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RESEARCH PAPER
1 Molecular Genetics Program, Wadsworth Center, New York State Department of Health and School of Public Health, State University of New York at Albany, Albany, New York 12201, USA; 2 Institute for Cellular and Molecular Biology, Department of Chemistry and Biochemistry and Section of Molecular Genetics and Microbiology, School of Biological Sciences, University of Texas at Austin, Austin, Texas 78712, USA
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Abstract |
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[Keywords: Retroelement; retrotransposon; RNase H; Pol I; Pol III; repair polymerases]
Received June 14, 2005; revised version accepted August 15, 2005.
; Lambowitz and Zimmerly 2004). Retrohoming pathways have been studied in detail for two related yeast mitochondrial introns (aI1 and aI2) and two bacterial introns (Ll.LtrB and RmInt1) (Belfort et al. 2002; Lambowitz and Zimmerly 2004; Martinez-Abarca et al. 2004). The Ll.LtrB intron, which derives from Lactococcus lactis (Mills et al. 1996; Shearman et al. 1996), was shown to be functional in both splicing and retrohoming in Escherichia coli (Mills et al. 1997; Cousineau et al. 1998). In all organisms, the retrohoming of group II introns occurs by a process in which the excised intron RNA reverse splices into one strand of a DNA target site and is then reverse transcribed by the intron-encoded protein (IEP). This process is mediated by a ribonucleoprotein (RNP) particle that is formed during RNA splicing and contains the IEP and the excised intron lariat RNA. In addition to catalytically active intron RNA, retrohoming of the Ll.LtrB intron is dependent upon three activities of the IEP (Belfort et al. 2002; Lambowitz and Zimmerly 2004; Lambowitz et al. 2005). These are RNA maturase, to stabilize the catalytically active structure of the intron RNA for RNA splicing and reverse splicing, DNA endonuclease, for cleavage of the target DNA to generate a primer for reverse transcription, and reverse transcriptase (RT) for making a cDNA copy of the intron RNA (Fig. 1).
Completion of the retrohoming pathway in bacteria is distinguished from the major pathway in yeast by its independence of homologous recombination between donor and recipient (Eskes et al. 1997; Mills et al. 1997; Cousineau et al. 1998; Martínez-Abarca and Toro 2000). After complete reverse splicing of the Ll.LtrB intron and endonucleolytic cleavage of the second strand, 9 nucleotides (nt) downstream of the intron-insertion site, full-length cDNA synthesis ensues in a process termed target DNA-primed reverse transcription (TPRT) (Fig. 1, steps 1-3). The later stages of retrohoming require degradation or displacement of the RNA strand, second-strand DNA synthesis, and possibly trimming of DNA ends, and ligation of junctions (Fig. 1, steps 4-7). However, the nature of these steps, and the enzymes involved, have not been defined for any group II intron.
Non-LTR-retrotransposons, which are evolutionarily related to mobile group II introns, also utilize a TPRT mechanism (Luan et al. 1993; Moran and Gilbert 2002). The protein encoded by the non-LTR-retrotransposons cleaves a DNA target site and then uses the cleaved 3' end as primer to synthesize a full-length cDNA of the element's RNA (Eickbush 2002). Here too, the mechanism of late steps in retrotransposition, including second-strand synthesis and the sealing of gaps, has remained obscure.
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). Reliance on the IEP, as well as the distinctive independence of homology between donor and recipient, and the absence of coconversion tracks, are all identical. Furthermore, in both systems retrohoming is independent of RecA function. For these reasons, and because of the general availability of DNA and RNA processing mutants in E. coli, we selected this host in which to examine the potential involvement of cellular factors in retrohoming. We thereby demonstrate how a retrotransposon parasitizes its host through exploitation of cellular nucleolytic, polymerization, and repair activities, to promote its own spread. |
Results |
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The plasmid-based assay described by Cousineau et al. (1998) was used to test the role of host accessory functions in retrohoming (Fig. 2A). In this assay, the group II intron donor plasmid contains drug-resistance marker PM1, and the intron contains an additional drug-resistance marker (IM), along with the group I td intron (I) in domain IV. The loss of the td intron by self-splicing reports the minimum number of homing events that have passed through an RNA intermediate. The compatible recipient plasmid contains the Ll.LtrB homing site (E1-E2) and a different drug-resistance marker (PM2). After induction of Ll.LtrB expression, plasmids are extracted and digested with restriction enzymes to destroy the donor plasmid, then retransformed into E. coli. Then, homing products are selected for the IM and recipient PM2 markers, and screened for sensitivity to the donor PM1. Homing frequencies in the 0.1%-0.6% range (Fig. 2B, crosses 1 and 2) could be increased to 
14% with expression of the ltrA gene downstream of exon 2 to generate a smaller intron (Fig. 2B, cross 3). The enhanced mobility frequency is thought to be due to decreased susceptibility of the smaller intron RNA to degradation by host nucleases (Guo et al. 2000).
A second assay, developed by Guo et al. (2000), was also used to check mutants with the most dramatic phenotypes (see Supplementary Tables S1-S3). In most cases, there was good agreement on host effects between the two assays, and where not, the disparities can be readily explained by the differences in assay conditions. A comparison between the two assays and related explanations are given in the Supplemental Material, where the assay described in the text is referred to as assay A, and the second assay as assay B.
To ensure that neither replication of the donor or recipient plasmids nor intron expression was compromised in each of the different hosts, we performed a gel assay on donor and recipient plasmid levels before and after induction of Ll.LtrB, as described (Cousineau et al. 1998). Conversion of the recipient plasmid to homing product and/or its disappearance due to cleavage by the RNP, with subsequent plasmid degradation by host nucleases, were interpreted as satisfactory expression. Additionally, LtrA expression was confirmed in many cases on protein gels. If either or both the replication and expression criteria were not satisfied, the result of the retrohoming assay was discarded. Loss of the td intron was also monitored to ensure that homing events had passed through an RNA intermediate.
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Table 1 lists the host mutants tested for DNA-processing activities, along with a brief description of the function of the mutated protein. The mutants were screened with cross 1, and those that showed a greater than threefold difference in homing frequency were considered to have a facilitatory or inhibitory effect on retrohoming. For each mutant, homing efficiency is expressed as the value relative to that in an isogenic parental host (Supplementary Table S4).
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Relationship of retrohoming efficiency to RNA-processing functions
Several general RNA-processing mutants were also screened for their ability to support retrohoming (Table 2). Although StpA, which promotes RNA annealing and strand exchange, appears not to affect retrohoming, RNase I and RNase E, degradative enzymes, do. Retrohoming was enhanced by greater than fourfold in the RNase I mutant, and elevated 
10-fold in a ts RNase E mutant. These increases likely reflect the fact that RNases I and E contribute to degradation of the intron RNA.
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). Mutation of RNase H1 (rnhA) caused a >30-fold drop in homing efficiency. In contrast, mutation of RNase H2 (rnhB) had only a twofold effect, while the RNase H1/H2 double mutant was again >30-fold depressed. Accordingly, this effect could be reversed by complementation with the rnhA but not the rnhB gene expressed from a compatible plasmid (Table 2, see footnote d). These results suggest that RNase H contributes to degradation of the intron RNA template, with RNase H1 playing the dominant role.
Pol I, the product of the polA gene, is a multifunctional protein that catalyzes lagging-strand DNA synthesis. Its 5'-3' exonuclease activity, which is involved in removing RNA primers from Okazaki fragments (Kornberg and Baker 1992), might be involved in intron RNA degradation before second-strand DNA synthesis. For testing Pol I mutants, a new donor and recipient pair with Bhr and pSC101 replication origins was constructed, because neither p15A nor ColE1 replicons can be maintained in polA hosts (Fig. 2B, cross 2). The polA107 mutant, which contains a point mutation that inhibits 5'-3' exonuclease activity, resulted in a fourfold reduction in retrohoming, whereas deletion of this domain in the 
polA::/F' klenow strain, eliminated mobility below detectable levels. Notably, RNase H1 overexpressed from a plasmid was unable to complement the Pol I-5'-3' exo deletion mutant (data not shown). Thus, as expected from their biochemical activities, RNase H1 and Pol I-5'-3' exo likely act at different steps in RNA degradation.
The LtrA protein has minimal DNA-dependent DNA polymerase activity in vitro
We next wished to identify the DNA polymerase that conducts second-strand cDNA synthesis. To test whether LtrA itself might play a role, we performed in vitro assays using the template-primer substrates shown in Figure 3 (I-IV). These assays used two substrates to test for DNA-dependent DNA polymerase activity: annealed synthetic DNA oligonucleotides that mimic a potential substrate for second-strand DNA synthesis in which the 3' end of E1 is used as a primer for top-strand synthesis (substrate I) and the artificial template/primer substrate poly(dA)/oligo(dT)18 (substrate II). As controls to assay RT activity, we used a previously described natural substrate mimic denoted Ll.LtrB/E2+10 (substrate III) and the artificial template/primer substrate poly(rA)/oligo(dT)18 (substrate IV). The former consists of Ll.LtrB RNA (an in vitro transcript containing the Ll.LtrB-ORF intron and flanking exons) with an annealed DNA primer (E2+10), whose 3' end corresponds to that of the cleaved bottom strand normally used as the primer for reverse transcription (Matsuura et al. 1997; Wank et al. 1999).
LtrA displayed high activities in both the bottom-strand RT and poly(rA)/oligo(dT) assays (Fig. 3, assays 5-7). However, no significant DNA-dependent DNA polymerase activity (i.e., incorporation above background) was detected with the top-strand synthesis substrate (I) and only very low activity was detected with poly(dA)/(dT)18 under different conditions, including high-salt (H) or low-salt (L) buffers (assays 1-4), further decreased salt concentrations, higher LtrA and dTTP concentrations, and reaction buffers optimal for Klenow or M-MLV-RT (see Fig. 3 legend). Furthermore, no significant DNA-dependent DNA polymerase activity with substrate I was found for RNPs, consisting of the Ll.LtrB lariat intron RNA and the LtrA protein (data not shown). As a control, Klenow showed high activities in the DNA-dependent DNA polymerase assays (assays 2-4), but not in the bottom-strand RT assay (assays 5 and 6). Klenow also displayed substantial activity with poly(rA)/oligo(dT)18 (assay 7), likely reflecting its cryptic RT activity (Springgate et al. 1973). Although we cannot exclude a difference between in vitro and in vivo conditions, the finding that LtrA has strong RT activity but little, if any, processive DNA-dependent DNA polymerase activity under a wide range of conditions, suggests that second-strand DNA synthesis is likely carried out by one or more host DNA polymerases.
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To determine whether replication of the recipient plasmid contributes to intron retrohoming, we used real-time PCR to assay retrohoming of the intron into the target site carried on a ts plasmid. For the mobility assay, pB102B-ltrB, a ts recipient plasmid, or its wild-type thermoresistant counterpart pB101B-ltrB (Fig. 4A; Supplementary Fig. S1C, cross 6), was transformed into cells containing the intron-donor plasmid pACD2 (Fig. 4A; Supplementary Fig. S1C, cross 5). Transformants were grown in LB medium at 30°C, the permissive temperature, or 37°C, the semirestrictive temperature for replication of the ts plasmid. Plasmid DNAs isolated from transformants grown for various times were subjected to real-time PCR to quantify intron homing. As shown in Figure 4A, intron integration into the ts recipient plasmid increased steadily at 30°C, but not at 37°C, while intron integration into the wild-type recipient plasmid increased at both temperatures. Although the reason for the fluctuation in homing frequencies at 37°C is not understood, the reduced mobility levels when the ts replicon is inhibited are reproducible, indicating that DNA replication is required for intron retrohoming.
We therefore wished to determine whether the major E. coli polymerases I (Pol I) and/or III (Pol III) are required for retrohoming. We first tested Pol I, the DNA polymerase that acts in lagging strand DNA synthesis and DNA excision repair, and found that loss of the polymerase and associated 3'-5' exonuclease activities do not significantly affect retrohoming (Table 3).
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-subunit of the Pol III core enzyme (Fig. 2B, cross 3), we showed that intron mobility was the same as that in the wild type at the permissive temperature of 30°C (Fig. 4B). However, retrohoming decreased approximately fourfold at the restrictive temperature of 37°C and decreased approximately fivefold at 42°C (Fig. 4B; Table 3). At 42°C, intron mobility in the wild-type strain also decreased, 10-fold from that at 30°Cor37°C, reflecting a general inhibitory effect on viability and homing when cells are grown at high temperature. For this reason, the 37°C numbers are reported in Table 3. The residual mobility in the dnaE mutant at 37°C and 42°C could result from the occurrence of retrohoming before the temperature shift, owing to leaky expression of the intron, from the involvement of other cellular polymerases, or from residual Pol III activity at elevated temperatures. Together, the data likely reflect not only the dependency of intron homing on DNA replication (Fig. 4A), but also the reliance of group II intron mobility on Pol III for second-strand cDNA synthesis.
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A possible role for the three SOS-inducible polymerases Pol II, Pol IV, and Pol V was also probed, because retrohoming may require activities similar to those that are recruited to repair damaged DNA. Pol II, the product of the polB gene, is a restart polymerase, which, in concert with a Pol III complex and a restart primosome complex, catalyzes error-free replication-restart (for review, see Goodman 2000; Sutton and Walker 2001). In contrast, Pol IV (dinB) copies undamaged DNA at stalled replication forks, which arise in the cell from mismatched or misaligned primer ends. Although Pol IV exhibits low processivity (6-8 nt before dissociation), association with Pol III causes a 3000-fold increase in DNA synthesis efficiency (Tang et al. 2000). Finally, Pol V, a product of the umuDC complex, is also nonprocessive, but is engaged in error-prone translesion synthesis (Sutton and Walker 2001).
Whereas Pol II and Pol IV single mutants were reduced threefold, the Pol V mutant was approximately 1.5-fold stimulated. The Pol II-Pol IV double mutant again yielded a threefold drop in retrohoming, whereas defects in Pol V together with Pol II or Pol IV mutations gave more dramatic results; the Pol II-Pol V, Pol IV-Pol V, and Pol II-Pol IV-Pol V mutants were 10-fold reduced in their ability to sustain retrohoming. Thus, in addition to a role identified for the replicative Pol III polymerase, the repair polymerases appear to have a substantial collective effect on retrohoming.
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A balance of inhibitory and stimulatory host functions in the initial steps of retrohoming
The first steps of reverse-splicing into the recipient DNA, second-strand DNA cleavage, and TPRT (Figs. 1, 5, steps 1-3) can occur in vitro and require only the catalytic activities of the intron RNA and the LtrA protein (Saldanha et al. 1999). These steps appear sensitive to host ribonucleases I and E (Table 2), probably due to intron degradation before reverse splicing or cDNA synthesis (Fig. 5, steps 1-3).
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), has any facilitatory effect, albeit small.
Another exonuclease to be considered, with an almost fourfold effect on retrohoming, is MutD (DnaQ), a 3'-5' exonuclease. MutD is a subunit (
) of Pol III holoenzyme, and carries out proofreading in the E. coli replication complex (Fersht and Knill-Jones 1983). Given that processive DNA synthesis is contingent upon this exonuclease subunit of the Pol III holoenzyme (Studwell and O'Donnell 1990), the phenotype of the MutD mutant fits well with the role of Pol III in second-strand cDNA synthesis (Figs. 4, 5, step 6). It is also possible that a 3'-5' exonuclease activity is required after removal of RNA, to cut back into the 5' exon, prior to second-strand synthesis by Pol III.
Retrohoming is reduced about fourfold in an SbcD mutant (Table 1). The SbcCD nuclease is involved in the structural maintenance of chromosomes, by cleaving DNA hairpins and other secondary structures that inhibit DNA replication (Connelly et al. 1998). Since the replication machinery is intimately involved in retrohoming, and stalled forks may well be intermediates in this process, we speculate that the role of SbcCD nuclease is in cleavage of inhibitory secondary structures at such forks.
Mutation of xthA, which encodes Exo III, elevates retrohoming by more than eightfold. This characteristic may result from Exo III's 3'-5' exonuclease activity degrading the newly synthesized cDNA, restoring the gap, and thereby inhibiting the repair process (Fig. 5, step 5). Alternatively, Exo III may degrade the top strand in the upstream exon and/or compete with Pol III for primers of second-strand synthesis (Fig. 5, step 6). Together, these results indicate that a delicate balance of inhibitory and facilitatory activities combine to effect, and possibly to regulate, retrohoming; then DNA ligase, with a fourfold effect in a ts mutant (Table 1), likely completes the process by sealing nicks left in the DNA (Fig. 5, step 7).
RNase H, Pol I, and the removal of intron RNA after reverse transcription
After reverse transcription, the intron RNA must be removed for synthesis of the second-strand using the cDNA as template (Fig. 5, step 5). Unlike retroviruses and LTR-retrotransposons, group II introns and non-LTR-retrotransposons do not encode their own RNases H (Malik and Eickbush 2001). We have shown here that of the two E. coli RNases H, RNase H1 plays an important role in retrohoming (Table 2; see also Supplementary Table S2), suggesting that group II introns can use a host RNase H to remove the RNA template after reverse transcription.
Two different Pol I mutants that lack the 5'-3' exonuclease activity, which may also act to remove the intron RNA template after reverse transcription, are strongly depressed in mobility. Whereas the rnhA gene, which encodes RNase H1, can complement an RNase H1 defect (Table 2), it fails to complement a Pol I 5'-3' defect, suggesting that the putative role of Pol I in RNA degradation is distinct from that of RNase H1. Indeed, whereas RNase H endonucleolytically cleaves the RNA strand in an RNA/DNA hybrid, Pol I is a 5'-3' exonuclease (Kornberg and Baker 1992). Furthermore, since Pol I 5'-3' exo and Pol III act in concert at replication forks (Lopez de Saro and O'Donnell 2001) and since our data support Pol III being responsible for second-strand synthesis, a role for Pol I 5'-3' exonuclease in the removal of RNA seems likely.
Pol III and second-strand DNA synthesis
Although the RTs of retroviruses and LTR retrotransposons have DNA-dependent DNA polymerase activity, this has not previously been tested quantitatively for members of the non-LTR retrotransposon superfamily, including group II introns. Although LtrA can copy the 5' overhang of the 3' exon DNA during initiation of TPRT (Saldanha et al. 1999), it has very low processive DNA-dependent polymerization activity on other substrates in vitro (Fig. 3), suggesting that second-strand synthesis may be carried out by a host polymerase.
The candidate functions are the two major polymerases in E. coli, Pol I and Pol III. Athough retrohoming was unaffected in a Pol I mutant lacking polymerization and 3'-5' exonuclease activities, Pol III was implicated (Table 3; Fig. 4B). A ts mutation in the catalytic subunit of Pol III, the 10-subunit processive host polymerase, resulted in a sharp, temperature-dependent reduction in intron mobility (Fig. 4B). This result, along with the need for MutD, the subunit of Pol III (Table 1), makes the major replicative enzyme of E. coli a primary candidate for second-strand cDNA synthesis in retrohoming (Fig. 5, step 6). The involvement of Pol III could explain the requirement for active DNA replication suggested by the real-time PCR experiment. This proposal is consistent with other results that imply a strong link between DNA replication and mobility in E. coli (Zhong et al. 2003; Coros et al. 2005).
Repair polymerases have a role in retrohoming
Mutations in Pol II and/or Pol IV, when combined with a mutation in Pol V, lead to a 10-fold reduction in retrohoming (Table 3), suggesting a need for repair polymerization across DNA lesions or DNA-RNA junctions. The physical association of all five polymerases and DNA ligase, through their interaction via the 
clamp, provides a molecular framework for the collaboration of these different enzymes (Lopez de Saro and O'Donnell 2001; Lopez de Saro et al. 2003; Plosky and Woodgate 2004).
Pol II, Pol IV, and Pol V provide a pool of accessory DNA polymerases with relaxed specificity, which assist the high-fidelity processive Pol III (Wagner et al. 2002). In various combinations, and with a great deal of functional redundancy, Pol II, Pol IV, and Pol V help bypass lesions when Pol III dissociates from a damaged primer-template (for review, see Plosky and Woodgate 2004; Tippin et al. 2004). Which of the three repair polymerases replaces the displaced Pol III in a complex depends on timing, enzyme availability, and the type of DNA lesion (Crowley and Courcelle 2002; Goodman 2002; Wagner et al. 2002). Our results indicate that in the Pol V mutant, retrohoming increases by 50% (Table 3), which may be consistent with the observation that Pol III can replicate efficiently past some DNA lesions when Pol V is inactivated (Borden et al. 2002). Although the lack of Pol II or Pol IV can reduce retrohoming by two-thirds, the Pol II-Pol IV double mutant does not have an additive effect. These results suggest that Pol II and Pol IV function similarly in retrohoming. However, in combination with a Pol V mutant, the Pol II and Pol IV mutants have 10-fold effects, underscoring the complex interdependencies of these enzymes (Sutton and Walker 2001). This functional enhancement by Pol V may be related to the finding that Pol II mutants are not sensitive to UV light, and Pol V mutants are only slightly sensitive, whereas Pol II-Pol V double mutants are extremely UV-sensitive (Goodman 2002).
There are at least three points in the retrohoming pathway at which repair polymerases might function. First, although LtrA can copy the 5' overhang of 3' exon DNA in vitro, given its low DNA polymerase activity, it is conceivable that repair polymerases contribute to this step in vivo (Fig. 5, intermediate a). Second, repair polymerases may be required to traverse the RNA-DNA junction of the template at the 5' splice site to continue DNA synthesis into the 5' exon (Fig. 5, intermediate b). Third, the repair polymerases may be needed to initiate second-strand synthesis (Fig. 5, intermediate c). If there is residual RNA attached to the top strand of the upstream exon, then the accommodating active site of a repair polymerase (Kunkel 2004) may more readily initiate second-strand synthesis than Pol III.
Although RecA is required for induction of SOS-dependent repair functions, constitutive levels of the repair polymerases Pol II and Pol IV are fairly high (Goodman 2002), explaining how retrohoming can still occur efficiently in a recA background. It remains puzzling, however, that we have not observed a high frequency of errors, even at the junctions of retrohoming events (D. Smith and M. Belfort, unpubl.). One possibility is that Pol II, which has an error-free pathway (Goodman 2000), is the major repair polymerase involved. A second possibility is that MutD, which is part of the Pol III holoenzyme, and which may play a role in retrohoming (Table 1), is involved in error correction. Regardless, the dependency of group II intron mobility on the repair polymerases suggests that the later steps of the retrohoming process may be viewed as a response to DNA damage.
Retroelements as molecular parasites that scavenge host functions
Group II introns are streamlined parasitic elements, carrying only those molecular features that are required to maintain themselves in a genome and to spread to others. Some bacterial group II IEPs, for example, lack the endonuclease module (Martínez-Abarca et al. 2000; Dai and Zimmerly 2002), and these introns may achieve mobility by utilizing a cellular replication pathway (Martinez-Abarca et al. 2004). Together with the recruitment of host replication and repair functions demonstrated here, it appears that group II introns scavenge much of their enzymatic machinery from the hosts they invade.
Features of the mechanism used by group II introns may be pertinent to non-LTR-retrotransposons, such as human LINE elements and insect R2 elements, and more generally to other non-LTR-retroelements, including retroplasmids and bacterial retrons. The replicative and repair polymerases have homologs not only in other bacteria, including Gram-positives from which the Ll.LtrB intron was derived, but also in phylogentically diverse eukaryotes (Crowley and Courcelle 2002; Goodman 2002; Plosky and Woodgate 2004; Tippin et al. 2004). It is therefore possible that replicative polymerases in a wide range of organisms are involved in second-strand synthesis, with specific steps aided by repair polymerases, or even that second-strand synthesis could occur during the normal course of DNA replication. To our knowledge, no evidence exists to the contrary. What these elements almost certainly have in common with group II introns is that they encode enzymes that promote initial steps in mobility, whereas later steps use host DNA recombination and repair machinery, thereby facilitating the element's dispersal.
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Strains used in this study, made lysogenic for 
DE3, are listed in Supplementary Table S4. Plasmids used as intron donors and recipients are listed in Figure 2B, with salient features, including drug resistances and origins of replication. Additionally, the length of the intron donor is noted. More details on these plasmids and their construction are in the Supplemental Material. The ts recipient plasmid pB102B-ltrB, which was used in real-time PCR experiments (Fig. 4A), was constructed similarly to pB101B-ltrB (Zhong and Lambowitz 2003), except that the ts replicon was amplified from pMAK705 (Hamilton et al. 1989).
Retrohoming assay
The retrohoming assay was performed as described (Cousineau et al. 1998) and is detailed in the Supplemental Material. Briefly, donor and recipient plasmids were cotransformed into the E. coli strain being tested (Fig. 2). Fresh cotransformants were grown overnight in TBYE (1% Bactone tryptone, 0.5% NaCl, 0.1% Bacto yeast extract) with antibiotics corresponding to intron and plasmid markers IM, PM1, and PM2. After outgrowth and induction of the donor intron with IPTG for 3 h, plasmid DNA was extracted, digested with the appropriate restriction enzymes, transformed into DH5 cells, and selected for IM and PM2.
Biochemical assays
DNA polymerase and RT assays were carried out with the primer-template substrates (S, I-IV) shown in Figure 3. Substrate I was made with 40 nM DNA oligonucleotide LtrBAs6 (see Supplementary Table S5 for the sequences of oligonucleotides), corresponding to bottom-strand 5'-exon nucleotides -18 to 72 of the Ll.LtrB intron, and 400 nM oligonucleotide LtrBDE3, corresponding to top strand 5'-exon nucleotides -18 to -1. Substrate III, denoted Ll.LtrB/E2+10, was made with 40 nM PAGE-purified Ll.LtrB-ORF intron precursor RNA and 400 nM 18-mer DNA oligonucleotide, ending at bottom-strand 3' exon nucleotide +10 (Wank et al. 1999). Substrates II and IV were 1 µg of poly(dA)/oligo(dT)12-18 or poly(rA)/oligo(dT)12-18, respectively, prepared as described (Matsuura et al. 1997).
Unless specified otherwise, reactions were for 10 min at 37°C in 10 µL of reaction mix containing 10 µCi [-32P]dTTP (3000 Ci/mmol; NEN-Dupont) with 200 µM dATP, dCTP, and dGTP added for substrates I and III. Reaction mixes were NMT450 (high salt) (450 mM NaCl, 5 mM MgCl2, 40 mM Tris-HCl at pH 7.5, 5 mM DTT, 100 µg/mL BSA, and 5% glycerol), which is optimal for LtrA reverse transcription of Ll.LtrB RNA/E2 DNA + 10 (substrate III); NMT100 (low salt) (100 mM NaCl, 5 mM MgCl2, 40 mM Tris-HCl at pH 7.5, 5 mM DTT, 100 µg/mL BSA, and 5% glycerol), for use of poly(rA)/oligo(dT)18 (substrate IV) (Wank et al. 1999); REact2 buffer (50 mM Tris-HCl at pH 8.0, 10 mM MgCl2, 50 mM NaCl), which is optimal for Klenow; or first-strand buffer (50 mM Tris-HCl at pH 8.3, 75 mM KCl, 5 mM MgCl2, and 1 mM DTT), which is optimal for M-MLV RT (Invitrogen). LtrA (20 nM) or Klenow (1 unit; Invitrogen) were added to the premixed substrates to initiate reactions. After incubation, 9 µL of the reaction mixture was spotted on DE81 filter paper, followed by five washes in 2x SSC. Dried filters were then counted for Cerenkov radioactivity.
Target DNA-primed reverse transcription was assayed using recipient plasmid pLHS, as described (Saldanha et al. 1999).
Intron mobility assay using quantitative real-time PCR
Recipient plasmid pB102B-ltrB (5 µg) was introduced into HMS174(DE3) containing the intron-donor plasmid pACD2 (plasmids described in Supplemental Material). After recovery in 5 mL of LB medium for 2 h at 30°C, cells were collected by centrifugation, washed with 7 mL of LB medium twice to remove the untransformed recipient plasmids, and resuspended in 50 mL of LB medium. Transformed cells were grown at 30 or 37°C, and 1.5-mL portions were removed at the indicated times for plasmid isolation. Plasmid DNA (2 µL) was used in a quantitative real-time PCR that contains 900 nM primers and 250 nM TaqMan probe (Applied Biosystems) to monitor homing of the intron into the target site. Briefly, primers HP1, HP2 with probe HPP, and primers R1, R2 with probe RP were used to quantify homing products, and the sum of the recipient plasmids and the homing products, respectively (sequence of primers and probes are listed in Supplementary Table S5). Real-time PCR was carried out using a TaqMan Universal PCR kit, and the products were analyzed in an ABI PRISM 7700 sequence detection system. Standard curves for both homing product and recipient plasmid were plotted from PCR of serial dilutions of plasmid pB102B-ltrBHP, which contains the Ll.LtrB-ORF intron inserted in the target site of pB102B-ltrB. Two duplicate PCRs were performed for each sample and the average threshold cycle (CT) was plotted on the standard curve to determine the relative quantity of initial PCR templates, either the homing products or the sum of the homing products and the recipient plasmids. Mobility frequencies were calculated as the ratio of homing product/(recipient plasmid + homing product).
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3 These authors contributed equally to this work. 
4 Present address: The Scripps Research Institute, Department of Molecular and Experimental Medicine, SBR-10, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
E-MAIL belfort{at}wadsworth.org; FAX (518) 474-3181.
Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1345105.
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and 
, respectively. (3) cDNA synthesis. (4-7) Extended cDNA synthesis, RNA degradation, second-strand DNA synthesis, and repair. The order of steps 4-7 is unknown.
