Nucleosome positioning at the replication fork
2001; Springer Nature; Volume: 20; Issue: 24 Linguagem: Inglês
10.1093/emboj/20.24.7294
ISSN1460-2075
Autores Tópico(s)Genomics and Chromatin Dynamics
ResumoArticle17 December 2001free access Nucleosome positioning at the replication fork Renzo Lucchini Renzo Lucchini Present address: Laboratorio Analisi Speciali, via Rovere 8, CH-6932 Breganzona, Switzerland Search for more papers by this author Ralf Erik Wellinger Ralf Erik Wellinger Institute of Cell Biology, ETH Hönggerberg, CH-8093 Zürich, Switzerland Present address: Laboratorio Analisi Speciali, via Rovere 8, CH-6932 Breganzona, Switzerland Search for more papers by this author José M. Sogo Corresponding Author José M. Sogo Institute of Cell Biology, ETH Hönggerberg, CH-8093 Zürich, Switzerland Search for more papers by this author Renzo Lucchini Renzo Lucchini Present address: Laboratorio Analisi Speciali, via Rovere 8, CH-6932 Breganzona, Switzerland Search for more papers by this author Ralf Erik Wellinger Ralf Erik Wellinger Institute of Cell Biology, ETH Hönggerberg, CH-8093 Zürich, Switzerland Present address: Laboratorio Analisi Speciali, via Rovere 8, CH-6932 Breganzona, Switzerland Search for more papers by this author José M. Sogo Corresponding Author José M. Sogo Institute of Cell Biology, ETH Hönggerberg, CH-8093 Zürich, Switzerland Search for more papers by this author Author Information Renzo Lucchini2, Ralf Erik Wellinger1,2 and José M. Sogo 1 1Institute of Cell Biology, ETH Hönggerberg, CH-8093 Zürich, Switzerland 2Present address: Laboratorio Analisi Speciali, via Rovere 8, CH-6932 Breganzona, Switzerland ‡R.Lucchini and R.E.Wellinger contributed equally to this work *Corresponding author. E-mail: [email protected] The EMBO Journal (2001)20:7294-7302https://doi.org/10.1093/emboj/20.24.7294 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info In order to determine the time required for nucleosomes assembled on the daughter strands of replication forks to assume favoured positions with respect to DNA sequence, psoralen cross-linked replication intermediates purified from preparative two-dimensional agarose gels were analysed by exonuclease digestion or primer extension. Analysis of sites of psoralen intercalation revealed that nucleosomes in the yeast Saccharomyces cerevisiae rDNA intergenic spacer are positioned shortly after passage of the replication machinery. Therefore, both the 'old' randomly segregated nucleosomes as well as the 'new' assembled histone octamers rapidly position themselves (within seconds) on the newly replicated DNA strands, suggesting that the positioning of nucleosomes is an initial step in the chromatin maturation process. Introduction Replication of eukaryotic chromosomes requires both the duplication of the parental DNA and its assembly into chromatin. Nascent DNA strands are reorganized into chromatin in a very rapid process (Gasser et al., 1996) characterized by the presence of nucleosomes in the vicinity of the elongation point (Cusick et al., 1984; Sogo et al., 1986). In order to provide the full complement of histone octamers on the nascent DNA strands, transfer of 'old' parental histones to the daughter strands must occur in coordination with the assembly of newly synthesized histones. In the first step of this process, the advance of the replication machinery destabilizes the nucleosomal organization of the chromatin fibre (Gasser et al., 1996) and the parental histone tetramers (H3/H4)2 are directly assembled on the newly synthesized daughter strands (Gruss et al., 1993) in a random fashion (for reviews see Krude, 1995; Sogo and Laskey, 1995). Re-association of either old or new H2A/H2B dimers to parental (H3/H4)2 tetramers (Jackson, 1990) completes the assembly of the so-called segregated parental nucleosomes. Newly synthesized histones H3 and H4 form de novo tetramers and associate with the nascent DNA strands (Jackson, 1990; Svaren and Chalkley, 1990). Chromatin assembly factor 1 (CAF-1)-mediated assembly of newly synthesized histones H3 and H4 into nucleosomes has been well documented by Stillman and co-workers (Smith and Stillman, 1989, 1991; Kaufman et al., 1995; Verreault et al., 1996; for reviews see Krude, 1995; Kaufman, 1996). Newly replicated chromatin appears to be less stable (Gasser et al., 1996) and more susceptible to degradation by nucleases than the corresponding sequences within bulk chromatin (Klempnauer et al., 1980; Cusick et al., 1984). Factors that could account for the behaviour of this so-called immature chromatin (Cusick et al., 1984) include histone composition (presence or absence of histone H1), histone modifications (reversible acetylation of the histones; for reviews see Annunziato, 1995; Wade et al., 1997), as well as the newly replicated DNA sequence itself. At least the assembly of the first nucleosome immediately behind the replication fork occurs asymmetrically with respect to DNA sequence on the nascent leading and lagging strands (Sogo et al., 1986). Thus, an altered distribution of nucleosomes on the different arms of a single replication fork was suggested (DePamphilis and Bradley, 1986). In this context, several intriguing questions remain to be answered, e.g. do nucleosomes of the sibling molecules find the same DNA sequence and if so when? Does this process occur on post-replicated chromosomes or are nucleosome positioning and replication elongation simultaneous processes? Since the main obstacle to investigating these questions is the lack of an available procedure to purify replicating chromatin, alternative techniques that allow an analysis of chromatin at the replication forks are required. An opportunity to examine replication in chromatin is provided by the psoralen technique routinely used in our group (Gruss and Sogo, 1992). However, analysis of individual replicating molecules by psoralen cross-linking followed by electron microscopy (Sogo et al., 1986; Avemann et al., 1988; Lucchini and Sogo, 1994, 1995; Gasser et al., 1996) does not provide the resolution necessary to accurately determine translational positioning of newly assembled nucleosomes. To overcome this limitation, we developed two complementary assays that allow precise mapping of nucleosomes along defined regions of living cells. Focusing on nucleosomes immediately behind the replication fork, we reveal that nucleosomes on the nascent strands are rapidly positioned after passage of the replication machinery. Results In vivo mapping of nucleosomes in the ribosomal spacer region using psoralen–DNA cross-linking and λ-exonuclease digestion Psoralens are small DNA-intercalating molecules which readily diffuse through cellular membranes (Cole, 1970). When chromatin is photoreacted with psoralen, cross-links are formed preferentially in the linker DNA between adjacent nucleosomes (Hanson et al., 1976; Conconi et al., 1984). The position of these cross-links can be determined by digestion of DNA fragments with exonuclease since psoralen–DNA cross-links serve as a roadblock for this enzyme (Widmer et al., 1988). Further digestion with S1 nuclease leads to DNA fragments of nucleosomal and polynucleosomal size, which are expected to carry psoralen cross-links at both ends. As summarized in Figure 1A, this approach was modified by substituting S1 nuclease with mung bean nuclease, since the latter enzyme does not cleave nicked duplex DNA (see Materials and methods). Using the indirect end-labelling technique (Nedospasov et al., 1989; Wu, 1989), the position of nucleosomes along a given DNA sequence can then be determined unambiguously (for details see Materials and methods). When the technique was applied to the intergenic spacer of the yeast rRNA gene locus, two defined domains with respect to chromatin organization were found. In a region that spans the 5S gene and the 5′ end of the 35S transcription unit, four positioned nucleosomes were mapped, as indicated by the empty boxes in Figure 1D (middle panel). To test the fidelity of the technique described, we prepared crude nuclei in a parallel experiment, digested them with micrococcal nuclease (MNase) and mapped the nuclease cleavage sites by indirect end-labelling (Livingstone-Zatchej and Thoma, 1999). MNase digestion of isolated nuclei confirmed the result obtained by psoralen cross-linking. Four nucleosomes were mapped at the same locations between the 5S gene and the 5′ end of the 35S transcription unit (Figure 1D, left panel). In contrast, nucleosome mapping of the region between the 5S gene and the 3′ end of the 35S coding region revealed the same pattern of cleavage in chromatin as in control deproteinized DNA (Figure 2C; see also Fritze et al., 1997). It seems that in this second domain, nucleosomes are randomly distributed. These results are confirmed by data of Vogelauer et al. (1998). In their study, a similar nucleosomal organization of the rRNA gene intergenic spacer was described. An important difference was detected in the nucleosomal organization of the rDNA-ARS (rARS) region. In contrast to the results of Vogelauer et al. (1998), where the rARS cis-element is placed within the linker of two adjacent nuclesomes, in the yeast strain used for this study the rARS element spanning 107 bp determined by Miller and Kowalski (1993) was located within a region that was modestly accessible to MNase digestion and to psoralen cross-linking (grey box in Figure 1D, see also Figure 4C; M.Muller, unpublished data). Although a putative nucleosome could fit into this less protected region [approximate map units (MU) −499 to MU −679 in Figure 1C], the absence of a classical nucleosomal footprint might be explained by another possibility. It is also conceivable that the ORC proteins, which are likely to cover the rARS throughout the cell cycle (Santocanale and Diffly, 1996), render the rARS element more accessible to MNase and psoralen (Lipford and Bell, 2001). We decided to maintain the nomenclature of Vogelauer et al. for nucleosomes 1, 3, 4 and 5, and leave out a designation for nucleosome 2. Figure 1.Mapping of nucleosome positions in the ribosomal intergenic spacer by the psoralen–exonuclease assay. (A) Schematic representation of the method. Crosses represent sites of psoralen cross-links in duplex DNA corresponding to the linker regions between nucleosomes (the preferential sites of psoralen cross-linking). (B) Structural organization of the spacer region. Restriction sites (upright and downright arrows), functional elements (boxes) and the transcription start site (+1) are indicated. A BstEII–AvaII fragment used as a probe for indirect end-labelling is shown (striped box). (C) Positioned nucleosomes (numbered boxes 1–5) and the corresponding linkers (roman numerals) are indicated. Positions of the linkers are given with respect to the transcriptional start site. The grey box represents the ORC binding site and adjacent sequences. The large empty box denotes randomly distributed nucleosomes towards the 3′ end of the rDNA coding unit. (D) Nucleosome mapping between the 5S gene and the transcription start site by indirect end-labelling from the BstEII site close to the 5S gene. In the left panel, the untreated BstEII fragment (N, lane 1), MNase cutting sites in chromatin (C, lanes 3 and 4) or in deproteinized DNA (D, lane 2) are shown. Chromatin (lanes C) was digested for 10 min with 25 U/μl (lane 3) or 500 U/μl (lane 4) MNase. In the right panel, psoralen cross-linking sites in chromatin (C, lanes 5 and 6) and deproteinized DNA (D, lane 7) were determined by the psoralen–exonuclease assay. λ-exonuclease entry sites were created by digesting purified cross-linked DNA for 2 min with 2 U/μl (lane 6) or 10 U/μl (lane 5) MNase [see (A)]. The pBR328 DNA fragments (BglI–HinfI) used as size markers are shown. Download figure Download PowerPoint Figure 2.Chromatin structure of the ribosomal intergenic spacer in replicating molecules with arrested forks. (A) Structural organization of the 4.5 kb BglII fragment containing the rRNA intergenic spacer. The y-shaped molecule represents replication intermediates blocked at the RFB. (B) Preparative 2D gel of BglII-digested rDNA from psoralen cross-linked S-phase cells. Linear fragments (L) and replication intermediates arrested at the RFB have been excised from the gel. The expected migration pattern (left) and Southern blot analysis of the gel are shown. (C) Nucleosome mapping towards the 3′ site. λ-exonuclease entry sites were created by digesting the DNA with HpaI, and mapping of the psoralen cross-links was achieved by indirect end-labelling from the AvaII site close to the 5S gene. DNA eluted from the gel plug (RFB) was subjected to the psoralen–exonuclease assay. As controls, DNA eluted from the gel plug L (lane 2) or cross-linked deproteinized DNA (lane 1) were used. Note that the random position of nucleosomes in this region is inferred from the very similar cross-linking pattern of chromatin and deproteinized DNA. The asterisk indicates the position immediately behind the branch point in RIs with arrested forks. (D) Nucleosome mapping towards the 5′ site. λ-exonuclease entry sites were created by digesting the DNA with CfoI, whereas mapping was performed from the BstEII site close to the 5S gene. Gel lanes are as in (C). The λ-DNA fragments (EcoRI–HindIII) used as size markers are shown. Download figure Download PowerPoint Nucleosome mapping of replicative intermediates (RIs) shows intact nucleosome positioning in long-lived replicative molecules The efficacy of the psoralen–exonuclease technique for chromatin mapping encouraged us to examine the nucleosomal organization of RIs. We first concentrated on molecules where leftward moving forks were stalled near the 3′ end of the 35S coding region at the replication fork barrier ('RFB' molecules; Figure 2A bottom; Gruber et al., 2000). In these long-lived molecules, newly replicated intergenic spacers are visualized by electron microscopy as rows of single-stranded (ss) bubbles, consistent with their packaging into nucleosomes (for details see Lucchini and Sogo, 1994). We therefore attempted to map the translational positions of nucleosomes on these RIs using the psoralen–exonuclease technique. The analysis of a specific class of replicative chromatin is a two-step process. First, the positions of nucleosomes are marked at the DNA level by psoralen cross-linking of chromatin in living cells. Then, the purified DNA molecules are separated according to their mass and shape on two-dimensional (2D) agarose gels (Brewer and Fangman, 1987). In such 2D gels, the location of a replication fork relative to the DNA sequence in a particular fragment is defined by its mobility in the gel. In brief, S-phase cells were psoralen photoreacted, the isolated rDNA was enriched, digested with BglII and fractionated in preparative 2D agarose gels (Figure 2A and B). DNA corresponding to linear fragments and RIs with arrested forks were excised from the 2D gel (Figure 2B, right panel), subjected to the exonuclease assay, and the mono- and polynucleosomal fragments generated were detected in a native agarose gel by indirect end-labelling (Figure 2C and D). Upstream of the 5S gene, no difference in the banding pattern of control deproteinized DNA and chromatin from non-replicated monomers could be detected (Figure 2C, compare lanes 1 and 2). This is consistent with MNase mapping studies, which suggest that nucleosomes are randomly distributed in this area. The banding pattern of linear non-replicating molecules was also compared with that of the homogeneous class of partially replicated molecules that accumulate at the RFB (Figure 2C, lane 3). In these molecules, the fork is arrested in a defined sequence (RFB; Figure 2A) which coincides with the HpaI cutting site (Gruber et al., 2000). Interestingly, the two patterns vary only in the region immediately behind the elongation point (the pre-nucleosomal DNA), which exhibited hypersensitivity to psoralen (Figure 2C, asterisk). When the 5S gene downstream region was analysed in RFB molecules, four positioned nucleosomes were detected (Figure 2D, lane 3). The positions of these nucleosomes correlate strictly with those determined for the non-replicated intergenic spacers (Figure 2D, lane 2, see also Figure 1D, lanes 5 and 6). This suggests that the nucleosomes re-assembled after the passage of the replication fork rapidly adopt the translational positions observed in non-replicated chromatin. The nucleosomal pattern of the four positioned nucleosomes between the 5S gene and 35S promoter is established immediately after passage of the replication machinery In the RIs stalled at the RFB, both left and rightward moving forks have already passed the region between the 5S gene and the 35S promoter (Figure 2A, bottom; for more details see Figure 3A, fork 5). We designate them 'long-lived' RIs since the fork persists at the RFB for up to several minutes. As was shown above, the positioning pattern of the four nucleosomes between the 5S gene and the 35S promoter in the RFB molecules (Figure 2D, lane 3) and control non-replicated chromatin (Figure 2D, lane 2) is indistinguishable. However, analysis of the positioning pattern of long-lived RIs does not reveal what the situation was immediately before and during the passage of the replication machinery. We therefore examined the passively replicating 4.7 kb NheI rDNA restriction fragment, in which the timing of nucleosome formation can be followed (Figure 3A, forks 1–4). These molecules containing the intergenic spacer were expected to generate the characteristic Y-arc in a 2D agarose gel (Figure 3B, left side). In principle, DNA fragments present in the Y-arc result from rightward moving forks entering an intergenic spacer where the upstream ARS element was not activated as an origin (Figure 3A, forks 1–4). The 4.7 kb fragments containing an active origin of replication (left intergenic spacer in Figure 3A) generate either a bubble-arc (Figure 3B) or a prominent spot on the Y-arc (Figure 3B, plug 5). As expected, Southern blot analysis of a 2D agarose gel shows a classical Y- and bubble-arc (Figure 3B, right side). Except for the RFB molecules, the DNA fragments migrating in the Y-arc mainly contain rightward moving forks, since in yeast most of the rRNA genes replicate in the same direction as transcription (Brewer and Fangman, 1988; Linskens and Huberman, 1988; Muller et al., 2000). In order to isolate pre- and post-replicative chromatin in the region spanning the 5S gene to the 35S promoter element (Figure 3A, slashed region), replicative molecules were isolated from preparative 2D gels at distinct sites within the Y- and bubble-arc. At the inflection point of the Y-arc (Figure 3B, plug 3), Y-shaped molecules containing arms with the same length accumulate. In these molecules, the expected location of the fork is within the 5S gene and ARS. Therefore, this region is most likely to be involved in the process of replication. In contrast, molecules isolated from the ascending (Figure 3B, plugs 1 and 2) or descending (Figure 3B, plugs 4 and 5) part of the Y-arc are pre- or post-replicative molecules with respect to the hatched region in Figure 3A (right side). Following the same criteria, another class of post-replicative molecules is found in the most retarded part of the bubble-arc (Figure 3B, plug 6). Figure 3.Chromatin structure of the intergenic spacer during replication. (A) Replication mode of the yeast rDNA. The top line represents the 35S coding region (thick line) flanked by intergenic spacers. Origin of replication (Ori; active initiation of replication), RFB, ARS element and NheI cutting sites are indicated. Left- and rightward moving forks (1–6) are localized at different positions along the 4.7 kb NheI restriction fragment containing the intergenic spacer (note that the ARS element is passively replicated). Replicating molecules with leftward moving forks arrested at the RFB are shown (5). The hatched zone marks the region of chromatin analysed. (B) Schematic representation of the expected mobility for the 4.7 kb NheI replicating fragments in an analytical 2D gel (left). Numbers indicate the positions predicted for the replication intermediates indicated in (A). In the right panel, NheI-digested rDNA from psoralen cross-linked S-phase cells was digested with NheI and separated on a preparative 2D gel (the arrow represents partially digested replicative intermediates). Small plugs containing a variety of replication intermediates were excised. Southern blot analysis of the gel is shown. (C) Exonuclease mapping of DNA eluted from the gel plugs. The analysis has been performed is as in Figure 2D. Download figure Download PowerPoint Figure 4.Nucleosome mapping by the psoralen–primer extension assay. (A) Schematic representation of the method. Enzymatic digestion steps and linear amplification are indicated. Note that the density of cross-links is very low. (B) Structural organization of the intergenic spacer region between the 5S gene and the 5′ end of the 35S coding region. Relevant restriction sites, primer 1317 (straight arrow) and strand-specific probe 1496–1317 (striped box) are indicated. (C) Schematic representation of the mapped nucleosomes. (D) Total DNA from cross-linked exponentially growing cells (C, lanes 3, 4 and 5) or deproteinized cross-linked DNA (D, lane 2) was digested with AvaI and AvaII and subjected to the psoralen–primer extension assay. As a control for the primer extension reaction, the non-treated AvaI fragment was used (N, lane 1). Note that only nucleosomes N1–N4 were mapped. Deproteinized DNA (D) was psoralen cross-linked with 0.08 kJ/m2 (lane 2), while the chromatin (C) was cross-linked with 0.9, 1.8 and 5.4 kJ/m2 (lanes 3, 4 and 5). Download figure Download PowerPoint The nucleosome positioning of the RIs described was analysed by λ-exonuclease digestion of the psoralen cross-linked DNA (Figure 3C). To our surprise, in all samples isolated from the Y-arc (Figure 3C, lanes 1–4) the nucleosomal banding pattern was indistinguishable. In addition, the pattern resembles those obtained either from control non-replicated or long-lived replicative molecules (Figure 3C, lanes L and RFB, respectively). Since nucleosome assembly of the leading and lagging strands is asymmetrical (Cusick et al., 1984; Sogo et al., 1986), this result is consistent with an extremely rapid positioning of nucleosomes after passage of the replication machinery. The nucleosomal organization on bubble-shaped molecules in which the intergenic spacer has just been replicated (Figure 3C, lane 6) was expected to confirm this interpretation. However, in lane 6, the banding pattern is practically absent. Most likely, the amount of purified material was not sufficient to allow the detection of the nucleosomal pattern. In order to improve the sensitivity of the analysis and to confirm the present result, we decided to analyse RIs by a similar exonuclease assay coupled to a primer extension reaction. Primer extension confirms the nucleosomal pattern obtained in replicating chromatin An outline of the approach is summarized in Figure 4A. Yeast cells were weakly psoralen cross-linked, then the DNA was isolated and digested with an appropriate restriction enzyme. Further treatment of the DNA with λ-exonuclease generated templates for primer extension reactions. Psoralen cross-links act as a roadblock for the Taq polymerase; therefore, the reaction products define the length between the priming site of the oligonucleotide and the psoralen cross-link. As shown previously, the linkers between nucleosomes can be mapped by this method (for details see Wellinger and Sogo, 1998). In contrast to the assay described in Figure 1, linear amplification of the reaction products can be achieved by repeated cycles of primer extension. Thus, the sensitivity of the mapping procedure is significantly enhanced. Nucleosome mapping by this method within the ribosomal spacer is shown in Figure 4D. Note that due to the position of the primer used (Figure 4B), only three nucleosomes were mapped. The calculated positions of these three nucleosomes (Figure 4C) were compared with those obtained previously (Figure 1C). With both techniques (Figures 1A and 4A), nucleosomes were mapped to the same positions within the resolution of the two techniques. In order to confirm the results obtained by the λ-exonuclease digestion of RIs, weakly psoralen cross-linked RIs were prepared as outlined in Figure 3. The replication intermediates were isolated from preparative 2D agarose gels and subjected to a primer extension reaction. Again, in all samples analysed, the banding pattern remained very similar, independent of whether the material was eluted from areas of the 2D gel containing non-replicated, early, mid or late replicated molecules (Figure 5A). Importantly, the amount of material excised from the bubble-arc was then sufficient for mapping nucleosomes along nascent strands (Figure 5A, lane 6). In summary, we could clearly confirm that nucleosomes rapidly occupy their translational position after the corresponding DNA sequence is duplicated. Figure 5.Mapping of nucleosomes in the replicating ribosomal intergenic spacer. (A) Replication intermediates of the 4.7 kb NheI fragment were isolated as described in Figure 3B. The eluted samples were subjected to the psoralen–primer extension assay and the cross-links were mapped as described in Figure 4A. As a control for the primer extension reaction, the non-treated AvaII fragment was used (N). The diagram to the right represents positioned nucleosomes behind the elongation point. Marker (M) represents multiples of 256 bp. (B) Interpretation of the results. Nucleosomes are depicted as short cylinders. The schematic drawing represents rightwards moving forks in a population of 4.7 kb replicating molecules isolated from a gel plug. As a single gel plug corresponds to approximately one-sixth of the total Y-arc (see the autoradiograph in Figure 3B), the branch points of the replication forks are uniformly distributed along a region of ∼750 bp (between dashed lines). The black–grey box at the bottom gives an estimate of the nucleosomal density along the replicating region. Download figure Download PowerPoint At first sight, our results showing positioned nucleosomes during or immediately after the replication process (lane 3 in Figures 3C and 5A) conflict with previous observations demonstrating non-nucleosomal DNA immediately behind the elongation point (Cusick et al., 1984). In addition, we showed in an earlier study that at least the first nucleosome close to the elongation point re-associates asymmetrically on the newly replicated DNA branches (Sogo et al., 1986). However, this apparent discrepancy can be explained by the somewhat heterogeneous position of the replication fork within the various classes of intermediates purified from the preparative 2D gel. In fact, a single gel plug contains a subpopulation of replication intermediates representing a pool of individual molecules where the replication-elongation point is localized at any position along a DNA stretch of ∼750 bp (see Figure 5B). Even if the replication machinery transiently disrupts up to three nucleosomes in the vicinity of the fork (Gasser et al., 1996), chromatin mapping of this heterogeneous population of molecules will never detect a region completely devoid of nucleosomes. Discussion A combination of DNA cross-linking by psoralen and subsequent preparative 2D gel analysis allowed the first direct assessment of the timing and extent of nucleosome positioning after the passage of the replication fork in vivo. This was achieved by selectively isolating rDNA replicative molecules from psoralen cross-linked yeast chromatin. Our analysis revealed a rapid repositioning of nucleosomes after passage of the replication fork. Psoralen as a tool to investigate nucleosome positioning in vivo Previous work established psoralen–DNA cross-linking as a useful tool to study the nucleosomal organization of chromatin. These studies included the investigation of bulk inactive (Hanson et al., 1976; Conconi et al., 1984; Widmer et al., 1988; Sogo and Thoma, 1989), transcriptionally active (Conconi et al., 1989; Lucchini and Sogo, 1997) and replicating chromatin (Gruss and Sogo, 1992; Sogo and Laskey, 1995). An intrinsic property of psoralen is its ability to mark the structural information of the in vivo organized chromatin at the level of the DNA. After UV irradiation of psoralen-treated cells, intercalated psoralen remains fixed on the isolated deproteinized DNA. However, although the DNA molecule is (reversibly) altered, its basic helical structure remains intact (Sinden and Hagerman, 1984). Remarkably, psoralen cross-links are restricted to the linker DNA between nucleosomes. This is best visualized when DNA is purified from cross-linked chromatin, spread, and mounted for electron microscopy under denaturing conditions. The nucleosomal DNA repeat can then be recognized as rows of ss-bubbles connected by small double-stranded regions. Thereby, the chromatin organization of a given domain can be deduced by direct visualization of the corresponding psoralen-marked DNA sequence. However, mapping of the resulting ss-bubbles does not allow the translational position of the nucleosomes to be determined. In order to improve the resolution of linker detection and to analyse the nucleosome positioning in a whole population of molecules, we developed a novel technique based on a biochemical approach. This psoralen–exonuclease assay was successfully tested on the rDNA locus in yeast. Additionally, we have shown that the sensitivity of linker detection
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