- Open Access
Dynamic usage of transcription start sites within core promoters
© Kawaji et al.; licensee BioMed Central Ltd. 2006
- Received: 31 July 2006
- Accepted: 12 December 2006
- Published: 12 December 2006
Mammalian promoters do not initiate transcription at single, well defined base pairs, but rather at multiple, alternative start sites spread across a region. We previously characterized the static structures of transcription start site usage within promoters at the base pair level, based on large-scale sequencing of transcript 5' ends.
In the present study we begin to explore the internal dynamics of mammalian promoters, and demonstrate that start site selection within many mouse core promoters varies among tissues. We also show that this dynamic usage of start sites is associated with CpG islands, broad and multimodal promoter structures, and imprinting.
Our results reveal a new level of biologic complexity within promoters - fine-scale regulation of transcription starting events at the base pair level. These events are likely to be related to epigenetic transcriptional regulation.
- Core Promoter
- Shape Class
- Restriction Landmark Genomic Scanning
- Base Pair Level
- Single Dominant Peak
There is great interest in elucidating the control of transcription initiation, because these controls are major components of the gene regulatory networks that underlie the development and diversity of animals [1, 2]. The standard view is that regulatory action takes place at distal and proximal enhancer and repressor cis elements, which are bound by transcription factors that interact with the basal transcription machinery at the core promoter to influence transcription. In this view, core promoters themselves are functionally simple, but recent data reveal that they are structurally complex, with a range of alternative transcription start sites (TSSs) at the base pair level [3–5]. A key issue is whether these complex structures are just 'biologic noise' from imprecise binding of basal transcription factors or whether TSS selection is precisely regulated.
Cap analysis of gene expression (CAGE) is a method used to identify TSSs and, at the same time, to measure their expression levels by counting a large number of sequenced 5' ends of full-length cDNAs, termed CAGE tags [6, 7]. The advantage of this method is that it provides a view at base pair level of the expression profiles of TSSs even within a promoter. In contrast, the most commonly used high-throughput methodology for measuring gene expression, namely the microarray, profiles transcript expression without distinguishing between alternate 5' ends. Expressed sequence tag (EST) and full-length cDNA sequencing characterize end structures of transcripts, but their quantification ability is limited because of their cost. Additionally, some cDNA libraries are subtracted or normalized for exploration of novel transcripts, and these libraries cannot provide a quantitative view of expression [8, 9].
In the FANTOM3 (functional annotation of mouse 3) project, the CAGE method was applied to more than 20 tissues from mouse and human [4, 10]. More than seven million mouse CAGE tags were sequenced and mapped to the mouse genome, and so many core promoters are represented by many CAGE tags. This gives unprecedented opportunities to resolve the internal structures of core promoters.
As with cDNA sequencing, sequencing a large number of CAGE tags may capture errors, such as degraded transcripts or incomplete cDNA synthesis events. Extensive experimental and statistical validation of the CAGE set analyzed in this study, presented elsewhere (see the report by Carninci and coworkers  and its supplementary material), demonstrated good reliability even for single CAGE tags. A potential weakness with the method is the tag length (20-21 base pairs [bp]); with only a few sequencing errors, mapping tags back to the genome can be problematic. In the present study we used only unequivocal tag mappings  and focused on core promoters with more than 100 co-occurring tags. Another general issue with all tag-based technology is how to reliably associate tags with their corresponding full-length transcript; however, this is not a CAGE-specific problem and similar challenges are faced when using array-based methods.
Interestingly, transcription initiation was found to occur at multiple nucleotide positions within a core promoter region in many cases, although the start sites are more tightly clustered (but still not uniquely defined) for a subset of promoters with an over-representation of TATA boxes. Thereby, most core promoters do not have a single TSS but rather an array of closely located initiation sites. For clarity, this is conceptually different from alternative promoters, in which core promoters are separated by clear genomic space. In order to analyze arrays of tags corresponding to core promoters it is necessary to cluster adjacent tags . A tag cluster is defined as a segment of a chromosome, on either the forward or reverse strand, where each 20 bp subregion contains at least one transcript 5' end identified by RIKEN full-length cDNAs, RIKEN-5' ESTs , GIS ditags , GSC ditags , or CAGE tags .
A basic issue that must be addressed if we are to understand such broad transcription start regions is whether start site selection is precisely regulated or whether TSS usage is driven by nonspecific binding of basal transcription factors . If TSS selection is regulated, then broad start regions could be caused by varying concentrations of transcription factors that favor initiation at different sites  or by epigenetic mechanisms such as DNA methylation, histone modifications, and chromatin remodeling [15–20]. If this is true, then it would be possible for the cell to modify the start site selection within a promoter in different contexts (such as tissues). On the other hand, if start site selection is primarily driven by the properties of the genomic sequence, then we would not expect major differences in TSS selection between tissues in a given broad promoter.
To address this issue, we examine tissue specificity at the base pair level, or fine-grained tissue-specific usage of TSSs. Note that our focus is not on alternative promoters, which are multiple promoters used by the same gene [4, 21]. Rather, we investigate alternative TSSs within a core promoter region.
Here, we show that there are distinct, tissue-specific modes of start site selection within core promoters. To suggest possible mechanisms for this phenomenon, we show that such fine-grained tissue specificities of TSSs are associated with some expression contexts, such as tag cluster shapes, and genomic imprinting candidates.
Tested tag clusters
We will be able to identify reliably only large usage biases if a tag cluster has few tags from each tissue, whereas more subtle biases will be reliably detectable if a tag cluster has many tags from some tissues. From this viewpoint, we use 8,157 tag clusters with 100 or more CAGE tags for statistical analysis. These clusters have previously been classified into the four shape classes based on CAGE tag distributions . The mean length of these tag clusters is 134.2 bp, and 95% of them are under 250 bp in length. The mean lengths of the four classes based on their shapes or CAGE tag distributions are as follows: 87.0 bp for the single dominant peak, 146.7 bp for the broad distribution with a dominant peak, 180.5 bp for the multimodal distribution, and 129.1 bp for the general broad distribution. The mean length for the multimodal class is the longest among the four classes, being over twice the mean length for the single dominant peak.
Positionally biased promoters
In our exploration of tissue specificities within a tag cluster in which transcripts are initiated over a continuous region, we have no clear border to distinguish subregions to be compared with each other. The situation is different from exploration of alternative promoters, where each promoter is clearly separated by a certain genomic space. To cope with this issue, we adopt two strategies to explore fine-grained tissue specificity as comprehensively as possible: first, we explore differences in central (or median) TSS position depending on tissue; and second, we explore subregions whose expression profiles are different from the rest of the tag cluster. The first strategy can identify an intuitive type of fine-grained tissue specificity, namely overall bias of centered position, such as shown Figure 2b. There remain other types of tissue specificity, such as shows in Figure 2c, which has some internal regions with distinct tissue specificities but no clear differences in terms of the centered position. The second strategy was devised to find these cases.
Given the above, we employed a statistical test with no in-built assumption about distributions, namely the Kruskal-Wallis one-way analysis of variance by ranks. It tests the null hypothesis that several samples come from populations with the same median  (this is essentially a nonparametric variant of the classical analysis of variance test). Thus, rejection of the null hypothesis implies that at least one of the underlying tag distributions has a distinct center point. The null hypothesis was rejected (P < 0.01) for 2,491 out of 8,157 tag clusters (30%), and we term these cases 'positionally biased'. The test does not indicate which tissues differ in median, just that they are not all the same.
Regionally biased promoters
Second, we identified tissue-specific subregions of 21 bp within tag clusters, using a Bayesian statistics based method developed previously for analysis of alternative splicing (see Materials and methods, below) .
An example of a regionally biased cluster is shown in Figure 4b. A tag cluster located at the 5' end of ORF61, which encodes a 574 amino acid protein of unknown function, has a broad shape, and the median TSS locations are positioned roughly in the center of the tag cluster. Although there is no significant difference of medians among tissues, the CAGE tag distributions in its subregions are different from each other depending on tissues. For example, upstream TSSs are used frequently in embryo whereas downstream TSSs are used frequently in liver. Tissue specificities change along the genome, but the other TSSs in the intermediate region and at both ends contribute to no significant difference in central TSS position.
Associations with CpG islands and CAGE tag shape classes
Statistical significance of associations with CpG islands, CAGE tag shape classes, promoter expression, and imprinting candidates
4.11 × 10-25*
1.65 × 10-56*
2.22 × 10-113*
CAGE tag shape class
Single dominant peak
2.13 × 10-182*
Broad distribution with a dominant peak
1.92 × 10-02
3.72 × 10-01
9.89 × 10-01
2.37 × 10-12*
1.49 × 10-02
General broad Distribution
6.70 × 10-01
3.19 × 10-79*
Maternal imprinting candidates
7.94 × 10-01
1.86 × 10-04*
9.97 × 10-01
Paternal imprinting candidates
6.65 × 10-04*
2.77 × 10-01
9.69 × 10-01
9.99 × 10-01
7.08 × 10-06*
We also examined their relations with shapes of CAGE tag distributions (Table 1). A significant association of positional bias with the multimodal shape class suggests that the multiple peaks are superimposed prominent TSSs utilized in a tissue-specific manner, implying that tag clusters with multimodal shapes consist of multiple and overlapping promoters. This can be expected from the definition of tag clusters, where two proximal and distinct promoters are joined if rarely used TSSs are located between them. Interestingly, Table 1 also shows a significant association of the regionally biased class with the general broad tag distribution. This reveals distinct tendencies between positional and regional biases, and that tag clusters without remarkable peaks are also regulated tissue specifically on a fine-grained scale. Nonspecific DNA binding of transcription factors  is unlikely to explain these tag clusters.
Associations with imprinting
Genomic imprinting is epigenetic modification of genes whose expression is determined according to their parent of origin . The key molecular mechanism is DNA methylation, which can repress transcription by direct and indirect mechanisms, such as inhibiting the binding of specific transcription factors, and recruiting methyl-CpG-binding proteins associated with repressive chromatin remodeling . Interestingly, different machineries for maternal and paternal silencing have been suggested: maternal repression is effected by promoter methylation of a target transcript, and paternal repression by inactivation of its antisense transcript by maternal methylation . Analysis of Eed mutant mice suggests that paternally and maternally inherited chromosomes can use different chromatin silencing mechanisms [27, 28]; however, the details remain unclear.
To explore links between dynamic TSS usage and imprinting, we used candidate imprinted transcripts stored in the EICO database , which were identified by differential expression dependent upon chromosomal parent of origin using cDNA microarrays . The sensitivity of the method was demonstrated by identification of previously reported imprinted genes . It should be emphasized that the EICO database lists candidate imprinted transcripts and non-imprinted transcripts under the control of imprinted transcripts by identification of differential expression between parthenogenotes and androgenotes [30, 31].
We found that 328 of the 8,157 tag clusters used in this study are located at 5' ends of the imprinting candidates, and 115 (35%) and 104 (31%) of them are classified as positionally and regionally biased, respectively. Table 1 shows the statistical significances of their associations with these candidates, which indicates that paternally and maternally imprinted transcripts are associated with positional and regional biases. We also found that paternal and maternal imprinting candidates are associated with the general broad shape class with P values of 0.04 and 1.6 × 10-5, where Fisher's exact test is used for the null hypothesis that paternal imprinting (or maternal imprinting) and the general broad shape class do not have any positive association. It is surprising that paternally imprinted promoters with positional bias are not associated with the multimodal shape class, which is a characteristic of positional bias in general. Although these paternally imprinted promoters are just special cases of positional bias, maternally imprinted promoters may be more representative cases of regional bias.
Associations with tissue-specific differentially methylated regions
Methylation is involved in tissue-specific expression in some cases, as well as genomic imprinting. Genome-wide analysis of DNA methylation status using restriction landmark genomic scanning (RLGS)  identified chromosomal regions that are differentially methylated in a tissue-specific manner [35, 36]. Quantitative real-time PCR and bisulfite genomic sequencing revealed associations of DNA methylation with tissue-specific expression and partial methylation in some examples .
To explore the possibility that the fine-grained tissue specificities are associated with differential methylation, we compared these 150 differentially methylated regions identified by Song and coworkers  with our classification. Most of the regions are located at promoters and CpG islands, and 29 of the tag clusters used here overlap the differentially methylated regions. Of the 29 tag clusters, 13 (44%) and 11 (37%) are classified as positionally and regionally biased, respectively. These fractions are substantially larger than the fractions of all tag clusters (30% for positional bias and 25% for regional bias) and the fractions of CpG related tag clusters (34% for positional bias and 29% for regional bias), but additional data are required to prove the association with differential methylation rigorously. Given these initial results, we hypothesize that differences in DNA methylation due to cellular context is one of several mechanisms responsible for the observed difference in TSS selection between tissues.
We found that TSSs are tissue-specifically utilized within a tag cluster, rather than uniformly among tissues, in about half of all tag clusters in this study. Tag clusters with multiple and prominent CAGE tag peaks and positionally biased tissue specificity can be interpreted as distinct and overlapping promoters. On the other hand, a substantial number of tag clusters contain broad TSSs with regionally biased tissue specificity. Although detailed understanding of their regulation will require further experimentation, our comparisons with genome imprinting candidates raise the hypothesis that some of these tissue-specific TSS usages are regulated via DNA methylation and/or subsequent chromatin remodeling.
Our study is based on a limited number of 22 tissues profiled by CAGE, and the number of tag clusters with fine-grained tissue specificities is bound to increase when more tissues and conditions are added. Our results give rise also to questions about TSSs and transcript 5' ends. In general, the transcripts with the most upstream 5' ends have been utilized to define TSSs of genes [37, 38]. However, our findings imply that this methodology is biologically relevant only in some cases, because specific transcription starts frequently from nearby but distinct sites depending on tissue preferences. Comprehensive detection of TSSs in all tissues and conditions will be required to gain a complete understanding of transcriptional regulation and of the logic behind specific recruitment of transcription factors within core promoter elements.
This study highlights a property of core promoters that is little explored and less understood; it is clear that start site selection within promoters is a highly regulated process and that core promoters cannot be considered simply as standard templates serving to integrate signals from other cis regulatory elements.
Utilized tissues and their CAGE tag counts in mouse
Total CAGE tags
Regionally biased tissue specificity
Here, we aimed to test the null hypothesis that a tag cluster does not contain any internal regions with different tissue specificity from the remaining part. Although a large number of CAGE tags are used, some regions inside tag clusters have few tags, because of our tag cluster definition stating that any region with at least one tag is a part of a tag cluster. To achieve a reliable test in cases with such a small number of CAGE tags, we used the tissue specificity score (TS) and the negative log value of its relative change (rTS), which was devised for finding tissue-specificity of alternative splicing from EST libraries . Bayesian statistics is used to make a reliable detection even among tissues with small numbers of ESTs.
Call an internal region in a tag cluster Rint, the remaining part Rrem, a tissue T, and all of the other tissues U. Let the hidden or true frequency of CAGE tag counts in Rint derived from T be θint,T, and similarly for the other variables to yield θint,U, θrem,T and θrem,U. They are normalized and should fulfill the following equations:
θint,T + θrem,T = 1
θint,U + θrem,U = 1
The tissue specificity score (TS) is calculated from the observed CAGE tag counts as follows:
TS = 100 (P [θint,T > 0.5 | obs] - P [θrem,T > 0.5 | obs])
Let the observed CAGE tag counts be Nint,T in the internal region derived from T, and the negative log value of its relative change (rTS) is defined as follows:
rTS = -log10 (ΔTS/TS)
Where ΔTS = | TS(Nint,T) - TS(Nint,T - 1) |. A high TS score indicates that the internal region is much preferred in the tissue in comparison with the all of the other tissues, and a high rTS value indicates that the TS value is stable even if a single CAGE tag is not sequenced by chance.
This examination of the null hypothesis, that the internal region in the tag cluster does not exhibit different tissue specificity from the remaining part, is applied for each tissue. Each 21 bp subregion around a genome position where any CAGE tag alignment starts is tested, and the tested subregions can overlap. Because of this evaluation being conducted repeatedly in a tag cluster, we adopted more rigorous thresholds than were used in the original publication of this method, namely TS score above 90 and rTS score above 0.9.
Statistical test for associations
Associations of the fine-grained tissue specificities with CpG islands, shapes of CAGE tag distribution, and genome imprinting candidates were evaluated by one-sided Fisher's exact test. A 2 × 2 contingency table for two sets of tag clusters is constructed, and the P value for the null hypothesis that the two sets do not have any positive association is evaluated.
The following additional data are available with the online version of this paper. Additional file 1 is a document including all of our classifications of the tag clusters and their attributes in tab-delimited format.
We should like to thank G McLachlan for advice on statistics; B Lenhard, DA Hume, V Bajic, and SL Tan for useful discussions about promoter analysis; T Kasukawa for scientific and technical discussion; A Karlsson for English editing; K Nakano and H Murakami for building computational systems; K Yoshida and K Murata for support; and all members of the FANTOM consortium. This study was supported by Research Grant for the RIKEN Genome Exploration Research Project from the Ministry of Education, Culture, Sports, Science and Technology of the Japanese Government to YH; Research Grant for Advanced and Innovational Research Program in Life Science to JK; a grant of the Genome Network Project from the Ministry of Education, Culture, Sports, Science and Technology, Japan to YH; and a Grant for the Strategic Programs for R&D of RIKEN to YH. MCF is a University of Queensland Postdoctoral Fellow.
- Levine M, Davidson EH: Gene regulatory networks for development. Proc Natl Acad Sci USA. 2005, 102: 4936-4942. 10.1073/pnas.0408031102.PubMedPubMed CentralView ArticleGoogle Scholar
- Levine M, Tjian R: Transcription regulation and animal diversity. Nature. 2003, 424: 147-151. 10.1038/nature01763.PubMedView ArticleGoogle Scholar
- Suzuki Y, Taira H, Tsunoda T, Mizushima-Sugano J, Sese J, Hata H, Ota T, Isogai T, Tanaka T, Morishita S, et al: Diverse transcriptional initiation revealed by fine, large-scale mapping of mRNA start sites. EMBO Rep. 2001, 2: 388-393.PubMedPubMed CentralView ArticleGoogle Scholar
- Carninci P, Sandelin A, Lenhard B, Katayama S, Shimokawa K, Ponjavic J, Semple CA, Taylor MS, Engstrom PG, Frith MC, et al: Genome-wide analysis of mammalian promoter architecture and evolution. Nat Genet. 2006, 38: 626-635. 10.1038/ng1789.PubMedView ArticleGoogle Scholar
- Smale ST, Kadonaga JT: The RNA polymerase II core promoter. Annu Rev Biochem. 2003, 72: 449-479. 10.1146/annurev.biochem.72.121801.161520.PubMedView ArticleGoogle Scholar
- Kodzius R, Kojima M, Nishiyori H, Nakamura M, Fukuda S, Tagami M, Sasaki D, Imamura K, Kai C, Harbers M, et al: CAGE: cap analysis of gene expression. Nat Methods. 2006, 3: 211-222. 10.1038/nmeth0306-211.PubMedView ArticleGoogle Scholar
- Shiraki T, Kondo S, Katayama S, Waki K, Kasukawa T, Kawaji H, Kodzius R, Watahiki A, Nakamura M, Arakawa T, et al: Cap analysis gene expression for high-throughput analysis of transcriptional starting point and identification of promoter usage. Proc Natl Acad Sci USA. 2003, 100: 15776-15781. 10.1073/pnas.2136655100.PubMedPubMed CentralView ArticleGoogle Scholar
- Carninci P, Shibata Y, Hayatsu N, Sugahara Y, Shibata K, Itoh M, Konno H, Okazaki Y, Muramatsu M, Hayashizaki Y: Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes. Genome Res. 2000, 10: 1617-1630. 10.1101/gr.145100.PubMedPubMed CentralView ArticleGoogle Scholar
- Carninci P, Waki K, Shiraki T, Konno H, Shibata K, Itoh M, Aizawa K, Arakawa T, Ishii Y, Sasaki D, et al: Targeting a complex transcriptome: the construction of the mouse full-length cDNA encyclopedia. Genome Res. 2003, 13: 1273-1289. 10.1101/gr.1119703.PubMedPubMed CentralView ArticleGoogle Scholar
- Carninci P, Kasukawa T, Katayama S, Gough J, Frith MC, Maeda N, Oyama R, Ravasi T, Lenhard B, Wells C, et al: The transcriptional landscape of the mammalian genome. Science. 2005, 309: 1559-1563. 10.1126/science.1112014.PubMedView ArticleGoogle Scholar
- Ng P, Wei CL, Sung WK, Chiu KP, Lipovich L, Ang CC, Gupta S, Shahab A, Ridwan A, Wong CH, et al: Gene identification signature (GIS) analysis for transcriptome characterization and genome annotation. Nat Methods. 2005, 2: 105-111. 10.1038/nmeth733.PubMedView ArticleGoogle Scholar
- Harbers M, Carninci P: Tag-based approaches for transcriptome research and genome annotation. Nat Methods. 2005, 2: 495-502. 10.1038/nmeth768.PubMedView ArticleGoogle Scholar
- Coleman RA, Pugh BF: Evidence for functional binding and stable sliding of the TATA binding protein on nonspecific DNA. J Biol Chem. 1995, 270: 13850-13859. 10.1074/jbc.270.23.13850.PubMedView ArticleGoogle Scholar
- Hochheimer A, Tjian R: Diversified transcription initiation complexes expand promoter selectivity and tissue-specific gene expression. Genes Dev. 2003, 17: 1309-1320. 10.1101/gad.1099903.PubMedView ArticleGoogle Scholar
- Biel M, Wascholowski V, Giannis A: Epigenetics: an epicenter of gene regulation: histones and histone-modifying enzymes. Angew Chem Int Ed Engl. 2005, 44: 3186-3216. 10.1002/anie.200461346.PubMedView ArticleGoogle Scholar
- Futscher BW, Oshiro MM, Wozniak RJ, Holtan N, Hanigan CL, Duan H, Domann FE: Role for DNA methylation in the control of cell type specific maspin expression. Nat Genet. 2002, 31: 175-179. 10.1038/ng886.PubMedView ArticleGoogle Scholar
- Jaenisch R, Bird A: Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Nat Genet. 2003, 245-254. 10.1038/ng1089. 33 SupplGoogle Scholar
- Jones PA, Takai D: The role of DNA methylation in mammalian epigenetics. Science. 2001, 293: 1068-1070. 10.1126/science.1063852.PubMedView ArticleGoogle Scholar
- Sutherland JE, Costa M: Epigenetics and the environment. Ann N Y Acad Sci. 2003, 983: 151-160.PubMedView ArticleGoogle Scholar
- Wolffe AP, Matzke MA: Epigenetics: regulation through repression. Science. 1999, 286: 481-486. 10.1126/science.286.5439.481.PubMedView ArticleGoogle Scholar
- Kimura K, Wakamatsu A, Suzuki Y, Ota T, Nishikawa T, Yamashita R, Yamamoto J, Sekine M, Tsuritani K, Wakaguri H, et al: Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Genome Res. 2006, 16: 55-65. 10.1101/gr.4039406.PubMedPubMed CentralView ArticleGoogle Scholar
- Siegel S, Castellan NJ: Nonparametric Statistics for the Behavioral Sciences. 1988, New York: McGraw-Hill, 2Google Scholar
- Xu Q, Modrek B, Lee C: Genome-wide detection of tissue-specific alternative splicing in the human transcriptome. Nucleic Acids Res. 2002, 30: 3754-3766. 10.1093/nar/gkf492.PubMedPubMed CentralView ArticleGoogle Scholar
- Wilkins JF: Genomic imprinting and methylation: epigenetic canalization and conflict. Trends Genet. 2005, 21: 356-365. 10.1016/j.tig.2005.04.005.PubMedView ArticleGoogle Scholar
- Robertson KD: DNA methylation and chromatin: unraveling the tangled web. Oncogene. 2002, 21: 5361-5379. 10.1038/sj.onc.1205609.PubMedView ArticleGoogle Scholar
- Reik W, Walter J: Genomic imprinting: parental influence on the genome. Nat Rev Genet. 2001, 2: 21-32. 10.1038/35047554.PubMedView ArticleGoogle Scholar
- Ferguson-Smith AC, Reik W: The need for Eed. Nat Genet. 2003, 33: 433-434. 10.1038/ng0403-433.PubMedView ArticleGoogle Scholar
- Mager J, Montgomery ND, de Villena FP, Magnuson T: Genome imprinting regulated by the mouse Polycomb group protein Eed. Nat Genet. 2003, 33: 502-507. 10.1038/ng1125.PubMedView ArticleGoogle Scholar
- Nikaido I, Saito C, Wakamoto A, Tomaru Y, Arakawa T, Hayashizaki Y, Okazaki Y: EICO (Expression-based Imprint Candidate Organizer): finding disease-related imprinted genes. Nucleic Acids Res. 2004, 32: D548-D551. 10.1093/nar/gkh093.PubMedPubMed CentralView ArticleGoogle Scholar
- Nikaido I, Saito C, Mizuno Y, Meguro M, Bono H, Kadomura M, Kono T, Morris GA, Lyons PA, Oshimura M, et al: Discovery of imprinted transcripts in the mouse transcriptome using large-scale expression profiling. Genome Res. 2003, 13: 1402-1409. 10.1101/gr.1055303.PubMedPubMed CentralView ArticleGoogle Scholar
- Mizuno Y, Sotomaru Y, Katsuzawa Y, Kono T, Meguro M, Oshimura M, Kawai J, Tomaru Y, Kiyosawa H, Nikaido I, et al: Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray. Biochem Biophys Res Commun. 2002, 290: 1499-1505. 10.1006/bbrc.2002.6370.PubMedView ArticleGoogle Scholar
- Shemer R, Birger Y, Riggs AD, Razin A: Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern. Proc Natl Acad Sci USA. 1997, 94: 10267-10272. 10.1073/pnas.94.19.10267.PubMedPubMed CentralView ArticleGoogle Scholar
- Hajkova P, Erhardt S, Lane N, Haaf T, El-Maarri O, Reik W, Walter J, Surani MA: Epigenetic reprogramming in mouse primordial germ cells. Mech Dev. 2002, 117: 15-23. 10.1016/S0925-4773(02)00181-8.PubMedView ArticleGoogle Scholar
- Hatada I, Hayashizaki Y, Hirotsune S, Komatsubara H, Mukai T: A genomic scanning method for higher organisms using restriction sites as landmarks. Proc Natl Acad Sci USA. 1991, 88: 9523-9527. 10.1073/pnas.88.21.9523.PubMedPubMed CentralView ArticleGoogle Scholar
- Hattori N, Abe T, Hattori N, Suzuki M, Matsuyama T, Yoshida S, Li E, Shiota K: Preference of DNA methyltransferases for CpG islands in mouse embryonic stem cells. Genome Res. 2004, 14: 1733-1740. 10.1101/gr.2431504.PubMedPubMed CentralView ArticleGoogle Scholar
- Song F, Smith JF, Kimura MT, Morrow AD, Matsuyama T, Nagase H, Held WA: Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression. Proc Natl Acad Sci USA. 2005, 102: 3336-3341. 10.1073/pnas.0408436102.PubMedPubMed CentralView ArticleGoogle Scholar
- Pruitt KD, Tatusova T, Maglott DR: NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res. 2005, 33: D501-D504. 10.1093/nar/gki025.PubMedPubMed CentralView ArticleGoogle Scholar
- Curwen V, Eyras E, Andrews TD, Clarke L, Mongin E, Searle SM, Clamp M: The Ensembl automatic gene annotation system. Genome Res. 2004, 14: 942-950. 10.1101/gr.1858004.PubMedPubMed CentralView ArticleGoogle Scholar
- CAGE Analysis Database. [http://fantom31p.gsc.riken.jp/cage_analysis/]
- Kawaji H, Kasukawa T, Fukuda S, Katayama S, Kai C, Kawai J, Carninci P, Hayashizaki Y: CAGE Basic/Analysis Databases: the CAGE resource for comprehensive promoter analysis. Nucleic Acids Res. 2006, 34: D632-D636. 10.1093/nar/gkj034.PubMedPubMed CentralView ArticleGoogle Scholar
- Karolchik D, Baertsch R, Diekhans M, Furey TS, Hinrichs A, Lu YT, Roskin KM, Schwartz M, Sugnet CW, Thomas DJ, et al: The UCSC Genome Browser Database. Nucleic Acids Res. 2003, 31: 51-54. 10.1093/nar/gkg129.PubMedPubMed CentralView ArticleGoogle Scholar
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.