INTRODUCTION

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Long terminal repeat-containing retrotransposons are closely related to retroviruses in structure and life cycle (6). Briefly, the retrotransposon RNA transcript is translated and the protein products assemble into viruslike particles (VLPs) in the cytosol. During this process, no double-strand (ds) breaks are created in the host genome because the original retrotransposon is not excised. The full-length RNA transcript contained within the VLP is then reverse transcribed by the retroelement-encoded reverse transcriptase (RT) into a linear dsDNA molecule, which is then inserted into the host genome by the retroelement-encoded integrase. In all of the cases characterized, integrase catalyzes direct nucleophilic attack by a 3' hydroxyl of the transposable element onto a target DNA phosphodiester bond (12). Again, this does not result in ds breaks in the host genome. Instead, the product of the integration reaction is the retroelement flanked by single-stranded (ss) DNA gaps that are then thought to be repaired by host factors (6).

It has been demonstrated that a reaction mechanism very similar to that of transposable element integration is employed by the RAG1 and RAG2 proteins in the first steps of V(D)J recombination, a site-specific genomic rearrangement process that helps generate the diversity of antigen-binding sites of immunoglobulin and T-cell receptor proteins (46). V(D)J recombination is severely debilitated in cell lines or animals defective in components of the DNA-dependent protein kinase (DNA-PK; 33, 43). DNA-PK is made up of a catalytic subunit (DNA-PKcs) and a DNA-binding protein (Ku), which is a heterodimer of ~70- and ~80-kDa subunits (Ku70 and Ku80, respectively; 18, 24). Ku and DNA-PKcs also function in the repair of radiation- or restriction enzyme-induced DNA ds breaks in mammalian cells (33, 43). Given that V(D)J recombination is similar mechanistically to retrotransposition and retroviral integration, we speculated that Ku and DNA-PKcs might play a role in retroelement life cycles. A second reason to consider a role for Ku in this process is that during retroelement life cycles, ds ends and ss gaps are created as products of reverse transcription and integration into the genome, respectively, and Ku has been shown to bind with strong affinity to these structures in vitro (19, 43). While no direct homologue of DNA-PKcs has been identified in Saccharomyces cerevisiae, there are homologues of Ku70 and Ku80 (the genes for these are termed YKU70 or HDF1, and YKU80 or HDF2, respectively) and these yeast factors have been shown to be involved in the repair of DNA ds breaks (13, 27). We investigated the potential role of Ku in Ty1 retrotransposition in S. cerevisiae, and we discuss the results in terms of the mechanism of action of Ku in this and related processes.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Disruption constructs. A BamHI-EcoRI fragment from pFA6a-kanMX4 (47) was cloned into the BamHI-EcoRI sites of pGEM-Ku80 (9) to create the p80::KAN disruption construct. The yku80::URA3 disruption construct pJDG80U was created by cloning a URA3-containing EcoRI-KpnI fragment from pBSURA3 into the EcoRI and KpnI sites of pGEM-Ku80 (9). A BamHI-EcoRI fragment containing the TRP1 gene from pJA52 (2) was inserted into the BglII-EcoRI sites of pJDGS3F to create the SIR3 disruption construct pJDGS3KO. The RAD50 disruption construct was created by excising the XbaI fragment of pGEM-50 and replacing it with an XbaI fragment containing the LEU2 gene from pJA51 (2) to create prad50::LEU. The full-length YKU70 gene and its promoter were excised from p413-fl70 (7) with BamHI and XhoI and inserted into the same sites of pRS414 to create p414-fl70.

Yeast strains. Yeast strains were maintained in accordance with standard protocols in synthetic complete (SC) medium with the appropriate selection (45). Unless otherwise stated, 2% glucose was used as the carbon source. Strains W303 (wild type) and hdf1 (yku70::LEU2) were gifts from H. Feldmann and E. L. Winnacker. All disruption strains were made in W303-derived strains by transforming 1 to 2 µg of restriction-digested disruption construct plasmid DNA by the standard lithium acetate transformation method (5), and the transformation reactions were plated on the appropriate selective medium. YKU80-disrupted strains were created by transforming strain W303 or the yku70 mutant strain with p80::KAN digested with NotI and selected on G418 plates as previously described (47). RAD52-disrupted strains were created by transforming strain W303 and the yku70 mutant strain with SalI-digested pR52T (Gift of D. Weaver). SGS1-disrupted strains were created by transforming W303 with pPWSGS1 (Gift of I. Hickson) digested with NcoI and PstI. SIR3-disrupted strains were created by transformation of W303 with ApaI- and SacI-digested pJDGS3KO. Disruptions were confirmed by PCR using one gene-specific primer and one marker-specific primer. Strain Y661 (wild type) and mec1-21, tel1, and mec1-21/tel1 mutant strains were gifts from S. Elledge. Strain JCY297 was a gift of J. Curcio, and YKU80 was disrupted in this strain with NotI-digested pJDG80U to create strain JDY15.

Ty1 retrotransposition assays. Yeast strains were transformed with pGTy1-H3mHIS3AI (14) (referred to as pGTy1 later in the text and in the figures) and plated on SC-ura (SC medium without uracil). These plasmids contain a Ty1 element under the control of the galactose-inducible GAL1 promoter and possess a HIS3 gene with an artificial intron. Expression of HIS3 is dependent on Ty retrotransposition (see Results for details). Colonies were picked and grown in SC-ura containing either glucose or galactose overnight at 23°C. Cells were counted by taking the optical density at 600 nm (OD₆₀₀) and plating them on nonselective medium to ensure that the OD was measuring viable cells. Equal numbers of viable cells were plated on SC-his (without histidine) containing glucose, and transposition levels were calculated as His⁺ colonies/total cells. Complementation of the yku70 mutant phenotype was performed by transforming p414-fl70 into yku70 mutant cells already containing the pGTy1 plasmid. Retrotransposition assays were performed exactly as described above but with selection for the p414-fl70 plasmid maintained by eliminating tryptophan from the medium. All assays were conducted a minimum of three times.

-Galactosidase activity measurements. Wild-type or yku70 mutant yeast cells were transformed with pJK101, which contains the lacZ gene under the control of the GAL1 promoter. Transformed cells were grown overnight in SC-ura containing glucose at 23°C. The OD₆₀₀ was measured, and cells were diluted to a density corresponding to an OD₆₀₀ of 0.2. The cells were then grown in SC-ura containing galactose at 23°C. At the indicated times, 200-µl aliquots were taken and -galactosidase activity was measured by o-nitrophenyl--D-galactopyranoside (ONPG) cleavage as previously described (41). Measurements were taken for three independent transformants of each strain.

VLP isolation and RT activity levels. The protocol for isolation of VLPs was adapted from reference 20. Briefly, 50 ml of an overnight yeast culture containing pGTy1 (grown in SC-ura containing glucose) was pelleted, washed with water, and used to inoculate 500 ml of SC-ura containing either glucose or galactose. After growing for 24 h at 22°C, cells were harvested, washed with water, and lysed by glass bead disruption in the presence of 2 ml of buffer B/Mg (10 mM HEPES [pH 7.6], 15 mM KCl, 3 mM dithiothreitol, Boehringer Mannheim complete protease inhibitors, 5 mM MgCl₂). Lysate was centrifuged at 12,000 × g, and the supernatant was loaded onto a sucrose gradient (consisting of 1 volume [1 or 5 ml] of 70% sucrose in buffer B without MgCl₂ and with 10 mM EDTA, 1 volume [1 or 5 ml] of this solution containing 30% sucrose, and 4 volumes [4 or 20 ml] of this solution containing 20% sucrose). Gradients were centrifuged in a Beckman SW-40 rotor at 4°C for 4 h. Fractions (0.75 ml) were collected and tested for RT activity as previously described (20). Positive fractions were pelleted at 50,000 × g overnight at 4°C, resuspended in 10 µl of buffer B/Mg, and stored at 4°C.

Western blot analysis. For analysis of sucrose gradient fractions, either 2 µl (for integrase analysis) or 5 µl (for Ku analysis) of each 10-µl pelleted sucrose gradient fraction was analyzed by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) and transferred to a nylon membrane. The membrane was incubated with either monoclonal antibody 8B11 directed against a portion of integrase (gift of J. Boeke; 20) or rabbit polyclonal anti-Yku70p serum and visualized with horseradish peroxidase-coupled anti-mouse or anti-rabbit immunoglobulin G and enhanced chemiluminescence (Amersham).

Immunoprecipitations from VLP preparations. Nine microliters of a VLP preparation from either strain W303 or the yku70 mutant strain was used for each immunoprecipitation. One microliter of the VLP preparation was diluted to 100 µl with buffer B/Mg and processed for either DNA or protein analysis as the input (I) fraction. Samples to be immunoprecipitated were incubated with 5 µl of anti-Yku70p antibody, rotating, for 1 h at 4°C. One hundred microliters of a 25% (vol/vol) solution of protein A-Sepharose beads was added, and the samples were incubated, rotating, for 1 h at 4°C. The samples were pelleted, washed 10 times with 1.5 ml of buffer B/Mg, and resuspended in 100 µl of buffer B/Mg. The immunoprecipitated pellet (P) fractions were processed for either DNA isolation or protein analysis. For DNA analysis, 10 µl of 10-mg/ml proteinase K in 0.25 M EDTA and 10 µl of 10% SDS were added to 50 µl of the I or P fraction. The samples were incubated for 3 h at room temperature. These were extracted once with phenol-chloroform and once with chloroform. The DNA was ethanol precipitated in the presence of 10 µg of glycogen, washed with 70% ethanol, and resuspended in 25 µl of 10 mM Tris · Cl (pH 8.0). One microliter was used for PCR analysis with primers Kai3 (5'-TCGTACAGTGAAAATGAGACTAATCATACA) and His3-3 (5'-GATTGTCTGCGAGGCAAGAATG). For protein analysis, 5 µl of 10× SDS loading buffer was added to 50 µl of the I or 50 µl of the P fraction and incubated for 5 min at 95°C, and 15 µl was analyzed by SDS-PAGE and Western blotting as described above.

Northern blot analysis. RNA was isolated from 5-ml cultures of JC297 or JDY15 grown to mid-log phase at room temperature by using the Qiagen RNeasy reagents and protocol. The RNA was quantitated by measuring the OD₂₆₀, and equal amounts of total RNA were electrophoresed on a 0.8% formaldehyde-agarose gel. The gel was transferred overnight in 20× SSC (1× SSC is 0.15 M NaCl plus 0.015 M sodium citrate) transfer buffer onto Amersham Hybond-N nylon membrane. The RNA was UV cross-linked to the membrane and hybridized overnight at 68°C in 6× SSC-2× Denhardt's reagent-0.1% SDS-100 µg of ss DNA per ml. The membrane was washed three times for 30 min each time at 65°C in 0.1× SSC-0.1% SDS and exposed to film. Probes against the Ty1 element and actin were generated by random prime labeling (Prime-a-Gene labeling system; Promega).

In vivo formaldehyde cross-linking. One-hundred-milliliter cultures of the wild-type and yku70 mutant strains were grown under the indicated selective or inductive conditions and subjected to in vivo formaldehyde cross-linking (38, 44). Briefly, formaldehyde was added to the cultures to a final concentration of 1% and incubated with shaking at room temperature for 15 min. Glycine was added to a final concentration of 125 mM, and cultures were incubated at room temperature for 5 min. Cells were harvested by centrifugation, washed twice with Tris-buffered saline, and resuspended in 800 µl of lysis buffer (50 mM HEPES [pH 7.4], 140 mM NaCl, 1 mM EDTA, 1% Triton X-100, Boehringer Mannheim complete protease inhibitors). Eight hundred microliters of glass beads was added, and the cells were lysed by vortexing 20 × 1 min with 1 min on ice between bursts. The lysate was moved to a microcentrifuge tube and clarified by centrifugation for 15 min at maximum speed in a microcentrifuge at 4°C.

Immunoprecipitation of whole-cell extracts prepared from formaldehyde-treated cultures. Ten microliters of whole-cell extract was transferred to a new microcentrifuge tube and diluted to 100 µl with 10 mM Tris · Cl (pH 8.0) to be analyzed as I fractions. Five microliters of preimmune serum was added to the remaining whole-cell extract and incubated, rotating, for 1 h at 4°C. One hundred microliters of 50% protein A-Sepharose beads (vol/vol) was added, and the tubes were rotated for 1 h at 4°C. The samples were centrifuged, and the supernatants were moved to new tubes. To these, 5 µl of anti-Yku70p antibody was added and the tubes were incubated, rotating, for 3 h at 4°C. One hundred microliters of 50% (vol/vol) protein A-Sepharose beads was added, and the tubes were rotated for 1 h at 4°C. The immunoprecipitates were pelleted and washed vigorously by inverting and vortexing the tubes for 5 × 5 min with 1.4 ml of lysis buffer, 2 × 5 min with lysis buffer containing 500 mM NaCl, 2 × 5 min with lysis buffer containing 600 mM NaCl, and 5 min with 10 mM Tris · Cl (pH 8.0). The pellets were resuspended in 100 µl of 10 mM Tris · Cl (pH 8.0). To both the I and P fractions, 1.25 µl of 10% SDS and 1.25 µl of 10-mg/ml proteinase K in 0.25 M EDTA were added. Samples were incubated overnight at 37°C and for a further 6 h at 65°C. Samples were extracted once with phenol-chloroform, the organic phase was back extracted with 100 µl of 10 mM Tris · Cl (pH 8.0), and the combined products were extracted once with chloroform. The DNA was ethanol precipitated in the presence of 20 µg of glycogen and resuspended in 25 µl of 10 mM Tris · Cl (pH 8.0). One microliter was used in PCRs using primers His3-4 (5'-AACCAAGTTCGACAACTGCG) and His3-5 (5'-GCAGAAGCAGTAGCAGAACA). These primers amplify a region of the HIS3 marker present in the pGTy1 plasmid across the site of the artificial intron. The product from the plasmid is 422 bp, while the product from the cDNA in which the intron has been spliced out is 318 bp. PCR products were electrophoresed on a 5% nondenaturing polyacrylamide gel, and the region between the 396- and 220-bp molecular size markers was excised and transferred onto nylon membrane (the region of the gel was excised to avoid overwhelming signal levels from the PCR product of plasmid DNA that was present at significant levels in the whole-cell extract). The membrane was analyzed by Southern blotting with radiolabeled His3-5 as the probe.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Ku facilitates Ty1 retrotransposition. To test whether Ku affects Ty retrotransposition, we used a Ty1 retrotransposition assay developed by Curcio and Garfinkel (14; Fig. 1). In this assay, yeast strains that are mutated in HIS3 are transformed with a plasmid that directs the expression of Ty1 RNA from a galactose-inducible promoter. This Ty1 element contains a HIS3 gene that is interrupted by an artificially inserted intron in reverse (antisense) orientation so that it cannot be spliced, and yeast cells containing this plasmid are phenotypically His. However, the intron is in sense orientation with respect to the galactose-inducible promoter, so it is removed by splicing of the Ty1 RNA. If this spliced product is reverse transcribed and integrated into the yeast genome, the resulting strain is His⁺ (Fig. 1). Therefore, the rate of His⁺ colony generation can be used as a measure of the retrotransposition rate in yeast (14).

View larger version (24K): [in this window] [in a new window]   FIG. 1.   Schematic of the Ty1 construct (pGTy1H3mHIS3AI or pGTy1 [14]) used to assay transposition frequencies. The artificial intron is in the sense direction relative to the transcription of full-length Ty1 but in the antisense direction relative to HIS3. Therefore, expression of functional HIS3 mRNA is primarily dependent on transcription, splicing, and integration of the reverse-transcribed Ty1 element into the yeast genome.

View larger version (27K): [in this window] [in a new window]   FIG. 2.   Inactivation of YKU70 or YKU80, but not other DNA maintenance genes, impairs Ty1 retrotransposition frequencies. (A) Transposition frequencies of Ty1 are decreased in a yku70 mutant background, and this is complemented by an episomal plasmid bearing YKU70. Frequencies are shown relative to that of the wild type, which had a mean Ty1 transposition frequency of 1.5 × 104. (B) Ty1 transposition frequencies in yku80, yku70/yku80, rad52, and sgs1 mutant strains relative to that of the wild type. (C) Ty1 transposition frequencies in lig4, rad50, and sir3 mutant strains relative to that of the wild type. (D) Ty1 transposition frequencies in tel1, mec1, and tel1/mec1 mutant strains relative to that of wild-type strain Y661. (E) Ty1 transposition frequencies in yku70, yku70/rad52, and yku70/rad52 strains with Ty1-in2600 relative to that of the wild type.

The role of Ku in Ty1 retrotransposition is specific. The yeast homologues of mammalian ligase IV (termed Lig4p or Dnl4p), Rad50p, and Sir3p have been shown to work in the same pathway as Ku in repairing DNA ds breaks in yeast (13, 27). Additionally, Ku has been shown to play a role in telomeric silencing (8, 32, 37) and telomeric length maintenance (9, 35, 40) in a manner that is epistatic with Sir3p and Rad50p, respectively. In order to determine whether these other members of the Ku-associated DNA maintenance pathways are involved in facilitating retrotransposition, we examined strains that have disruptions in either RAD50, LIG4, or SIR3. Perhaps surprisingly, rad50, lig4, and sir3 mutant strains showed no significant decrease in retrotransposition rates relative to wild-type cells (Fig. 2C). Taken together, these results show that Ku facilitates retrotransposition in a manner that is distinct from its previously characterized roles and that the effect of Ku on Ty1 retrotransposition is not likely to be an indirect consequence of a defect in DNA ds break repair or telomeric maintenance.

7

Loss of Ku does not impair Ty1 transcription or VLP assembly. In mammalian systems, there is evidence that Ku has a role in regulating transcription (23, 30, 31). This raised the possibility that the reduced rates of retrotransposition in the absence of Ku are due to a reduction in transcription of the Ty1 element. To address this possibility, we examined the levels of transcription in yku70 mutant cells by using a reporter plasmid containing the lacZ gene under the control of the same galactose-inducible promoter used in the pGTy1 construct. When this reporter construct was used, no reduction of -galactosidase activity was observed in the absence of Ku (Fig. 3A), suggesting that the lower levels of retrotransposition are not the result of lower levels of Ty1 transcription.

View larger version (24K): [in this window] [in a new window]   FIG. 3.   VLP formation is normal in yku70 mutant cells. (A) Transcription levels in wild-type (squares) and yku70 mutant (diamonds) cells assayed by using a reporter plasmid containing a lacZ construct under the control of the same galactose-inducible promoter that is on the Ty1 plasmid construct. Cells were grown in the presence of galactose and assayed at various time points after induction for -galactosidase activity by measuring ONPG cleavage. (B) RT activity profile of sucrose gradient fractions. Whole-cell extracts of the wild-type and yku70 mutant strains containing pGTy1 and grown under inducing conditions were run over sucrose gradients and analyzed for RT activity. (C) Southern analysis of Ty1 cDNA prepared from VLPs from the wild-type and yku70 mutant strains. The DNA was hybridized to a radiolabeled fragment of the pGTy1 plasmid. One and 10 ng, respectively, of the BamHI-XhoI fragment of pGTy1 are shown in the last two lanes. (D) Ty1 cDNAs isolated from VLPs from the wild-type and yku70 mutant strains were digested with SpeI, radiolabeled, and analyzed by nondenaturing PAGE. (E) SpeI cleavage pattern of the Ty1 element. (F) Western blot analysis of VLPs prepared from the wild-type and yku70 mutant strains using monoclonal antibody 8B11 directed at a portion of the integrase (IN) coding sequence (20). It recognizes both the TYA/TYB precursor protein and the mature form of integrase (p90-TYB; IN).

Ku cofractionates with Ty1 VLPs. Because Ku is able to bind specifically to DNA ds ends, and since the Ty1 RNA is reverse transcribed in the VLPs to produce a ds linear DNA element, we decided to investigate whether Ku is associated with the Ty1 VLPs. To do this, we fractionated VLPs by sucrose gradient sedimentation and then tested the resulting fractions for RT activity (Fig. 4A) and for the presence of Ku by Western blot analysis using a polyclonal antiserum directed against Yku70p (Fig. 4B; antibody specificity is demonstrated by detection of Yku70p in extracts of wild-type but not yku70 mutant cells). Yku70p was thus detected in sucrose gradient fractions 1 and 2 derived from wild-type cells either lacking or containing an induced Ty1 element (Fig. 4B). Moreover, Yku70p was also detected in fraction 8 of Ty-containing wild-type extracts. This is the same fraction that contains peak RT activity (Fig. 4B, top panel). In contrast, Yku70p was not detected in the equivalent fraction derived from cells lacking Ty1 (Fig. 4B, bottom panel). The presence of Yku70p was found consistently in fractions containing peak RT activity levels in independent VLP preparations, suggesting that Ku and the Ty1 VLPs can associate with one another.

View larger version (26K): [in this window] [in a new window]   FIG. 4.   Yku70p cofractionates with Ty1 VLPs. (A) Whole-cell extracts prepared from wild-type cells containing the induced Ty1 element (circles), wild-type cells without an induced Ty1 element (squares), and yku70 mutant cells containing the induced Ty1 element (triangles) were fractionated over a sucrose gradient and assayed for RT activity. (B) Western blot analysis of sucrose gradient fractions from panel A with anti-Yku70p antibody. Nuclear extracts from the wild-type (Wt) and yku70 (70) strains were also analyzed. Yku70p is an ~67-kDa protein recognized in wild-type extracts but not seen in yku70 extracts and is indicated by an arrow.

View larger version (24K): [in this window] [in a new window]   FIG. 5.   Ku is associated with the Ty1 cDNA and integrase. (A) Immunoprecipitations were performed with a polyclonal antibody directed against Yku70p. These were done with VLPs prepared from the wild-type strain containing VLPs (W303 + pGTy1, lanes 3 and 4), the yku70 mutant strain (yku70 + pGTy1, lanes 5 and 6), or analogous fractions from the wild-type strain without pGTy1 (W303, lanes 1 and 2). DNA was isolated from the I and P fractions and analyzed by PCR using primers that amplify a portion of pGTy1. PCR products are shown from reactions containing pGTy1 (lane 7) or no DNA (lane 8). (B) Western blot analysis of the I, supernatant (S), and P fractions of the immunoprecipitations performed as described for panel A using monoclonal antibody 8B11 (20) directed against the integrase (IN) protein.

Ku associates with Ty1 VLPs in vivo. To investigate the physiological relevance of the association detected between Ku and Ty1 VLPs, in vivo formaldehyde cross-linking experiments were performed. In these studies, wild-type and yku70 mutant strains containing the pGTy1 plasmid were grown in the presence of either glucose or galactose and then treated with formaldehyde. Whole-cell extracts were prepared, immunoprecipitations were performed by using the anti-Yku70p polyclonal antibody, and DNA was isolated from the I and immunoprecipitated P fractions. This DNA was analyzed for the presence of Ty1 cDNA by PCR, followed by Southern blotting. Because these experiments were performed with whole-cell extracts, we designed primers around the site of the artificial intron in the pGTy1 plasmid so that PCR products from the plasmid and the reverse-transcribed Ty1 cDNA could be distinguished from one another. With these primers, a product of 422 bp is generated with the pGTy1 plasmid DNA as a substrate (data not shown), whereas if the artificial intron has been spliced out and the RNA is subsequently reverse-transcribed, the expected PCR product is 318 bp. To avoid the overwhelming signal due to plasmid DNA present in the whole-cell extracts, only the region of the gel encompassing the anticipated product size for the spliced cDNA was analyzed by Southern blotting.

View larger version (18K): [in this window] [in a new window]   FIG. 6.   Ku is associated with the Ty1 cDNA in vivo. (A) In vivo formaldehyde cross-linking was performed on the wild-type and yku70 mutant strains, both carrying the pGTy1 plasmid. Whole-cell extracts were prepared and used in immunoprecipitation reactions with an antibody directed against Yku70p. DNA from the I or immunoprecipitated P fraction was isolated and analyzed by PCR and Southern blotting using primers that give a specific product for the Ty1 cDNA. Lanes: 1 and 2, I and P fractions from yku70 mutant cells grown in glucose; 3 and 4, I and P fractions from yku70 mutant cells grown in galactose; 5 and 6, I and P fractions from wild-type cells grown in glucose; 7 and 8, I and P fractions from wild-type cells grown in galactose. PCRs using DNA isolated from a partially purified VLP fraction (lane 9), plasmid DNA (pGTy1, lane 10), and the P fraction from wild-type yeast not containing the pGTy1 plasmid (W303, lane 11) as the substrate are shown, demonstrating the specificity of the PCR product. (B) Whole-cell extracts prepared from formaldehyde-treated wild-type cells not carrying the pGTy1 plasmid (W303) were mixed with whole-cell extracts from formaldehyde-treated yku70 mutant cells carrying the pGTy1 plasmid (yku70/Ty1). Immunoprecipitations and Ty1 DNA analysis using the mixed extracts were performed as described above, and I and P fractions are shown in lanes 1 and 2. In lanes 3 and 4, as a positive control, the immunoprecipitation and Ty1 DNA analysis were performed in parallel by using wild-type cells carrying the pGTy1 plasmid (W303/Ty1). (C) In vivo formaldehyde cross-linking and immunoprecipitations were performed as described above on strain JDY1 (rad52::TRP1) containing integration-deficient pGTy1-in2600 (lanes 1 and 2), JC297 (containing the genomic HIS3AI-marked Ty1 element under the control of its endogenous promoter [11]; lanes 3 and 4), or JDY15 (yku80::URA3 in JC297; lanes 5 and 6). (D) Transposition levels were measured for the genetically marked endogenous Ty1 element in wild-type (JC297) and yku80 mutant (JDY15) yeast strains. Measurements were done five times for each strain. (E) Northern blot analysis of 10 µg of total RNA using probes directed against either the Ty1 element or actin.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

The results presented here indicate a role for yeast Ku in Ty1 retrotransposition. In contrast, the absence of other proteins that are involved in DNA repair and its maintenance, including other components of the Ku-mediated DNA ds break repair pathway, does not lead to markedly impaired retrotransposition in these assays. Furthermore, although Ku has been shown to affect telomere length and telomeric transcriptional silencing, other proteins examined in this assay that share these activities do not markedly affect Ty1 retrotransposition. Taken together, these observations suggest that the manner in which Ku facilitates retrotransposition is distinct from its other defined cellular roles and argue that the observed reduction of retrotransposition in Ku-deficient cells is not likely to be an indirect consequence of the perturbation of these processes. In addition, our data indicate that the reduction of retrotransposition in the absence of Ku does not result from impaired galactose-inducible transcription or defective VLP assembly. These results suggest that it is likely that Ku plays a role in the retrotransposon life cycle subsequent to VLP formation.

There are various ways in which Ku could potentiate integration of the retrotransposon. First, since Ty1 integrates preferentially into regions upstream of genes transcribed by RNA polymerase III (16), it is possible that Ku functions by targeting Ty1 to such locations. However, we found that Ty3 transposition, which is targeted to different sites in the genome from Ty1 (29), is also reduced significantly in the absence of Ku (48). This therefore argues that Ku is unlikely to facilitate Ty1 retrotransposition solely by targeting the retrotransposition machinery to specific sites in the genome and furthermore suggests that Ku might have a general role in retrotransposition processes.

Another possible role for Ku is suggested by our finding that it is associated with the Ty1 VLPs in vivo. Although this may reflect an association with VLP proteins, an attractive model is one in which Ku binds directly to the Ty1 cDNA. In this way, Ku might serve to prevent degradation of the Ty1 DNA by cellular nucleases, a possibility supported by the fact that Ku does protect dsDNA ends from nuclease-mediated degradation in vitro (17) and by the observation that Ty1 cDNA is susceptible to nuclease attack (15). Since a specific terminal structure of the retroelement DNA is necessary for efficient integration (21, 36), it is conceivable that even limited degradation of the Ty1 DNA in the absence of Ku might result in the loss of viable retroelements. We did not, however, find any significant or reproducible differences in either the amount or the apparent integrity of the Ty1 cDNA isolated from yeast lacking Ku. Nevertheless, it remains a possibility that degradation in the absence of Ku is limited to the few terminal bases of the linear retroelement DNA and/or that Ku protects against nuclease digestion only the subset of Ty1 cDNA that enters the nucleus on its way to integration into the host genome.

An additional potential role for Ku is during the Ty1 integration reaction itself. In this regard, in vitro studies have demonstrated that Ku can bind to DNA ss gaps with affinity comparable to that with which it binds to dsDNA ends (22, 39), raising the possibility that it is involved in the repair of the ss gaps that arise as retrotransposition intermediates. Through binding to such structures and displacement of integrase, Ku could also prevent the reversal of the transposition reaction, disintegration, which results in the removal of the newly integrated product from the substrate DNA. If Ku did function in any of these regards, it would make sense that, in order to be maximally effective, the retroelement would want to ensure that Ku is already present when it initiates its progression toward integration into the host genome. The binding of Ku to VLPs might reflect such a mechanism. Consistent with a role for Ku in facilitating integration of retroelement DNA, Ku and DNA-PKcs have been recently demonstrated to facilitate retroviral integration in mammalian cells (15a). Because transcription, translation, and viral-particle formation occur prior to infection of the new host cell, Ku must play a role in the retroviral life cycle subsequent to reverse transcription but prior to integration. These data are consistent with the role proposed here for Ku during Ty1 element retrotransposition and suggest that Ku may be involved in facilitating the integration of other retroelements in a diversity of eukaryotes.

Finally, previous work has established that Ku plays a role in Drosophila P-element DNA transposition (4). In DNA transposition, the transposable element is excised from one part of the genome before being integrated into a new site by the element-encoded transposase. Therefore, the decrease in P-element transposition rates in the absence of Ku might, at least in part, reflect a requirement for Ku to repair the DNA ds break in the host DNA after the transposable element has been excised. Similarly, it has been suggested that the mechanism by which Ku facilitates V(D)J recombination is repair of the DNA ds breaks created by the RAG1 and RAG2 proteins. Recent findings suggest that the V(D)J recombination machinery is evolutionarily related to that of DNA transposable elements (1, 26), implying that Ku could provide the same type of DNA ds break repair function in both of the above-described processes. Although ds break repair may be the only function of Ku in these processes, it is noteworthy that the mechanism by which retroelement integrases integrate the element into a new target site is essentially the same as that used by the RAG proteins and DNA transposon transposases, and we found a role for Ku in the Ty1 retrotransposon life cycle, where there is no obvious requirement for DNA ds break repair activity. This, therefore, raises the possibility that Ku has a common role in all of these events. It will be of great interest to investigate the association of Ku with V(D)J and DNA transposition intermediates and whether it plays a direct role in integrating these and other transposable elements into the host chromosome.