Intasome architecture and chromatin density modulate retroviral integration into nucleosome
© Benleulmi et al.; licensee BioMed Central. 2015
Received: 25 September 2014
Accepted: 19 January 2015
Published: 7 February 2015
Retroviral integration depends on the interaction between intasomes, host chromatin and cellular targeting cofactors as LEDGF/p75 or BET proteins. Previous studies indicated that the retroviral integrase, by itself, may play a role in the local integration site selection within nucleosomal target DNA. We focused our study on this local association by analyzing the intrinsic properties of various retroviral intasomes to functionally accommodate different chromatin structures in the lack of other cofactors.
Using in vitro conditions allowing the efficient catalysis of full site integration without these cofactors, we show that distinct retroviral integrases are not equally affected by chromatin compactness. Indeed, while PFV and MLV integration reactions are favored into dense and stable nucleosomes, HIV-1 and ASV concerted integration reactions are preferred into poorly dense chromatin regions of our nucleosomal acceptor templates. Predicted nucleosome occupancy around integration sites identified in infected cells suggests the presence of a nucleosome at the MLV and HIV-1 integration sites surrounded by differently dense chromatin. Further analyses of the relationships between the in vitro integration site selectivity and the structure of the inserted DNA indicate that structural constraints within intasomes could account for their ability to accommodate nucleosomal DNA and could dictate their capability to bind nucleosomes functionally in these specific chromatin contexts.
Thus, both intasome architecture and compactness of the chromatin surrounding the targeted nucleosome appear important determinants of the retroviral integration site selectivity. This supports a mechanism involving a global targeting of the intasomes toward suitable chromatin regions followed by a local integration site selection modulated by the intrinsic structural constraints of the intasomes governing the target DNA bending and dictating their sensitivity toward suitable specific nucleosomal structures and density.
The retroviral replication requires the integration of viral DNA into the host genome. This step, catalyzed by retroviral integrase (IN), is performed within a nucleoprotein structure, the pre-integration complex (PIC), which must reach the nucleus and gain access to the target DNA in a nucleosomal compacted structure [1,2]. During the integration process, IN first removes two nucleotides from both 3′ ends of the long terminal repeats generated during reverse transcription, which is called the 3′ processing reaction. The newly exposed 3′OH groups are then used in the concerted nucleophilic attack of two phosphodiester bonds across the major groove of the host DNA, a reaction termed joining or strand transfer [3-6]. Post-integration DNA reparation (PIR) of this integration intermediate, leading to the establishment of the provirus, generates short target DNA duplications. The size of these duplications varies among retroviruses: 4 bp in the case of the Spumaretrovirus, prototype foamy virus (PFV) and the Gammaretrovirus, murine leukemia virus (MLV), 5 bp for the Lentivirus, human immunodeficience virus (HIV) and 6 bp for the Alpharetrovirus, avian sarcoma virus (ASV) and some Beta- and Deltaretroviruses . This size corresponds to the distance between the phosphodiester bonds of cellular DNA attacked by the two viral DNA ends during concerted integration process. This distance is dictated by physical constraints within the intasomes, as the space between the two functional catalytic sites, governing the bending of the target DNA [8-10].
Retroviral INs comprise three distinct structural and functional domains: the N–terminal domain (which is preceded by an additional domain, the N-terminal extension domain (NED), in Spumaretroviral, Gamma- and Epsilonretroviral INs), adopts an HTH-fold and is characterized by the presence of an HHCC zinc finger–like motif; the core domain, structurally related to Escherichia coli RNase H and other polynucleotidyl-transferases, contains the invariant acidic triad DDE involved in the coordination of the catalytic cofactors; and the C–terminal domain, the least conserved among retroviral INs, includes an SH3-fold [11,12] for recent reviews). Although numerous partial structures of INs from different retroviral genera have been determined, only PFV IN has been crystallized in its full-length form, in the presence of its DNA substrates, providing unprecedented details on the organization of the successive nucleoprotein complexes involved in the integration process, from the stable synaptic complex (SSC, also referred to as the intasome) to the strand transfer complex (STC) [8-10]. In agreement with these structural data, previous biochemical studies performed on INs from different retroviruses have also concluded that the integration reaction was carried out by an IN tetramer [13-15], although the global architecture of the intasome and the STC might vary from a system to another [16,17]. Although IN alone can catalyze integration in vitro, other cellular or viral proteins have been found to play an important role in infected cells within the pre-integration complex (PIC) or during transit to the nucleus (for a review on the IN cofactors see ). Furthermore some post-translational modifications of HIV-1 IN have been reported that could also affect the enzyme activity and its cellular behavior [19,20].
The integration boundaries mark the definitive position of the provirus, and the site selection is highly important for the outcome of the infection. Integration into a region of active transcription promotes viral gene expression, whereas integration into transcriptionally repressed chromatin could potentially promote viral latency [21-23]. If HIV-1 DNA is integrated into actively transcribed genes, the viral genes would need to be repressed to allow persistence of the infection. The mechanisms that control viral gene expression are not yet understood fully. Several factors are involved in the infection of latent and resting cells and in the preferential integration found at the periphery of the nucleus in such latent T cells [24-26]. On the other hand, for the host, integration events can lead to the activation of proto-oncogenes or the inactivation of essential cellular genes . For all these reasons it appears essential to elucidate the molecular mechanisms governing integration site selection to set up safe and efficient gene therapy approaches.
To this end, genome-wide studies have been undertaken and have revealed that retroviruses target different regions of the host chromatin. These studies have shown that some members of the Spumaretrovirus and Gammaretrovirus families favor transcription start sites of actively transcribed genes (TSSs) and CpG islands, the Lentiviruses that have been studied integrate preferentially into active transcription units (TUs), the Alpha– and Deltaretroviruses tested exhibit only a weak preference for TUs, and some Betaretroviruses integrate in an almost random fashion (reviewed in ). Globally, retroviruses can thus be classified into three separate categories: those that preferentially target TSSs and CpG islands, those that display a strong bias toward integration into TUs and those that exhibit little or no particular preference for any chromosomal feature. Interestingly these three groups comprise viruses that share the same target site duplication signature as mentioned above. This raises the question of the relationship between these genomic signatures, closely linked to intasome structures and target DNA bending, and integration selectivity.
HIV-1 and MLV integration site preferences have been shown to rely essentially on the interaction of IN with specific host cell factors - i.e. lens epithelium-derived growth factor (LEDGF/p75) (see  for a review) and bromodomain and extraterminal domain (BET) proteins [30,31], respectively - that recognize defined transcription-associated histone modifications. On the other hand, cellular data obtained from a murine LEDGF/p75 knock-out (KO) model have shown that LEDGF/p75 was not involved in the local target DNA sequence preference associated with HIV-1 integration [32-34]. Thus, despite its ability to bind histone tails through its PWWP domain , LEDGF/p75 is unlikely the sole protein responsible for targeting integration into nucleosomal DNA which may require additional intasome/nucleosome interactions and/or chromatin-remodeling activities . Recently it has been shown that dissociating the interaction between MLV integrase and BET proteins did not change the local integration site sequence selection . Furthermore, in the lack of LEDGF/p75, the local HIV-1 integration sequence selectivity was also shown unchanged [38,39]. Taken together all these data suggest that integrase protein plays a role in the local targeting to the nucleosomal locus after targeting of the intasome into suitable regions of the chromatin thanks to its interaction with cellular cofactors. We, thus, focused our work on the better determination of this final local association between IN and nucleosomes.
The functional interaction between retroviral intasomes and nucleosomes in cells remains elusive. There are no preferential positions for nucleosomes across the majority of the human genome . Consequently, the dynamic nature of chromatin makes it difficult to accurately predict the positions of nucleosomes in the cell. For this reason, in vitro approaches based on the use of chromatinized templates, in which nucleosome positioning is exclusively sequence-driven, are valuable for understanding the specific influence of the chromatin structure on retroviral integration site selectivity. Early results showed that DNA distorsion and nucleosome could favor retroviral integration in vitro [41-46]. More recently, in vitro study using chromatinized template has shown that HIV-1 integration into nucleosomes could be modulated by chromatin structure and dynamics . Additionally, partial one end and physiological two ends concerted HIV-1 integration reactions were shown to be affected differently by chromatin in vitro suggesting that the structure of the different intasomes catalyzing these various integration reactions could impact their sensitivity to nucleosomal DNA .
In order to determine how integration could be modulated both by chromatin structure and intasome architecture, we compared the ability of various retroviral intasomes to accommodate different chromatin structures both in vitro and in vivo. We selected retroviral integrases that vary in their integration site preference in infected cells and in the size of the duplicated target site sequence governed by the distance separating the two active sites of the intasome and, thus, the architecture of the IN catalytic pocket. To determine the intrinsic sensitivity of the selected integrases toward chromatin compactness was determined by analyzing their integration efficiency, selectivity and fidelity in naked and nucleosomal DNA in vitro using specific biochemical conditions allowing efficient full site integration reactions in the lack of cofactors. Our results indicate that the impact of the chromatin structure at the integration site is mainly driven by intrinsic physical constraints within the retroviral intasomes. These constraints could thus dictate their capability to bind nucleosomes functionally in specific chromatin contexts after targeting into specific regions of the host genome via the interaction with cellular cofactors.
In vitro integration catalyzed on chromatin by integrases from various retroviral genera
The overall chromatin structure of the plasmid was first checked by DNase 1 protection after nucleosomes assembly with increasing amounts of the native core histones, H3, H4, H2A and H2B (Additional file 2: Figure S2B). Then, typical restriction assays (REA) using restriction enzymes cutting distinctively in both regions (see Additional file 2: Figure S2A and S2C) showed that the 5S-G5E4 containing domain 1 was poorly accessible, unlike region 2 which remained highly sensitive to DNA cleavage. This confirmed the two distinct chromatin structural regions (regions 1, densely occupied and region 2 sparsely occupied), as predicted from the nucleosome positioning prediction algorithm. Finally, the accurate nucleosome positioning in the 5S-G5E4 region 1 was confirmed by agarose nucleosome gel shift assay performed on EcoRI cleaved 5S fragments (Additional file 2: Figure S2D), demonstrating the formation of evenly spaced mononucleosomes of the same size accurately positioned in known sites.
To confirm that different retroviral INs could be affected differently by chromatin in vitro¸ ASV enzyme was tested under its previously reported optimal conditions . Under these conditions, ASV IN was found to be more active on naked DNA than HIV-1, PFV and MLV enzymes catalyzing the formation of a greater amount of integration products (Figure 2A and quantification in 2B). Cloning and quantification of the circular FSI forms, the most representative for the physiological integration reaction observed in cells, confirmed that ASV IN was more active in vitro (Figure 2C) and preferentially displayed the expected 6 bp target site duplication (Additional file 3: Figure S3). However, despite its higher activity found on naked DNA, ASV integration was strongly inhibited by nucleosomes assembly as observed for HIV-1 IN (see Figure 2A and quantification in 2B). Additionally, specific quantification of the circular FSI products also revealed a strong decrease in the number of integrants on nucleosomal templates even at low histones concentrations (Figure 2C). Similar results were obtained using different enzyme constructs, preparations, purification procedure and various viral DNA substrates (see data reported for HIV-1 IN in Additional file 4: Figure S4).
To better ascertain the relationship between integration, nucleosomes positions and chromatin structure, we mapped more precisely the integration sites obtained from retroviral integrases on the different chromatin structures of the acceptor plasmid.
Effect of nucleosomes density on in vitro HIV-1, PFV, ASV and MLV integration selectivity
HIV-1 and ASV integration sites carrying the physiological duplications (respectively 5 and 6 bp) obtained under the same reaction conditions and using the p5S vector assembled with a similar 1/1.3 DNA/histones ratio (w/w) were then analyzed. The integration experiment was reproduced a sufficient number of times to obtain a similar amount of 50 integrants carrying integration sites in the 5S-G5E4 region for both enzymes. As shown in Figure 4B and D, a strong bias toward regions of low nucleosome occupancy, especially the linker regions separating the nucleosomes, was found in the 5S-G5E4 region. The mean nucleosome occupancy found at the HIV-1 and ASV integration sites was 2-fold lower than the global mean found for the overall plasmid sequence (Figure 5A). Again, this distribution was not due to a sequence bias since a random distribution was found in the naked plasmid (Additional file 5: Figure S5 and Figure 5B). This indicates that both HIV-1 and ASV integration are preferred in regions containing poorly dense nucleosomes and that nucleosomes localized in organized and stable regions are not favored substrates for HIV-1 and ASV in vitro integration in contrast to MLV and PFV.
As shown in Additional file 3: Figure S3 and Additional file 6: Figure S6A HIV-1 IN also catalyzed in vitro integration events displaying 4 bp target site duplications, in addition to the correct 5 bp duplications. As discussed below and shown in , these integration events are assumed to be catalyzed by differently structured intasomes. While no bias was found in the distribution of the 4 bp integration loci in the naked DNA (Additional file 6: Figure S6B), a strong bias for the 5S region was observed for these events (Additional file 6: Figure S6C) with a strong preference for nucleosomes dense regions of the plasmid. Since these 4 bp and 5 bp integration events were catalyzed by intasomes from the same enzyme preparation this result strongly suggests that the differences found in the sensitivity of the various INs for nucleosomes are not due to differences in reaction conditions or activity. Moreover these data also suggest that the differences found in nucleosome sensitivity between the various integrases are mainly due to local constraints in the catalytic pocket of the various intasomes that define the target DNA duplication.
In vitro PFV IN sensitivity to nucleosome is not dependent on its N-terminal extension domain (NED)
Since MLV and PFV integrases both contain an additional N-terminal extension domain (NED) compared to HIV-1 IN and ASV , we wondered whether it could be responsible for the difference in the impact of chromatin structures on in vitro integration. A PFV IN deleted for this NED domain was thus expressed and purified according to the same procedure as for wt IN and its in vitro integration activity was compared using naked and chromatinized templates. Wt and the NED-deleted INs were found to be equally active under standard conditions using the naked p5S acceptor plasmid, as it was expected from previous data obtained using short donor DNA . This indicates that both enzymes share a similar functional structure even on long donor DNA. Analysis of the integration site structure also indicated that both enzymes shared the same target site duplication of 4 bp (Additional file 3: Figure S3), confirming that this duplication is mainly governed by the arrangement of viral ends in the catalytic sites involved in the strand transfer reaction.
Comparison between integration sites in infected cells and predicted nucleosome occupancy
In order to investigate whether the sensitivity to dense nucleosomes regions found in vitro for the retroviral enzymes could be relevant in a more physiological context we analyzed the positions of cellular integration sites from two retroviruses showing distinct and opposite in vitro selectivity. HIV-1 and MLV were chosen since they present highly divergent in vitro and in vivo integration profiles. Furthermore their integration profiles in infected cells were extensively reported and, thus, a sufficient number of integration sites could be recovered from literature allowing a statistically relevant analysis.
The sequence surrounding 41 435 and 32 631 non redundant HIV-1 and MLV integration sites respectively obtained in human infected cells and selected from previous studies [55,56] were mapped into the human genome and submitted to a nucleosome-position prediction algorithm developed previously by Milani et al. . This algorithm was chosen since it has been shown to provide predictions that are in good agreement with nucleosome positioning determined in vitro by physical and biochemical approaches [53,57,58]. This has been further validated on our in vitro receptor templates by showing a good correlation with the experimentally determined nucleosomes positions (see Additional file 2: Figure S2). Actually, the performance of this method is as good as the more commonly used approach developed by Segal and Widom’s groups  (the mean Pearson correlation between genome-wide experiments and prediction is > 0.75).
Consequently, our results indicate a preferential integration into a nucleosome in infected cells for both MLV and HIV-1. However the nucleosome targeted by both viruses appear located in differently dense chromatin contexts. This shows that MLV and HIV-1 present distinct and opposite preferences for chromatin density surrounding the nucleosomal integration site supporting a modulation of retroviral integration by the chromatin density surrounding the targeted nucleosome as suggested by our in vitro data.
Discussion and conclusion
Retroviral integration selectivity is thought to be regulated by viral and cellular determinants and some of them are specific of the retrovirus. Among all retroviruses, the IN protein and component of the Gag polyprotein have been shown to be involved in integration selectivity . Interactions between these viral components and chromatin structure are thought to affect the selectivity of retroviral integrases. Early experiments performed in vitro using recombinant enzymes and reconstituted nucleosomal DNA indicated that nucleosomes were a preferential target for in vitro integration [42-46]. Compaction of a polynucleosome template by histone H1 was also shown to affect differently integration catalysed by two different INs (HIV and ASV) . Concerted integration assays were more recently employed to investigate the influence of chromatin structure on integration site selectivity [61,36]. These data confirmed that HIV-1 global integration was favoured into nucleosomal DNA  and demonstrated that the chromatin structure and dynamics could influence the physiological full-site integration reaction . This was then confirmed in a selectivity assay using a mixture of vectors with different nucleosome densities indicating that full-site HIV-1 integration was favoured in less dense polynucleosomal template . Taken together these data obtained in different nucleosomal models with different chromatin structures and various retroviral integrases, in addition to the differences found in in vivo integration selectivity from one retrovirus to another one suggest that intrinsic properties of the viral intasome as well as the structure, density and dynamics of the chromatin around the targeted nucleosome play an important role in the integration site selection.
To determine the importance of this regulation in the local association of the intasome with nucleosomes, we focused our present work on the intrinsic properties of different retroviral integrases that can affect the final intasome•nucleosomal DNA functional interaction. We have chosen various retroviral integrases belonging to distinct genera displaying different in vivo selectivity and target sequence duplications marks. These enzymes were tested in vitro for their integration activity on chromatinized template in the lack of cellular cofactors. For this purpose we have selected reaction conditions allowing efficient concerted integration for all the enzymes tested in the work without the need of additional cofactors. Two main in vitro integration conditions were described in the literature using either long donor substrates, PEG and low enzyme concentration [48,49] either short donor substrate without PEG but requiring higher enzyme concentration and cellular cofactors, as LEDGF/p75, for efficient integration activity . Since our main aim was to study the impact of chromatin on retroviral INs without their cofactors we have chosen conditions including PEG and allowing efficient integration for all the enzymes tested. To avoid biases due to the choice of these specific reaction conditions (presence of non-physiological components as PEG) we focused our analyses on the physiological full site integration products catalyzed by the retroviral enzyme. Indeed, these events are undoubtedly catalyzed only by functional intasomes and, thus, the experimental conditions were not expected to impact the choice of the integration sites. Under these conditions, we found that HIV-1, PFV, ASV and MLV enzymes were not affected equally by nucleosomes. PFV and MLV integration efficiencies were increased in a chromatinized template, whereas HIV-1 and ASV integrations were inhibited by stable and compact chromatin. Furthermore PFV and MLV integration events occurred preferentially in the 5S-G5E4 positioning region of our plasmid with a significant preference for the stably associated nucleosomes. In contrast, HIV-1 and ASV integration events were found preferred in regions of low nucleosomes occupancy especially in the less dense region of our acceptor DNA. These differences were not found dependent on the purification procedure nor reaction conditions since same profiles were always found for the various retroviral INs when purified or tested in distinct conditions (concentration, presence of detergent, use of donor DNA containing various viral U3/U5 ends combination, see Additional file 4: Figure S4). Even if we can not completely rule out any bias link to the reaction conditions selected for the study (presence of PEG for example) the focus of the analysis on the full site integration products is expected to limit this bias. Indeed, even if the formation of a catalytically proficient intasome remains a limiting step with regard to integration efficacy, the reaction conditions should only affect the amount of functional intasomes formed and not the choice of the integration site dictated both the architecture of the intasome and the local target DNA structure. This is supported by the fact that the differences in the sensitivity toward nucleosomal density were found independent on the efficiency of concerted integration. Indeed, ASV was found more active than PFV on naked DNA but was also found inhibited by stable chromatin as HIV-1 (less active than PFV in catalyzing concerted integration events).
Furthermore, the differences found between HIV-1/ASV and PFV/MLV INs were not dependent on the presence of the additional NED domain in PFV, indicating that the differential effect of chromatin on these enzymes in vitro is probably mainly due to local differences in the architecture of the catalytic pocket within the functional intasomes and not to global structural differences between the complexes. This is supported by the differences found between the HIV-1 integration reactions, leading to different staggered cuts in the target DNA. Indeed we previously showed that full site and half site integration could be impacted differently by nucleosome assembly in vitro . Interestingly, differences were also found in this work regarding the effect of nucleosomes on the selectivity of HIV-1 integration reactions leading to 4 bp, 5 bp or 6 bp target DNA duplications (see Additional file 6: Figure S6). Indeed, while 5 bp and 6 bp integration reactions were highly disfavored in the stable chromatin region of the acceptor plasmid, 4 bp events were more widespread in the backbone with a clear preference for the high nucleosome density region. Since the ratio of chromatin assembly did not influence the proportion of these “non-physiological” integration events (Additional file 3: Figure S3), the latter are most likely catalyzed by aberrant intasomes structures as previously demonstrated . Consequently, the most reasonable hypothesis that could account for their enrichment in nucleosome dense regions would be that the IN sensitivity toward chromatin is mainly driven by the structure of the IN/viral DNA complex that can or cannot accommodate nucleosomal DNA depending on the relative position of the active sites.
Because no bias in the PFV integration site positions was found in the naked version of the acceptor plasmid (Figure 5 and Additional file 5: Figure S5), our data indicate that the PFV and MLV intasomes can fit with compacted chromatin, in contrast to HIV-1 and ASV INs. The structure of the target DNA, and especially its bending, in the retroviral intasome is expected to be governed by the space between the two catalytic sites involved in the staggered cut leading to different target DNA duplication size [8-10]. This target DNA curvature varying in the different intasomes could, thus, impact the nucleosome sensitivity of the retroviral enzymes. This is supported by the differences found between the retroviral enzymes tested here catalyzing different target sequence duplication and by the differential effect of nucleosomes on the selectivity of HIV-1 integration reactions leading to 4 bp, 5 bp or 6 bp target DNA duplication. Interestingly, recent work highlighted the importance of the presence of flexible pyrimidine/purine steps between the attacked phosphate groups during the strand transfer reaction in promoting DNA bending and thus allowing the target DNA to adopt a conformation compatible with its capture by the intasome, with a minimal energetic expense  and reviewed in . The extent to which the target DNA must be bent depends on the relative position of the IN active sites responsible for the pair-wise strand transfer reaction within the intasome. In the context of a nucleosome, the target DNA is already structurally constrained, therefore, its engagement into the target DNA capture complex would depend on the conformational rearrangements required, hence on the intasome structure. Indeed, this bending of the target DNA in linked to the position of the IN active sites for the pair-wise strand transfer reaction. This bendability is also expected to be affected by the nucleosome structure and chromatin environment which can allow DNA extrusion and facilitate its optimal curvature for integration. Both intrinsic structural properties of the enzymes and nucleosome structure may, thus, play an important role in the final integration site selection. Especially all these data confirm that intasome structural constraints, as the distance between catalytic sites, participate in the local selection of the integration site within chromatin by modulating the functional affinity of the integration complex with nucleosomal DNA in specific chromatin structure.
Additional interactions between intasomes and nucleosomes could also be modulated by the chromatin density at the insertion locus. Especially histone tails could be more or less accessible depending on the compaction of the surrounding nucleosomes. Comparison of the relationship between integration sites from two retroviral paradigms (HIV- and MLV) and nucleosome occupancy in cells (Figure 7) indicates that, both retroviral insertion loci were associated locally with high nucleosome occupancy probability. This suggests that in both cases the selected integration site is probably occupied by a nucleosome which is in contrast to what was observed for HIV-1 in nucleosome dense regions of the receptor templates used in vitro. The apparent discrepancy found for the local preference of HIV-1 IN for nucleosomes between in vitro and in vivo data could be due to the fact that, in the cells, additional remodeling machineries could be involved during the integration process, especially in the highly transcribed regions of viral DNA insertion as supported by previous data , as well as the lack of cellular tethering cofactors in the biochemical assays used in this work. However, when the chromatin structure surrounding the integration sites was analyzed a significant preference for region of higher nucleosome occupancy was found for MLV comparing to HIV-1 IN that preferred less dense regions of the host DNA. This cellular phenotype appears compatible with the intrinsic sensitivity of the retroviral enzymes toward nucleosomes and their capability to accommodate dense or less dense chromatin structure as found in vitro. Thus, even in cellular context, when targeting factors are present, the IN-specific preference found in vitro for regions of variable nucleosomes density can also be detected. Even if the role of the IN cofactors in the local association between intasome and nucleosome remains to be established, our data suggests that the intrinsic sensitivity of retroviral INs toward specific chromatin structure may play an important role in the local selection of the integration site in infected cells in addition to their targeting toward specific region of the host genome by the host cofactors. Taken together all these data support a preferential retroviral integration into a nucleosome but in different chromatin contexts in a mechanism that will depend both on the integrases structures and modulations by the chromatin environment of the targeted nucleosome.
Consequently, the retroviral integration targeting toward nucleosomes appears as a multiple steps process that includes a targeting of the retroviral intasome toward suitable regions of the chromatin as promoter or gene body due to specific interaction between INs and their targeting factors as LEDGF/P75 or BET proteins; and a more local targeting toward the suitable integration site governed by the intrinsic sensitivity of the retroviral INs to specific target DNA bending and chromatin density surrounding the integration locus. These last steps are expected to be governed by the physical constraints within the intasomes modulating its functional interaction with the targeted nucleosome. This model is strongly supported by several data from the literature. Knock out experiments have previously established that LEDGF/p75 was not essential for HIV-1 integration in vivo  and, in the absence of LEDGF/p75, the weak consensus associated with HIV-1 integration is maintained and integration is (though to a lower extent) still associated to active transcription units. Furthermore, a C-terminal deletion derivative of MLV IN, unable to bind BET proteins, still allowed integration catalysis, in vivo, and does not show changes in its local integration selectivity . These data, in addition to our work, support the dependence on the structure of the intasome in its functional association with nucleosomes after the initial targeting step mediated by cellular cofactors (e.g. LEDGF/p75 and BET proteins). Consequently, taken together, these results point out the retroviral intasome, itself, as an important actor in the integration site selection process.
Other additional key parameters are also known to be important in integration site selection, such as the three dimensional localization of the chromatin in the nucleus in comparison to the PIC nuclear entry site  or the involvement of chromatin remodeling proteins that can be found in the integration locus area and expected to affect the nucleosomes stability. Global analyses of the HIV-1 integration site showed that integration occurs in the active region of the chromatin carrying nucleosomes bearing the H3K36me3 modification that promotes transcription and remodeling . In silico comparison of the integration sites found in infected cells and nucleosome positioning show that the process occurs in a region of low nucleosomes density within the chromatin . These data suggest that, for HIV-1 integration to occur, a nucleosomal DNA structure could be required at the integration site but in a context of dynamic chromatin. In this context, the DNA extrusion from the nucleosome is expected to be facilitated, especially during remodeling, allowing the required degree of bending. The position of the integration sites on the surface of the nucleosome  also suggests that other proteins inducing local remodeling of the DNA in the nucleosome nucleoprotein complex and/or supplementary intasome/nucleosome interactions could be involved, in addition to the anchoring factor LEDGF/p75. This would makes the cellular integration process more complex than just involving a direct binding of the retroviral intasomes to the DNA at the nucleosome surface and would highlight the importance of the chromatin context around the targeted nucleosome modulating additional contacts between the integration partners.
PFV and ASV INs were purified from E.coli BL21 bacteria using the same procedure than described previously  . HIV-1 IN was purified either from bacteria using the same procedure as described for PFV enzyme  either from yeast was purified as previously reported . MLV IN was purified using the procedure reported by .
ASV_U3_SupF5′ 5′AATGTAGTCTTATGCAATACTCTTGTAGTCTTGCAATTAACGTTGCCCGGATCCGGTCGCGC 3′, ASV_U3_SupF3′ 5′AATGTAGTCTTATGCAATACTCTTGTAGTCTTGCAAGCGGCGCGTCATTTGATATGATGCG 3′PFVSupF5′ 5′ ATTGTCATGGAATTTTGTATATTGATTATCCTTTAACGTTGCCCGGATCCGGTCGCGC 3′, PFVSupF3′ 5′ ATTGTCATGGAATTTTGTATATTGATTATCCTGCGGCGCGTCATTTGATATGATGCG 3′. MLVSupF5′ 5′TATGAAAGACCCCACCTGTAGTTAACGTTGCCCGGATCCGGTCGCGC 3′
MLVSupF3′ 5′ TATGAAAGACCCCCGCTGACGCGGCGCGTCATTTGATATGATGCG 3′, respectively.
The amplified fragments were purified from a 1% agarose gel using the PROMEGA Wizard SV gel and PCR cleanup system and 5′ radiolabelled using the T4 polynucleotide DNA kinase (PROMEGA). The different donor DNA are described in Additional file 1: Figure S1.
Polynucleosome templates were assembled using purified HeLa core histones (H3, H4, H2A and H2B)  by gradient salt dialysis . Structure of regions I and II of the p5S vector was previously checked by ab initio prediction of nucleosome occupancy throughout the DNA sequence performed by computing the free-energy landscape associated with the bending of DNA around histone octamers to form nucleosomes  (see Figure 1). Nucleosome assembly was checked by DNase I protection, REA assay and mono- and di-nucleosome gel shift, as done before  and described in Additional file 2: Figure S2.
Standard concerted integration reactions were optimized from conditions described previously  in order to allow efficient catalyse of full site integration reaction in absence of other cellular cofactors. For this purpose we used 5′-end-labeled donor DNA (10 ng) and naked or chromatinized circular target DNA plasmids (50 ng) and purified INs (typically 100 nM) previously diluted to 1 μM in 1 M NaCl, 20 mM HEPES 1 M pH7, 10 mM DTT for 30 minutes on ice. Then 200 nM IN were incubated 30 minutes on ice with 10 ng of donor DNA and 50 ng of acceptor plasmid in 5 μl final volume. Reaction was then started by adding 5 μl of the reaction buffer (final concentrations 100nM IN, 15% DMSO, 8% PEG, 10 mM MgCl2, 20 μM ZnCl2, 100 mM NaCl, 10 mM DTT). After the reaction, integration products were loaded onto 1% agarose gel. The gel was then dried and autoradiographied. Quantification of the integration activity was performed using the Image J software with the following procedure: the bands corresponding to the free substrate (S), the donor/donor (d/d), linear FSI (FSI) and circular HSI + FSI (HSI + FSI) were quantified. The percentage of HSI + FSI integration activity was calculated as (HSI + FSI)/[(FSI) + (HSI + FSI) + (d/d) + (S)] × 100. Percentage of FSI integration activity was determined as (FSI)/[(FSI) + (HSI + FSI) + (d/d) + (S)] × 100. The global FSI activity was estimated from the amount of linear FSI products which has previously been shown to be representative of the circular FSI form. The circular FSI reaction efficiency was then quantified by cloning the integration products in bacteria according to the same protocol as described previously  with some minor modifications. The integration reaction performed with unlabelled donor DNA and the corresponding acceptor plasmids was 15 times scaled up and the integration products were loaded on 1% agarose gel after deproteinization using protease K 1 mg/ml (ROCHE) and phenol/chloroform/isoamyl alcohol (24/25/1, v/v/v). The open circular forms of the products were purified using the PROMEGA Wizard SV gel and PCR cleanup system and 2–5 μl aliquots of the purified DNA were used to transform electrocompetent MC1060/P3 E. coli strain which contained ampicillin-, tetracycline- and kanamycin-resistance genes. Integration clones carrying the supF gene were selected in the presence of 40 μg/ml ampicillin, 10 μg/ml tetracycline and 15 μg/ml kanamycin. Integration loci determination was performed by isolating plasmids from triple-resistant colonies and PCR sequencing (ABI Prism big dye terminator cycle sequencing ready reaction kit, Applied Biosystems) using the corresponding HIV-1, PFV, ASV and MLV primers described above. The number of experiments was adjusted to reach the required amount of integrants for statistically significant analyses.
Nucleosome occupancy prediction
The work was supported by the French National Research Agency (ANR, RETROSelect program), the French National Research Agency against AIDS (ANRS), the Centre National de la Recherche Scientifique (CNRS), the University Victor Segalen Bordeaux 2, the French Research Group GDR 3546 “Les Eléments Génétiques Mobiles : du mécanisme aux populations, une approche integrative”, and the ECOS-CONICYT C12B03 program. The authors are deeply grateful to Dr Simon Litvak for fruitful discussions and constant encouragement and to Prof. R. Cooke (University Victor Segalen Bordeaux 2) for proofreading the manuscript.
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