Mammalian splicing factor SF1 interacts with SURP domains of U2 snRNP-associated proteins

Splicing factor 1 (SF1) recognizes the branch point sequence (BPS) at the 3′ splice site during the formation of early complex E, thereby pre-bulging the BPS adenosine, thought to facilitate subsequent base-pairing of the U2 snRNA with the BPS. The 65-kDa subunit of U2 snRNP auxiliary factor (U2AF65) interacts with SF1 and was shown to recruit the U2 snRNP to the spliceosome. Co-immunoprecipitation experiments of SF1-interacting proteins from HeLa cell extracts shown here are consistent with the presence of SF1 in early splicing complexes. Surprisingly almost all U2 snRNP proteins were found associated with SF1. Yeast two-hybrid screens identified two SURP domain-containing U2 snRNP proteins as partners of SF1. A short, evolutionarily conserved region of SF1 interacts with the SURP domains, stressing their role in protein–protein interactions. A reduction of A complex formation in SF1-depleted extracts could be rescued with recombinant SF1 containing the SURP-interaction domain, but only partial rescue was observed with SF1 lacking this sequence. Thus, SF1 can initially recruit the U2 snRNP to the spliceosome during E complex formation, whereas U2AF65 may stabilize the association of the U2 snRNP with the spliceosome at later times. In addition, these findings may have implications for alternative splicing decisions.


INTRODUCTION
Pre-mRNA splicing is essential for eukaryotic gene expression and one of the most versatile mechanisms to increase proteome diversity through alternative splice site choices (1).The reaction is catalyzed by the spliceosome, a multimegadalton complex (2).Five small nuclear ribonucleopro-tein particles (U1, U2, U4, U5 and U6 snRNPs) and more than 100 non-snRNP proteins assemble in a step-wise fashion on the pre-mRNA through networks of RNA-RNA, RNA-protein and protein-protein interactions to form the catalytic center of the spliceosome for intron removal.
Essential sequence elements at the 5 and 3 splice sites are recognized at the onset of spliceosome assembly (2).U1 snRNP binds to the 5 splice site, whereas SF1 and the U2 snRNP auxiliary factor (U2AF) recognize distinct sequences at the 3 splice site.SF1 and the large subunit of U2AF (U2AF65) interact with one another and cooperatively bind the branch point sequence (BPS) and the adjacent polypyrimidine tract, respectively (3)(4)(5)(6)(7)(8).The small U2AF subunit (U2AF35) recognizes the 3 splice site AG dinucleotide (9).Together these interactions assemble the early complex E, which is converted into pre-splicing complex A by incorporation of the U2 snRNP.This is accomplished through interaction of the U2 snRNP-associated SF3b155 with U2AF65 (10), binding of U2 snRNP proteins to and adjacent to the BPS (11)(12)(13) and base pairing of the U2 snRNA with the BPS.These events are thought to displace SF1 from the spliceosome (14).In addition, displacement of the Saccharomyces cerevisiae ortholog of SF1, termed branch point-binding protein (BBP; also known as MSL5 or YLR116W) is thought to require the DExD-box helicase Sub2p (15)(16)(17).The following steps of spliceosome assembly involve binding of the remaining snRNPs and additional non-snRNP proteins, juxtaposition of the splice sites and dynamic remodeling of the complexes leading to the formation of the catalytic center, followed by intron removal in two catalytic steps (2).
SF1 was initially identified as a protein required for prespliceosome assembly (18,19).It is evolutionarily conserved and yeast BBP was shown to function in the formation of the early commitment complex CC2, which together with CC1 is the equivalent of the human E complex (14).SF1 is essential in S. cerevisiae, Caenorhabditis elegans and mammalian cells (4,(20)(21)(22)(23), but surprisingly, initial RNA interference-mediated knockdown of SF1 in human cells did not affect the splicing of several pre-mRNAs tested (22).Similarly, biochemical or genetic depletion of SF1/BBP from human extracts or yeast cells only marginally affected splicing activity, possibly due to a kinetic role for SF1 in spliceosome assembly (14,24).Later experiments demonstrated that SF1 is not involved in the splicing of all introns, but influences alternative splicing decisions (25)(26)(27)(28).Thus, altered or mis-splicing of essential genes in the absence of SF1 could reflect its requirement for viability.In addition to its role in splicing, SF1 has been implicated in nuclear pre-mRNA retention and transcriptional repression (29,30), functions that may contribute to or be the cause of SF1's essential phenotype.
To better understand SF1 function in splicing and potentially other processes, we set out to identify interacting proteins by co-immunoprecipitation (co-IPs) from HeLa cell nuclear extracts combined with mass spectrometry (MS) and in yeast two-hybrid (Y2H) screens with human SF1.Our results confirm that the major role for SF1 is in early stages of the splicing reaction.We demonstrate a novel function of SF1, which is essential for efficient spliceosome assembly, in the initial recruitment of the U2 snRNP through direct interactions with two U2 snRNP-associated proteins.The isolation of Y2H partners moreover suggests interactions of SF1 with additional proteins implicated in splicing, but also in other processes and identifies domains potentially mediating these interactions.

Co-IP of SF1-interacting proteins and MS
HeLa cell nuclear extract (corresponding to 2 mg of total protein) was incubated in the absence or presence of 0.3 mg/ml RNase A (Sigma) for 15 min at room temperature followed by pre-clearing for 1 h at 4 • C with Protein G Sepharose (GE Healthcare) equilibrated in IP buffer (50 mM Tris-HCl, pH 7.9, 100 mM NaCl, 0.05% Nonidet P-40 [NP-40] and 0.5 mM dithiothreitol [DTT]).Unbound material was incubated for 1 h at 4 • C with Protein G Sepharose-coupled anti-SF1 (Abnova; H7536-MO1A) or control mouse IgG (Sigma, P4810), followed by centrifugation at 2000 rpm in a microfuge for 2 min at 4 • C. Unbound material was saved and the beads were washed three times with 1 ml IP buffer.Bound material was eluted with NuPAGE LDS sample buffer (Life Technologies) and separated in NuPAGE Novex 4-12% Bis-Tris protein gels (Life Technologies), followed by Coomassie blue staining.Proteins were in-gel trypsin-digested and extracted according to Shevchenko et al. (31).Peptides were analyzed in an LTQ Orbitrap XL mass spectrometer (Thermo Fisher Scientific) under standard conditions.Proteins were identified by searching fragment spectra against the NCBI nonredundant database using Mascot as search engine.The number of product ion spectra (total spectrum count) of identified peptides was compared between anti-SF1 and control-IgG samples.Proteins with more than 15% of spectra in control IgG versus anti-SF1 were eliminated.Proteins with five or more spectrum counts are shown in Table 1; those with less than five spectrum counts, in addition to proteins assumed to represent common contaminants, are listed in Supplementary Table S1.

Y2H analysis
Y2H screens were performed with the partial coding sequence of human SF1 (amino acids 1-441; GenBank accession number gi: 295842308), which was PCR-amplified and cloned into pB27 as a C-terminal fusion to LexA (N-LexA-SF1-C).The construct was verified by sequencing and used as a bait to screen random-primed and dT-primed cDNA libraries constructed in pP6 (Table 2) with a mean insert size of 900 bp.Library construction has been described (32).pB27 and pP6 are derived from pBTM116 and pGADGH, respectively (33,34).
Baits were screened using a mating approach with YHGX13 (Y187 ade2-101::loxP-kanMX-loxP, mat␣) and L40 Gal4 (mata) yeast strains as described (35).The number of clones tested and histidine-positive clones are listed in Table 2. Prey fragments of positive clones were PCRamplified and sequenced at the 5 and 3 junctions.Preys from the dT-primed library were only sequenced at the 5 junctions.The resulting sequences were used to identify the corresponding interacting proteins in the GenBank database (http://www.ncbi.nlm.nih.gov/gene/) with a fully automated procedure.A confidence score (Predicted Biological Score, PBS) was attributed to each interaction as described (32).

Data set
The protein interactions from this publication have been submitted to the IntAct Molecular Interaction Database (36) at the International Molecular Exchange Consortium (IMEx; http://www.imexconsortium.org/)and assigned the identifier IM-23671.The data are presented in Supplementary Tables S2-9 and Supplementary Figures S4-S11 and can also be browsed with the PIMRider data analysis software at https://pimr.hybrigenics.com/(SF1 project).

Cloning procedures
DNAs were amplified with the Expand High Fidelity PCR System (Roche) according to the manufacturer's instructions and suitable primers.Correct cloning was verified by sequencing (Microsynth, Switzerland).
Plasmids for bacterial expression of SF1 proteins were cloned as follows: C-terminal truncations carrying Nterminal His 6 -tags were cloned into the BamHI and EcoRI sites of pTrcHisA (Life Technologies).N-terminal deletions were cloned into the NcoI and EcoRI sites of pETMBP-1a (a gift of Michael Sattler, Helmholtz Center and Technical University, Munich), encoding proteins with N-terminal His 6 -MBP tags.Internal deletions of SF1-C370 in pETMBP-1a were generated by replacing the deleted sequences with one ( 306-326 and Zn) or two ( KH) KpnI sites, encoding Gly and Thr.Internal sequences of SF1 (127-302, 295-335 and 304-326) were cloned into the NcoI/EcoRI sites of pETMBP-1a.
For transient expression of N-terminal GFP fusion proteins in HeLa cells, SF1 sequences were cloned into the Gateway vector pDEST53 (Life Technologies).
Templates for in vitro transcription of 3 splice site pre-mRNAs were generated by HindIII and BstEII digestion of a pBluescript plasmid encoding the region spanning exons 1 and 2 of AdML pre-mRNA (37).The 3 overhangs were blunt-ended with T4 DNA polymerase (Promega) followed by religation.The resulting pre-mRNA contains 51 nts of vector sequences, 75 nts of the 3 end of AdML intron 1 and 38 nts of exon 2. This plasmid was used to mutate the original AdML BPS (UACUUAU) to a consensus (UACUAAC) or weak (AAUUCAC) BPS with the Gene-Tailor Site-Directed Mutagenesis System (Life Technologies).

Bacterial expression and purification of recombinant proteins
Plasmids encoding GST-tagged SURP domains and His 6 -MBP-tagged SF1 proteins were transformed into E. coli strain BL21 by heat shock.Plasmids encoding GST, GST-U2AF65-UHM and His 6 -tagged SF1 proteins were transformed into E. coli strain XL1-Blue by heat shock.Proteins were expressed for 4 h at 37 • C after addition of isopropyl-␤-D-thiogalactopyranoside (IPTG) to a final concentration of 1 mM.Cells were harvested by centrifugation at 5000 × g for 10 min.
Cells expressing GST-tagged proteins were lysed in PBS supplemented with complete protease inhibitors (Roche) by sonication on ice and supplemented with Triton X-100 to a final concentration of 1%.Proteins were purified with 500 l of a 50% suspension of glutathione agarose (Sigma) equilibrated in PBS.Unbound proteins were removed by washing three times with 10 ml PBS and GST-tagged proteins were eluted with 5 mM glutathione and 50 mM Tris-HCl, pH 8.0.
Cells expressing His 6 -or His 6 -MBP-tagged proteins were lysed in 10 mM Tris-HCl, pH 8.0, 100 mM NaCl, 50 mM Na phosphate, 8 M urea and complete protease inhibitors.Proteins were purified on TALON Metal Affinity Resin (BD Biosciences).Unbound material was removed by three washes with lysis buffer containing 0.4 M NaCl and 20 mM imidazole and bound proteins were eluted with 0.1 M EDTA, pH 8.0.
All recombinant proteins were dialyzed against D buffer (38) supplemented with 3 mM MgCl 2 and stored at −80 • C. Purified proteins were quantified by SDS-PAGE and Coomassie blue staining.

GST pull-down assays
Reactions containing 20 l of packed glutathione-agarose beads (Sigma) and 0.056 nmole (corresponding to ≈2 g) of GST fusion proteins in a total volume of 200 l NETN (20 mM Tris-HCl, pH 8.0, 50 mM NaCl, 0.5% NP-40, 0.5 mM EDTA) were incubated for 30 min at 4 • C and washed twice with 500 l NETN.His 6 -or His 6 -MBP tagged pro-teins were added in a two-fold molar excess and the reaction mixture was incubated for 45 min at 4 • C in a total volume of 200 l NETN.Where indicated, purified proteins were treated with 0.3 mg/ml of RNase A for 20 min at room temperature and centrifuged at maximal speed in a microfuge for 5 min prior to GST pull-down.Unbound proteins were removed by three NETN washes.Proteins were eluted from the beads with SDS sample buffer for 5 min at 95 • C and separated by SDS-PAGE followed by western blotting (39).Input and bound proteins were detected with mouse monoclonal anti-His 6 (Sigma; H1029); the amount of GST-tagged proteins was verified by incubation with rabbit anti-GST (A.K., unpublished).Goat anti-mouse and anti-rabbit IRDye800 and 680LT (LI-COR) were used as secondary antibodies and immune complexes were visualized with the Odyssey Fc imaging system (LI-COR Biosciences).

Cell culture, transient transfection and preparation of HeLa cell lysates and nuclear extract
HeLa cells were grown at 37 • C with 5% CO 2 in DMEM (Sigma) supplemented with 10% FBS (Sigma), 2 mM Lglutamine (Gibco), 100 u/ml penicillin and 100 g/ml streptomycin (Gibco).Cells were plated in 10-cm culture dishes 24 h prior to transfection.Cells were transfected at 60-70% confluency with polyethylenimine (Brunschwig) according to the manufacturer's instructions and collected 72 h later.Whole cell lysates were prepared by lysis of transfected cells in 50 mM Tris-HCl, pH 7.5, 100 mM NaCl, 1% NP-40, 1 mM DTT, 2 mM EDTA and complete protease inhibitors for 30 min at 4 • C followed by centrifugation at 16 000 x g for 5 min at 4 • C. HeLa cell nuclear extracts were prepared according to Dignam et al. (38) and dialyzed against buffer D.

Co-IPs
HeLa cell nuclear extract was incubated with 0.3 mg/ml RNase A (Sigma) for 20 min at room temperature and centrifuged in a microfuge at maximal speed for 5 min.The supernatant (corresponding to 100 g of total protein) was incubated for 1 h at 4 • C with Dynabeads Protein G (Invitrogen) coated with anti-SF1 or control mouse IgG.The unbound fraction was kept for western blotting and beads were washed four times with 1 ml of 50 mM Tris-HCl, pH 7.5, 100 mM NaCl, 0.05% NP-40 and 0.5 mM DTT. Bound proteins were eluted with SDS sample buffer for 5 min at 95 • C. Input, unbound and bound material were separated by SDS-PAGE followed by western blotting with the following antibodies: mouse monoclonal anti-CHERP (Santa-Cruz; Sc-100650), rabbit anti-H1 (Santa-Cruz; Sc-10806), mouse monoclonal anti-SF1 (Abnova; H7536-MO1A), rabbit anti-SF3a60 (40), mouse monoclonal anti-SF3a66 (41), rabbit anti-SF3a120 (42), rabbit anti-SFSWAP (Aviva; ARP 40524) and mouse monoclonal anti-U2AF65 (Sigma; U4758).Secondary antibodies and detection of immune complexes were as above.
For precipitation of transiently expressed GFP-tagged SF1 and associated proteins, HeLa whole cell lysate (corresponding to 6 mg of total protein per reaction) was treated with RNase A as above and incubated for 1 h at 4 • C with Dynabeads Protein G-coupled goat anti-GFP (a gift of Karla Neugebauer, Yale University).Washing, elution, SDS-PAGE and western blotting were performed as above.Proteins were detected with anti-SF3a120, anti-U2AF65 and rabbit anti-GFP (Invitrogen; A-11122).

Immunodepletion
SF1 was immunodepleted from HeLa cell nuclear extract adjusted to 600 mM KCl by three passages over Dynabeads Protein G-coupled anti-SF1.The depleted extract was dialyzed against buffer D (38) and stored at −80 • C. Mock depletions were performed as above in the absence of antibody.

Spliceosome assembly
AdML pre-mRNAs with a consensus or weak BPS were synthesized with T3 RNA polymerase (Promega) in the presence of [␣-32 P]UTP and gel-purified (37,43).Biological triplicates of spliceosome assembly were performed in 10-l reactions in the presence of 10% untreated, mock-or SF1-depleted HeLa nuclear extract, 10 mM Hepes-KOH, pH 7.9, 50 mM KCl, 0.05 mM EDTA, 0.25 mM DTT, 1 g tRNA and 1.6 pmol pre-mRNA at 30 • C for the times shown in the figure legends.Where indicated, reactions were complemented with 0.022, 0.22 or 2.2 pmol SF1-C370 or SF1-302.Reaction products were separated in native 4% polyacrylamide gels (44).Gels were dried and exposed to PhosphorImager screens.Quantification was done with the Molecular Imager FX (BioRad) and software Quantity One V 4.2.1 (BioRad).

UV cross-linking and IP of U2AF65
Spliceosome assembly was performed as above in 20-l reactions in the presence of 25% mock-or SF1 depleted extract and 18 pmol pre-mRNA.Samples were incubated at 30 • C for 15 min, UV cross-linked and treated with RNase A as described (45).Dynabeads Protein G coupled with control IgG or anti-U2AF65 and 100 l buffer D (38) were added and samples were incubated for 1.5 h at 4 • C with rotation.After centrifugation, the beads were washed four times with 600 l of 50 mM Tris-HCl, pH 7.5, 0.5 M NaCl, 1% NP-40 and 0.5 mM DTT, and once with 50 mM Tris-HCl, pH 7.5 and 1% NP-40.Bound material was eluted by boiling in SDS loading buffer for 5 min, followed by centrifugation and separation by 10% SDS-PAGE.Gels were dried, exposed to a PhosphorImager screen and signals were quantified as above.

The U2 snRNP co-immunoprecipitates with SF1
To identify potential novel partners of SF1, we performed co-IPs of HeLa cell nuclear extracts followed by MS.Extracts were incubated in the absence or presence of RNase A, pre-cleared on Protein G Sepharose and aliquots were incubated with Protein G Sepharose-coupled control mouse IgG or a monoclonal antibody directed against the Nterminal 110 amino acids of SF1.Eluted proteins were separated by 1D PAGE (Supplementary Figure S1), in-gel trypsin-digested and analyzed by liquid chromatography tandem mass spectrometry (LC-MSMS).
A total of 58 proteins were specifically precipitated by anti-SF1 (Table 1), four of which were previously reported to directly interact with SF1: FBP11/PRPF40A, PUF60, SPF45/RBM17 and U2AF65/U2AF2, (3,4,20,(46)(47)(48). Forty-seven proteins are represented in a list of 244 annotated spliceosomal proteins (see 49).Among these, 29 are associated with the U1 or U2 snRNPs or function in presplicing complex A assembly.Eight are part of the U4/U6, U5 or U4/U6.U5 snRNPs or function after A complex formation.Three members of the SR family of proteins with functions early and late during spliceosome assembly were found, in addition to six proteins with roles in mRNA export or mRNA binding and one miscellaneous protein associated with the spliceosome.Thus, consistent with the function of SF1 at the initial steps of spliceosome assembly, more than half of the proteins co-precipitating with SF1 are components of early spliceosomes, compared to 52 of the annotated early spliceosomal proteins (excluding SR and hnRNP proteins), whereas only a small percentage (eight of 103 proteins) are associated with later complexes.An additional 14 spliceosome-associated proteins were detected below the cut-off used for the data in Table 1 and are listed in Supplementary Table S1, together with proteins not known to be part of the spliceosome or to be common contaminants.
A closer inspection of the early spliceosomal proteins precipitated by anti-SF1 revealed the presence of nine of the 12 U2 snRNP-specific proteins, as well as nine of 11 proteins more loosely associated with the U2 snRNP (Table 1, U2 and U2-related, respectively; see 50).This finding was surprising, since the U2 snRNP is thought to replace SF1 from the spliceosome during the complex E to A transition by binding of the U2 snRNP-associated SF3b155 to the U2AF65-UHM, a site occupied by SF1 in complex E (14,(51)(52)(53) and base pairing of the U2 snRNA with the BPS.Moreover, SF1 has not been found among U2 snRNPassociated proteins (50).However, although the U2 snRNA base-pairs with the BPS only in complex A (54), the U2 snRNP has been detected already in complex E (55)(56)(57).
Eleven proteins isolated by co-IP are not known to be related to splicing (Table 1).Most are nuclear proteins with functions in RNA binding and/or transcription.The presence of some of these proteins may be due to interactions with other components of the splicing machinery that are directly or indirectly associated with SF1.
human and three mouse tissues or cell lines fused to the Gal4 activation domain were tested for interactions (Table 2).As summarized in Table 3 (and listed in detail in Supplementary Tables S2-S9), previously described SF1 partners were detected in the Y2H screens (ABL1/2, PRPF40A/FBP11, RBM17/SPF45, U2AF65 and UHMK1/KIST ; 3,4,20,46,48,58,59), with U2AF65 showing an expectedly high confidence score (Predicted biological score, PBS; Table 3).Several spliceosomeassociated proteins and other proteins with roles in splicing were among the potential partners.However, only few proteins found in complex with SF1 by co-IP/MS were detected, suggesting that the majority of these were not direct binding partners, but co-precipitated with SF1 from HeLa cell extracts due to the numerous protein-protein interactions in the spliceosome (2).
The highest PBS was found for KPNA2 (Table 3), a subunit of the nuclear import complex.Other members of the same complex were also detected, but with a lower PBS depending on the subunit or cell type.Moreover, KIAA0907 was found as a SF1 partner with very high confidence in all cell types tested.Roles in splicing for this protein, also termed BLOM7, have been described (60).It contains a KH domain, similar to a few other proteins found in the Y2H screens with a lower PBS.Apart from these, SF1 may also directly interact with proteins containing RNA recognition motifs (RRMs) or zinc fingers.A possible relation of these proteins to SF1 function will be described in the discussion.
Among the preys with reported roles in splicing are two U2 snRNP-associated proteins: splicing factor SF3A subunit 1 (SF3A120/SF3a1) and calcium homoeostasis endoplasmic reticulum protein (CHERP; Table 3).SF3a120 is part of a heterotrimeric complex with SF3a66 and SF3a60 and essential for U2 snRNP function in spliceosome assembly (61).CHERP was originally identified as an endoplasmic reticulum protein involved in the regulation of intracellular Ca 2+ homoeostasis (62), but is also loosely associated with the U2 snRNP, and has been reported to localize to the nucleus and function in alternative splicing (50,63,64).
Together, these data suggest that SF1 binds U2 snRNPassociated proteins and SFSWAP via SURP domainmediated interactions.

SF1 directly binds SURP domains of SF3a120, CHERP and SFSWAP
To validate binding of SF1 to SURP domains, we first performed co-IPs with anti-SF1 coupled to Dynabeads Protein G from RNase A-treated HeLa cell nuclear extracts and western blotting with antibodies against the potential interacting proteins.Figure 1B shows that SF3a120, as well as SF3a60 and SF3a66 were co-precipitated with SF1; thus, the entire SF3a heterotrimer was bound.CHERP was also found in the precipitate; however, SFSWAP was not detected.U2AF65, known to interact with SF1 (4,20) and used as a positive control, was bound to SF1, whereas histone H1, a negative control, was not.None of the proteins were bound to Dynabeads Protein G coated with nonspecific IgG.These results show that SF3a120 and CHERP can be co-precipitated with SF1 from HeLa cell extracts, whereas an interaction with SFSWAP was not detected.
To determine whether SF1 binding to SF3a120, CHERP and SFSWAP was mediated by direct interactions with the SURP domains identified in the Y2H screens, we performed GST pull-down assays with GST-tagged SURP domains and recombinant His 6 -tagged SF1-C370 (containing amino acids 1-370, i.e. the region common to all SF1 isoforms).His 6 -SF1-C370 was bound by the SURP domains of SF3a120, CHERP and SFSWAP, as well as by the positive control, GST-U2AF65-UHM, but not by GST alone (Figure 1C).The interactions were insensitive to RNase A treatment prior to GST pull-down, demonstrating that SURP domain binding of SF1 was not mediated by RNA.Thus, SURP1 of SF3a120, the single SURP domain of CHERP and SURP2 of SFSWAP are sufficient for direct SF1 binding, confirming the results of the Y2H screens.

An evolutionarily conserved domain in SF1 is essential for SURP domain binding
The region of SF1 responsible for the SURP domain interaction was analyzed in GST pull-down assays with His 6tagged C-and N-terminal as well as internal deletion mutants of SF1 (Figure 2A).Compared to SF1-C370, binding to GST-SF3a120-SURP1, CHERP-SURP and SFSWAP-SURP2 was slightly weakened with SF1-C327 and strongly reduced upon deletion to amino acid 320 (Figure 2B).Binding of SF1-C315 was barely detectable and further deletion of SF1 residues completely abolished the SURP domain interaction.Thus, the C-terminal border of the SURP interaction domain (ID) lies between SF1 residues 315 and 327.
SF1 mutants with N-terminal His 6 and maltose-binding protein (MBP) tags were used to further delimit the SF1 SURP-ID.N-terminal deletions up to, and including the zinc knuckle (N127 to N292; Figure 2C) did not abolish binding of SF1 to the SURP domains.Thus, neither the SF1 KH/QUA2 domain nor the zinc knuckle are involved in the interaction, which was confirmed with SF1 mutants carrying internal deletions of these domains ( KH and Zn).SF1 residues 295-335 were barely sufficient for the interaction and amino acids 127-302 or 304-326 did not bind the SURP domains.Moreover, an internal deletion of residues 306-326 abolished binding.The C-terminal or internal deletions did not affect binding to GST-U2AF65-UHM, used as a positive control, whereas none of the N-terminal deletions interacted with GST-U2AF65-UHM, since the U2AF ligand motif (ULM) of SF1 was not present.Binding to GST alone was not observed.Together, these data indicate that the region between residues 293 and 327 of SF1 is required for the interaction with SURP domains.
To further test the relevance of this domain for SURP binding, GFP-tagged SF1-C370 and -C302 were transiently expressed in HeLa cells.RNase A-treated whole cell lysates were immunoprecipitated with Dynabeads Protein G-coupled anti-GFP.SDS-PAGE and western blotting with anti-SF3a120 showed that endogenous SF3a120 interacted with GFP-SF1-C370 but not -C302, whereas U2AF65 bound both proteins (Figure 2D).Thus, the SF1 SURP-ID identified in vitro with recombinant proteins is also essential for binding SF3a120 in HeLa cell lysates.
A multiple sequence alignment of SF1 revealed the presence of a region well-conserved from Drosophila to humans (amino acids 293-326 of human SF1; Figure 2E) encompassing the residues that eliminated the SURP domain interaction.This region is highly conserved in mammals, Xenopus and zebrafish, and partial conservation of key residues (amino acids 301-321) is seen in other organisms, including Arabidopsis, Schizosaccharomyces pombe and Dictyostelium, with the exception of S. cerevisiae.From these results we conclude that an evolutionarily conserved domain in SF1, spanning amino acids 293-327 is essential for binding SURP domains.

The SF1/SURP interaction is required for efficient early spliceosome assembly
The above results demonstrate that SF1 can bind the U2 snRNP through direct interactions with SF3a120 and CHERP.SF1 recognizes the BPS in complex E and the U2 snRNP is weakly bound to this complex before base pairing of the U2 snRNA to the BPS and pre-mRNA binding of several U2 snRNP-associated proteins in complex A (5,10,13,56,57).To test the possibility that SF1 is involved in the recruitment of the U2 snRNP to the pre-mRNA, we compared spliceosome formation in HeLa cell nuclear extracts and SF1-depleted extracts in the absence or presence of recombinant SF1 proteins with or without the SURP-ID.To facilitate quantification of the results, spliceosome assembly was analyzed with an AdML pre-mRNA lacking the 5 splice site and containing 75 nts of the 3 end of intron 1 and part of exon 2. Similar splicing substrates are efficiently assembled into a 3 splice site complex related to pre-splicing complex A (termed A3' complex hereafter) but not converted to complex B (43).In addition, the original BPS of AdML intron 1 was changed to the yeast consensus BPS, UACUAAC, which is the optimal BPS for mammalian splicing (74) and also the preferred binding site of SF1 (5,25,75).
Immunodepletion with anti-SF1 bound to Dynabeads Protein G resulted in a 91% reduction of different SF1 isoforms compared to untreated or mock-depleted nuclear extracts (Figure 3A).Other proteins, such as U2AF65 or SF3a120, were not co-depleted (Supplementary Figure S2A).A3' complex formation tested by incubation for 30 min at 30 • C in triplicate experiments was reduced to an average of 44% of that seen in the mock-depleted extract (Figure 3B).The SF1-depleted extract was then complemented with equivalent concentrations of His 6 -SF1-C370 or -C302 (Supplementary Figure S3), containing or lacking the SURP-ID, respectively (Figure 2A and B).Addition of SF1-C370 rescued A3' complex formation to 160% compared to mock-depleted extract in a dose-dependent man-  ner, whereas complex formation in the presence of SF1-C302 was less efficient (126%; Figure 3B).The observation that the recombinant proteins rescued A3' complex assembly to more than 100% could be due to the fact that their concentration exceeded that of endogenous SF1.Comparison of protein levels of endogenous and recombinant proteins is difficult, because endogenous SF1 exists in multiple isoforms (Figure 3A; 76) and their exact contribution to splicing is not established.
A rather modest effect of SF1 depletion on spliceosome formation, despite an at least 98% reduction in SF1 protein has been reported by Guth and Valcárcel (24).The same authors showed that the effect of SF1 depletion was more pronounced with a pre-mRNA containing a weak as compared to a strong BPS.Similarly, depletion of SF1 in yeast causes more severe splicing defects with reporters containing mutated splice sites (14).We therefore repeated the experiment with the same pre-mRNA as above, but containing the weak IgM BPS (AAUUCAC; 24,77).Compared to mock-treated extract, SF1 depletion reduced complex formation to about 23% (Figure 3C).Complementation with SF1-C370 rescued A3' complex formation to nearly mockdepleted levels (98%), whereas addition of SF1-C302 resulted in a significantly reduced rescue of 58%.Thus, the region of SF1 necessary for the interaction with U2 snRNP proteins is also required for efficient A3' complex assembly.The more marked effect seen with the pre-mRNA containing a suboptimal BPS can be explained by the fact that the consensus BPS is the preferred SF1 binding site (5,25,75).
Previous studies suggested a kinetic role for SF1 in spliceosome assembly (14,24).The above results indicate that SF1 binds two U2 snRNP proteins and the SF1 SURP-ID is required for efficient A3' complex formation.To test whether the SF1-U2 snRNP interaction underlies the kinetic role of SF1, we performed a time course of A3' complex formation.Pre-mRNAs with a consensus or weak BPS were incubated with mock-or SF1-depleted HeLa nuclear extract supplemented with His 6 -SF1-C370 or -C302.Representative results of experiments performed in triplicate are shown in the top panels of Figure 4A and B. A3' complex formation was quantified and normalized to the values for the 60-min time points of the mock-depleted extract (bottom panels).SF1 depletion resulted in a 65 or 76% reduction in A3' complex assembly with pre-mRNAs containing a consensus or weak BPS, respectively.Addition of SF1-C370 rescued complex formation to the levels of mock-depleted extract with both pre-mRNAs.When reactions were complemented with SF1-C302, A3' complex formation with the consensus BPS substrate was reduced only at the 45 and 60-min time points, plateauing at 70%.In contrast, A3' complex formation performed in the presence of SF1-C302 and the pre-mRNA with a weak BPS was less efficient at all time points, with a maximum level of 43% at 60 min.Thus, the interaction between SF1 and the U2 snRNP is essential for efficient A3' complex formation, especially when U2 snRNA/BPS base pairing is suboptimal.This observation can explain the previously reported kinetic effect on spliceosome assembly (24).
The absence of the SF1 SURP-ID does not compromise U2AF65 binding to the RNA SF1 and U2AF65 cooperatively bind the pre-mRNA and increase each others affinity for RNA (3).Thus, SF1 depletion also causes decreased binding of U2AF65 to the polypyrimidine tract with a concomitant decrease in spliceosome assembly (24), which likely contributes to the lower levels of A3' complex formation seen above.To rule out the possibility that RNA binding of U2AF65 is affected in a SF1-depleted extract complemented with recombinant SF1 proteins, we performed UV cross-linking of U2AF65 in 15-min reactions containing mock-or SF1depleted extracts and pre-mRNAs with a consensus or weak BPS.Triplicate samples were UV cross-linked, RNase Atreated and incubated with Dynabeads Protein G-coupled control IgG or anti-U2AF65.Bound material was analyzed by SDS-PAGE and the fraction of RNA bound to U2AF65 was quantified (Figure 5).U2AF65 efficiently cross-linked to both pre-mRNAs in the mock-depleted samples.Only background cross-linking was detected in IPs performed with control IgG.As expected from previous results (24), pre-mRNA binding of U2AF65 was partially reduced upon SF1 depletion.However, addition of either His 6 -SF1-C370 or -C302 increased U2AF65/RNA binding to the levels seen in mock-depleted extract, consistent with the fact that both proteins contain the ULM and thus can bind U2AF65 (Figure 2B).We therefore conclude that the reduced levels of A3' complex formation observed in SF1-depleted extracts complemented with SF1-C302 are due to the lack of interaction of SF1 with the U2 snRNP and not caused by decreased pre-mRNA binding of U2AF65.

DISCUSSION
Results from co-IP/MS experiments and Y2H screens have provided information about novel and, in part, unexpected partners of SF1.The co-IP/MS experiment demonstrated that about half of the proteins co-precipitated with SF1 from HeLa cell nuclear extracts are involved in early steps of spliceosome assembly, confirming an early role for SF1 in splicing (19,20).Surprisingly, most of the U2 snRNPassociated proteins were co-precipitated with SF1.Y2H screens revealed potential interactions of SF1 with the SURP domain-containing, U2 snRNP-associated proteins SF3a120 and CHERP, as well as the alternative splicing factor SFSWAP.Direct binding of SF1 to SURP domains of the three proteins were confirmed in GST pull-down assays and the interaction domain was mapped to an evolutionarily conserved, central region of SF1.We furthermore show that the SF1/U2 snRNP interaction is necessary for efficient spliceosome assembly, suggesting a role for SF1 in the early recruitment of the U2 snRNP to the pre-mRNA.

A novel role for SF1 in U2 snRNP recruitment
Consistent with a role for SF1 at the onset of spliceosome assembly (19,20), anti-SF1 antibodies precipitated more than half of the proteins present in early splicing complexes, compared to only 8% of proteins associated with later complexes or functioning in splicing catalysis and post-splicing events (Table 1; 2,49).However, although only five of 18  annotated A complex components were co-precipitated, almost all U2 snRNP-associated proteins were present.This finding was unexpected, since the events leading to stable pre-mRNA binding of the U2 snRNP at the time of A complex assembly are thought to trigger the release of SF1 at the same time.In S. cerevisiae SF1 (BBP) was detected in the ATP-independent commitment complex 2, but not the pre-spliceosome (14).In the human system proteins in the ≈80-kDa range, most likely representing SF1 isoforms, cross-link to the BPS in a U1 snRNP-dependent and ATP-independent manner at very early times of spliceosome assembly (78).These cross-links disappear in the presence of ATP and are replaced by cross-links to proteins of 14, 35 and 150 kDa, which persist in complex A. The 14-kDa protein is SF3b14a/p14, a U2 snRNP protein directly binding to the BPS adenosine (11,12,78).The 150-kDa protein probably represents SF3b155, a U2 snRNP component binding upstream and downstream of the BPS and interacting with the U2AF65-UHM, the same site occupied by SF1 (10,51,53).In addition, a 'U2 mimic', an oligoribonucleotide base-pairing to the BPS and neighboring sequences, prevents BPS binding of SF1 (3).Finally, SF1 has only been detected in small amounts in A complexes isolated from HeLa cells under physiological conditions and the material used could have contained small amounts of E complexes (79).These findings imply that the SF1/U2 snRNP interaction occurs prior to A complex formation.Since the U2 snRNP has been detected in complex E (55)(56)(57), our data strongly suggest that SF1, binding to the SURP domains of SF3a120 or CHERP, aids the initial recruitment of the U2 snRNP to the assembling spliceosome.We envision the following series of events: SF1 and U2AF65 interact with one another, involving the ULM at the N terminus of SF1 and the UHM of U2AF65 (51).This is followed by their cooperative binding to the BPS and the polypyrimidine tract (3).SF1 binds the BPS through its KH domain (6), leaving the SURP-ID available for binding SF3a120 or CHERP.The SF1/BPS interaction prebulges the BPS adenosine, whereas other nucleotides are accessible for U2 snRNA base pairing (6).In principle, SF1 could interact with the U2 snRNP before or after binding to U2AF65; in either case it would position the U2 snRNP close to the BPS.The transition to complex A then occurs through replacement of the SF1/U2AF65 interaction by binding of SF3b155 to the U2AF65 UHM, binding of SF3b14a/p14 to the BPS adenosine, base pairing of U2 snRNA to the BPS and binding of SF3a and SF3b subunits to the pre-mRNA on both sides of the BPS, tethering the U2 snRNP for later steps (10,11,13,53,78).In this scenario, SF1 initiates U2 snRNP recruitment and facilitates the events required for A complex formation by placing the U2 snRNP into the vicinity of the BPS and U2AF65, whereas U2AF65 stabilizes the association of the U2 snRNP with the spliceosome once SF1 is released.
The interaction of SF1 with U2 snRNP-associated proteins is required for efficient spliceosome assembly, since A3' complex formation is strongly reduced following SF1 depletion and can be restored by addition of SF1 containing, but less so by addition of SF1 lacking the SURP-ID (Figures 3 and 4).This effect is not due to the disruption of the SF1/U2AF65 interaction, since both SF1 proteins contain the ULM and pre-mRNA binding of U2AF65 was not compromised in the presence of either protein (Figure 5).Guth and Valcárcel (24) suggested a function of SF1 in addition to increasing the affinity of U2AF65 for the polypyrimidine tract.The results presented here strongly suggest that this additional role is the binding of SF1 to the U2 snRNP, thereby directly promoting the U2 snRNP/BPS interaction.
Although SF1 has long been considered a constitutive splicing factor, it is not required to splice all introns (22,25).In these cases, U2AF65 may be sufficient to recruit the U2 snRNP, perhaps helped by other proteins (80).Also, U2AF65 may not be necessary for the recognition of 12% of functional human 3 splice sites (81); thus, SF1 may play a major role in the recruitment of the U2 snRNP to introns that are not bound by U2AF65.

The interaction of SF1 with SURP domains
The Y2H screens identified SURP1 of SF3a120, the single SURP domain of CHERP and SURP2 of SFSWAP as SF1 interaction partners, which was confirmed with recombinant proteins (Table 3, Figure 1 and Supplementary Fig- ures S4-S11).The remaining SURP domains of SF3a120 and SFSWAP could not be tested, since the bacterially expressed proteins were insoluble (data not shown).However, the following points argue that SF1 only interacts with the SURP domains tested.First, although some of the cD-NAs isolated in the Y2H screens completely or partially included the other SURP domains of SF3a120 and SFSWAP, SF3a120 SURP1 and SFSWAP SURP2 were present in all cDNAs recovered.Second, Kuwasako et al. (66) only obtained SURP2 of SF3a120 in soluble form when coexpressed with SF3a60.In analogy to these experiments, coexpression of SF1 and SF3a120 SURP2 did not yield soluble SURP2 (data not shown), suggesting that SF1 does not interact with SF3a120 SURP2.Third, SURP domains can be classified into two evolutionarily related subgroups (66).The SURP domains of SF3a120, SFSWAP and CHERP isolated in the SF1 Y2H screens belong to subgroup 1, whereas SF3a120 SURP2 and SFSWAP SURP1 belong to subgroup 2. It is therefore highly likely that SF1 only interacts with SURP domains of subgroup 1, but not those of subgroup 2.
The SF1 SURP-ID is located immediately C-terminal to the zinc knuckle (Figure 2).Its sequence is almost invariant in mammals and conserved to a lesser extent in A. thaliana and S. pombe, but it is not present in S. cerevisiae SF1.BLAST searches did not identify a related sequence in other mammalian proteins.SF3a60 binds SURP2 of SF3a120 and single amino acid changes in SURP2 and SURP1 swap the identity of the domains, i.e. prevent SURP2 binding of SF3a60 but allow for SURP1 binding (66).It is therefore intriguing to speculate that the interaction sites in SF3a60 and SF1 show a certain degree of similarity.A sequence alignment between the SF1 and SF3a60 SURP-IDs does not reveal obvious homology (data not shown).The SF3a60 SURP-ID forms a long amphipathic ␣-helix (66) and an equivalent interaction surface has been described between the S. cerevisiae orthologs (68).Analysis with the Phyre2 protein fold recognition server (82) also predicts a helical structure for the SF1 SURP-ID (data not shown).Differences in the mode of interaction would however be expected, since SF3a forms a stable heterotrimer (41), whereas the SF1/SF3a120 interaction is dynamic and resolved at the time of A complex assembly.Future structural stud-ies should define similarities and differences in the binding modes of SF3a60 and SF1 to SF3a120.

Lack of conservation of the SF1 SURP-ID in S. cerevisiae
Somewhat as a surprise, the SF1 SURP-ID is not conserved in S. cerevisiae SF1 (BBP).In addition, SURP1 of the yeast SF3a120 ortholog Prp21p lacks four amino acids close to a 3 10 helix present in the human protein (66), which could change the spatial organization of the interaction site.This may suggest that BBP and Prp21p do not interact.In fact, Y2H interactions between BBP and Prp21p have not been detected (J.-C.R., unpublished results) and are also not documented in the Saccharomyces Genome Database (http://www.yeastgenome.org/).
Could the BBP/Prp21p interaction be dispensable in S. cerevisiae?The vast majority of yeast introns contain the consensus BPS, UACUAAC, (83) with a perfect complementarity to the BPS-interacting sequence of U2 snRNA (G-UAGUA; the dash indicates the missing complementarity to the bulged-out BPS adenosine).Given our observation that the SF1/U2 snRNP interaction is more important for efficient splicing of introns with a weak BPS, SF1 may thus not be required for U2 snRNP recruitment in yeast.

The SF1/SFSWAP interaction
SFSWAP was identified as an additional partner of SF1 in Y2H screens from mouse tissues.SF1 binding to its SURP2 domain was confirmed in GST pull-down assays, but we did not detect the interaction by anti-SF1 IP from HeLa cell lysates.SFSWAP is an alternative splicing regulator that also autoregulates the splicing of its own pre-mRNA (65,(69)(70)(71)(72); however, targets of its regulation remain largely unknown.Given that SF1 also acts as an alternative splicing factor (25)(26)(27)(28), the two proteins may physically interact to regulate the splicing of perhaps only a few pre-mRNAs or only in certain tissues, which could explain the failure to detect the interaction in HeLa cells.Finding common splicing substrates with appropriate methods could solve this question.

Additional potential partners of SF1
Anti-SF1 antibodies co-precipitated only few proteins without a reported connection to splicing (Table 1).Some of these are involved in transcription, which may be related to the published role for SF1 in transcription repression (84,85).Similarly, several transcription factors were identified as potential partners of SF1 in the Y2H screens (e.g.zinc finger-containing proteins).
The Y2H screens were informative concerning other potential SF1 partners and structural domains mediating interactions with SF1 (Table 3).KPNA2 was found as a prey in all cell types tested with the highest-confidence PBS observed.Other members of this family of nuclear import factors were also detected, but with lower PBS.SF1 is a nuclear protein and therefore its interaction with the nuclear import machinery may not be surprising.However, Y2H screens with other nuclear proteins did not find KPNAs in such abundance (J.-C.R., unpublished data).The shortest Nucleic Acids Research, 2015, Vol. 43, No. 21 10471 selected interaction domain ( SID) of the KPNAs comprises armadillo repeats, which are also found in the nuclear pore complex protein Nup155, another prey of SF1.Therefore, SF1 may have a thus far unknown function related to nuclear import.
Another protein with a high PBS found in all cell types analyzed is KIAA0907/BLOM7.It was initially identified in Y2H screens with a component of the human Prp19 complex and has been shown to increase splicing in HeLa cell nuclear extracts and regulate alternative splice site decisions (60).BLOM7 contains two KH domains, the second of which is comprised in the SF1 SID.Six additional proteins with KH domains covered by the SID were found as SF1 preys (KHDRBS1/SAM68; KHDRBS3/SLM-2; KHSRP/FUBP2; hnRNPK; FUBP3; QKI), most of which play roles in splicing (86)(87)(88)(89)(90). Interestingly, SF1 itself contains a KH domain of the same type as those of KHDRBS1, KHDRBS2, QKI and BLOM7.KIAA0562/CEP104 is a centrosomal protein of 104 kDa and another example of a prey identified in all cell types with a high PBS.The SID of CEP104 does not comprise any known structural domain and a potential role for a SF1/CEP104 interaction is elusive.
In addition to these proteins, SF1 preys include RRMcontaining proteins, most of which with reported functions in splicing.Interestingly, the SIDs of these proteins often comprise tandem RRMs.This observation may suggest that SF1 not only binds proteins with non-canonical RRMs of the UHM class (47,48,51,91), but also other types of RRMs.Taken together, the Y2H screens have provided a vast amount of information about possible SF1 partners and novel interaction domains, the relevance of which remains to be investigated.
To conclude, our data demonstrate a new role for SF1 in the recruitment of the U2 snRNP to the spliceosome by interaction with SURP domain-containing proteins and the potential to regulate alternative splicing events through a SURP domain-mediated interaction with SFSWAP.Our findings moreover stress the function of SURP domains as protein-protein interaction modules and future studies may identify additional proteins interacting with SURP domains.Furthermore, the Y2H screens identified potential novel partners of SF1.Studying these interactions may reveal additional functions of SF1 in splicing and other cellular pathways.

Figure 1 .
Figure 1.Analysis of the interaction of SF1 with SURP domain-containing proteins.(A) Scheme of SURP domain-containing proteins identified in Y2H screens.The domain structure of SF3a120, CHERP and SFSWAP is shown with SURP domains indicated in dark grey.Other domains are shown in light grey: CID, RNA polymerase II-binding domain; G-patch, G-patch domain; RS domain, Arg/Ser-rich domain; UBL, ubiquitin-like domain.Numbering was taken from UniProt entries (www.uniprot.org).The smallest selected interaction domain ( SID) deduced from cDNAs found in the Y2H screens is indicated below the proteins (numbering according to human proteins).(B) Co-IP.HeLa cell nuclear extract was incubated with Dynabeads Protein G coated with anti-SF1 or control IgG.Input (I; 10% of total), bound (B) and unbound (U) fractions were separated by 7.5% SDS-PAGE (10% for anti-H1) followed by western blotting with antibodies against the proteins indicated on the right side of each panel.(C) GST pull-down.His 6 -tagged SF1-C370 was incubated with GST alone, GST-tagged U2AF65-UHM, SF3a120-SURP1, CHERP-SURP or SFSWAP-SURP2 bound to glutathione-agarose as indicated above the figure.GST-tagged proteins were mock-treated (−) or digested with RNase A (+) as shown.The His 6 -SF1-C370 input (I; 10% of total) and bound proteins were separated by 10% SDS-PAGE and western blotted with anti-His 6 (top) and anti-GST antibodies (bottom).The migration of protein markers is indicated in kDa on the left.

Figure 2 .Figure 3 .
Figure 2. Determination of the SURP-ID of SF1.(A) Scheme of mutant SF1 proteins.Boxes represent known protein domains: ULM, UHM ligand motif; KH/QUA2, K-homology/Quaking2 domain; Zn, zinc knuckle.Numbering above full-length SF1 refers to amino acids.The names of SF1 mutants are shown on the left; numbers on the right refer to the residues comprising the proteins.(B) and (C) GST pull-down of mutant SF1 proteins with SURP domains.GST-tagged SF3a120-SURP1, CHERP-SURP, SFSWAP-SURP2, U2AF65-UHM and GST alone, bound to glutathione agarose (as indicated on the right), were incubated with mutant His 6 -(B) or His 6 -MBP-tagged (C) SF1 proteins as indicated above the figures.Bound proteins were separated by 10% SDS-PAGE and western blotted with anti-His 6 (top panels) and anti-GST (bottom panels).The input (10% of the total) is shown at the bottom.(D) Co-IP.GFP-tagged SF1-C370 and -C302 were transiently expressed in HeLa cells.Total cell lysates were RNase A-treated and incubated with Dynabeads Protein G-coupled anti-GFP.Input (I; 0.5% of the total) and bound proteins (B) were separated by 7.5% SDS-PAGE and western blotted with anti-SF3a120, anti-U2AF65 and anti-GFP as indicated on the right.The migration of protein markers (in kDa) is shown on the left.(E) Multiple sequence alignment of SF1 proteins.SF1 sequences taken from the UniProt database (www.uniprot.org)were aligned with ClustalW2 (www.ebi.ac.uk/Tools/msa/clustalw2/). The region from the zinc knuckle of human SF1 and 40 amino acids C-terminal of this domain is shown.Numbering is given for human SF1.Amino acids identical in more than 50% of the sequences are marked.

Figure 4 .
Figure 4. Deletion of the SF1 SURP-ID affects the kinetics of spliceosome assembly.Splicing reactions with AdML 3 splice site pre-mRNAs containing a consensus (A) or weak BPS (B) were performed in triplicate at 30 • C for the times indicated in the presence of mock-or SF1-depleted ( SF1) nuclear extract supplemented with 2.2 pmol His 6 -SF1-C370 or -C302 as shown.Samples were separated in native 4% polyacrylamide gels, which were dried and exposed to PhosphorImager screens.Representative gels are shown in the top panels.The results are quantified in the bottom panels.'% A3' complex' represents the ratio of A3' complex to total lane intensities.Values were normalized to those of mock-treated extracts at the 60-min time points.Error bars indicate SEM.

Figure 5 .
Figure 5. Deletion of the SF1 SURP-ID does not reduce U2AF65 binding to the pre-mRNA.(A) and (B) U2AF65 UV cross-linking to AdML 3 splice site substrates.Splicing reactions containing radio-labeled RNA with a consensus (A) or weak (B) BPS, mock or SF1-depleted ( SF1) extracts complemented with 2.2 pmole His 6 -SF1-C370 or -C302 as indicated were incubated at 30 • C for 15 min.Samples were UV cross-linked, RNase A-treated and immunoprecipitated with control IgG or anti-U2AF65, as indicated.RNA-protein complexes were separated by 10% SDS-PAGE.Gels were dried and exposed to PhosphorImager screens.The top panels show representative results of triplicate experiments; quantifications are shown in the bottom panels.'% U2AF65-bound RNA' indicates the percentage of the intensity of the cross-linked RNAs normalized to the RNA immunoprecipitated with anti-U2AF65 from mock-treated extract.Data are shown as mean value ± SEM.

Table 1 .
Proteins immunoprecipitated with anti-SF1 antibodies from HeLa cell nuclear extracts (49)up is described in the Materials and Methods section.SF1 or IgG, proteins precipitated by anti-SF1 antibodies or control IgG coupled to Protein G Sepharose; -RNase or + RNase, HeLa extracts were incubated without (−) or with (+) RNase A prior to IP. Raw data were filtered (see Materials and Methods section) and the final list was compared to 244 spliceosomal proteins annotated in Supplementary TableS1of Hegele et al.(49).1Proteinnamecommonlyused in the splicing field.Proteins shown in bold are known SF1 partners; underlined, proteins also found in Y2H screens (Table3); *, proteins with SURP domains. 2 NCBI ENTREZ symbol.3NCBIENTREZ GeneID.

Table 2 .
Libraries used in Y2H screens