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The comprehensive updated regulatory network of Escherichia coli K-12
BMC Bioinformatics volume 7, Article number: 5 (2006)
Escherichia coli is the model organism for which our knowledge of its regulatory network is the most extensive. Over the last few years, our project has been collecting and curating the literature concerning E. coli transcription initiation and operons, providing in both the RegulonDB and EcoCyc databases the largest electronically encoded network available. A paper published recently by Ma et al. (2004) showed several differences in the versions of the network present in these two databases.
Discrepancies have been corrected, annotations from this and other groups (Shen-Orr et al., 2002) have been added, making the RegulonDB and EcoCyc databases the largest comprehensive and constantly curated regulatory network of E. coli K-12.
Several groups have been using these curated data as part of their bioinformatics and systems biology projects, in combination with external data obtained from other sources, thus enlarging the dataset initially obtained from either RegulonDB or EcoCyc of the E. coli K12 regulatory network. We kindly obtained from the groups of Uri Alon and Hong-Wu Ma the interactions they have added to enrich their public versions of the E. coli regulatory network. These were used to search for original references and curate them with the same standards we use regularly, adding in several cases the original references (instead of reviews or missing references), as well as adding the corresponding experimental evidence codes. We also corrected all discrepancies in the two databases available as explained below.
One hundred and fifty new interactions have been added to our databases as a result of this specific curation effort, in addition to those added as a result of our continuous curation work. RegulonDB gene names are now based on those of EcoCyc to avoid confusion due to gene names and synonyms, and the public releases of RegulonDB and EcoCyc are henceforth synchronized to avoid confusion due to different versions. Public flat files are available providing direct access to the regulatory network interactions thus avoiding errors due to differences in database modelling and representation. The regulatory network available in RegulonDB and EcoCyc is the most comprehensive and regularly updated electronically-encoded regulatory network of E. coli K-12.
Escherichia coli is a reference organism because of the rich knowledge of its biology. The group of Collado-Vides has been curating regulation of transcription initiation and operon organization during the last ten years [1–3]. This effort feeds two databases, RegulonDB and EcoCyc [4, 5]. This information is freely and openly available, and has been used by several groups to perform different types of analyses, in bioinformatics and systems biology.
For instance, this dataset was used a few years ago by the group of Uri Alon to identify statistically over-represented topological motifs of gene-regulatory relationships within the network . The notion of statistically significant motifs proposed therein has been widely used in subsequent analyses of networks. More recently, a team led by An-Ping Zeng in Braunschweig has analyzed topological properties of this network . These two groups have enlarged this dataset with their own addition of interactions.
Additional uses of this dataset include novel or expanded computational methods of promoters; operons [8–10]; microarray analyses [11, 12]; and chip-chip experiments ; formal models of transcriptional processes ; metabolic and regulatory network reconstruction ; and experimental studies [16, 17], among others.
In order to avoid a multiplication of slightly different versions of the E. coli regulatory network, we have integrated the interactions from the Alon and Zeng groups – data generously provided by them – and have flat files publicly available that contain in a direct and simple way the set of regulatory interactions either at the gene or at the protein level.
Ma et al have extracted from EcoCyc and from RegulonDB the regulatory network of interactions and the transcriptional links of sigma factors and their regulated genes. They describe in their Figure 1 an important number of differences in the network obtained from each database. There are several reasons for these differences, summarized below, but an important one derives from the different ways of encoding the interactions in the schemas of EcoCyc and RegulonDB. Furthermore, they used the two versions available then, version 8.0 of EcoCyc and version 4.0 of RegulonDB which were not synchronized and therefore had a different content. As mentioned below, since version 9.0 of EcoCyc and 4.4 of RegulonDB, the public versions of both databases are synchronized to prevent these problems. Version 9.6 of EcoCyc will correspond to version 5.0 of RegulonDB.
In the following we describe the specific differences and curation involved, and in the last sub-section we describe the final files available with the updated network as well as those apparent interactions that were not incorporated.
Unified use of gene names and synonyms
Some of the differences in the network observed by Ma et al derive from discrepancies in gene names and in interactions when comparing each database. Differences in gene content are mostly due to the use of different names and synonyms in each database. They have been corrected, and we now make uniform use of gene names and synonyms, mostly incorporating the curated gene annotations of EcoCyc into RegulonDB in future releases.
Ma et al found 370 interactions present in RegulonDB and absent in EcoCyc and 336 present in EcoCyc and absent in RegulonDB. As summarized in Table 2, after eliminating repetitions in both databases that derive from the existence of heterodimer proteins (i.e. IHF encoded by himA and himD genes, rcsA and rscB genes that encode for protein RcsB), separating the set of sigma factor interactions with their corresponding promoters as a different type of interactions, as well as those that are already present in both databases as curation continued, we were left with 69 interactions unique to RegulonDB and 77 unique to EcoCyc.
Out of the 69 considered unique to RegulonDB, 24 interactions are in fact present in both databases but they were missed by Ma et al. because the gene names are different. Some gene names in one database are synonyms in the other. We have unified the names in both databases with the first one in the following list of pairs being the current name, followed by its synonym: atsC-argM, mngA-hrsA, mngR-farR, mazF-chpA, mazE-chpR, rrnA-rrsA, rrnC-rrsC, rrnD-rrsD, rrnE-rrsE, rrnG-rrsG, rrnH-rrsH, csiR-gabC, glnG-ntrC, astC-argM, nfnB-nfsB, alsR-rpiR.
Out of the interactions reported as unique to EcoCyc, six were in fact present in both databases but with different regulated gene names, although present as synonyms. The pair of gene names and synonyms is the following: mlc-dgsA, icdA-icd, lpdA-lpd. Since mlc encodes a TF, and it regulates 3 other genes, its name change affects 3 interactions. Furthermore, lpdA is regulated by two different Tfs (ArcA and Fis) thus again one gene name affects two TF-gene interactions.
Ma reports interactions present in one database and not in the other one. However, in our analyses they are absent in both. There are 17 such interactions with no promoter associated, therefore they do not belong to any known TU, and we do not consider them as validated interactions.
Finally, 28 specific regulator-regulated gene interactions, affecting 27 regulated genes, (two interactions affect gcvB), implied correcting only 15 interactions as encoded in the databases because four operons (sufABCDSE, galETKM, rtcBA and guaBA) account for 14 TF-regulated gene interactions, in addition to 11 interactions of genes transcribed monocistronically.
77 interactions are reported as unique to EcoCyc. These involve 19 proteins affecting 61 genes. In addition to those due to different gene names mentioned above, there are 8 interactions involving glnL, which encodes a sensor protein NtrB. In fact all these genes are regulated by NtrC, encoded by glnG. These are interactions wrongly derived from EcoCyc that were never present in the databases and are not present in the current website.
The knowledge in the databases is sometimes incomplete, such as in some cases, annotated promoters, for which there is no clear evidence of the extent of the TU they transcribe. In EcoCyc such promoters are linked with the downstream TU, even if there is no experimental evidence for the existence of the TU. This generates differences in the number of interactions, accounting for 16 additional interactions present in EcoCyc and absent in RegulonDB. It is up to the criteria of the modeler of the network to assume that such likely interactions exist, or from a more conservative approach, to eliminate them. In the website mentioned below, they are not included.
18 interactions were in fact corrected before, first deleted in RegulonDB, but present in version 8.0 of EcoCyc and deleted in subsequent releases.
We corrected 11 operons which involve 29 TF-regulated gene interactions. These affect a total of 23 genes -again because some of them are regulated by more than one TF-. 17 of the 29 specific interactions are grouped in four operons: pdhR-aceEF-lpdA, deoABCD, glpTQ and fimAICDFGH.
Final datasets of the regulatory network and of transcription by different types of RNAPs based on their sigma factors
The RegulonDB and EcoCyc data web pages will be updated systematically as part of the periodic releases of EcoCyc and RegulonDB. Both the team of Uri Alon and the team of An-Ping Zeng have agreed to link to our urls from their respective public sites.
The datasets produced as a result of the curation described above, are the following:
Interactions available both in EcoCyc and RegulonDB
File 1 RegulonDB-EcoCyc interactions, contains the set of regulatory interactions at the level of transcription initiation. Each line describes the name of the transcription factor (TF), the regulatory gene, the name of the regulated gene, and the corresponding function (activator or repressor). In the case of heterodimers, we kept them in one line, with for instance, IHF, followed by himA/himD genes. Thus, the total counting corresponds to the number of proteins affecting the expression of individual genes. Note that these are exclusively regulatory interactions affecting the initiation of transcription.
File 2 Gene Sets Transcribed by common Sigma Factors contains the set of seven sigma factors present in E. coli, and their corresponding transcribed genes. These are not regulatory interactions, but sets of genes transcribed by the same RNA polymerase holoenzyme.
Interactions not found in E. coli K-12
File 3 and File 4, have those interactions for which we found no evidence and were not therefore added to the databases. File 3 has 19 interactions from Alon for which we found no published evidence. File 4 has 31 interactions from Ma et al.
12 interactions that are not of transcriptional regulation (pending curation), 10 based on microarray experiments which we cannot know if are direct or indirect, and 9 for which we found no reference of experimental evidence. Table 1 summarizes the literature revision performed to what initially were 346 interactions of Alon and 93 of Zeng that were absent in RegulonDB and EcoCyc. As mentioned before, after curation of these two datasets we have 150 new interactions that have been curated.
Access to the regulatory network
Access to more complete data on transcriptional regulation and operon organization can be found at RegulonDB  and EcoCyc  web sites. The public releases of both databases are now synchronized.
As mentioned before, the data sets available from RegulonDB and EcoCyc web pages shall facilitate investigators to generate the full regulatory network of E. coli. The remaining few differences between the databases will disappear as curation of the data now occurs within EcoCyc and is immediately propagated to RegulonDB. We will extract from EcoCyc the annotations of genes and incorporate them for the genome annotation in RegulonDB. Furthermore, the releases of both databases have been synchronized, to avoid different versions of the data content. There will be a corresponding equivalent version of each database.
Collado-Vides J, Magasanik B, Gralla JD: Control site location and transcriptional regulation in Escherichia coli . Microbiol Reviews 1991, 55: 371–394.
Gralla JD, Collado-Vides J: Organization and Function of Transcription Regulatory Elements. In Cellular and Molecular Biology: Escherichia coli and Salmonella. Volume Chap 79. 2nd edition. Edited by: American Society for Microbiology, Washington, D.C. Neidhardt FC, Curtiss III R, Ingraham J, Lin ECC, Low KB, Magasanik B, Reznikoff W, Schaechter M, Umbarger HE, Riley M; 1996:1232–1245.
Huerta AM, Salgado H, Thieffry D, Collado-Vides J: RegulonDB: A Database on Transcription Regulation in Escherichia coli . Nucleic Acids Res 1998, 26: 55–60. 10.1093/nar/26.1.55
Keseler IM, Collado-Vides J, Gama-Castro S, Ingraham J, Paley S, Paulsen IT, Peralta-Gil M, Karp PD: EcoCyc: a comprehensive database resource for Escherichia coli . Nucleic Acids Res 2005, 33: D334–337. 10.1093/nar/gki108
Salgado H, Gama-Castro S, Martínez-Antonio A, Díaz-Peredo E, Sánchez-Solano F, Peralta-Gil M, Garcia-Alonso D, Jiménez-Jacinto V, Santos-Zavaleta A, Bonavides-Martínez C, Collado-Vides J: RegulonDB (version 4.0): Transcriptional Regulation, Operon Organization and Growth Conditions in Escherichia coli K-12. Nucleic Acids Res 2004, 32: 303–306. 10.1093/nar/gkh140
Shen-Orr SS, Milo R, Mangan S, Alon U: Network motifs in the transcriptional regulation network of Escherichia coli . Nat Genet 2002, 31: 64–68. 10.1038/ng881
Ma HW, Kumar B, Ditges U, Gunzer F, Buer J, Zeng AP: An extended transcriptional regulatory network of Escherichia coli and analysis of its hierarchical structure and network motifs. Nucleic Acids Res 2004, 16: 6643–6649. 10.1093/nar/gkh1009
Zwir I, Shin D, Kato A, Nishino K, Latifi T, Solomon F, Hare JM, Huang H, Groisman EA: Dissecting the PhoP regulatory network of Escherichia coli and Salmonella enterica . Proc Natl Acad Sci USA 2005, 102(8):2862–2867. 10.1073/pnas.0408238102
Li H, Rhodius V, Gross C, Siggia ED: Free in PMC Identification of the binding sites of regulatory proteins in bacterial genomes. Proc Natl Acad Sci USA 2002, 99(18):11772–11777. 10.1073/pnas.112341999
Gordon L, Chervonenkis AY, Gammerman AJ, Shahmuradov IA, Solovyev VV: Sequence alignment kernel for recognition of promoter regions. Bioinformatics 2003, 19(15):1964–1971. 10.1093/bioinformatics/btg265
Sabatti C, Rohlin L, Oh MK, Liao JC: Co-expression pattern from DNA microarray experiments as a tool for operon prediction. Nucleic Acids Res 2002, 30(13):2886–2893. 10.1093/nar/gkf388
Cooper TF, Rozen DE, Lenski RE: Parallel changes in gene expression after 20,000 generations of evolution in Escherichia coli . Proc Natl Acad Sci USA 2003, 100(3):1072–1077. 10.1073/pnas.0334340100
Herring CD, Raffaelle M, Allen TE, Kanin EI, Landick R, Ansari AZ, Palsson BO: Immobilization of Escherichia coli RNA polymerase and location of binding sites by use of chromatin immunoprecipitation and microarrays. J Bacteriol 2005, 187(17):6166–6174. 10.1128/JB.187.17.6166-6174.2005
Sneppen K, Dodd IB, Shearwin KE, Palmer AC, Schubert RA, Callen BP, Egan JB: A mathematical model for transcriptional interference by RNA polymerase traffic in Escherichia coli . J Mol Biol 2005, 346(2):399–409. 10.1016/j.jmb.2004.11.075
Herrgard MJ, Covert MW, Palsson BO: Reconstruction of microbial transcriptional regulatory networks. Curr Opin Biotechnol 2004, 15(1):70–77. 10.1016/j.copbio.2003.11.002
Nickels BE, Mukhopadhyay J, Garrity SJ, Ebright RH, Hochschild A: The sigma 70 subunit of RNA polymerase mediates a promoter-proximal pause at the lac promoter. Nat Struct Mol Biol 2004, 11(6):544–550. 10.1038/nsmb757
Adams MA, Jia Z: Structural and biochemical evidence for an enzymatic quinone redox cycle in Escherichia coli : identification of a novel quinol monooxygenase. J Biol Chem 2005, 280(9):8358–8363. 10.1074/jbc.M412637200
The development of RegulonDB is funded by grant RO1-GM71962 from the NIH National Center of General Medical Sciences, and that of EcoCyc is funded by grant 1-R01-RR07861-01 from the NIH National Center for Research Resources. We acknowledge data analysis assistance by César Bonavides and Suzanne Paley, and Irma Martínez-Flores for the coordination assistance in the curation.
HS carried out the data analysis, synchronized the regulatory network data sets and drafted and revised the manuscript. AS participated and coordinated the curation of data, SG, MP and MIP participated in the curation and analysis of data, AM participated at the beginning of the project in its coordination and drafted a first manuscript, PDK was involved in drafting the manuscript and revising it critically, JC conceived the study, and drafted and revised the manuscript.
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Salgado, H., Santos-Zavaleta, A., Gama-Castro, S. et al. The comprehensive updated regulatory network of Escherichia coli K-12. BMC Bioinformatics 7, 5 (2006). https://doi.org/10.1186/1471-2105-7-5
- Regulatory Network
- Transcription Initiation
- Sigma Factor
- Public Release
- Flat File