Cis Element:dif
Cis element summary table
<protect>
Standard Name |
dif |
---|---|
Synonyms |
deletion-induced filamentation |
Function |
Recombination site in terminus |
Location |
|
SO terms |
|
edit table |
</protect>
Notes
Location and Sequence
<protect>
See Help:Gene_location for help entering information in the Gene Location and DNA sequence table.
Strain | Map location | Genome coordinates | Genome browsers | Sequence links |
---|---|---|---|---|
34.2 minutes |
MG1655: 1588774..1588801 |
|||
edit table |
</protect>
Notes
The dif site is a 28bp sequence located within a 30kb region of the terminus known as the "dif activity zone" (DAZ) and is involved in Chromosome Dimer Resolution involving XerCD[2][3][4]. dif must be located in the terminus region for proper function and may be functionally replaced by loxP if the Cre recombinase is supplied in trans[5]. XerC binds the dif left half site while XerD binds the dif right half site- these sites are not interchangeable[6].
Interactions
<protect>
See Help:Product_interactions for help entering or editing information about gene product interactions in this section of EcoliWiki.
Partner Type | Partner | Notes | References | Evidence |
---|---|---|---|---|
Protein |
XerC |
|||
Protein |
XerD |
| ||
edit table |
</protect>
Notes
Sites where XerCD bind and cleave dif can be found in Blakely et al. (1997)[9].
Mutant alleles and phenotypes
<protect>
Allele | Nt change(s) | Phenotype: Type | Phenotype: Description | Reference | Availability | Comments |
---|---|---|---|---|---|---|
Δdif |
Growth Phenotype |
Filamentation- >15% of cells |
||||
Δdif |
Growth Phenotype |
|
||||
Δdif rarA |
Growth Phenotype |
Filamentation- >15% of cells |
| |||
edit table |
</protect>
Notes
Genetic Resources
<protect>
See Help:Gene_resources for help entering information into the Genetic Resources table.
Resource | Resource Type | Source | Notes/Reference |
---|---|---|---|
pSDC124 |
Plasmid Clone |
pUC18-based dif reporter |
|
pFC238 |
Plasmid Clone |
pGB2-based dif reporter |
|
pFH127 |
Plasmid Clone |
pGB2ts-based dif reporter carrying one dif site |
|
NL Strains |
Strain |
This paper lists a variety of different dif deletions and other constructs designed to test the dif locus |
|
pUC-dif |
Plasmid Clone |
pUC18-based dif reporter |
|
GR35 |
Strain |
AB1157difΔ6 |
|
GR47 |
Strain |
AB1157lexA3difΔ6 |
|
pGB201 |
Plasmid Clone |
dif1-1 containing plasmid |
|
pGB102 |
Plasmid Clone |
Reporter plasmid with directly repeateddif1-1 sites |
|
pGB204 |
Plasmid Clone |
Reporter plasmid containing two right half sites of dif1-1 (dif1-1DD) |
|
pGB103 |
Plasmid Clone |
Reporter plasmid with inverted dif1-1 sites |
|
pGB105 |
Plasmid Clone |
Reporter plasmid with inverted dif sites |
|
pGB203 |
Plasmid Clone |
Reporter plasmid containing two left half sites of dif1-1 (dif1-1CC) |
|
pGB205 |
Plasmid Clone |
Reporter plasmid containing isolated right half site of dif1-1 (dif1-1D) |
|
pGB206 |
Plasmid Clone |
Reporter plasmid containing isolated left half site of dif1-1 (dif1-1C) |
|
pGB408 |
Plasmid Clone |
Reporter plasmid containing two right half sites of dif (difDD) |
|
edit table |
</protect>
Notes
- One way to test the resolution competency at the dif activity zone (DAZ) or individual dif sites is to perform plasmid dimer resolution assays[16], or dif-Km-dif excision assays[17]. Steiner and Kuempel (1998) used a density label assay to analyze dif recombination[18][19].
Accessions
<protect>
See Help:Gene_accessions for help with entering information into the Gene Accessions table.
Database | Accession | Notes |
---|---|---|
EcoCyc: |
Escherichia coli str. K-12 substr. MG1655 | |
EcoGene: |
Escherichia coli str. K-12 substr. MG1655 | |
RegulonDB: |
Escherichia coli str. K-12 substr. MG1655 | |
EchoBASE: |
Escherichia coli str. K-12 substr. MG1655 | |
ASAP: |
Escherichia coli str. K-12 substr. MG1655 | |
edit table |
</protect>
Notes
References
See Help:References for how to manage references in EcoliWiki.
- ↑ 1.0 1.1 Kuempel, PL et al. (1991) dif, a recA-independent recombination site in the terminus region of the chromosome of Escherichia coli. New Biol. 3 799-811 PubMed
- ↑ Tecklenburg, M et al. (1995) The dif resolvase locus of the Escherichia coli chromosome can be replaced by a 33-bp sequence, but function depends on location. Proc. Natl. Acad. Sci. U.S.A. 92 1352-6 PubMed
- ↑ Cornet, F et al. (1996) Restriction of the activity of the recombination site dif to a small zone of the Escherichia coli chromosome. Genes Dev. 10 1152-61 PubMed
- ↑ Kuempel, P et al. (1996) Use of a transposon (Tndif) to obtain suppressing and nonsuppressing insertions of the dif resolvase site of Escherichia coli. Genes Dev. 10 1162-71 PubMed
- ↑ 5.0 5.1 Leslie, NR & Sherratt, DJ (1995) Site-specific recombination in the replication terminus region of Escherichia coli: functional replacement of dif. EMBO J. 14 1561-70 PubMed
- ↑ Smith, MR & Cook, RT (1977) Urea reduces the thermal stability of polyanion-treated chromatin. Biochem. Biophys. Res. Commun. 74 1475-82 PubMed
- ↑ 7.0 7.1 Barre, FX et al. (2000) FtsK functions in the processing of a Holliday junction intermediate during bacterial chromosome segregation. Genes Dev. 14 2976-88 PubMed
- ↑ 8.0 8.1 Sherratt, DJ et al. (1995) Site-specific recombination and circular chromosome segregation. Philos. Trans. R. Soc. Lond., B, Biol. Sci. 347 37-42 PubMed
- ↑ Blakely, GW et al. (1997) Binding and cleavage of nicked substrates by site-specific recombinases XerC and XerD. J. Mol. Biol. 265 30-9 PubMed
- ↑ 10.0 10.1 Sherratt, DJ et al. (2004) Recombination and chromosome segregation. Philos. Trans. R. Soc. Lond., B, Biol. Sci. 359 61-9 PubMed
- ↑ Blakely, G et al. (1991) Escherichia coli XerC recombinase is required for chromosomal segregation at cell division. New Biol. 3 789-98 PubMed
- ↑ 12.0 12.1 12.2 Recchia, GD et al. (1999) FtsK-dependent and -independent pathways of Xer site-specific recombination. EMBO J. 18 5724-34 PubMed
- ↑ Hayes, F & Sherratt, DJ (1997) Recombinase binding specificity at the chromosome dimer resolution site dif of Escherichia coli. J. Mol. Biol. 266 525-37 PubMed
- ↑ Grainge, I et al. (2007) Unlinking chromosome catenanes in vivo by site-specific recombination. EMBO J. 26 4228-38 PubMed
- ↑ 15.0 15.1 15.2 15.3 15.4 15.5 15.6 15.7 15.8 Blakely, G et al. (1993) Two related recombinases are required for site-specific recombination at dif and cer in E. coli K12. Cell 75 351-61 PubMed
- ↑ Yates, J et al. (2003) Species specificity in the activation of Xer recombination at dif by FtsK. Mol. Microbiol. 49 241-9 PubMed
- ↑ Pérals, K et al. (2000) Functional polarization of the Escherichia coli chromosome terminus: the dif site acts in chromosome dimer resolution only when located between long stretches of opposite polarity. Mol. Microbiol. 36 33-43 PubMed
- ↑ Steiner, WW & Kuempel, PL (1998) Cell division is required for resolution of dimer chromosomes at the dif locus of Escherichia coli. Mol. Microbiol. 27 257-68 PubMed
- ↑ Steiner, WW & Kuempel, PL (1998) Sister chromatid exchange frequencies in Escherichia coli analyzed by recombination at the dif resolvase site. J. Bacteriol. 180 6269-75 PubMed