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AraC DNA-binding transcriptional dual regulator

Synonyms: AraC-α-L-arabinopyranose, AraC, AraC-D-fucose
Summary:
The "arabinose regulator," AraC, is a transcription factor that regulates transcription of several genes and operons involved in arabinose catabolism and transport. It coregulates with another transcriptional regulator, CRP; both are transcription factors involved in l-arabinose degradation. These regulators bind cooperatively to activate transcription of five operons related to transport, catabolism, and autoregulation of l-arabinose. Transcription of these operons is induced when E. coli is grown in the absence of glucose and when the physiological inducer, l-arabinose, binds to the AraC regulator. In the absence of glucose, cellular cyclic AMP levels are high and cyclic AMP forms a dimeric complex with CRP to coregulate with AraC [6, 9, 13, 14, 17, 20, 21] AraC binds to five target sites in the araBp region. AraC binds to the less-conserved site (-42.5) with less strength; this binding occurs only in the presence of arabinose, and it is absolutely required for expression of araBp [5, 22, 23, 24, 25] AraC binding to the distal site (-123.5) has been shown to down-regulate expression of araBp and araCp [4, 23] In the absence of arabinose, AraC is unable to activate araBp, but it regulates its own expression by repressing araCp and araBp simultaneously [22, 23, 24] Arabinose triggers AraC-dependent activation of araBp and relieves AraC-dependent repression of araCp [23, 24] The araBAD operon is located upstream of araC and in the opposite direction. In the presence of arabinose, this regulator activates transcription by overlapping the -35 box of the core promoters, and the central position of the binding site is located near bp -41.5.
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Transcription factor      
TF conformation(s):
Name Conformation Type TF-Effector Interaction Type Apo/Holo Conformation Evidence Confidence level (C: Confirmed, S: Strong, W: Weak) References
AraC Functional   Apo [EXP-IDA], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] S [1], [2], [3], [4], [5], [6]
AraC-α-L-arabinopyranose Functional Allosteric Holo [EXP-IDA], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] S [1], [2], [3], [4], [5], [6]
AraC-D-fucose Non-Functional Allosteric Holo nd nd nd
Evolutionary Family: AraC/XylS
TFBs length: 17
TFBs symmetry: inverted-repeat
Sensing class: Sensing external and internal signals
Connectivity class: Local Regulator
Gene name: araC
  Genome position: 70387-71265
  Length: 879 bp / 292 aa
Operon name: araC
TU(s) encoding the TF:
Transcription unit        Promoter
araC
araCp


Regulon       
Regulated gene(s) araA, araB, araC, araD, araE, araF, araG, araH, araJ, xylA, xylB, ydeM, ydeN, ygeA
Multifun term(s) of regulated gene(s) MultiFun Term (List of genes associated to the multifun term)
carbon compounds (11)
membrane (3)
Porters (Uni-, Sym- and Antiporters) (2)
Transcription related (1)
activator (1)
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Regulated operon(s) araBAD, araC, araE-ygeA, araFGH, araJ, xylAB, ydeNM
First gene in the operon(s) araB, araC, araE, araF, araJ, xylA, ydeN
Simple and complex regulons AraC,CRP
AraC,CRP,XylR
AraC,GadX,NagC
Simple and complex regulatory phrases Regulatory phrase (List of promoters regulated by the phrase)
[AraC,-](4)
[AraC,+](6)


Transcription factor regulation    


Transcription factor binding sites (TFBSs) arrangements
      

  Functional conformation Function Promoter Sigma factor Central Rel-Pos Distance to first Gene Genes Sequence
LeftPos RightPos Evidence Confidence level (C: Confirmed, S: Strong, W: Weak) References
  AraC repressor araBp Sigma70 -275.0 -302.0 araB, araA, araD
attcagagaaGAAACCAATTGTCCATAttgcatcaga
70342 70358 [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [2], [6], [6], [7], [8], [8], [9], [10], [11]
  AraC-α-L-arabinopyranose repressor araBp Sigma70 -138.0 -165.0 araB, araA, araD
caaaaacgcgTAACAAAAGTGTCTATAatcacggcag
70205 70221 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS], [EXP-IMP-SITE-MUTATION] C [4], [4], [9], [11]
  AraC-α-L-arabinopyranose repressor araBp Sigma70 -117.0 -144.0 araB, araA, araD
tctataatcaCGGCAGAAAAGTCCACAttgattattt
70184 70200 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS], [EXP-IMP-SITE-MUTATION] C [4], [4], [9], [11]
  AraC repressor araBp Sigma70 -64.0 -91.0 araB, araA, araD
tgctatgccaTAGCATTTTTATCCATAagattagcgg
70131 70147 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [1], [1], [6], [7], [8], [8], [9], [10], [11], [12]
  AraC-α-L-arabinopyranose activator araBp Sigma70 -64.0 -91.0 araB, araA, araD
tgctatgccaTAGCATTTTTATCCATAagattagcgg
70131 70147 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [1], [1], [6], [7], [8], [8], [9], [10], [11], [12]
  AraC-α-L-arabinopyranose activator araBp Sigma70 -43.0 -70.0 araB, araA, araD
tccataagatTAGCGGATCCTACCTGAcgctttttat
70110 70126 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [1], [1], [2], [5], [6], [7], [8], [8], [9], [12]
  AraC-α-L-arabinopyranose activator araCp Sigma70 -105.0 -269.0 araC
ataaaaagcgTCAGGTAGGATCCGCTAatcttatgga
70110 70126 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [1], [2], [2], [5], [8], [8], [9], [12]
  AraC repressor araCp Sigma70 -84.0 -248.0 araC
ccgctaatctTATGGATAAAAATGCTAtggcatagca
70131 70147 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [1], [8], [8], [9], [10], [11], [12]
  AraC-α-L-arabinopyranose activator araCp Sigma70 -84.0 -248.0 araC
ccgctaatctTATGGATAAAAATGCTAtggcatagca
70131 70147 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [1], [8], [8], [9], [10], [11], [12]
  AraC-α-L-arabinopyranose repressor araCp Sigma70 -31.0 -195.0 araC
aaataatcaaTGTGGACTTTTCTGCCGtgattataga
70184 70200 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS], [EXP-IMP-SITE-MUTATION] C [4], [4], [9], [11]
  AraC-α-L-arabinopyranose repressor araCp Sigma70 -10.0 -174.0 araC
ctgccgtgatTATAGACACTTTTGTTAcgcgtttttg
70205 70221 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS], [EXP-IMP-SITE-MUTATION] C [4], [4], [9], [9], [11]
  AraC repressor araCp Sigma70 128.0 -37.0 araC
tctgatgcaaTATGGACAATTGGTTTCttctctgaat
70342 70358 [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [2], [6], [8], [9], [10], [11]
  AraC-α-L-arabinopyranose activator araEp Sigma70 -65.0 -91.0 araE, ygeA
cgacatgtcgCAGCAATTTAATCCATAtttatgctgt
2982265 2982281 [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [9], [13], [13]
  AraC-α-L-arabinopyranose activator araEp Sigma70 -44.0 -70.0 araE, ygeA
tccatatttaTGCTGTTTCCGACCTGAcacctgcgtg
2982244 2982260 [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [9], [13], [13]
  AraC-α-L-arabinopyranose activator araFp1 Sigma70 -166.0 -276.0 araF, araG, araH
ccaaagacaaCAAGGATTTCCAGGCTAatcttatgga
1986396 1986412 [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [9], [14], [14], [15], [15]
  AraC-α-L-arabinopyranose activator araFp1 Sigma70 -145.0 -255.0 araF, araG, araH
aggctaatctTATGGATTAATCTGCTGtgcattcgac
1986375 1986391 [COMP-AINF-SIMILAR-TO-CONSENSUS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [3], [9], [14], [14], [15], [15]
  AraC-α-L-arabinopyranose activator araFp1 Sigma70 -91.0 -201.0 araF, araG, araH
ggctttccctTATGTCTTTTCCCGCTAaatttatgca
1986321 1986337 [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [9], [14], [14], [15], [15]
  AraC-α-L-arabinopyranose activator araFp1 Sigma70 -70.0 -180.0 araF, araG, araH
ccgctaaattTATGCACGTTCTCACTGtaattctgcg
1986300 1986316 [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [3], [14], [14], [15], [15], [16]
  AraC-α-L-arabinopyranose activator araFp3 Sigma38 -166.0 -276.0 araF, araG, araH
ccaaagacaaCAAGGATTTCCAGGCTAatcttatgga
1986396 1986412 [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [9], [14], [14], [15], [15]
  AraC-α-L-arabinopyranose activator araFp3 Sigma38 -145.0 -255.0 araF, araG, araH
aggctaatctTATGGATTAATCTGCTGtgcattcgac
1986375 1986391 [COMP-AINF-SIMILAR-TO-CONSENSUS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [3], [9], [14], [14], [15], [15]
  AraC-α-L-arabinopyranose activator araFp3 Sigma38 -91.0 -201.0 araF, araG, araH
ggctttccctTATGTCTTTTCCCGCTAaatttatgca
1986321 1986337 [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS], [EXP-IMP-SITE-MUTATION] C [9], [14], [14], [15], [15]
  AraC-α-L-arabinopyranose activator araFp3 Sigma38 -70.0 -180.0 araF, araG, araH
ccgctaaattTATGCACGTTCTCACTGtaattctgcg
1986300 1986316 [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [3], [14], [14], [15], [15], [16]
  AraC-α-L-arabinopyranose activator araJp Sigma70 -64.0 -112.0 araJ
aataactattCAGCAGGATAATGAATAcagaggggcg
412585 412601 [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [9], [14], [14], [17]
  AraC-α-L-arabinopyranose activator araJp Sigma70 -43.0 -91.0 araJ
tgaatacagaGGGGCGAATTATCTCTTggccttgctg
412564 412580 [COMP-AINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] S [9], [14], [14], [17]
  AraC-α-L-arabinopyranose repressor xylAp nd -48.0 -90.0 xylA, xylB
attatctcaaTAGCAGTGTGAAATAACataattgagc
3730847 3730863 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-HINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS] S [18], [18]
  AraC-α-L-arabinopyranose repressor xylAp nd -25.0 -67.0 xylA, xylB
taacataattGAGCAACTGAAAGGGAGtgcccaatat
3730824 3730840 [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [EXP-IDA-BINDING-OF-CELLULAR-EXTRACTS] W [18], [18]
  AraC-α-L-arabinopyranose repressor ydeNp Sigma70 nd nd ydeN, ydeM nd nd [EXP-IEP-GENE-EXPRESSION-ANALYSIS] W [19]



High-throughput Transcription factor binding sites (TFBSs)
      

  Functional conformation Function Object name Object type Distance to first Gene Sequence LeftPos RightPos Center Position Growth Condition Evidence Confidence level (C: Confirmed, S: Strong, W: Weak) References
  AraC repressor ytfQRT-yjfF Transcription-Unit nd
agacggtataCAGAGCAGGAAAATCCATAAccgtagccgc
4449772 4449791 4449781.0 nd [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-AINF-SIMILAR-TO-CONSENSUS], [EXP-IMP-SITE-MUTATION] W [19]


Alignment and PSSM for AraC TFBSs    

Aligned TFBS of AraC   
  Sequence
  CACAGCAGATTAATCCATAA
  CGCAGCAATTTAATCCATAT
  TACAGTGAGAACGTGCATAA
  CATAGCATTTTTATCCATAA
  CACGGCAGAAAAGTCCACAT
  TTTAGCGGGAAAAGACATAA
  TTCAGCAGGATAATGAATAC
  AGCAGTGTGAAATAACATAA
  AAGAAACCAATTGTCCATAT
  CGTAACAAAAGTGTCTATAA
  ATTAGCCTGGAAATCCTTGT
  TCAGGTCGGAAACAGCATAA
  GATTAGCGGATCCTACCTGA
  AAGAGATAATTCGCCCCTCT
  CCCTTTCAGTTGCTCAATTA

Position weight matrix (PWM). AraC matrix-quality result   
A	4	7	1	11	3	2	6	5	5	9	6	8	6	2	3	2	12	0	11	9
C	6	2	7	0	0	8	5	1	0	0	0	3	3	1	9	12	2	1	1	1
G	1	3	2	2	11	1	3	6	8	1	1	1	5	1	3	0	0	0	2	0
T	4	3	5	2	1	4	1	3	2	5	8	3	1	11	0	1	1	14	1	5

Consensus   
;	consensus.strict             	cacaGccggatagtCCaTaa
;	consensus.strict.rc          	TTATGGACTATCCGGCTGTG
;	consensus.IUPAC              	cayaGcmrrwwartCCaTaw
;	consensus.IUPAC.rc           	WTATGGAYTWWYYKGCTRTG
;	consensus.regexp             	ca[ct]aGc[ac][ag][ag][at][at]a[ag]tCCaTa[at]
;	consensus.regexp.rc          	[AT]TATGGA[CT]T[AT][AT][CT][CT][GT]GCT[AG]TG

PWM logo   


 


Evolutionary conservation of regulatory elements    
     Note: Evolutionary conservation of regulatory interactions and promoters is limited to gammaproteobacteria.
TF-target gene evolutionary conservation
Promoter-target gene evolutionary conservation




Reference(s)    

 [1] Bustos SA., Schleif RF., 1993, Functional domains of the AraC protein., Proc Natl Acad Sci U S A 90(12):5638-42

 [2] Huo L., Martin KJ., Schleif R., 1988, Alternative DNA loops regulate the arabinose operon in Escherichia coli., Proc Natl Acad Sci U S A 85(15):5444-8

 [3] Johnson CM., Schleif RF., 1995, In vivo induction kinetics of the arabinose promoters in Escherichia coli., J Bacteriol 177(12):3438-42

 [4] Lee DH., Huo L., Schleif R., 1992, Repression of the araBAD promoter from araO1., J Mol Biol 224(2):335-41

 [5] Lee N., Francklyn C., Hamilton EP., 1987, Arabinose-induced binding of AraC protein to araI2 activates the araBAD operon promoter., Proc Natl Acad Sci U S A 84(24):8814-8

 [6] Seabold RR., Schleif RF., 1998, Apo-AraC actively seeks to loop., J Mol Biol 278(3):529-38

 [7] Lobell RB., Schleif RF., 1991, AraC-DNA looping: orientation and distance-dependent loop breaking by the cyclic AMP receptor protein., J Mol Biol 218(1):45-54

 [8] Niland P., Huhne R., Muller-Hill B., 1996, How AraC interacts specifically with its target DNAs., J Mol Biol 264(4):667-74

 [9] Gallegos MT., Schleif R., Bairoch A., Hofmann K., Ramos JL., 1997, Arac/XylS family of transcriptional regulators., Microbiol Mol Biol Rev 61(4):393-410

 [10] Lee DH., Schleif RF., 1989, In vivo DNA loops in araCBAD: size limits and helical repeat., Proc Natl Acad Sci U S A 86(2):476-80

 [11] Lee NL., Gielow WO., Wallace RG., 1981, Mechanism of araC autoregulation and the domains of two overlapping promoters, Pc and PBAD, in the L-arabinose regulatory region of Escherichia coli., Proc Natl Acad Sci U S A 78(2):752-6

 [12] Reeder T., Schleif R., 1993, AraC protein can activate transcription from only one position and when pointed in only one direction., J Mol Biol 231(2):205-18

 [13] Stoner C., Schleif R., 1983, The araE low affinity L-arabinose transport promoter. Cloning, sequence, transcription start site and DNA binding sites of regulatory proteins., J Mol Biol 171(4):369-81

 [14] Hendrickson W., Stoner C., Schleif R., 1990, Characterization of the Escherichia coli araFGH and araJ promoters., J Mol Biol 215(4):497-510

 [15] Lu Y., Flaherty C., Hendrickson W., 1992, AraC protein contacts asymmetric sites in the Escherichia coli araFGH promoter., J Biol Chem 267(34):24848-57

 [16] Johnson CM., Schleif RF., 2000, Cooperative action of the catabolite activator protein and AraC in vitro at the araFGH promoter., J Bacteriol 182(7):1995-2000

 [17] Reeder T., Schleif R., 1991, Mapping, sequence, and apparent lack of function of araJ, a gene of the Escherichia coli arabinose regulon., J Bacteriol 173(24):7765-71

 [18] Desai TA., Rao CV., 2010, Regulation of arabinose and xylose metabolism in Escherichia coli., Appl Environ Microbiol 76(5):1524-32

 [19] Stringer AM., Currenti S., Bonocora RP., Baranowski C., Petrone BL., Palumbo MJ., Reilly AA., Zhang Z., Erill I., Wade JT., 2014, Genome-scale analyses of Escherichia coli and Salmonella enterica AraC reveal noncanonical targets and an expanded core regulon., J Bacteriol 196(3):660-71

 [20] Hendrickson W., Flaherty C., Molz L., 1992, Sequence elements in the Escherichia coli araFGH promoter., J Bacteriol 174(21):6862-71

 [21] Miyada CG., Stoltzfus L., Wilcox G., 1984, Regulation of the araC gene of Escherichia coli: catabolite repression, autoregulation, and effect on araBAD expression., Proc Natl Acad Sci U S A 81(13):4120-4

 [22] Lobell RB, Schleif RF, 1990, DNA looping and unlooping by AraC protein., Science, 250(4980):528 10.1126/science.2237403

 [23] Hamilton EP., Lee N., 1988, Three binding sites for AraC protein are required for autoregulation of araC in Escherichia coli., Proc Natl Acad Sci U S A 85(6):1749-53

 [24] Martin K, Huo L, Schleif RF, 1986, The DNA loop model for ara repression: AraC protein occupies the proposed loop sites in vivo and repression-negative mutations lie in these same sites., Proc Natl Acad Sci U S A, 83(11):3654 10.1073/pnas.83.11.3654

 [25] Carra JH, Schleif RF, 1993, Variation of half-site organization and DNA looping by AraC protein., EMBO J, 12(1):35 10.1002/j.1460-2075.1993.tb05629.x

 [26] Tischer A, Brown MJ, Schleif RF, Auton M, 2019, Arabinose Alters Both Local and Distal H-D Exchange Rates in the Escherichia coli AraC Transcriptional Regulator., Biochemistry, 58(26):2875 10.1021/acs.biochem.9b00389

 [27] Rodgers ME, Schleif R, 2009, Solution structure of the DNA binding domain of AraC protein., Proteins, 77(1):202 10.1002/prot.22431

 [28] Gallegos MT, Michán C, Ramos JL, 1993, The XylS/AraC family of regulators., Nucleic Acids Res, 21(4):807 10.1093/nar/21.4.807

 [29] Cole SD, Schleif R, 2012, A new and unexpected domain-domain interaction in the AraC protein., Proteins, 80(5):1465 10.1002/prot.24044

 [30] Soisson SM, MacDougall-Shackleton B, Schleif R, Wolberger C, 1997, The 1.6 A crystal structure of the AraC sugar-binding and dimerization domain complexed with D-fucose., J Mol Biol, 273(1):226 10.1006/jmbi.1997.1314

 [31] Soisson SM, MacDougall-Shackleton B, Schleif R, Wolberger C, 1997, Structural basis for ligand-regulated oligomerization of AraC., Science, 276(5311):421 10.1126/science.276.5311.421

 [32] Rodgers ME, Holder ND, Dirla S, Schleif R, 2009, Functional modes of the regulatory arm of AraC., Proteins, 74(1):81 10.1002/prot.22137

 [33] Seedorff J, Schleif R, 2011, Active role of the interdomain linker of AraC., J Bacteriol, 193(20):5737 10.1128/JB.05339-11

 [34] Malaga F, Mayberry O, Park DJ, Rodgers ME, Toptygin D, Schleif RF, 2016, A genetic and physical study of the interdomain linker of E. Coli AraC protein--a trans-subunit communication pathway., Proteins, 84(4):448 10.1002/prot.24990



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