INTRODUCTION

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The carboxy-terminal domain (CTD) of the largest subunit of RNA polymerase II (pol II) consists of multiple repeats of the heptapeptide sequence YSPTSPS (2, 24). The CTD is found in pol II from a variety of species but is not present on pol I or pol III, indicating a role in mRNA biogenesis (22, 23). Deletion studies have demonstrated that the CTD is essential for cell viability in yeast, Drosophila, and mammalian cells (3, 4, 55, 75). While roles in transcription activation, enhancer function, and pre-mRNA processing have been proposed, the essential role of the CTD remains elusive.

The CTD contains an uncommonly high density of potential phosphorylation sites (26, 27). Both hyper- and hypophosphorylated pol II can be detected in vivo, but the distribution of phosphates among the more than 100 potential sites has not been determined. Substitution of alanine for serines in either position 2 or 5 of each repeat is lethal in yeast, suggesting that phosphorylation of both of these sites is essential (70).

In vitro transcription experiments have led to the hypothesis that the CTD is reversibly phosphorylated with each transcription cycle (26, 27). One role of phosphorylation may be to disrupt contacts between the unphosphorylated CTD and components of the holoenzyme. In addition, phosphorylation may prepare the CTD for a role subsequent to initiation. Indeed, transcription elongation is CTD dependent (1, 44) and is temporally linked to CTD phosphorylation (1, 31, 44, 56, 69).

Yeast two-hybrid screens have led to the identification of a family of CTD-binding proteins containing serine/arginine-rich motifs (17, 64, 74). The SCAFs (SR-like CTD-associated factors) contain conserved N-terminal or C-terminal CTD-interacting domains (25). We have previously shown that the C-terminal CTD-interacting domain of SCAF1 (formerly rA1 [74]) binds either highly or partially phosphorylated pol II.

In this paper, we demonstrate that SCAF8 (formerly rA8 [74]) interacts specifically with a highly phosphorylated form of the CTD. We also show that a protein recognized by an antibody directed against the CTD-binding domain of SCAF8 coimmunoprecipitates with pol II0. Consistent with these biochemical findings, a fraction of SCAF8 colocalizes with sites of active transcription and partially colocalizes with phosphorylated pol II in nuclei of whole cells as well as in cells extracted for nuclear matrix. Finally, we show that SCAF8 is enriched in a nuclear matrix fraction known to contain proteins involved in pre-mRNA processing (13, 54).

	MATERIALS AND METHODS

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Plasmids and strains. Plasmids for expression of glutathione S-transferase (GST) consensus CTDs and serine-substituted CTDs are derived from a set of hemagglutinin-tagged yeast CTD mutants constructed earlier (70) and are described in detail elsewhere (57). The CTD-interacting domains of SCAF8 (residues 2 to 200) and SCAF4 (residues 2 to 200) were expressed as a histidine-tagged proteins with the pTrcHis(B) expression vector (Invitrogen).

Purification of SCAF8 CTD-interacting domain. His-tagged SCAF8 and SCAF4 CTD-interacting domain (CID) fusion proteins were purified by metal affinity chromatography with Ni²⁺-agarose (Pharmacia) or Co²⁺-agarose (Clontech). Escherichia coli BL21 expressing His-tagged fusion protein was grown to an optical density at 600 nm of 0.8, induced by addition of isopropyl--D-thiogalactopyranoside (IPTG) to 0.1 mM, and grown for an additional 4 h. Cells were harvested by centrifugation, resuspended in 200 ml of buffer A (50 mM Tris-HCl [pH 8], 150 mM NaCl, 2 µM pepstatin A, 0.6 µM leupeptin, 2 mM benzamidine HCl, and 1 mM phenylmethylsulfonyl fluoride [PMSF]). After addition of Triton X-100 to 0.1%, the cells were lysed by freezing overnight at 20°C and thawing at room temperature. Thawed lysate was sonicated for 10 min and centrifuged at 4°C for 1 h at 12,000 × g. The supernatant was incubated with Ni²⁺-agarose or Co²⁺-agarose for 1 h at 4°C with shaking. Beads were collected by centrifugation at 1,500 × g for 10 min and washed with two column volumes of buffer A containing 10 mM imidazole, resuspended in the same buffer, packed onto a column, and washed with 10 column volumes of buffer A containing 10 mM imidazole. Bound protein was eluted with two column volumes of buffer A containing 100 mM imidazole. The affinity-purified SCAF8 fusion protein was greater than 90% pure as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE [10% polyacrylamide]) (Fig. 1A).

View larger version (57K): [in this window] [in a new window]   FIG. 1.   Fusion proteins used in binding studies. (A) Coomassie blue staining of recombinant SCAF8 CID. Five micrograms of purified SCAF8 CID was run on SDS-PAGE (10% polyacrylamide) and stained with Coomassie blue. Lane 1, marker proteins; lane 2, SCAF8 CID. (B) Coomassie blue staining of GST-CTD fusion proteins. Five micrograms of the affinity-purified proteins was run on SDS-PAGE (10% polyacrylamide) and stained with Coomassie blue. Lane 1, wild-type CTD (16 repeats); lane 2, A5 mutant CTD (15 repeats); lane 3, A2 mutant CTD (14 repeats).

Purification and phosphorylation of CTD fusion proteins. E. coli (DH5) strains expressing GST-CTD fusion proteins were grown overnight to saturation. Cultures were diluted 10-fold in fresh L-broth containing 100 µg of ampicillin per ml and grown for 1 h before addition of IPTG to 0.1 mM. After 4 h of induced expression, cells were collected by centrifugation and sonicated, and the fusion protein was purified by glutathione-agarose (Pharmacia) affinity chromatography as described previously (57). Purified GST fusions containing 16 copies of the wild-type heptapeptide YSPTSPS, 15 copies of YSPTAPS (A5), or 14 copies of YAPTSPS (A2) (mutated residues are underlined) were separated by SDS-PAGE (10% polyacrylamide) and stained with Coomassie blue dye (Fig. 1B).

CTD binding assay. About 2 µg of the GST fusion protein or human pol II was applied to a 15-µl Ni-agarose column containing 8 µg of bound SCAF8-CID. The column was washed with six sequential 50-µl aliquots of binding buffer (100 mM NaCl, 10 mM Tris-HCl [pH 7.9], 10 mM imidazole, 0.1% Nonidet P-40, 2 µM pepstatin A, 0.6 µM leupeptin, 2 mM benzamidine HCl, and 1 mM PMSF), and bound protein was eluted with sequential 50-µl aliquots of SDS-PAGE sample buffer. All samples were separated by SDS-PAGE (10% polyacrylamide) and subjected to Western blotting. The blots were probed with MAb 12CA5, which recognizes both phosphorylated and unphosphorylated GST-CTD fusion proteins, or with antiphosphotyrosine antibody to detect c-Abl-phosphorylated CTD. Gels containing ³²P-labeled proteins were directly subjected to autoradiography.

MAbs. MAb 8WG16 is an anti-CTD immunoglobulin G (IgG) described by Thompson et al (65). MAb H14 is an IgM directed against phosphoepitopes on the CTD (18, 19) and was a gift of Steve Warren (Nexstar Pharmaceuticals, Boulder, Colo.), while MAb B3 (49) is a mouse IgM that recognizes a partially overlapping set of CTD phosphoepitopes on the hyperphosphorylated CTD (57). MAb 230.F1E1 (F1E1) is an IgG raised in mice against the His-tagged SCAF8 CID with the help of Dennis Wilson (Johns Hopkins).

Immunoprecipitation of SCAF8 complexes. Tissue culture supernatant containing MAb F1E1 (about 25 µg) was allowed to bind protein A/G agarose beads (50 µl; Pierce) overnight and washed three times with 500 µl of IP100 buffer (100 mM NaCl, 50 mM Tris-HCl [pH 7.6], 0.05% Nonidet P-40, 0.5 mM dithiothreitol, 5 mM MgCl₂, 5 mM NaF, 5 mM -glycerol phosphate). Beads (20 µl, containing approximately 10 µg of antibody) were incubated with 25 µl of HeLa cell nuclear extract for 1 h at 4°C with shaking. The beads were washed four times with 500 µl of IP100 buffer, and bound proteins were eluted with 50 µl of 2× SDS-PAGE loading buffer, and subjected to SDS-PAGE followed by Western blot analysis (57).

Immunostaining and laser scanning confocal microscopy. Mouse 3T3 fibroblasts were grown on coverslips for 48 h. Cells were then fixed in 3% paraformaldehyde on ice for 2 min, permeabilized with 0.5% Triton X-100 in TBS buffer (10 mM Tris-HCl [pH 7.4], 150 mM NaCl, 5 mM MgCl₂) for 1 min on ice, blocked with 5% goat serum, and then incubated consecutively with MAbs B3 and F1E1 at room temperature for 1 h. Cells were then treated with biotin-conjugated goat anti-mouse IgG Fc fragments (Jackson ImmunoResearch Laboratories, Inc.) at 1:50 dilution at room temperature for 30 min, washed three times with TBS-Tween buffer, and incubated with a mixture of fluorescein isothiocyanate (FITC)-conjugated goat anti mouse IgM (µ chain specific, Sigma) at 1:50 and Texas red-conjugated streptavidin (GIBCO) at 1:50 at room temperature for 30 min. After a final wash with TBS-Tween buffer, coverslips were mounted on slides, and images from 0.5-µm optical sections were collected with a Bio-Rad MRC-1024 confocal microscope. A krypton argon laser was used to excite FITC and Texas red simultaneously at 488 and 568 nm, respectively. The emitted light was collected with filter 522-DF32 for FITC and filter HQ598-40 for Texas red.

Isolation of nuclear matrix. Rat liver nuclei and nuclear matrix were isolated based on the procedures of Berezney and Coffey (11) and Basler et al. (6). Briefly, rat livers were excised and homogenized with a Potter-Elvehjem apparatus and centrifuged to isolate the nuclei. To obtain the rat liver nuclear matrix, the rat liver nuclei were digested with DNase I (5 U/mg of DNA), extracted with 2 M NaCl three times, and then further extracted with 0.4% Triton X-100. The final rat liver nuclear matrix pellet was resuspended in 10 mM Tris (pH 7.4)-0.2 mM MgCl₂-50% glycerol and stored in liquid nitrogen.

Double labeling of transcription sites and SCAF8 in permeabilized cells. Labeling of RNA synthesis sites was done according to published methods (41, 50, 68) with modifications. Briefly, Swiss 3T3 mouse fibroblast cells were grown on a coverslip in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum in 5% CO₂ for 24 to 48 h. Cells were then washed with ice-cold TBS buffer (10 mM Tris-HCl [pH 7.4], 150 mM NaCl, 5 mM MgCl₂) and further washed with glycerol buffer (20 mM Tris-HCl [pH 7.4], 25% glycerol, 5 mM MgCl₂, 0.5 mM EGTA, 0.5 mM PMSF) for 10 min on ice. Washed cells were permeabilized with 0.025% Triton X-100 in glycerol buffer with 25 U of RNasin (Promega) per ml on ice for 3 min and immediately incubated with RNA synthesis buffer (50 mM Tris-HCl [pH 7.4]; 10 mM MgCl₂; 150 mM NaCl; 25% glycerol; 0.5 mM PMSF; 25 U of RNasin per ml; 1.8 mM ATP; 0.5 mM CTP, GTP, and bromo-UTP; and 25 U of RNasin per ml) to label transcription sites. After incubation for 30 min at room temperature, the cells were washed twice with ice-cold 0.5% Triton X-100 in TBS buffer and immediately fixed in 100% methanol at 20°C for 20 min and further fixed with 3% freshly made formaldehyde in PBS on ice for 5 min. Fixed cells were washed twice with ice cold TBS-Tween buffer (10 mM Tris-HCl [pH 7.4], 150 mM NaCl, 0.2 mM MgCl₂, 0.2% Tween 20), and blocked with 5% goat serum on ice for 5 min before incubation with primary antibodies at room temperature for 1 h. For labeling RNA sites, Sera-Lab rat anti-bromodeoxyuridine (BrdU) MAb was used at a 1:5 dilution. Tissue culture supernatant containing MAb F1E1 was used to detect SCAF8. After incubation with the primary antibody, cells were washed three times and incubated with FITC-conjugated goat anti-rat IgG (Jackson ImmunoResearch Laboratories, Inc.) at a 1:50 dilution for 40 min at room temperature to visualize transcription sites. MAb F1E1 was detected as described in the previous section. After a final wash with TBS-Tween buffer, coverslips were mount on slides in Slow Fade (Molecular Probe) and examined under a laser scanning confocal microscope as described above.

	RESULTS

Top Abstract Introduction Materials & Methods Results Discussion References

SCAF8 interacts with serine-phosphorylated CTD. In previous work, we showed that the SCAF1 (rA1) CID binds hypophosphorylated RNA pol IIA and the hyperphosphorylated II0 form (74). Whether phosphorylation is necessary for this interaction could not be determined from these experiments, because both forms of pol II contained phosphorylated CTD residues. Here we show that phosphorylation of the CTD is required for the CTD-SCAF8 interaction. When a mixture of phosphorylated and unphosphorylated wild-type CTD fusion proteins is passed over a column containing the SCAF8 CID, most of the unphosphorylated CTD flowed through (Fig. 2A, lanes FT and W1 to W6). Bound phosphorylated GST-CTD fusion protein was eluted with SDS-PAGE sample buffer (lanes E1, E2, and E3). The SCAF8-CTD interaction is resistant to treatment with DNase or RNase, ruling out a nucleic acid "bridge" and suggesting a direct interaction between SCAF8 and the CTD (Fig. 2B). Figure 2B also shows that the SCAF8-CTD interaction is sensitive to 0.1% Sarkosyl and 1 M NaCl. The SCAF8 CID does not interact with tyrosine-phosphorylated CTD (Fig. 2C), indicating that the interaction does not reflect a general affinity for phosphorylated proteins.

View larger version (35K): [in this window] [in a new window]   FIG. 2.   SCAF8 CTD binding assays. (A) SCAF8 interacts with phosphorylated CTD fusion proteins. The binding assay for SCAF8 CID and the different CTD fusion proteins is described in Materials and Methods. All column fractions were separated by SDS-PAGE (10% polyacrylamide) and then subjected to Western blot analysis. Proteins were detected with monoclonal antibody 12CA5, which detects both phosphorylated and unphosphorylated CTD fusion proteins (indicated at left). The phosphorylated fusion protein can be distinguished by its retarded mobility. The column matrix is indicated to the right. Lane L, protein load; lane FT, flowthrough; lanes W1 to W6, column washes; lanes E1 to E3, SDS sample buffer eluates. (B) Binding controls. A binding assay similar to that described for panel A was performed in the presence of additional components indicated above the figure. In this experiment, the wild-type CTD fusion protein was phosphorylated with Cdc2 kinase in the presence of [-32P]ATP, and the bound fractions eluted with SDS sample buffer were pooled. (C) SCAF8 does not bind tyrosine-phosphorylated CTD (P-tyr CTD). A binding assay similar to that described for panel A was performed with tyrosine-phosphorylated CTD (Materials and Methods). Lanes are as indicated for panel A. (D) SCAF8 does not bind mutant CTDs. A binding reaction similar to that for panel A was performed with a mixture of phosphorylated A5 and A2 mutant CTD fusion proteins. The identity of the fusion protein (indicated at left) was determined by running them individually. Lanes are as described for panel A.

SCAF8 does not interact with serine-phosphorylated mutant CTDs. Our earlier studies indicated that serine-to-alanine substitutions in either position 2 or 5 of each consensus repeat is lethal in yeast (70). We have used the same mutant CTDs to study the specificity of the SCAF8-CTD interaction. Cdc2 kinase, which phosphorylates both positions 2 and 5 in the wild-type CTD (80), was used to phosphorylate mutant CTDs containing serine-to-alanine substitutions in serine 2 or 5 of each repeat. The resulting phosphorylated fusion proteins contain phosphates only in position 5 or 2, respectively. When a mixture of the phosphorylated mutant fusion proteins is passed over a SCAF8 CID column, we observe that most of the protein fails to bind (Fig. 2D), suggesting that SCAF8 interacts with CTD phosphorylated on serine residues in both positions 2 and 5.

SCAF8 interacts with phosphorylated pol II. The results described so far demonstrate that SCAF8 interacts with in vitro-phosphorylated CTD. To extend our observation to full-length pol II, we passed semipurified pol II derived from HeLa cells over a SCAF8 CID-Ni²⁺-agarose column and monitored the fate of the unphosphorylated (IIA) and phosphorylated (II0) forms by Western blotting. As shown in Fig. 3A, most protein flows through the column. The flowthrough contains essentially all of the pol IIA, while most of the pol II0 remains bound to the column (Fig. 3B), thus suggesting that SCAF8 interacts specifically with pol II containing the phosphorylated CTD.

View larger version (77K): [in this window] [in a new window]   FIG. 3.   SCAF8 interacts with phosphorylated pol II. The binding experiment using partially purified pol II is described in Materials and Methods. Proteins were separated by SDS-PAGE (5% polyacrylamide) and then subjected to either silver staining (A) or Western blotting (B). Lane L, column load; lane FT, column flowthrough; lanes W1 to W6, column washes; lanes E1 and E2, SDS sample buffer eluates.

SCAF8 binds phosphorylated pol II in vivo. To determine if SCAF8 interacts with pol II in vivo, we performed immunoprecipitation experiments with a MAb directed against the SCAF8-CID. MAb F1E1 was raised against a fusion protein containing the first 200 amino acids of SCAF8. Because the CIDs of SCAF4 and SCAF8 are similar (Fig. 4A), it was important to determine whether F1E1 cross-reacts with SCAF4. Figure 4B shows that F1E1 reacts with a SCAF8 CID fusion protein but not with a similar SCAF4 fusion protein. F1E1 recognizes a protein of around 170 kDa in Hela nuclear extract (Fig. 4C) and in total rat liver nuclear proteins (see Fig. 6B). A similar-sized protein is observed in insect cells infected with a baculovirus expressing SCAF8 but not in control cells (not shown). While the apparent molecular mass is slightly larger than the 140 kDa predicted from the cDNA sequence (74), we note that the protein is rich in proline residues (10%) and therefore may display aberrant mobility in SDS gel electrophoresis. In addition, phosphorylation of the SCAF8 Arg-Ser repeats may retard mobility in SDS gel electrophoresis.

View larger version (62K): [in this window] [in a new window]   FIG. 4.   SCAF8 interacts with phosphorylated pol II in vivo. (A) Alignment of SCAF8 and SCAF4 CTD interacting domains. These sequences were expressed as 6His-tagged fusion proteins as described in Materials and Methods. (B) MAb F1E1 detects the SCAF8 but not the SCAF4 CID. Partially purified 6His-tagged SCAF CID fusion proteins were separated by SDS gel electrophoresis and immunoblotted with anti-His tag antibody (BABCO) or with MAb F1E1. (C) Western blot analysis of HeLa nuclear extract (NE). SCAF8 was detected with MAb F1E1. (D) Immunoprecipitation of SCAF8 complexes. Immunoprecipitation of the SCAF8 complexes was carried out as described in Materials and Methods. The same blot was probed with MAb H14 (left panel) or with 8WG16 (right panel). The immunoprecipitating antibody is indicated above the lane, while the blotting antibody is indicated below the panel. Markers are indicated to both sides and between the blots. The right lane in the right panel contains nuclear extract to indicate the position of the unphosphorylated RNA pol II largest subunit (IIA).

SCAF8 colocalizes with transcription sites. Recent studies have shown that pol II transcription is distributed among several thousand nuclear sites which are revealed as small "dots" when cells pulse-labeled with BrUTP are stained with anti-BrdU antibody (36, 39, 41, 52, 68, 78). To determine whether SCAF8 localizes to these sites of transcription we labeled both transcription sites and SCAF8 in the same nuclei. Figure 5 shows that both transcription sites and SCAF8 are localized to numerous punctate extranucleolar staining regions. The merged images indicate a significant level of overlap at the light microscopy level of resolution. The expanded regions in the lower panels indicate that most, but not all, punctate extranucleolar staining regions overlap. Colocalization of SCAF8 with transcription sites is also detected over the nucleolar regions (left side of Fig. 5F). The SCAF8 decoration of nucleolar transcription sites is very weak, however, making the significance of this observation unclear.

View larger version (100K): [in this window] [in a new window]   FIG. 5.   SCAF8 is associated with transcription sites. Mouse Swiss 3T3 cells were permeabilized and incubated with BrUTP to label transcription sites in situ (Materials and Methods). Transcription sites were detected with rat anti-BrUTP antibody (Sera-Lab) and visualized with green (A). SCAF8 was detected with MAb F1E1 and then visualized with red (B), and the merged images are displayed in panel C. The boxed area, including both extranucleolar and nucleolar regions, is further enlarged and displayed in panels D (transcription sites), E (SCAF8), and F (merged images). The line through F indicates the boundary between the nucleolus (left) and the nucleus (right).

Association of SCAF8 with the nuclear matrix. Previous studies have shown that hyperphosphorylated pol II is associated with the nuclear matrix (49). Since purified SCAF8 binds to the phosphorylated CTD, it was of further interest to determine whether SCAF8 is also a nuclear matrix-associated protein. As a first step, we ran Western blots of total rat liver nuclei and nuclear matrix proteins prepared by classical procedures (6, 11) and probed with the F1E1 antibody. Figure 6A shows the total protein profiles stained with Coomassie blue. Approximately 25% of the total nuclear protein was recovered in the isolated nuclear matrix fraction, which was devoid of histones and enriched in higher-molecular-mass nuclear proteins. Immunoblot analysis of the total rat liver nuclear and nuclear matrix protein fractions revealed a single band with an apparent molecular mass of 170 kDa (Fig. 6B). The four- to fivefold enrichment of SCAF8 in the rat liver nuclear matrix versus the total nuclear fraction indicates a nearly quantitative association of SCAF8 with the nuclear matrix.

View larger version (36K): [in this window] [in a new window]   FIG. 6.   SCAF8 fractionates with nuclear matrix proteins. (A) Coomassie blue staining of rat liver nuclear (N) and nuclear matrix (M) proteins. Ten micrograms of protein from each sample was run on SDS-PAGE (12.5% polyacrylamide). The molecular mass markers (in kilodaltons) are displayed on the left side. (B) Western blot of rat liver nuclear and nuclear matrix proteins with FIEI antibody. (C) The distribution of the SCAF8 protein, RNA pol II0, and lamin B in the HeLa cytoplasmic fraction (C), purified nuclear fraction (N), nuclear matrix fraction (M), and salt-extracted nuclear proteins (S) was determined by Western blot analysis.

Spatial relationships between SCAF8 and pol II0. The distribution of SCAF8 with respect to a particular pol II phosphoisoform was studied by fluorescence laser scanning confocal microscopy. Consistent with the results shown in Fig. 5 and the immunoblot studies, the SCAF8 protein was detected exclusively in the interphase cell nucleus of BALB/c 3T3 mouse fibroblast cells, with no detectable signal in the cytoplasm (Fig. 7). Numerous granule-like foci were present in the extranucleolar regions of the nucleus, with far fewer distributed over the nucleoli. Extraction of the coverslip-grown cells preserving nuclear matrix (50) resulted in a strikingly similar pattern of decoration and staining intensity. This is consistent with the immunoblotting experiments, which indicated a nearly quantitative association of the SCAF8 protein with the isolated nuclear matrix, and further suggests that certain key features of the structural organization of SCAF8 observed in whole cells are also maintained in the cells extracted for nuclear matrix.

View larger version (120K): [in this window] [in a new window]   FIG. 7.   Double labeling of 3T3 cells and in situ-prepared nuclear matrix with B3 and FIEI antibodies. The hyperphosphorylated RNA pol II large subunit was recognized with the B3 antibody (green). SCAF8 antigen was recognized with the FIEI antibody (red). The merged image is displayed on the right. Five speckle regions indicated by the B3 staining were magnified and displayed underneath the whole images. The single red and green channel images for the magnified areas of the nucleus in the whole cell are also displayed above the merged magnified regional images. The 0.5-µm optical sections are displayed.

	DISCUSSION

Top Abstract Introduction Materials & Methods Results Discussion References

Recent studies have shown that the pol II CTD plays a role in coupling transcription and pre-mRNA processing (reviewed in references 25, 53 and 63), but the molecular details of the interface between the transcription and processing machinery have not been established. In this paper, we demonstrate that a recently discovered CTD-binding protein, SCAF8, interacts specifically with a phosphorylated form of pol II. We further show that SCAF8 colocalizes with sites of active transcription. These transcription sites are enriched in nuclear matrix preparations that have previously been shown to contain components of the processing machinery (reviewed in references 12, 13, and 54). The ability of SCAF8 to interact with both transcription and processing structures indicates that it could play a direct role in coupling these two processes.

The CTD is involved in pre-mRNA processing. Although in vitro transcription and pre-mRNA processing can occur in isolation, in vivo these processes occur in close proximity. Electron micrographs of active transcription units first demonstrated that intron removal can occur on elongating transcripts (14). Subsequent studies have supported a model in which nascent transcripts are cotranscriptionally processed (7, 8, 43, 79).

Pre-mRNA processing and the CTD phosphorylation cycle. The CTD is rich in potential phosphorylation sites and is reversibly phosphorylated during the transcription cycle in vivo, thus giving rise to at least two distinct forms of pol II (27). Pol IIA has an unphosphorylated or hypophosphorylated CTD and is involved in the formation of preinitiation complexes (27). CTD phosphorylation in the context of the preinitiation complex converts pol IIA to pol II0, coinciding with the elongation phase of the transcription cycle. The involvement of pol II0 in transcription elongation suggests that processing components will interact with the phosphorylated CTD. Indeed, capping activities have been shown to interact with the phosphorylated CTD (21, 46, 58, 73). Cleavage and polyadenylation factors also bind to the CTD, but here the role of phosphorylation is not clear (47). Loading the 3'-end-forming factors onto the transcription complex also requires the general transcription factor TFIID (28). Splicing small nuclear ribonucleoprotein particles (snRNPs) and members of the SR family of non-snRNP pre-mRNA splicing factors associate with hyperphosphorylated forms of pol II (20, 42, 49, 66), but in most of these cases, it is not known whether these splicing components interact directly with the CTD.

SCAF8 binds to the phosphorylated CTD. Yeast two-hybrid interaction screening has led to the identification of proteins that interact with the pol II CTD (17, 64, 74). These proteins resemble the SR proteins previously implicated in splicing (33) and have been designated SCAFs.

Subnuclear localization of transcription and pre-mRNA processing. Antibodies directed against splicing components stain mammalian nuclei in a nonuniform manner, suggesting the presence of subnuclear structures associated with pre-mRNA processing (62). Typical mammalian cells contain 20 to 50 such "speckles," which were first detected with an antibody directed against the splicing factor SC35 (34). The size and number of these structures can vary according to the staining conditions (52), with more dilute staining leading to smaller, more abundant speckles. The method of signal processing (32, 59) can also influence the perception of speckles. Careful quantification of SC35 distribution in the nucleus indicates that the local concentration varies by as little as twofold. Together, these factors make structural characterization of speckles difficult. The localization of green fluorescent protein-tagged proteins to speckle-like structures supports the nonuniform distribution of splicing factors in vivo (48).

SCAF8 and pol II0 are nuclear matrix proteins. The nuclear structure remaining after removal of soluble nuclear proteins and chromatin has been termed the nuclear matrix (10-13, 54). The nuclear matrix contains the majority of the heterogeneous nuclear RNA (38), and pulse-labeled transcripts also associate with the nuclear matrix (40), indicating that this structure contains transcription components. Nascent, unprocessed pre-mRNAs are apparently held in a functional state, because addition of soluble nuclear factors to matrix preparations leads to rapid processing of bound mRNA precursors (76, 77). In addition to RNA, the nuclear matrix contains proteins, including spliceosome components (67), a novel set of high-molecular-mass SR-like proteins (15, 16), phosphorylated pol II0 (20, 49, 66), and, as we show here, SCAF8.

Summary. The results presented here support two main conclusions. First, SCAF8 interacts directly with a highly phosphorylated form of pol II. This observation indicates that SCAF8 is not involved in transcription initiation but rather associates with pol II during elongation. The colocalization of SCAF8 with sites of active transcription supports this conclusion. Second, SCAF8 is present in the nuclear matrix. The second conclusion is consistent with the presence of large nuclear structures containing both transcription and pre-mRNA processing components. The role of SCAF8 could be to bind newly initiated pol II and recruit processing factors to the elongation complex. In this case, SCAF8 (and possibly other SCAFs) would act as coupling factors, responding to CTD phosphorylation by linking transcription elongation complexes to an appropriate processing machine. The details of this mechanism and its potential regulatory function await further investigation.