In vivo recruitment of exon junction complex proteins to transcription sites in mammalian cell nuclei

INTRODUCTION

In eukaryotes, messenger RNAs are transcribed in the nucleus as precursor forms (pre-mRNAs). Immediately upon synthesis, nascent transcripts associate with proteins forming ribonucleoprotein (RNP) particles, the protein content of which evolves throughout the lifetime of a mRNA (for a recent review, see Dreyfuss et al. 2002). The proteins associated with messenger ribonucleoprotein particles (mRNPs) play key roles in all aspects of the RNA metabolism, from nucleocytoplasmic transport to cytoplasmic localization, translational efficiency, and decay. In particular, a specific subset of proteins including SRm160, RNPS1, Y14, Mago, DEK, REF/Aly, and UAP56 form the exon junction complex (EJC), which associates with mRNAs as a consequence of splicing (Blencowe et al. 1998; Mayeda et al. 1999; Kataoka et al. 2000; Le Hir et al. 2000a,b; McGarvey et al. 2000; Zhou et al. 2000; Luo et al. 2001). SRm160 and RNPS1 were originally characterized as activators of pre-mRNA splicing (Fleckner et al. 1997; Blencowe et al. 1998; Mayeda et al. 1999). More recently, SRm160 was shown to promote transcript 3′-end cleavage (McCracken et al. 2002), whereas RNPS1 couples splicing to nonsense-mediated decay (Lykke-Andersen et al. 2001). Y14 is involved in mRNA quality control via the nonsense-mediated mRNA decay (NMD) pathway (Lykke-Andersen et al. 2001), and together with Mago, is required for the proper cytoplasmic localization of oskar mRNA during Drosophila development (Hachet and Ephrussi 2001; Mohr et al. 2001). Y14 and Mago form a tight heterodimer in vivo (Lau et al. 2003), and the association between the two proteins is essential for function in NMD (Fribourg et al. 2003). DEK has been involved in multiple functions ranging from splicing (McGarvey et al. 2000) to chromatin structure (Alexiadis et al. 2000) and transcriptional regulation (Faulkner et al. 2001). REF/Aly has been identified as a chaperone that regulates the activity of bZIP transcription factors (Virbasius et al. 1999), and also as a factor that facilitates the nuclear export of mRNA by interacting with the export receptor NXF1/TAP (for review, see Reed and Hurt 2002). UAP56 is a putative RNA helicase also implicated as a splicing factor required for early spliceosome assembly (Kistler and Guthrie 2001; Libri et al. 2001; Zhang and Green 2001). Contrasting with NXF1/TAP and UAP56, the depletion of which causes nuclear accumulation of mRNA, REF/Aly, RNPS1, SRm160, and Y14 are dispensable for bulk mRNA export (Gatfield and Izaurralde 2002; Longman et al. 2003; MacMorris et al. 2003). Accordingly, SR proteins were identified recently as adaptors that, in addition to REF/Aly, can mediate the interaction between NXF1/TAP and cellular mRNAs (Huang et al. 2003).

Translocation of mRNAs through the nuclear pore complex requires binding of an heterodimer composed of NXF1/TAP and NXT1/p15 (Mex67 and Mtr2 in Saccharomyces cerevisiae). NXF1/TAP, which interacts both with RNA-binding adapter proteins and components of the nuclear pore complex, is believed to be the major receptor for the export of mRNAs to the cytoplasm (for recent reviews, see Izaurralde 2002; Lei and Silver 2002b; Reed and Hurt 2002; Cullen 2003; Stutz and Izaurralde 2003). Another protein that interacts simultaneously with mRNPs and nucleoporins is Dbp5/Rat8 (Snay-Hodge et al. 1998; Tseng et al. 1998). Although in yeast Dbp5 is essential for mRNA export to the cytoplasm (Snay-Hodge et al. 1998; Tseng et al. 1998), depletion of the Drosophila homolog of Dbp5 does not result in the bulk nuclear retention of mRNAs (Gatfield et al. 2001).

How export-competent mRNPs assemble in the living cell nucleus and travel to the nuclear pores remains poorly understood. Here, we visualize the localization of EJC proteins and mRNA export factors in the nucleus of mammalian cells producing abundant pre-mRNA transcripts. First, we analyzed HeLa cells infected with adenovirus, because this virus recruits the host transcription and processing machinery to the sites of viral pre-mRNA synthesis (Jimenez-Garcia and Spector 1993; Pombo et al. 1994). In addition, we made use of murine erythroleukemia (MEL) cells stably transfected with the human β-globin gene under the control of the locus control region (LCR). The human β-globin gene, which integrates in the host cell genome as a tandem array, expresses at physiological levels upon induction of MEL cells to undergo terminal erythroid differentiation (Collis et al. 1990). Using in situ hybridization and confocal microscopy, we observe colocalization of EJC proteins (REF/Aly, Y14, SRm160, UAP56, RNPS1, and Magoh) and core spliceosome components (U snRNPs) at sites in the nucleus containing nascent adenoviral and β-globin transcripts. In contrast, the export factors NXF1/TAP, p15, and Dbp5 are not detected at sites of transcription. The results further show that REF/Aly, SRm160, UAP56, and spliceosomal snRNPs fail to accumulate at the site of transcription of a processing-defective β-globin mutant. Taken together, these data suggest that EJC proteins bind cotranscriptionally to mRNPs, and that efficient pre-mRNA processing is required for assembly of EJC proteins onto nascent transcripts in vivo.

RESULTS

Components of the EJC, but not NXF1/TAP, p15, or Dbp5, are recruited to sites of adenoviral transcription in the nucleus of infected HeLa cells

Adenovirus type 2 (Ad2) causes a productive infection of HeLa cells that proceeds through an infectious cycle of ~36 h. This cycle is conventionally divided into early and late stages, separated by the onset of viral DNA replication (for review, see Philipson et al. 1975). Adenoviruses enter the host cells by receptor-mediated endocytosis, penetrate the cytoplasm from endosomes, and deliver their DNA genome into the nucleus (Greber et al. 1993). Upon entry in the nucleus, transcription of the viral genome starts immediately, and the viral mRNAs transcribed at this early stage direct the synthesis of a small number of proteins that promote viral DNA replication. After the onset of viral DNA replication, which occurs at ~8 h post-infection, the remaining viral genomic information is expressed, yielding large quantities of the structural proteins that will eventually constitute new virus particles (Philipson et al. 1975; Flint 1986). During this period, the normal nuclear architecture undergoes a series of progressive changes (for review, see Pombo and Carmo-Fonseca 1995). The replication of Ad DNA produces single-stranded intermediates (ssDNA) that accumulate, forming viral inclusions in the nucleoplasm. These inclusions are readily identified using antibodies against the viral ssDNA-binding protein DBP. Following incorporation of a modified uridine-analog, it is possible to visualize by fluorescence microscopy the sites of RNA synthesis in the nucleus (Pombo et al. 1994). In noninfected cells, newly synthesized RNAs incorporating bromouridine are detected widespread throughout the nucleoplasm (Fig. 1A). In infected cells, nascent transcripts form ring-like structures (Fig. 1B) that surround the inclusions containing viral ssDNA (Fig. 1C). Previous work has indicated that these ring-like structures represent nascent viral mRNA transcripts (Pombo et al. 1994).

Consistent with previous evidence for cotranscriptional processing of pre-mRNA obtained in noninfected cells (Beyer and Osheim 1988; LeMaire and Thummel 1990; Wu et al. 1991; Xing et al. 1993; Bauren and Wieslander 1994; Zhang et al. 1994; Tennyson et al. 1995; Bauren et al. 1996; Huang and Spector 1996; Neugebauer and Roth 1997), in situ evidence suggests that splicing of Ad mRNAs occurs cotranscriptionally. Namely, spliceosome components including snRNPs and non-snRNP splicing proteins are recruited to the sites of viral mRNA synthesis (Pombo et al. 1994; Bridge et al. 1995; Gama-Carvalho et al. 1997,, 2003). Furthermore, spliced major late-viral mRNAs are detected in the ring-like structures formed by the nascent transcripts (Bridge et al. 1996; Gama-Carvalho et al. 2003, Fig. 1D–F).

Here we analyzed whether protein components of the EJC become concentrated at sites of Ad transcription. The results show that in noninfected cells, REF/Aly, Y14, SRm160, UAP56, RNPS1, and Magoh are localized throughout the nucleoplasm with higher concentration in nuclear speckles, and excluding nucleoli (Fig. 1G; data not shown), as previously described (Blencowe et al. 1998; Loyer et al. 1998; Gatfield et al. 2001; Le Hir et al. 2001a; Rodrigues et al. 2001). At 14–16 h post-infection, each of these proteins is predominantly concentrated in ring-like structures (Fig. 1H–L). Double-labeling experiments confirm that EJC proteins colocalize with spliced Ad mRNA and spliceosomal snRNPs at the ring-like structures formed by nascent viral transcripts (Fig. 2A–C). In contrast to REF/Aly, Y14, SRm160, UAP56, RNPS1, and Magoh, the protein DEK appears more homogeneously distributed throughout the nucleoplasm with less pronounced accumulation in either nuclear speckles in noninfected cells or ring-like structures in Ad-infected cells (Fig. 2D–F).

Unlike EJC components, the proteins NXF1/TAP, p15, and Dbp5 do not accumulate in nuclear speckles of noninfected cells, but rather, distribute homogeneously throughout the nucleoplasm with higher concentration at the nuclear rim (Schmitt et al. 1999; Bachi et al. 2000; Herold et al. 2000). Following treatment with TritonX-100 prior to fixation, the nucleoplasmic pool of NXF1/TAP, p15, and Dbp5 is largely solubilized and the proteins are predominantly detected at the nuclear rim (Fig. 3A–C). This localization reflects interactions with the nuclear pore complexes, as previously described (Schmitt et al. 1999; Bachi et al. 2000; Herold et al. 2000). At 14–16 h after adenoviral infection, NXF1/TAP, p15, and Dbp5 remain predominantly localized at the nuclear rim (Fig. 3D–F). Neither of these proteins is detected in the ring-like structures that concentrate spliceosomal snRNPs (Fig. 3G–I).

In summary, our results show that REF/Aly, Y14, SRm160, UAP56, RNPS1, and Magoh are all recruited to sites of adenoviral mRNA synthesis in the nucleus of infected HeLa cells. In contrast, NXF1/TAP, p15, and Dbp5 are not detected at sites of viral transcription.

Components of the EJC, but not NXF1/TAP or p15, are recruited to sites of β-globin transcription in the nucleus of MEL cells

Having shown that EJC components accumulate at sites of adenoviral transcription, we next sought to visualize recruitment of these proteins to nascent cellular transcripts. As a model system, we used murine erythroleukemia (MEL) cells stably transfected with the human β-globin gene. The clone used in this study (MELβWT) harbors ~14 copies of the transgene as a tandem array (Custódio et al. 1999). Detection of the human β-globin transcripts by FISH was performed with a probe complementary to the transcribed sequence of the gene (RNA probe, Fig. 4A, a). Expression of the human β-globin transgenes was induced by dimethylsulfoxide, which triggers terminal erythroid differentiation of the MEL cells (Antoniou 1991). In cells induced for 2 d, nascent β-globin transcripts are detected as a focus in the nucleus (Fig. 4A, b). After induction for 4 d, the cells contain a focus in the nucleus corresponding to nascent β-globin transcripts and additional cytoplasmic staining (Fig. 4A, c). To determine whether EJC proteins colocalize with nascent β-globin transcripts, MELβWT cells were induced to differentiate and sequentially hybridized with the RNA probe and immunolabeled with antibodies against SRm160 and REF (Fig. 4B, a and b). Alternatively, cells were transfected with plasmids encoding tagged versions of Y14 and UAP56 (Fig. 4B, c and d). The results indicate that each EJC protein colocalizes with the β-globin RNA focus in the nucleus. Quantification of the fluorescence intensity along a line that spans the nucleus across the RNA focus shows that the concentration of EJC proteins at the site of βglobin transcription is higher than in surrounding areas of the nucleoplasm (Fig 4B, a′–d′). Similar results were obtained for MEL cells labeled with antibodies against Sm proteins (Fig. 4C, a and a′) or U2snRNP B″ protein (Fig. 4C, b and b′).

Next, MELβWT cells expressing tagged NXF1/TAP or p15 were hybridized with the β-globin RNA probe (Fig. 4D, a and b). NXF1/TAP and p15 are both detected homogeneously distributed throughout the nucleoplasm with higher accumulation at the nuclear rim, reflecting interactions with the nuclear pore complexes. Quantification of the fluorescence intensity along a line across the RNA focus clearly shows that NXF1/TAP and p15 do not concentrate at the site of β-globin transcription (Fig. 4D, a′ and b′).

EJC proteins are not recruited by splicing-defective mutant β-globin transcripts

Current biochemical evidence indicates that EJC proteins are deposited onto mRNAs as a consequence of splicing (Le Hir et al. 2000a,b, 2001b; Kataoka et al. 2001; Kim et al. 2001). To study the role of splicing on recruitment of EJC proteins to sites of transcription in the nucleus, we have made use of MEL cells stably transfected with a human β-globin mutant gene that contains a normal first intron but is devoid of the second intron (termed βIVSI).

To analyze the processing of βIVSI pre-mRNAs in the nucleus of MEL cells, we performed RNase protection assays using nuclear RNA fractions from 4-day-induced cells and ³²P-labeled antisense RNA probes (Fig. 5A). The protection products were quantified by PhosphorImager, and the results show that for the wild type β-globin transcripts (βWT), the percentage of splicing of introns I and II is 65 and 68, respectively (Fig. 5B, lane 1). Thus, splicing of both introns has occurred in the majority of wild type β-globin transcripts (βWT) present in the nucleus. Consistent with the genomic deletion of the second intron in the βIVSI mutant, no intron II sequences are detected in the corresponding transcripts (Fig. 5B, lane 2). Unexpectedly, the first intron remains unspliced in all βIVSI transcripts (Fig. 5B, lane 2). Furthermore, and according to data reported previously (Collis et al. 1990; Antoniou et al. 1998), the efficiency of 3′-end cleavage is reduced from 93% in βWT RNA to 32% in βIVSI transcripts (Fig. 5B, lanes 3,4).

We have previously shown that βIVSI transcripts are not exported to the cytoplasm, being retained at the site of transcription (Custódio et al. 1999). We consider it unlikely that the reduced cleavage efficiency is the primary cause of nuclear retention, as another β-globin splicing mutant possessing a 5′-splice site mutation (GT→AC) in intron II, is correctly cleaved at normal rates, yet is also stalled at the site of transcription (Custódio et al. 1999). However, we cannot rule out the possibility that inefficient 3′-end processing contributes to retention of nascent β-globin RNA at the site of transcription.

Having determined that there is no splicing of βIVSI transcripts in the nucleus of MEL cells, we next performed double-labeling experiments using a probe to detect β-globin RNA and antibodies or GFP to detect SRm160, REF, UAP56, and Sm. The results clearly show no significant colocalization of the RNA and protein signals (Fig. 6a–d). Quantification of the fluorescence intensity along a line that spans the nucleus across the RNA focus confirms that there is no accumulation of EJC or Sm proteins at the site of transcription of the mutant β-globin gene (Fig. 6a′–d′). This suggests that, in the absence of efficient pre-mRNA processing, both spliceosomal components and EJC proteins fail to be properly assembled onto nascent β-globin transcripts in the nucleus.

DISCUSSION

In this work, we used a microscopy approach to study recruitment of the EJC to nascent transcripts in the nucleus of mammalian cells. We find that EJC proteins colocalize with protein components of the spliceosome at sites of transcription and splicing in the nucleoplasm, providing in vivo evidence that the EJC binds cotranscriptionally to mRNPs. We further report that mutant β-globin pre-mRNAs that are neither spliced nor released from the site of transcription fail to recruit spliceosome snRNPs and EJC proteins. This suggests that splicing of β-globin pre-mRNAs is required for efficient recruitment of the EJC and subsequent targeting of the resulting mRNP to the nuclear export pathway.

We show that the EJC proteins SRm160, RNPS1, Y14, Magoh, REF/Aly, and UAP56 accumulate in the nucleus at sites of abundant adenoviral and β-globin pre-mRNA synthesis. This is consistent with reports that the yeast homolog of REF/Aly, Yra1, associates with transcribed chromatin (Lei et al. 2001; Lei and Silver 2002a), and that both Yra1 and Sub2 (the yeast counterpart of UAP56) associate with the THO transcription complex (Strasser et al. 2002). A different result is observed for DEK, which appears more homogeneously distributed throughout the nucleoplasm, with no clear concentration at transcription sites. Remarkably, recent immunopurification analysis of nuclear mRNPs detected all EJC components except DEK (Lykke-Andersen et al. 2001; Lejeune et al. 2002). The failure to detect DEK using both microscopic and biochemical approaches suggests that either DEK associates loosely with the EJC or it is not part of this complex in vivo.

In contrast to EJC proteins, Dbp5, NXF1/TAP, and p15 fail to concentrate in the nucleus at sites of abundant pre-mRNA synthesis. Dbp5 was identified originally in yeast as a DEAD-box helicase implicated in mRNA export (for review, see Reed and Hurt 2002). Although early studies suggested that the function of metazoan Dbp5 is conserved, more recent analysis using RNA interference indicate that this protein is not essential for mRNA export in Drosophila (Gatfield et al. 2001). Like the yeast protein, human Dbp5 (hDbp5) shuttles between the nucleus and the cytoplasm, but at steady state, it is detected mainly in the cytoplasm (Schmitt et al. 1999). The Dbp5/hDbp5 protein appears enriched at the nuclear periphery, where it interacts with nucleoporins located at the cytoplasmic fibrils of nuclear pore complexes (Hodge et al. 1999; Schmitt et al. 1999; Strahm et al. 1999). Here, we observe that Dbp5 distribution is not altered upon infection of HeLa cells with adenovirus (Fig. 3C,F). No Dbp5 labeling was detected at sites of nascent viral pre-mRNAs, suggesting that in mammalian cells, this protein is recruited to mRNPs shortly before or after release from the sites of transcription. However, a recent report indicates that a Dbp5 homolog in the dipteran Chironomus tentans (Ct-Dbp5) binds to the Balbiani ring pre-mRNP cotranscriptionally and accompanies the mRNP to and through the nuclear pores (Zhao et al. 2002). An involvement of yeast Dbp5 during the early steps of transcription was also suggested on the basis of genetic and physical interactions with the transcriptional factor IIH (Estruch and Cole 2003). Due to the sensitivity limits of our assay, we cannot exclude that some Dbp5 molecules may associate with nascent transcripts.

The heterodimer formed by vertebrate NXF1/TAP and NXT1/p15 represents to date the most important receptor involved in export of mRNA from the nucleus to the cytoplasm (Izaurralde 2002; Lei and Silver 2002b; Reed and Hurt 2002; Cullen 2003; Stutz and Izaurralde 2003). Several EJC proteins, including REF/Aly, Y14, and Magoh can bind to NXF1/TAP, suggesting that these factors may act as adaptors that recruit the export receptor to mRNAs (Dreyfuss et al. 2002; Reed and Hurt 2002). However, our observation that NXF1/TAP and NXT1/p15 do not accumulate at sites of transcription suggests that binding of the EJC proteins to the mRNA is not sufficient to recruit the TAP-p15 heterodimer. This is consistent with the recent finding that REF/Aly and other components of the EJC are dispensable for export of bulk mRNA in Drosophila (Gatfield and Izaurralde 2002) and Caenorhabditis elegans (Longman et al. 2003; MacMorris et al. 2003), indicating that additional adaptor proteins mediate the interaction between NXF1/TAP and mRNAs in metazoan. SR proteins were recently identified as adaptors that, in addition to REF/Aly, can mediate the interaction between NXF1/TAP and cellular mRNAs (Huang et al. 2003).

Although REF/Aly can interact directly with NXF1/TAP (Strasser and Hurt 2000; Stutz et al. 2000), and NXF1/TAP coimmunopurifies with EJC proteins in nuclear mRNP fractions (Lejeune et al. 2002), there is no evidence that the TAP-p15 heterodimer is recruited to mRNAs cotranscriptionally. In fact, NXF1/TAP was reported to bind very weakly to purified spliced mRNPs in vitro (Zhou et al. 2000). Our observation that NXF1/TAP and p15 do not concentrate at the sites of pre-mRNA transcription, therefore, favors the view that this heterodimer is recruited efficiently at a later stage in the export pathway.

At present, it is well established that EJC proteins are deposited onto mRNAs as a consequence of splicing (Le Hir et al. 2000a,b,, 2001b; Kataoka et al. 2001; Kim and Dreyfus 2001). More recent studies described the timing of EJC assembly on spliced mRNA (Lejeune et al. 2002; Reichert et al. 2002). REF/Aly was shown to interact with pre-mRNA prior to spliceosome assembly, whereas Y14, Magoh, RNPS1, UAP56, and SRm160 are found in intermediate-containing spliceosomes (Reichert et al. 2002). Upon exon ligation, association of RNPS1, UAP56, and SRm160 are destabilized, whereas REF/Aly, Y14, and Magoh remain stably bound to the spliced exons (Reichert et al. 2002).

In a previous study, we have shown that transcripts encoded by a human β-globin mutant gene (βIVSI) that is devoid of the second intron fails to be released from the site of transcription (Custódio et al. 1999). Although pre-mRNAs encoded by this mutant contain a normal first intron, RNase protection assays show that splicing of this intron is almost completely inhibited in βIVSI transcripts (Fig. 5B). Thus, the βIVSI mutant gene generates pre-mRNAs that are not spliced. Notably, βIVSI transcripts conserve the normal sequence spanning the second and third exons, but this exon–exon junction is no longer the product of a splicing reaction. In clear contrast with the results observed in MEL cells expressing normal human β-globin transcripts, βIVSI pre-mRNAs do not colocalize with SRm160, REF, UAP56, or Sm proteins. This argues that the accumulation of EJC proteins at transcription sites requires efficient pre-mRNA processing. However, there is previous evidence indicating that REF/Aly can associate with the region 20–24 nucleotides upstream of exon–exon junctions independent of splicing (Reichert et al. 2002), that UAP56 binds to nascent transcripts independent of the localization of introns (Kiesler et al. 2002), and that both REF/Aly and UAP56 are part of the TREX (transcription/export) complex, which is thought to be recruited during transcription (Strasser et al. 2002). Possibly, in our microscopic assay we fail to visualize proteins that are loosely associated with the RNA and detect only stable complexes. According to this view, our results would argue that the initial binding of REF/Aly and UAP56 to nascent transcripts is not sufficient for stable EJC assembly.

In addition to being splicing deficient, βIVSI transcripts are not properly 3′-end cleaved. This is consistent with recent findings showing that splicing stimulates mRNA biogenesis by enhancing mRNA 3′-end processing (Lu and Cullen 2003; Nott et al. 2003). Because this effect appears to be mediated by the EJC (Wiegand et al. 2003), failure of βIVSI transcripts to recruit EJC proteins may contribute to their inefficient cleavage.

In conclusion, we find that EJC proteins colocalize with protein components of the spliceosome at sites of transcription and splicing in the nucleoplasm, providing in vivo evidence that the EJC binds cotranscriptionally to mRNPs. We further report that mutant β-globin pre-mRNAs that are neither correctly processed nor released from the site of transcription fail to concentrate spliceosome snRNPs and EJC proteins. This suggests that processing of β-globin pre-mRNAs is required for efficient recruitment of the EJC and also for subsequent targeting of the resulting mRNP to the nuclear export pathway.

MATERIALS AND METHODS

HeLa cell culture, transfections, and Adenovirus infection

HeLa cells from ECACC were cultured as monolayers in minimum essential medium (MEM, GIBCO-BRL) supplemented with 10% fetal calf serum (FCS, GIBCO-BRL) and nonessential amino acids (Invitrogen Corporation). Experiments were performed with cells grown on 10 × 10 mm glass coverslips. Transfections were performed on subconfluent cells using FuGENE 6 reagent (Roche Biochemicals), and cells were fixed for analysis 24 h after transfection. Infections with Adenovirus Type 2 (Ad2, strain wt900) were performed as described previously (Pombo et al. 1994). Briefly, cells were incubated with Ad2 for 2 h in serum-free medium, and then supplemented with 10% FCS. For simultaneous Ad2 infection and transfection, the transfection mixture was added to the cells immediately after the addition of the FCS. For in situ detection of sites of transcription, the cells were incubated for 1 h in culture medium supplemented with 2 mM BrU (Sigma-Aldrich), and fixed for analysis.

MEL cell culture and transfections

The maintenance and induction of erythroid differentiation of the MEL cell lines were described previously (Antoniou 1991; Custódio et al. 1999). Transient transfections were performed with either FuGENE 6 reagent (Roche Biochemical) or Tfx-50 reagent (Promega). The erythroid differentiation was induced 5–6 h after transfection by the addition of 2% (v/v) DMSO to the culture medium, and allowed to proceed for 48 h.

DNA clones for transient transfections

The plasmids used for expression in HeLa and MEL cells were kindly provided by Elisa Izaurralde (EMBL-Heidelberg). NXF1/TAP, RNPS1, UAP56, Magoh, and Dbp5 full-length cDNAs were cloned in pEGFP (Clontech). Y14 and p15 cDNAs were cloned in the pRN3zz vector. The zz tag was detected by indirect immunofluorescence with an antibody against protein A.

In situ hybridization

HeLa cells were grown on glass coverslips, and MEL cells were washed in serum-free medium and allowed to adhere onto poly-L-lysine (Sigma) coated glass coverslips. Cells were fixed and permeabilized according to one of the following alternative protocols: (1) permeabilized with 0.5% Triton X-100 in CSK buffer (Fey et al. 1986) containing 0.1 mM PMSF for 1 min on ice, and fixed with 3.7% paraformaldehyde in CSK buffer for 10 min at room temperature; (2) fixed in 3.7% paraformaldehyde in PBS for 10 min, and permeabilized with 0.5% Triton X-100 in PBS for 10 min at room temperature.

Spliced major late adenoviral mRNAs were visualized using a 5′-biotinylated DNA oligonucleotide probe, as previously described (Bridge et al. 1996). Oligonucleotides are particularly suited to identify spliced mRNA molecules, as probes complementary to exon–exon splice junctions form unstable hybrids with the unspliced primary transcripts. The probe (termed SJ1) has the following sequence: CAACCGCGAGCCCAACAGCTG. All in situ hybridization procedures were based on the protocols previously described (Bridge et al. 1996), and the hybrids were detected with Cy3 avidin (1/200, Jackson ImmunoReseach Labs, Inc).

To detect the human β-globin transcripts, MEL cells were hybridized as previously described (Custódio et al. 1999). The probe used consists of a plasmid containing the genomic sequence of the human β-globin gene labeled with either digoxigenin-11-dUTP (Roche) or Cy3-AP3-dUTP (Amersham Pharmacia) by nick translation. Digoxigenin detection was either with Fluorescein-conjugated sheep anti-digoxigenin (1/100, Roche), followed by AlexaFluor488-conjugated goat anti-Fluorescein (1/200, Molecular Probes), or Cy3 conjugated mouse anti-digoxin (1/250, Jackson ImmunoReseach Labs, Inc.). After the detection steps, cells were fixed with 1% formaldehyde in PBS for 10 min, washed with PBS, and processed for indirect immunofluorescence.

Immunofluorescence

The following primary antibodies were used for immunofluorescence. Rabbit polyclonals directed against (1) SRm160 (1/250, Blencowe et al. 1998); (2) DEK (1/300, Fornerod et al. 1995); (3) REF (1/100, Rodrigues et al. 2001); (4) protein A (1/2000, Sigma); (5) adenoviral protein DBP (Linné et al. 1977). Mouse monoclonals directed against (1) Sm antigen of SnRNPs (mAb Y12; Lerner et al. 1981); (2) U2 snRNP specific protein B″ (mAb 4G3; Habets et al. 1989). Bromo-uridine incorporation was detected with a sheep polyclonal antibody directed against BrdU (1/200, Abcam).

The secondary antibodies used were AlexaFluor488-conjugated goat anti-rabbit IgG (1/200), TRITC-conjugated donkey anti-rabbit IgG (1/100, Jackson ImmunoResearch Labs, Inc.), AlexaFluo488-conjugated goat anti-mouse IgG (1/200, Jackson), Cy3-conjugated goat anti-mouse IgG (1/300, Jackson), FITC-conjugated goat anti-human IgG (1/100, Jackson), Cy5-conjugated rabbit anti-human IgG (1/100, Jackson), and FITC-conjugated donkey anti-sheep IgG (1/100, Jackson).

Microscopy

Images were acquired on a Zeiss LSM 510 confocal microscope using the PlanApochromat 63×/1.4 objective. FITC and AlexaFluor488 fluorescence was detected using the 488-nm line of the argon ion laser. The 543-nm line of the helium-neon laser was used to excite Cy3 and TRITC and the 633-nm line to excite Cy5.

RNase protection assay

Nuclear and cytoplasmic fractionation of MEL cells was as previously described (Antoniou et al. 1998). The nuclei were lysed with 4 M guanidinium thiocyanate, 25 mM tri-sodium citrate, 0.5% (w/v) N-lauryl sarcosine, 0.1 mM dithiothreitol (Huang and Carmichael 1996), and the homogenate sonicated (30 pulses using a small-diameter probe) to shear the DNA. The RNA was purified by phenol:chloroform (2.8:1) extraction, isopropanol and ethanol precipitations, and DNase digestion (RNase free, Roche). Human β-globin RNase protection probes (McCracken et al. 1997) were prepared by in vitro transcription with T7 RNA polymerase in the presence of [α-³²P]UTP, and gel-purified prior to use. RNase protection assays were performed as previously described (McCracken et al. 2002). Briefly, 3 μg of nuclear RNA were incubated with the antisense RNA probe overnight at 50°C, and the hybridization products were digested with a mixture of RNase T1 (5 μg/mL) and RNase A (0.5 μg/mL) at 37°C for 1 h. The protected fragments were resolved on a 6% denaturing polyacrylamide gel, and the intensity of the bands quantified using a BioRad PhosphorImager. Following quantification of each gel band, background was subtracted and the values normalized for U content of the protected probe fragment.