- Methodology article
- Open Access
Escherichia coli MW005: lambda Red-mediated recombineering and copy-number induction of oriV-equipped constructs in a single host
© Westenberg et al; licensee BioMed Central Ltd. 2010
- Received: 17 July 2009
- Accepted: 29 March 2010
- Published: 29 March 2010
Escherichia coli strain EL350 contains chromosomally integrated phage lambda Red recombinase genes enabling this strain to be used for modifying the sequence of resident clones via recombineering. BAC and fosmid clones are highly suitable for modification by recombineering but, because they are present at low (1-2) copies per cell, the DNA is difficult to isolate in high yield and purity. To overcome this limitation vectors, e.g. pCC1FOS, have been constructed that contain the additional replication origin, oriV, which permits copy-number to be induced transiently when propagated in a suitable host strain, e.g. EPI300, that supplies the cognate trans-replication protein TrfA. Previously, we used EL350 and EPI300 sequentially to recombineer oriV-equipped fosmid genomic clones and, subsequently, to induce copy-number of the resulting recombinant clone. To eliminate these intervening DNA isolation and transformation steps we retrofitted EL350 with a PBAD-driven trfA gene generating strain MW005 that supports, independently, both recombineering and copy-number induction.
The PBAD-driven copy of cre in EL350 was replaced seamlessly with a copy of trfA, PCR-amplified from EPI300 chromosomal DNA, to generate MW005. This new strain has been used to both generate, via recombineering, a number of reporter gene fusions directly from pCC1FOS-based Caenorhabditis elegans genomic clones and to transiently induce copy-number of fosmid and BAC clones prior to DNA preparation.
By retrofitting EL350, an established 'recombineering' E. coli strain, with a tightly regulated copy of trfA we have produced a new strain, MW005, which combines recombineering capacity with the useful ability to transiently induce copy-number of oriV-equipped clones. By coupling these two steps in a single strain, use of MW005 will enable the more rapid recombineering-mediated production of recombinant clones in the yield and quality necessary for many downstream purposes.
- Genomic Clone
- Fosmid Clone
- Recombineering Step
- Replacement Cassette
- deoR recA1
Recombineering (recombinogenic engineering) is a relatively recently described technique of homologous recombination (HR)-based genetic engineering performed within an E. coli host and mediated by transient expression of phage-encoded recombinases [reviewed in ref ]. Both lambda Red  and the Rec E/T  recombinase systems have been developed into recombineering tools for transient, controlled expression of the respective recombinase activities. Whilst recombineering can be used to modify the host chromosome the technique is more commonly applied to episomal replicons including low-copy-number BACs or fosmids and intermediate and multicopy plasmids. Modifications are targeted and precise and can range from single base-pair deletions or insertions to the addition or deletion of sequences in the kilobase-pair range. Bacteria containing the target are transformed with linear, double- or single-stranded, donor DNA molecules bearing the desired sequence changes. These donor molecules are generated, as PCR-amplicons, restriction fragments or oligonucleotides, that contain, at each end, appropriate regions of homology to the circular target. In contrast to RecA-mediated genetic engineering only short (~50 bp) homologies are required to mediate efficient HR between donor and target molecules. These "homology arms" can be built easily into a donor by PCR. Recombineering is particularly useful when manipulating larger target molecules, such as BACs or fosmids, which, because of their size, will likely lack the required range of unique and appropriately positioned restriction enzyme sites necessary to achieve subtle modifications. Recombineering is gaining wider acceptance as a genetic engineering tool and may be viewed as a viable alternative to more traditional restriction enzyme/ligase-based approaches particularly when modifying large target molecules.
The nematode C. elegans is a genetically tractable model animal that, since its initial introduction , has become the experimental system of choice for many laboratories. Determining the expression pattern for a gene-of-interest (goi) by analysing β-galactosidase or fluorescent protein reporter expression in C. elegans transformed with a goi::reporter fusion gene is a commonly performed procedure. In a so-called transcriptional reporter gene fusion the expression of the reporter protein alone is driven by DNA fragments known, or presumed, to contain all or part of the goi's promoter. In C. elegans this usually comprises 1-4 kb from immediately 5' of the translational start codon. Such constructions will, by definition, exclude any regulatory elements that lie outside the assayed genomic DNA fragment. In contrast, in a translational reporter gene fusion the reporter gene is fused, in-frame, to all, or part, of the goi's protein coding region to encode a fusion protein. Such a translational reporter gene fusion would, ideally, contain not only all in the immediate vicinity of the goi's protein coding region but also significant stretches of 5' and 3' flanking DNA, and so include more distantly located regulatory elements.
As discussed, recombineering is ideal for engineering large targets and a number of protocols designed to generate translational-style reporter gene fusions directly from C. elegans genomic clones have been described [5–8]. Additionally, we , and others , have combined recombineering with counter-selection to enable the reporter sequence to be inserted seamlessly into the target. Such counter-selection strategies are, however, limited to fosmid or other low-copy-number vector targets because the relative inefficiency of the recombineering method makes it difficult otherwise to select negatively for desired recombinants. The C. elegans genome is covered extensively with genomic clones from a library constructed in the copy-number-inducible fosmid vector pCC1FOS (CopyControl, Epicentre, Madison, USA; Moerman D., pers. comm.). In addition to the F factor system, that maintains pCC1FOS-based clones at 1-2 copies per chromosome, pCC1FOS also contains an oriV replication origin. When propagated in a suitable host strain, e.g. EPI300 (Epicentre), that carries trfA encoding the associated replication protein TrfA, the oriV replication origin allows copy-number to be induced to approximately 50-100 copies per host chromosome. If trfA transcription is tightly controlled, for example by the L-arabinose-regulated araC-PBAD system, then oriV-equipped fosmid copy-number is only increased "on-command" when high yields of good-quality DNA need to be isolated for downstream events .
The counter-selection protocol applied by us [5, 10] utilises E. coli host strains, e.g. EL250 and EL350  and derivatives there from, that provide recombineering capacity via a chromosomally integrated defective lambda prophage. The prophage contains the Red recombinase genes arranged in their natural context and tightly regulated by the temperature-sensitive cI857 repressor . Although recombinase functions can be supplied [for example ref ] via plasmids the tighter control and coordinated expression of the integrated prophage approach is considered more efficient and controllable. Our counter-selection approach  utilizes a dicistronic counter-selection cassette (the RT-cassette), containing the respective positive and negative markers tetA(C) and rpsL driven by the hypo-osmotically up-regulated ompF promoter to provide stringent positive and negative selection for single-copy vectors . The RT-cassette, inserted at the target site by an initial recombineering step using positive selection for recombinants, is replaced with the desired sequence in a second round of recombineering using negative selection. Positive selection is provided by tetA(C) conferring tetracycline (Tc) resistance (TcR) whereas, when expressed in a rpsL- host, the wild-type rpsL+ gene provides the negative marker. Mutations in the chromosomal rpsL, that encodes the ribosomal protein S12, confers streptomycin [Sm], resistance (SmR). When both mutant and wild-type rpsL alleles are co-expressed a dominant Sm sensitive (SmS) phenotype results. Because EL250 and EL350 are rpsL- and thus SmR, the introduction, via the RT-cassette, of a rpsL+ allele confers SmS. Consequently, non-recombinants following the second recombineering step will remain SmS and are selected against whereas desired recombinants are SmR revertants.
Whilst efficient in mediating recombineering, a strain such as EL350 does not permit copy-number induction of resident oriV-equipped clones. Thus, our present protocol requires an additional fosmid DNA isolation step and transformation into a TrfA-producing strain to enable transient copy-number induction. In order to combine recombineering and copy-number induction in a single strain we have retrofitted the chromosome of EL350 with a copy of trfA under control of the araC-PBAD regulatory system. The resulting strain, MW005, enables recombineering and copy-number induction to be performed in a single host with significant improvements in speed and productivity. We have used MW005 successfully to create a number of reporter gene fusions in pCC1FOS-based genomic clones. We describe here construction details for MW005 and demonstrate its use in supporting controlled copy-number induction of oriV-equipped fosmid and BAC genomic clones. In addition, we also illustrate its use in recombineering in the construction of a pCC1FOS-based translational GFP reporter gene fusion for the C. elegans transcription factor gene ceh-12.
The coupled pCC1FOS-based genomic clone recombineering and copy-number induction described here have validated the use of MW005 as a convenient host strain in which to perform both recombineering-based genetic engineering and copy-number induction. As there is some evidence for very low levels of "leaky" cre expression in EL350  we were concerned initially that if trfA expression was similarly leaky in MW005 this may result in pCC1FOS-based clone copy-number being increased above its normal range of 1-2 copies per cell with knock-on effects for clone stability and/or recombineering efficiency. However, restriction enzyme digestion of fosmid and BAC clones isolated from MW005 minicultures (Fig.2 and data not shown) indicated these clones were stably propagated in this strain. In addition to the clone modification described here, MW005 has been used successfully to perform recombineering on more than twenty additional pCC1FOS-based C. elegans genomic clones and there is no evidence that recombination efficiency differs from the parental strain EL350. Estimates of such efficiency (number of colonies with selection/total viable cell count) × 100 indicate a range of approx. 0.01-0.05% for both EL350 and MW005.
The only experimental proviso on the use of MW005 is that incubation temperatures must not exceed 32°C at any time except during the brief heat-shock needed to de-repress transcription of the Red gene cluster. This is not a significant inconvenience as culture growth rates are slowed only marginally. As we retrofitted strain EL350, MW005 cannot be used for recombineering with a galK counter-selection cassette  nor can it be used to excise loxP-flanked sequences as the chromosomal copy of cre is now replaced with trfA. We believe MW005, available from the non-profit plasmid repository Addgene, will prove useful to a number of labs using recombineering to modify oriV-equipped clones. For clones lacking an oriV this sequence can be easily retrofitted into the clone either by recombineering or by standard genetic engineering techniques or, and perhaps more straightforwardly, via random Tn5 transposon-mediated insertion  (EZ-Tn5 system, Epicentre).
We have described the construction of a new E. coli strain, MW005, retrofitted with a PBAD-driven copy of trfA encoding the trans-activating replication protein TrfA. Use of MW005 permits researchers to perform both lambda Red-mediated recombineering and subsequent copy-number induction of recombinant DNAs, if these are equipped with oriV, in a single host thereby negating the requirement for additional clone isolation and transformation steps. When large number of clones are being modified by recombineering this can translate into significant time saving.
Generation of MW005
PCR-amplification and cloning of trfA
PCR-amplification of the rpsL-tetA(C) and trfArecombineering cassettes
The rpsL-tetA(C) counter-selection cassette (RT-cassette)  was generated by PCR using a gel-purified 2.7 kb NcoI fragment of pBAC-RT  as template (5 ng) and ODNs 6090 and 6091 (Table 1). These "recombineering" ODNs were PAGE-purified (IDT, Leuven, Belgium) and contain 50-nt 5' homology arms corresponding to sequences directly flanking the single NcoI and HindIII sites of pBADcre  (Fig. 1A), respectively, and designed to enable replacement of the PBAD-driven cre gene in EL350  with trfA. The trfA replacement cassette was generated by PCR using pMW010 DNA (5 ng) as template and ODNs 6088 and 6089 (Table 1) that contained homology arms equivalent to those of 6090 and 6091 (Table 1) (Fig. 1B). Both PCR products were purified (Wizard SV columns, Promega) then quantified, by visualisation against a DNA mass ladder (1 kb ladder, NEB), prior to use.
Recombineering-mediated generation of MW005
Heat-shock-mediated induction of Red activities, preparation of electrocompetent E. coli cells and all subsequent recombineering steps were performed essentially as described . Briefly, non-induced (control) or Red-induced electrocompetent EL350 cells were electroporated (Eppendorf 2510) with 500 ng of the PCR-generated RT-cassette and cells recovered (SOC [-Mg] medium, 32°C, 220 rpm, 2.5 h). Recovered cells were serially diluted (M9 salts), aliquots (50 μl) spread on either selective (Tc, 5 μg/ml) or non-selective (for cell viability determination) LB-agar plates and incubated (32°C, 48 h). Five discrete Tc-resistant colonies were re-streaked on Tc-selective LB-agar plates and incubated further (32°C, 48 h). Those colonies in which the RT-cassette had been inserted correctly into the host chromosome were identified by colony-PCR using the insertion site-flanking ODNs 6102 and 6103 (Table 1). The RT-cassette-containing EL350 strain was named MW004.
In the subsequent replacement recombineering step the PCR-generated trfA gene sequence (500 ng) was introduced into non- or Red-induced MW004 cells by electroporation and, subsequently, recovered cells were spread on either selective (Sm, 500 μg/ml) or non-selective LB-agar plates and incubated (32°C, 48 h). As above, a number of discrete Sm-resistant colonies were re-streaked to fresh Sm-selective plates and incubated further (32°C, 48 h). Those colonies in which the RT-cassette had been replaced with the trfA sequence were identified, initially by colony-PCRs, with ODNs 6102 and 6103 (Table 1) and subsequently by direct sequencing of the resulting PCR products. The new strain, MW005, has the PBAD-driven chromosomal cre sequence replaced with that encoding trfA.
Copy-number induction of pCC1FOS- and pCC1BAC-based genomic clones in MW005
Construct fUL#SB28 (see below), two additional C. elegans pCC1FOS-based genomic clones WRM0636aA04 and WRM067aC01 and Lates calcarifer pCC1BAC-based genomic clones A02_CBP0333, A10_CBP1191 and H12_CBP0642  were electroporated into MW005 and EPI300 and recovered bacteria plated on selective (Chl, 12.5 μg/ml) LB-agar plates. Aliquots of overnight cultures (10 ml LB, Chl 12.5 μg/ml, 32°C, 220 rpm), each inoculated with a single colony, were mixed with fresh medium (LB, Chl 12.5 μg/ml) to give a final volume of 20 ml and OD600 of 0.4. Each diluted culture was divided equally into two 10 ml aliquots with 10 μl of CopyControl induction solution (Epicentre) being added to one aliquot before all were incubated for an additional 4 h (32°C, 220 rpm). Cell densities (OD600) were measured enabling DNA to be isolated, by standard alkali lysis and isopropanol precipitation, from the same number of bacterial cells (equivalent to 5 ml at an OD600 of 3.0) per culture. DNA was resuspended (50 μl TE) and aliquots (5 μl) incubated with either BamHI or NcoI. Non-diluted and 2-fold serial dilutions of the digested DNA from, respectively, non-copy-number-induced and copy-number-induced cells were subject to agarose gel (0.7% w/v) electrophoresis (Fig. 2).
Construction of a fosmid-based ceh-12::gfpreporter gene fusion in MW005
The generation of the linear RT and gfp replacement cassettes differed slightly from that described above and previously  in that the counter-selection RT-cassette was flanked by 50 bp regions corresponding to the extreme 5' and 3' ends of the gfp coding sequence. This enabled the replacement gfp cassette to be provided as a simple restriction-fragment excised from a suitable gfp-containing plasmid . Briefly, a target specific [5-gfp-RT-gfp-3']-cassette was amplified by PCR using, as a template, a plasmid containing a 5'-gfp-RT-gfp-3' sequence , and ODNs S0316 & S0317 (Table 1). These primers contained 50-nt 5' homology arms designed to insert the [5'-gfp-RT-gfp-3']-cassette immediately upstream of the translation termination codon of the C. elegans ceh-12 gene. The amplified [5'-gfp-RT-gfp-3']-cassette was electroporated into recombineering-competent MW005 E. coli that had been previously transformed with the pCC1FOS-based genomic clone, WRM0611dH08. The 33.5 kb insert of this clone contains the entire ceh-12 locus plus significant 3' (>25 kb) and 5' (>6 kb) flanking genomic DNA (Fig. 3A). Following recovery, cells were spread on Tc-selective LB-agar plates and restreaked. Fosmids containing a [5'-gfp-RT-gfp-3']-cassette inserted correctly at the target site were identified by colony-PCR using the insertion site-flanking ODNs S0015 and S0016 (Table 1). Replacement of the 5'-gfp-RT-gfp-3' sequence with gfp within electro- and recombineering-competent MW005 was carried out as described above except a restriction fragment, encoding the complete gfp coding sequence, minus the termination codon, was used  and cells were selected on LB-agar plates containing both Sm (500 μg/ml) and chloramphenicol (Cm) (12.5 μg/ml). A recombinant fosmid clone containing the correctly recombineered ceh-12::gfp fusion sequence was identified by colony-PCR, using PCR primers flanking the insertion site, and detailed restriction digestion (data not shown) and was called fUL#SB28 (Fig. 3C). Sequencing across the insertion site was deemed unnecessary as the replacement sequence was introduced into MW005 as a restriction fragment  rather than a PCR product as used previously .
C. eleganstransformation and observation
Following copy-number induction, performed as described above, and DNA isolation transformation of C. elegans N2 worms with fUL#SB28 and plasmid pRF4 was performed by microinjection into adult syncytial gonads as described . GFP expression in adult hermaphrodites from independently derived lines was observed by fluorescence microscopy as described (Fig. 3D) .
We thank the Wellcome Trust (ref. WT078981) and the BBSRC (ref. BB/E008038/1) for support and Dr G.H. Yue (National University of Singapore) for Lates calcarifer BAC genomic clones.
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