Flechner L, Su AI, Hogenesch JB, Montminy M: Genome–wide analysis of CREB target genes reveals a core promoter requirement for cAMP responsiveness. Mol Cell 2003, 11: 1101–1108.View ArticlePubMed
              16. Hughes JD, Estep PW, Tavazoie S, Church GM: Computational identification of cis–regulatory elements associated with groups of functionally related genes in Saccharomyces cerevisiae . J Mol Biol 2000, 296: 1205–1214.View ArticlePubMed
              17. FitzGerald PC, Shlyakhtenko A, Mir AA, Vinson C: Clustering of DNA sequences in human promoters. Genome Res 2004, 14: 1562–1574.View ArticlePubMed
              18. Tweedie S, Charlton J, Clark V, Bird A: Methylation of genomes and genes at the invertebrate–vertebrate boundary. Mol Cell Biol 1997, 17: 1469–1475.PubMed
              19. Bird AP: CpG–rich islands and the function of DNA methylation. Nature 1986, 321: 209–213.View ArticlePubMed
              20. Bird A, Taggart M, Frommer M, Miller OJ, Macleod D: A fraction of the mouse genome that is derived from islands of nonmethylated, CpG–rich DNA. Cell 1985, 40: 91–99.View ArticlePubMed
              21. Gardiner–Garden M, Frommer M: CpG islands in vertebrate genomes. J Mol Biol 1987, 196: 261–282.View ArticlePubMed
              22. Antequera F: Structure, function and evolution of CpG island promoters. Cell Mol Life Sci 2003, 60: 1647–1658.View ArticlePubMed
              23. Burden AF, Manley NC, Clark AD, Gartler SM, Laird CD, Hansen RS: Hemimethylation and non–CpG methylation levels in a promoter region of human LINE–1 (L1) repeated elements. J Biol Chem 2005, 280: 14413–14419.View ArticlePubMed
              24. Benbrook DM, Jones NC: Different binding specificities and transactivation of variant CRE's by CREB complexes. Nucleic Acids Res 1994, 22: 1463–1469.View ArticlePubMed
              25. Drust DS, Troccoli NM, Jameson JL: Binding specificity of cyclic adenosine 3',5'–monophosphate–responsive element (CRE)–binding proteins and activating transcription factors to naturally occurring CRE sequence variants. Mol Endocrinol 1991, 5: 1541–1551.View ArticlePubMed
              26. Medcalf RL, Ruegg M, Schleuning WD: A DNA motif related to the cAMP–responsive element and an exon–located activator protein–2 binding site in the human tissue–type plasminogen activator gene promoter cooperate in basal expression and convey activation by phorbol ester and cAMP. J Biol Chem 1990, 265: 14618–14626.PubMed
              27. Kruyt FA, Folkers G, van den Brink CE, van der Saag PT: A cyclic AMP response element is involved in retinoic acid–dependent RAR beta 2 promoter activation. Nucleic Acids Res 1992, 20: 6393–6399.View ArticlePubMed
              28. Evers BM, Wang X, Zhou Z, Townsend CM Jr, McNeil GP, Dobner PR: Characterization of promoter elements required for cell–specific expression of the neurotensin/neuromedin N gene in a human endocrine cell line. Mol Cell Biol 1995, 15: 3870–3881.PubMed
              29. Matthews RP, McKnight GS: Characterization of the cAMP response element of the cystic fibrosis transmembrane conductance regulator gene promoter. J Biol Chem 1996, 271: 31869–31877.View ArticlePubMed
              30. Bannister AJ, Kouzarides T: The CBP co–activator is a histone acetyltransferase. Nature 1996, 384: 641–643.View ArticlePubMed
              31. Hinrichs AS, Karolchik D, Baertsch R, Barber GP, Bejerano G, Clawson H, Diekhans M, Furey TS, Harte RA, Hsu F, Hillman–Jackson J, Kuhn RM, Pedersen JS, Pohl A, Raney BJ, Rosenbloom KR, Siepel A, Smith KE, Sugnet CW, Sultan–Qurraie A, Thomas DJ, Trumbower H, Weber RJ, Weirauch M, Zweig AS, Haussler D, Kent WJ: The UCSC Genome Browser Database: update 2006. Nucleic Acids Res 2006, 34: D590–598.View ArticlePubMed
              32. UCSC Lift Genome Annotations [http://​genome.​ucsc.​edu/​cgi-bin/​hgLiftOver]
              33. Bird AP: methylation and the frequency of CpG in animal DNA. Nucleic Acids Res 1980, 8: 1499–1504.View ArticlePubMed
              34. Karolchik D, Hinrichs AS, Furey TS, Roskin KM, Sugnet CW, Haussler D, Kent WJ: The UCSC Table Browser data retrieval tool. Nucleic Acids Res 2004, 32: D493–496.View ArticlePubMed
              35. DiNardo DN, Butcher DT, Robinson DP, Archer TK, Rodenhiser DI: Functional analysis of CpG methylation in the BRCA1 promoter region. Oncogene 2001, 20: 5331–5340.View ArticlePubMed
              36. Mancini DN, Singh SM, Archer TK, Rodenhiser DI: Site–specific DNA methylation in the neurofibromatosis (NF1) promoter interferes with binding of CREB and SP1 transcription factors. Oncogene 1999, 18: 4108–4119.View ArticlePubMed
              37. Iannello RC, Gould JA, Young JC, Giudice A, Medcalf R, Kola I: Methylation–dependent silencing of the testis–specific Pdha–2 basal promoter occurs through selective targeting of an activating transcription factor/cAMP–responsive element–binding site. J Biol Chem 2000, 275: 19603–81960.View ArticlePubMed
              38. Iguchi–Ariga SM, Schaffner W: CpG methylation of the cAMP–responsive enhancer/promoter sequence TGACGTCA abolishes specific factor binding as well as transcriptional activation. Genes Dev 1989, 3: 612–619.View ArticlePubMed
              39. Simmen MW, Leitgeb S, Charlton J, Jones SJ, Harris BR, Clark VH, Bird A: Nonmethylated transposable elements and methylated genes in a chordate genome. Science 1999, 283: 1164–1167.View ArticlePubMed
              40. Matsuo K, Clay O, Takahashi T, Silke J, Schaffner W: Evidence for erosion of mouse CpG islands during mammalian evolution. Somat Cell Mol Genet 1993, 19: 543–555.View ArticlePubMed
              41. H – Invitation Database [http://​www.​h-invitational.​jp/​]
              42. NCBI Reference Sequences [http://​www.​ncbi.​nlm.​nih.​gov/​RefSeq/​]
              43. Mammalian Gene Collection [http://​mgc.​nci.​nih.​gov]
              44. Pan Y, Smith B, Fang H, Famili FA, Sikorska M, Walker R: Selection of putative cis–regulatory motifs through regional and global conservation. Proceedings of the 2004 IEEE Computational Systems Bioinformatics Conference (CSB 2004), August 16–19, 2004 Stanford, CA, USA, IEEE Computer Society 2004, 684–685.


              © Smith et al. 2007

              This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.