Abstract
Translation is tightly regulated in cells for keeping adequate protein levels, this task being notably accomplished by dedicated mRNA-binding proteins recognizing a specific set of mRNAs to repress or facilitate their translation. To select specific mRNAs, mRNA-binding proteins can strongly bind to specific mRNA sequences/structures. However, many mRNA-binding proteins rather display a weak specificity to short and redundant sequences. Here we examined an alternative mechanism by which mRNA-binding proteins could inhibit the translation of specific mRNAs, using YB-1, a major translation regulator, as a case study. Based on a cooperative binding, YB-1 forms stable homo-multimers on some mRNAs while avoiding other mRNAs. Via such inhomogeneous distribution, YB-1 can selectively inhibit translation of mRNAs on which it has formed stable multimers. This novel mechanistic view on mRNA selection may be shared by other proteins considering the elevated occurrence of multimerization among mRNA-binding proteins. Interestingly, we also demonstrate how, by using the same mechanism, YB-1 can form multimers on specific DNA structures, which could provide novel insights into YB-1 nuclear functions in DNA repair and multi-drug resistance.
INTRODUCTION
YB-1 was first described as an mRNA-binding protein expressed in all mammalian tissues to regulate translation (1–3). The functions of YB-1 in translation are most probably essential for mammalian development as YB-1 deficiency in mouse results in prenatal death (4). In the cytoplasm, YB-1 interacts directly and strongly with mRNA (KD∼nM, (5,6)) via its single cold-shock domain which possesses two highly conserved RNA recognition motifs (7), RNP-1 and RNP-2, and its unstructured and positively-charged C-terminal tail (8,9). As shown by atomic force microscopy, YB-1 can form multimers in the presence of mRNA and force mRNPs to adopt a beads-on-a-string structure (10). When YB-1 interacts with mRNA close to saturation, the resulting mRNP particles cannot be translated in cell free systems while, well below saturation, YB-1 favors translation (11,12). In line with its role as translation repressor, sucrose gradient analyses of various cell extracts have shown that YB-1 is mostly present in the non-polysomal fraction containing free mRNPs (13). For these reasons, YB-1 is considered as a major component of free mRNPs in the cytoplasm.
However, how YB-1 can exert its function in translation repression while a large amount of YB-1 (about 30 nucleotides per YB-1) is required to stop translation (9,14) remains an unanswered question. Rather than being homogenously distributed among mRNAs, a strong bias for the YB-1 binding to mRNAs may allow its accumulation on specific mRNA transcripts in order to prevent their translation. In line with such biased binding, it has been found that YB-1 orchestrates a selective translational repression in cells (13,15) like that of its own mRNA (16). Despite such YB-1-consuming mechanism, YB-1 can still target a significant number of transcripts in cells. For example, in mouse fibroblasts, about 2 × 106 copies of YB-1 were detected using SILAC technology (17). Therefore, assuming an average mRNA length of 2 × 103 nucleotides (18) and without taking into account the binding of YB-1 to others RNA than mRNA, the amount of YB-1 could be sufficient to repress the translation of at most 3–4 × 104 mRNA molecules. Even overestimated, the YB-1-repressed mRNAs may thus represent a non-negligible fraction of mRNPs if we consider that about 30% of the 2 × 105 mRNAs present in the cytoplasm are in their non-polysomal state, as measured in yeast (19). The preference of YB-1 for A/C-rich hexa/hepta nucleotides (16,20) or other mRNA sequences/structures (21–23) may provide the basis for the selective binding of YB-1 to mRNA. Upon binding to mRNAs containing specific sites, YB-1 could then accumulate on these mRNAs via a cooperative binding. This model thus provides a rational explanation for both YB-1-mediated repression of a specific set of mRNAs and the large amount of this protein per mRNA required to stop translation. In the present work, we explored whether there is a mechanistic model to support such hypothesis.
Another issue addressed in this study is the interaction of YB-1 with DNA as YB-1 is known as a DNA/RNA binding protein (24). Some reports have indeed revealed the translocation of YB-1 to the nucleus and have proposed putative nuclear functions for this protein (25). The nuclear translocation of YB-1 is observed following treatment with some anti-cancer drugs like cisplatin (26), possibly after the cleavage by the proteasome in its C-terminal domain (27) but other mechanisms have also been proposed (28). In the nucleus, YB-1 is present in pre-splicesomes and could participate in exon skipping (29) and regulate RNA splicing (20). In addition, YB-1 may also interact with the promoter regions of genes involved in DNA repair such as topoisomerase IIα (30) to regulate their transcription (31), a function more and more challenged due to the rather unspecific binding of YB-1 to DNA (32,33). The translocation of YB-1 to the nucleus also correlates with multidrug resistance (MDR) (25), which has attracted much interest (34,35) and revealed YB-1 as an important factor for DNA repair (36,37). However, despite its preferential binding to mismatches or damaged DNA (36), the interaction of YB-1 with dsDNA is weak (KD∼μM, (38,39)). We may then wonder whether YB-1 can compete with other DNA-binding proteins in the nucleus (40). As explored here, a possible mean for YB-1 to gain access to DNA is not to act as an isolated protein but rather as a multimer in order to effectively compete in the cellular context with other DNA-binding proteins despite its weak affinity to DNA as an isolated protein.
Using an original approach based on single molecule data extracted from atomic force microscopy images (41), we analyzed the relative role of the cold-shock domain and the unstructured C-terminal tail of YB-1 on its interaction with long mRNA and DNA molecules at a nanometric scale. These data combined with other obtained using classical techniques like gel mobility shift assay provide a novel mechanistic view on how YB-1 interacts with both mRNA and DNA. The interest of this approach lies in considering the role of YB-1 multimerization, which could not have been grasped by using short DNA and RNA nucleotides. We then took advantage of our findings to address the concerns raised regarding the selective translational repression mediated by YB-1 and its significant binding to dsDNA structures. We finally discuss the interests of this model to the more general issue of the translation regulation operated by mRNA-binding proteins. In addition, the results provide further insights into the putative role of YB-1 in DNA repair as we discovered its selective targeting of DNA crosses.
MATERIALS AND METHODS
Preparation of recombinant proteins
Recombinant YB-1 constructs were expressed in E. coli BL21 strain and proteins were purified as described (42,43). Briefly, YB-1 was synthesized in E. coli from the pET-3–1-YB-1 plasmid and purified by Heparin-Sepharose, MonoS and Superose 12 (GE Healthcare) chromatography. Fractions containing pure YB-1 were concentrated and dialyzed against 20 mM Hepes-KOH [pH 7.4], 0.5 M KCl. The pET-3–1-YB-1-tr plasmid was provided by Dr. Alexey Sorokin. YB-1-tr was purified the same way as YB-1 except that it was dialyzed against 20 mM Hepes-KOH [pH 7.4], 0.15 M KCl. Plasmids encoding AP-CSD, CSD (Cold-shock domain) and CTD (C-terminal domain) were provided by Dr. Sergey Guryanov. AP-CSD and CSD were isolated by ammonium sulfate fractionation and chromatography using SP-Sepharose, Phenyl-Sepharose and MonoS columns (GE Healthcare). AP-CSD and CSD were stored in 20 mM Hepes-KOH [pH 7.4], 0.2 M KCl or 50 mM potassium phosphate [pH 7.4], respectively. CTD was purified using TALON Metal Affinity Resin (Clontech) and Heparin-Sepharose chromatography. After, CTD was concentrated and dialyzed against 20 mM Hepes-KOH [pH 7.4], 0.5 M KCl. To construct plasmids for CTD1 and CTD2, the corresponding DNA fragments were PCR-amplified and inserted into the pET-22b plasmid. CTD1 and CTD2 were synthesized in E.coli and isolated by ammonium sulfate fractionation and chromatography using SP-Sepharose and Superose 12 columns. CTD1 and CTD2 were stored in 20 mM Hepes-KOH [pH 7.4], 0.5 M and 0.15 M KCl, respectively. The DNA fragment corresponding to the mutated YB-1 with two amino acids substitutions in CSD (Y72A F74A) was cloned into pET22b plasmid and purified by the same way as wild type YB-1. Concentrations were estimated from 280 nm absorbance using calculated extinction coefficients (ProtParam tool, http://expasy.org/tools/protparam.html). The OD280/OD260 ratios were ∼2, thus showing the absence of nucleic acids from the protein samples. Human recombinant G3BP was purchased from Novus Biological. Human PARP1 was a gift from Dr. Maria Sukhanova. The integrity of the recombinant proteins was tested after migration in a denaturating gel (Supplementary S1).
In vitro transcription and capping
Linearized plasmids, pT3Luc, pSP72–2Luc and pcDNA3-HA-YB-1 (provided by Dr. Dmitry Lyabin) were used as templates for RNA synthesis by T7 polymerase of Luc (∼1500 nt), 2Luc (∼3000 nt) and YB-1 mRNA (∼1500 nt), respectively. In vitro Transcription was performed by HiScribe T7 High Yield RNA Synthesis Kit (NEB). Short 91 nt RNA was synthesized by the same way using linearized plasmid pBluesript II SK encoding region (from 1339 nt to 1430 nt) of 3′UTR YB-1 mRNA (provided by Alexander Doronin). In order to obtain fluorescent mRNAs, linearized plasmids pcDNA3-HA-YB-1 and pSP72–2Luc were used as templates for RNA synthesis by T7 polymerase (NEB). The transcription mixture was supplemented with fluorescent nucleotides, Atto680-UTP (for 2Luc and Luc mRNAs) or DY776-UTP (for HA-YB-1 mRNA) (Jena Bioscience). Synthesized RNAs were purified using phenol extraction. mRNAs were capped using Vaccinia Capping System according to the manufacturer's recommendations (NEB).
Gel mobility shift assays
Indicated amounts of YB-1, its fragments and G3BP were incubated with 0.25 pmol of 2Luc mRNA, 0.5 pmol of Luc and YB-1mRNA, 7.5 pmol of 91 nt RNA or 70 fmol of pBR322 (NEB) in 10 μl of binding buffer (20 mM Hepes [pH 7.6], 50 mM KCl, 4 mM MgCl2) at 37°C for 10 min. Complexes were separated in 0.75% (2Luc, Luc, YB-1 mRNAs) or in 1.5% agarose gel (91 nt RNA) in 1X TBE buffer for gel shift with RNA and in 1% agarose gel in 1X TAE buffer for gel shift with DNA at room temperature at 25 V for 1 h and were stained with 0.5 μg/mLl EtBr or alternatively using Odyssey Visualizing System (Li-COR) when fluorescent RNAs were used.
Cross-linking assays
5 μg of YB-1 or its fragments were incubated in the 10 μl of buffer (20 mM Hepes-NaOH [pH 7.6], 50 mM NaCl, 0.5 mM PMSF) containing 0.1% glutaraldehyde for 10 min at room temperature. The reaction was stopped by the addition of 1 μl of 1M Tris-HCl [pH 7.9], and 4 μl of 4X SDS-PAGE sample buffer, and incubation at 95°C for 5 min. Cross-linked proteins were separated by 12% SDS-PAGE and visualized by Coomassie-blue staining.
Cell culture and transfection
NRK-52E cells (ATCC, Manassas, VA, USA) are rat kidney epithelial cells originating from proximal tubules. They were cultured in Dulbecco's modified Eagle's medium (DMEM) supplemented with 5% (v/v) fetal bovine serum (FBS), 2 mM L-glutamine and 1% antibiotics (penicillin and streptomycin) in a humidified 5% CO2 atmosphere at 37°C. Transient transfection of plasmid DNA was performed using Lipofectamine™ 2000 (Invitrogen). The cDNAs encoding the full-length YB-1, YB-1-tr, CSD, CTD, CTD1 and CTD2 were cloned into the XhoI and BamHI sites of the pEGFP-C3 vector (Clontech). The cDNA encoding G3BP was cloned into HindIII and BamHI of the pMRFP-C1 vector (gift from Cecile Gauthier). After transfection, cells were fixed with 4% PFA, 150 mM sucrose in PBS for 20 min at 37°C. For in situ hybridization, cell were fixed with 4% PFA (in PBS-sucrose) for 30 min at 37°C, incubated with 100% ice-cold methanol for 10 min at -20°C, in ice-cold 70% ethanol for 10 min at -20°C and then in 1 M Tris (pH = 8) for 5 min. We then added the Cy3-conjugated oligonucleotides (Ploy (T) of 40 nucleotides, Sigma) in the hybridization buffer (0.005% BSA, 1 mg/ml yeast RNA, 10% dextran sulphate, 25% formamide in 2X SSC) at 1 μg/μl. Slides were then placed in a humidity chamber for 1 h at 37°C and shacked. Following hybridization, cells were washed once with 4X SSC and once with 2X SSC. NRK cells were also labeled with anti-YB-1 antibody to detect stress granules.
Atomic Force microscopy
Ten microliters of each sample were deposited on freshly cleaved mica and dried with a filter paper for AFM imaging. The electrostatic adsorption of both protein:mRNA or protein:DNA complexes on mica was mediated by divalent magnesium cations which are present in the binding buffer (20 mM Hepes [pH 7.6], 50 mM KCl, 4 mM MgCl2). All AFM experiments were performed in intermittent contact mode with a multimode AFM instrument (Digital Instruments, Veeco, Santa Barbara, CA, USA) operating with a Nanoscope IIIa controller. We used AC160TS silicon cantilevers (Olympus, Hamburg, Germany) with resonance frequencies of around 300 kHz. The applied force was minimized as much as possible. Images were collected at a scan frequency of 1.5 Hz and a resolution of 512 × 512 pixels. The scan frequency was typically 1 Hz per line, and the modulation amplitude was of about a few nanometers. Statistical analyses were performed using the nanoScope analysis software.
Topoisomerase assay
Cell extracts with topoisomerase activity were purified as described before with minor modifications (44). Briefly, NRK cells were harvested with PBS-EDTA, washed twice with PBS and resuspended in low-salt buffer (20 mM Tris-HCl [pH 7.6], 5 mM KCl, 1 mM MgCl2, 10% Glycerol, 1 mM DTT, 1 mM PMSF). After 10 min incubation on ice, the plasma membrane was disrupted by Dounce homogenizer (narrow pestle) and intact nuclei were collected by centrifugation for 3 min at 15 000 × g. After nuclei were resuspended in high-salt buffer (law-salt buffer containing 0.5 M KCl), incubated for 80 min on ice and centrifuged for 10 min at 25 000 × g. Supernatant was tested for topoisomerase activity and was used in further experiments. Kinetoplast DNA was purchased from Topogen. Standart decatenation reactions (20 μl) contained 300 ng kDNA and in freshly prepared reaction buffer (20 mM Tris-HCl [pH 7.6], 50 mM KCl, 10 mM MgCl2, 1 mM ATP, 1 mM EDTA, 1 mM DTT and 30 μg/ml BSA). Reactions were stopped after 30 min by the addition of 5 μl of stop buffer (30% glycerol, 0.5% bromophenol blue and 1% SDS) and resolved on 0.8% agarose gel with 0.5 μg/ml EtBr.
Purification of proteins bound to poly (A) mRNAs
NRK cells were transfected with the pEGFP-C3 plasmid either empty or encoding different fragments of YB-1 (full-length YB-1, YB-1-tr, AP-CSD and CTD) using LipofectamineTM 2000. Twenty four hours after transfection, cells were washed twice with 1X PBS and scraped in the lysis buffer (Tris-HCL 20 mM, pH = 8.0, NaCl 150 mM, Triton X100 1% and complete protease inhibitor (Roche). Then, cells were centrifuged for 20 min 16 000 × g at 4°C and pellets were discarded. Supernatants were mixed with Oligo d (T)25 Magnetic Beads (NEB) in the lysis buffer and incubated overnight at 4°C. Finally, beads were three times washed with lysis buffer and mRNAs and proteins bound to them were eluted using 1.5X Laemli buffer. Fragments of YB-1 bound to poly (A) mRNAs were detected by western blotting using specific antibodies anti-GFP (Cell Signaling).
In vitro translation assays
Translation occurs in an incubation mixture (30 μl) containing 20 μl of nuclease-treated rabbit reticulocyte lysate (Promega), amino acids (20 μM) and mRNA as indicated in figure legends. Translation was performed at 30°C for the indicated amount of time. New synthetized proteins were visualized by western-blotting using specific antibodies (anti-luciferase, anti-HA).
RESULTS
The C-terminal tail of YB-1 is mostly responsible for the binding of YB-1 to mRNA in vitro and in cells while the cold-shock domain, by itself, does not significantly bind to mRNA
We first examined at the single molecule level by atomic force microscopy (AFM) the roles of two YB-1 domains on its binding to mRNA: (i) the cold-shock domain of YB-1 which has a β-barrel structure and contains two RNA-binding motifs (7); (ii) the unstructured C-terminal domain of YB-1 which is highly positively charged and thus binds to mRNA. Besides, it may also participate to YB-1 multimerization via the presence of alternate clusters of positive/negative residues (2,45). The alanine/proline rich domain (AP) located at the N-terminus of YB-1, which is not involved in the interaction of YB-1 with RNA (2) but rather with protein partners, is not further considered in this study. Surprisingly, albeit being the most studied, the role of the cold-shock domain in the binding of YB-1 to RNA remains elusive. Indeed, the cold-shock domain alone has a low affinity to mRNA (46) in vitro and, in contrast with the Unr protein which displays five cold-shock domains (47), a single cold-shock domain may hardly compete with other mRNA-binding proteins to gain access to mRNA. As previously reported (9), this is rather the highly positively charged C-terminal domain which binds strongly to mRNA via electrostatic interactions.
In order to reveal the respective roles of the CSDs and CTDs, we analyzed the binding to mRNA of several YB-1-derived constructs (Figure 1A): YB-1, full length; YB-1-tr, a truncated form comprising the first 219 amino acid residues which mimics the cleaved form of YB-1 by the 20S proteasome after stress (27); CSD, the cold-shock domain, or AP-CSD (AP+CSD domains), both giving the same results regarding their interaction with mRNA; CTD, the entire C-terminal domain; CTD1 and CTD2, two halves of the C-terminal domain which are separated following the 20S proteasome cleavage. So far, only the structure of full length YB-1:mRNA complexes was analyzed by AFM (10). For this analysis, we used a synthetic 2Luc mRNA of about 3000 nucleotides, which allows a better visualization of the YB-1:mRNA structure than shorter mRNA. A single YB-1 binds to about 30 ribonucleotides. At saturating YB-1 concentration (YB-1/2Luc mRNA molar ratio of 150), isolated mRNPs with typical beads-on-a-string structure were clearly detected by AFM (Figure 1B and C), in line with a previous report (10). A similar pattern was also observed for YB-1-tr after its interaction with mRNA. At the same molar ratio, the binding of CTD, CTD1 and CTD2 with mRNA could be also detected but, interestingly, CTD, CTD1 and CTD2 alone cannot induce the formation of beads-on-a-string structures. In contrast with the other constructs, the binding of CSD to mRNA was not detected by AFM under such conditions, which should be due to its weak affinity to mRNA.
We then explored whether the interactions of the various YB-1 constructs with mRNA detected in vitro by AFM are relevant in a cellular context using NRK cells transfected with plasmids encoding for the YB-1 constructs fused to a N-terminal GFP tag. To that end, we used oligo(dT)25 magnetic beads to isolate, from NRK cell extracts, poly (A) mRNA along with mRNA-binding proteins and other proteins indirectly interacting with mRNA (Figure 2A (48)). The results clearly indicate that GFP-YB-1, GFP-YB-1-tr and GFP-CTD probably interact with mRNA. In contrast, GFP-AP-CSD was not detected in the pull down fraction.
To further probe the affinity of YB-1 for mRNA but without disrupting the cell membrane, we took advantage of the spatial enrichment of mRNA in stress granules (49,50). Stress granules are non-polysomal mRNA-containing aggregates of micrometric size that appear in the cytoplasm of mammalian cells, either upon acute stress conditions (51) or after the expression of pro-aggregating RNA-binding proteins like TIA-1 or G3BP (52). The presence of YB-1 in stress granules can either be due to its binding to mRNA, owing to its high affinity for mRNA, or to its binding to other proteins found in stress granules, which cannot be excluded. In NRK cells expressing RFP-G3BP, we found that GFP-YB-1, GFP-YB-1-tr and GFP-CTD significantly accumulate in stress granules compared to GFP alone (Figure 2B and C). On the other hand, GFP-CSD was not found enriched in stress granules, its spatial distribution being similar to that of GFP alone. The affinity of CSD for mRNA is probably not sufficient to allow its accumulation in stress granules.
Due to the low affinity of CSD for mRNA, we then considered an alternative role for CSD and our attention turned to a putative role in a cooperative binding to mRNA since, in bacterial cold-shock proteins, the cooperative binding to RNA has been reported (53,54).
The cold-shock domain of YB-1 is critical for the cooperative binding of YB-1 to mRNA
To capture a putative cooperative binding of YB-1 to mRNA, we analyzed its interaction with 2Luc mRNA at the single molecule level by AFM and at a YB-1 concentration well below the saturation level (YB-1:2Luc mRNA molar ratio equals to 25). This method was previously developed to detect the cooperative binding of ssDNA-binding proteins to ssDNA (41). We rapidly noticed a striking inhomogeneous repartition of YB-1 among mRNA molecules (Figure 3A). Some mRNA formed typical beads-on-a-string structure as observed at saturating YB-1 concentration, while others mRNA appeared as free or in complex with few YB-1 molecules (Figure 3B). A cooperative binding of YB-1 to mRNA was also detected by AFM for YB-1-tr but not for CTD. Interestingly, the cooperative behavior observed for YB-1 is not shared by another mRNA-binding protein, G3BP, used as control (Figure 3A and B).
To ensure that the cooperative binding of YB-1 really takes place in the bulk solution and not only on the mica surface used for AFM, we analyzed its binding to mRNA by gel mobility shift assay (Figure 3C). At YB-1 concentrations below saturation, we noticed the appearance of two distinct bands in the gel which should result from the coexistence of saturated YB-1:mRNA complexes and of free or unsaturated mRNA, a typical feature of cooperative behavior. As known for proteins that bind to single-stranded DNA cooperatively (41), increasing the ionic strength reduces the cooperative binding of YB-1 to mRNA (Figure S2A). In contrast with YB-1, even at moderate ionic strength, G3BP binds to mRNA in a non-cooperative manner as indicated by the single migration band of the G3BP:mRNA complex and the progressive reduction of its electrophoretic mobility with increasing concentration of G3BP. Crosslinking experiments further indicate that mRNA serves as a scaffold for the multimerization of YB-1 and demonstrate YB-1 multimerization on mRNA via direct YB-1:YB-1 interactions (Figure S2B).
As both YB-1 and YB-1-tr bind to mRNA cooperatively, two domains, CSD and CTD1, may be involved in the molecular mechanism leading to cooperativity. CTD1 contains two clusters of positive charges (+ 6 e− for 11 residues and +10 e− for 20 residues) and one cluster of negative charges of low charge density (- 4 e− for 14 residues, see Figure S3). The many positive charges of CTD1 can hardly lead to an electrostatic self-attraction of CTD1 but rather to a strong self-repulsion. In line with this, CTD alone fails to display a cooperative binding to mRNA (Figure 3C). Albeit we cannot exclude the participation of CTD1, CSD probably play a central role in this cooperative binding process because both bacterial and mammalian CSD domains bind to RNA cooperatively (53–55). To explore this hypothesis, we analyzed protein multimerization in the absence of RNA after glutaraldehyde exposure and found a significant crosslinking between CSD but not between CTD molecules (Figure S4A) and obtained similar results by AFM (Figure S4B). The positive charges of YB-1 and YB-1-tr located in CTD and CTD1, respectively, most probably hinder multimerization owing to an electrostatic repulsion. Along with this, in 2M LiCl, YB-1 can form long fibrils and it was proposed that CSD plays a key role in the genesis of such fibrils (42).
To further examine the role of CSD in the cooperative binding of YB-1 to mRNA, we generated two point mutations on residues implicated in the binding of CSD to RNA (Y72A/F74A, (56)) and analyzed the binding of the double YB-1 mutant to mRNA by using gel mobility shift assays (Figure 3D). In contrast to YB-1, we observed a single migration band which indicates that the binding of the mutant protein to mRNA is still effective but no longer cooperative. In addition, high resolution imaging by AFM reveals the disappearance of the beads-on-a-string structures typical of saturated YB-1:mRNA complexes, which adds credits to the role of CSD in the cooperative binding of YB-1.
Interestingly, the cooperative binding of YB-1 evidenced for long mRNA was not observed for short 91 nt RNA (Figure 3C). YB-1 protein reduces the mobility of the short RNA via discrete steps typical of a non-cooperative behavior. As for many polymerization processes, a nucleus of critical size needs to be form prior to elongation. The two or three YB-1 which can bind to 91 nt RNA may not be sufficient to form a stable nucleus. This result demonstrates that long RNA should be used to probe the cooperative binding of YB-1 to mRNA.
In summary, we propose that CTD mostly participates in the binding of YB-1 to mRNA through its clusters of positive charges. When YB-1 is bound to mRNA, most of the CTD positive charges are neutralized by the negative charges of mRNA, which prevents the electrostatic self-repulsion of YB-1. The YB-1 self-attraction can then trigger the cooperative binding of YB-1 on mRNA via the CSD.
The cooperative binding of YB-1 to mRNA can take place in the presence of protein competitors
At the light of these results, we asked the question as to whether the cooperative binding of YB-1 to mRNA occurs in the presence of competitors present in the cytoplasm. Indeed many other mRNA-binding proteins may compete with YB-1 for the binding to mRNA and may thus hinder the proposed mechanism of cooperative binding. To examine this point, we chose G3BP for the following reasons: (i) G3BP is a cytoplasmic mRNA-binding protein like YB-1 (52); (ii) Our data show that G3BP binds to mRNA in a non-cooperative manner, in contrast with YB-1 (Figure 3C). We therefore analyzed the binding of YB-1 to preformed G3BP:mRNA complexes by gel mobility shift assay and observed the appearance of two bands in the presence of YB-1 below saturating concentration (Figure 4A). The presence of two bands indicates that YB-1 may bind to mRNA cooperatively even in the presence of G3BP. To ascertain this result, we performed a statistical analysis of the AFM data at the single molecule level under similar conditions. The saturated YB-1:mRNA complexes can be easily distinguished owing to their height larger than that of G3BP:mRNA complexes. Our measurements then reveal the presence of two different populations in the presence of YB-1 below saturating concentration which is typical of the cooperative binding of YB-1 to mRNA (Figure 4B and S5). The presence of G3BP is therefore not an obstacle for the cooperative binding of YB-1 to mRNA. A mechanism to account for this result is advanced in the discussion.
Saturated YB-1:mRNA complexes are stable when mixed with free mRNA which provides a basis for a selective translational repression
To decipher whether YB-1 can target specific mRNAs and thus selectively repress their translation, YB-1 was added to an equimolar mixture of two fluorescent mRNAs, YB-1 and 2Luc mRNAs, which are considered as specific and non-specific YB-1 targets, respectively (16). However, by gel mobility shift assays, we failed to evidence a preferential binding of YB-1 to its own mRNA (Figure 4C). In vitro, the use of long and naked mRNA with many non-specific nucleotide sequences may hinder the selective binding of YB-1 to specific RNA sequences. Other protein factors may also come into play to orient YB-1 multimerization on specific mRNAs.
To document whether YB-1 multimerization on specific mRNAs can provide a basis for mRNA selection, we designed a dedicated protocol. One of the two mRNAs, either 2Luc or YB-1 mRNA, was allowed to interact with YB-1 in a pre-incubation step before mixing the two mRNAs together for 15 min. As observed by gel mobility shift assays (Figure 4C), YB-1 forms saturated complexes exclusively with the mRNA that has been pre-incubated with it whatever it is YB-1 or 2Luc mRNA. On the other hand, when YB-1 was replaced by CTD, which does not bind to RNA cooperatively, we rather observed a homogenous and gradual reduction of the electrophoretic mobility for the two mRNAs despite the pre-incubation step. These results indicate that the YB-1 molecules are hardly released from mRNA once saturated YB-1:mRNA complexes have been formed. The energy benefit due to the cooperative binding of YB-1 to mRNA is probably an obstacle to the release of YB-1 from mRNA.
These results prompted us to further explore whether a selective multimerization of YB-1 on mRNAs can indeed lead to a preferential translation repression in vitro in rabbit reticulocyte system. As previously described, YB-1 inhibits translation in vitro at the initiation step and the CTD alone is sufficient to inhibit translation (9). After pre-incubating YB-1 with Luc or YB-1 mRNA, the two mRNAs were mixed together before being added to rabbit reticulocyte lysate for translation (Figure 4D). We clearly noticed a selective translational repression of the mRNA that has been pre-incubated with YB-1, whatever it is Luc or YB-1 mRNA. As a control, a selective translational repression was not observed in the absence of the pre-incubation step (Figure S6A). Furthermore, even with a similar pre-incubation step, the translation inhibition mediated by CTD is non-selective (Figure 4D). Altogether, these results indicate that the cooperative binding of YB-1 to mRNAs leads to the coexistence of untranslatable mRNAs, which have formed saturated and stable mRNA-YB-1 complexes, and translatable mRNAs, which are free or in complex with few YB-1. The cooperative binding of YB-1 to mRNA could thus provide a basis for a selective translational repression.
YB-1 binds preferentially to supercoiled DNA at DNA crosses
YB-1 is a dual RNA/DNA-binding protein. However, so far, no information about the structure of DNA:YB-1 complexes at the molecular level has been reported. As expected (38,39), we found that YB-1 binds to DNA with a low affinity compared to mRNA since no interaction with DNA was detected by AFM at YB-1 concentrations previously used to probe mRNA:YB-1 interactions (50 nM). We therefore used a higher YB-1 concentration (500 nM) to examine its interaction with DNA and probed the presence of YB-1 on both relaxed and supercoiled DNA. The point is to observe whether the affinity of YB-1 to DNA was regulated by the DNA topology. DNA topology should be considered while investigating DNA:protein interaction because of its critical impact on DNA recognition and processing in cells. Interestingly, we found that YB-1 binds much more efficiently to supercoiled than to relaxed DNA as shown by AFM (Figure 5A). In addition, we observed that YB-1 forms multimers along supercoiled DNA which are mostly, if not exclusively, located at DNA crosses. We also examined the selective binding of YB-1 and YB-1-tr to DNA using a mixture of linear and supercoiled DNA and compared the results with those obtained with G3BP used as control mRNA-binding protein. The results were striking: YB-1 multimers were barely detected on linear DNA but most often on supercoiled DNA, which confirms a selective YB-1 multimerization based on nucleation at DNA crosses (Figure 5B and S7). YB-1-tr displays the same selectivity toward DNA crosses as YB-1, as expected owing to its preserved cooperative binding. On the other hand, no significant binding or multimerization of G3BP on supercoiled DNA was observed.
The selective binding of YB-1 to supercoiled DNA was further demonstrated in a competitive gel mobility shift assay performed in the simultaneous presence of nicked and supercoiled DNA. Indeed, we clearly observed the disappearance of the band related to free supercoiled DNA while, at the same YB-1 concentrations, the intensity of the band corresponding to free nicked plasmid remained unchanged (Figure 5B). To further address the possible multimerization of YB-1 at DNA crosses, we finally performed crosslinking experiments which show that YB-1 indeed forms multimers on supercoiled DNA via direct YB-1:YB-1 interactions since they are resistant to DNAse once formed (Figure S2B).
To decipher which domains of YB-1 is responsible for its binding to DNA crosses and for the ensuing YB-1 multimerization, we probed the affinity of different YB-1 constructs to supercoiled DNA by AFM and gel mobility shift assay. YB-1-tr is of special interest because it mimics a possible YB-1 cleavage by the 20S proteasome which induces its nuclear translocation, as observed in transfected NRK cells (Figure 5C). CTD, CTD1 and CTD2 were also partially located in the nucleus, which is probably due their positive charges. The AFM results show that YB-1-tr can form multimers on supercoiled DNA, which are especially located at DNA crosses (Figure 5D), as in the case of full length YB-1. In addition, we detected a significant electrophoretic shift of the migration band corresponding to supercoiled DNA in the presence of YB-1-tr (Figure 5E). In contrast, the interaction of CSD with supercoiled DNA was not detected by AFM or gel mobility shift assay, in agreement with its weak affinity for DNA (7). In the presence of CTD, we detected the presence of large DNA aggregates by AFM, which is probably due to an electrostatic mechanism by considering its clusters of positive charges (Figure S3). Most probably for a similar reason, DNA aggregation could also occur in the presence of CTD1, as observed by gel mobility shift assay (Figure 5E). At CTD1 concentration sufficiently low to prevent DNA aggregation, no multimeric structure was detected on supercoiled DNA by AFM. CTD2, which is globally less charged than CTD1, does not form DNA aggregates. We noticed that CTD2 tends to localize at DNA crosses and also prefers to bind to supercoiled rather than relaxed DNA (Figure S8A), which may be attributed to the electrostatic benefit provided by forming salt bridge at the interface between two crossing DNA helices. On the other hand, in the presence of CTD2, we failed to detect long-ranged multimerization starting from DNA crosses by AFM. In line with this, the migration shift of the supercoiled DNA band is weak and displays little smear with CTD2 compared to what is observed for YB-1-tr or YB-1 (Figure 5E).
In summary only YB-1 and YB-1-tr have the capacity to multimerize at DNA crosses most probably because of the CSD self-attraction. The CTD positive charges preferentially localize at the interface between two crossing DNA helices to form a ‘salt bridge’ and this probably participates to the higher affinity of YB-1 for crosses.
YB-1 multimerization at DNA crosses leads to the self-alignment of the two facing DNA
As DNA crosses appear as preferred sites for the binding of YB-1, we explored whether YB-1 may lead to a higher-order assembly of DNA via its multimerization in between two DNA helices. We indeed noticed in AFM images a forced alignment of two interacting DNA helices in the presence of YB-1 multimers (Figure 6A). In addition, we measured by AFM that YB-1 multimers are not homogenously distributed along DNA and tend to be closer to each other than expected from random positioning (Figure 6B). When the YB-1 multimers are close to each other along supercoiled DNA, DNA helices are forced to adopt a parallel trajectory, which increases the occurrence of forming novel YB-1 multimers. In line with this, two parallel supercoiled DNA can be also associated into a single large filament thus indicating the YB-1 multimers can bridge two DNA helices from two different DNA molecules (Figure 6C).
To further ascertain that YB-1 multimerization takes place at the interface between two DNA helices and forces them to adopt a parallel trajectory, we examined the consequences of YB-1 multimerization on the high-order assembly of linear DNA, which has no topological constraint imposed by supercoiling and thus can theoretically be perfectly aligned through YB-1 multimerization. In the presence of YB-1 at high concentration (1 μM) to compensate for the lower affinity of YB-1 to linear than supercoiled DNA, we observed the presence of YB-1 multimers in structures that appear circular and in which many linear DNA tend to adopt a parallel trajectory (Figure 6D). We also noticed the scarce presence of YB-1 multimers on isolated DNA in contrast to its high concentration in multimolecular DNA structures. An inhomogeneous distribution of YB-1 on DNA further evidences the cooperative binding of YB-1 to nucleic acids either RNA or DNA. Interestingly, the circular structure made of many linear DNA molecules can also be compacted into regular toroids via YB-1 multimerization (Figure 6D).
In summary, YB-1 displays a striking affinity at the interface between two DNA crosses which serves as seeds for the cooperative binding and multimerization of YB-1 between two DNA helices.
YB-1 blocks topoisomerase II activity from NRK cell extracts
The specific targeting of YB-1 to DNA crosses prompted us to investigate the interference of YB-1 with topoisomerase II. To that end, we used kinetoplast (kDNA) which is a network of many circular DNAs. Topoisomerase II, but not topoisomerase I, has the ability to release circular DNAs from this network in a process called decatenation. We thus analyzed the conversion rate of kDNA into decatenated DNA circles mediated by topoisomerase II (Figure 7A). The results indicate that YB-1 significantly decreases the topoisomerase II activity from nuclear NRK cell extracts. In contrast, G3BP, used as control, does not prevent the topoisomerase II activity (Figure 7B). To further probe the relevance of the inhibition of the topoisomerase activity by YB-1, we used PARP-1, a DNA-binding protein which also displays a higher affinity for DNA crosses (57). We found that, in contrast with YB-1, PARP-1 is not an obstacle for the decatenation of kinetoplast DNA. As previously reported, PARP-1 may inhibit the topoisomerase activity but only when activated in the presence of NAD+ to produce Poly (ADP-ribose) (58). In the case of YB-1, its multimerization at DNA crosses could be an efficient mechanism to prevent the binding of topoisomerase II. In agreement with this, YB-1 does form multimers at crosses between catenated DNA circles, as revealed by AFM (Figure 7C). This result indicates that YB-1 and topoisomerase II may compete for the binding to DNA crosses. In addition, YB-1 does not progressively reduce topoisomerase activity but does it rather abruptly above a critical concentration of YB-1, which may reflect the multimerization of YB-1 above a threshold concentration.
DISCUSSION
Protein multimerization as a novel mechanism for selective translational regulation
Many mRNA-binding proteins display a weak specificity toward short and redundant RNA sequences/structures, in vitro, while having for many of them a significant selectivity toward specific mRNA in the cellular context (59). RNA selection by dedicated proteins is therefore the focus of ongoing investigations and, except for some RNA-binding proteins displaying a strong affinity for specific sequences (60), the molecular mechanisms at the heart of such selective binding remain elusive (22,61,62). In addition, as recently shown with the RNA-binding protein C5 (61), the selectivity is not necessarily driven by a strong affinity and case-by-case studies may be the key to unravel the probable various mechanisms adopted by RNA-binding proteins for an efficient selectivity. In light of the present results, we advance a novel mechanism leading to selectivity among transcripts using YB-1 as a model: a preferential protein multimerization based on a cooperative binding to mRNA (Figure 8A). YB-1 is a possible protein candidate to test this model because it possesses some critical characteristics for an efficient multimerization on mRNA. The cold-shock domain of YB-1 has a low affinity for RNA and can form multimers in solution (Figure 2 and S4). In the absence of RNA, the highly positively charged C-terminus of YB-1 is an obstacle to YB-1 multimerization via its cold-shock domain (Figure S4). However, when bound to negatively-charged mRNA, the electrostatic repulsion due the C-terminus of YB-1 is no longer effective, which enables YB-1 multimerization on mRNA (Figure S2B). In agreement with this, the experimental results indicate that the cold-shock domain plays a critical role for the cooperative binding of YB-1 to mRNA and the ensuing YB-1 multimerization (Figures 2, 3 and S2B).
If we assume that the residence time of YB-1 on specific RNA sites is longer than average, the chance to attract other YB-1 molecules via YB-1 self-attraction increases accordingly. Once YB-1 multimerization starts, the energy benefit in attracting others YB-1 molecules significantly increases because there are many YB-1 molecules on mRNA to interact with them. Owing to the energy benefit of YB-1 multimerization, a permanent regime may be reached where some mRNAs, which have preferential nucleation sites, form saturated YB-1:mRNA complexes while YB-1 is apparently kept at bay from non specific mRNAs. In a sense, the specificity of the initial nucleation is detected, amplified and energy-secure via a cooperative binding. A related mechanism has also been proposed to explain the specific packaging of viral RNA by proteins via a cooperative binding (63).
As a proof of concept of this model, we show that the cooperative binding of YB-1 to mRNA stabilizes saturated YB-1:mRNA complexes (Figure 4C). In addition, after mixing saturated complexes with other mRNAs, we obtained a preferential translation repression of the pre-incubated mRNAs compared to the other coexisting mRNAs in rabbit reticulocyte system. We therefore succeeded in manipulating translation selectively (Figure 4D).
At first sight, such model of protein multimerization on specific mRNAs could be challenged by other competing mRNA-binding proteins in vivo. To address this issue, we show that the presence of G3BP, a non-cooperative mRNA-binding protein, was not an obstacle for the cooperative binding of YB-1 to mRNA (Figure 4A and B). The point is that YB-1 multimerization most probably provides a huge energy benefit which enables to displace isolated RNA-binding proteins like G3BP.
Other RNA binding-proteins than YB-1 could orchestrate translation repression via a similar mechanism as protein self-attraction is an over-represented property among RNA-binding proteins, mostly due the high occurrence of low complexity sequences or prion-like domains (64–66). In line with this, multimerization on RNA-protein target has already been described for other RNA-binding proteins (65–70) like HuR and FUS. It is thus of interest to explore whether a similar mechanism of translation repression can take place for these proteins.
Finally, an unanswered issue, which applies to other selective translation mechanisms orchestrated by RNA-binding proteins, is whether the affinity of RNA-binding protein for short mRNA sequences results in a selective binding to mRNA. Indeed, while such preferential binding is well documented for short hexa/hepta nucleotides in vitro (22), it remains elusive for long mRNA molecules. The presence of many non-specific RNA sites in long mRNA probably hinders the preferential binding to specific sequences. In vitro approaches may require additional protein factors that may be lacking so far. For example, the initial recruitment of proteins like YB-1 may rely on interactions with other mRNA-binding proteins having a high affinity for specific mRNA sequences/structures, as proposed for DDX6 (71). These issues deserve to be considered in the future to further document the mechanisms of selective translation.
YB-1 binding to DNA and putative functions in DNA-related processes
So far, the proposed nuclear functions of YB-1 related to its interactions with DNA were based on its reported preferential binding to damaged DNA (36) and, possibly, to the promoter regions of many genes implicated in cell proliferation, multi-drug resistance or DNA repair (31). Albeit interesting, major concerns have been raised regarding the putative function of YB-1 as a transcription factor (32) based on its weak affinity to specific DNA sequences. Similarly, the molecular mechanism by which YB-1 participates to DNA repair despite the presence of many other DNA-binding proteins of higher affinity toward DNA than YB-1 remains to be clarified.
Here we advanced an alternative view which allows YB-1 to become a relevant competitor for the binding to DNA. YB-1 should not be considered as an isolated protein with a strong affinity to specific DNA structures but rather as a protein able to multimerize at specific DNA sites. The energy benefit in forming YB-1 multimers on DNA results from the sum of the YB-1:DNA and YB-1:YB-1 interactions, which should clearly reduce the chance of being displaced from DNA by other proteins. In line with this, we found a striking preferential multimerization of YB-1 at the interface between two parallel DNA helices starting from DNA crosses (Figure 5A and B). The difference in the persistence length between mRNA and DNA may provide a rational explanation for the preference of YB-1 for mRNA and DNA crosses compared to relaxed DNA (Figure 8B). The number of nucleotides separating two consecutive YB-1 molecules on mRNA is large (about 30–40 nucleotides), which roughly corresponds to the number of phosphate charges sufficient to neutralize the clusters of positive residues located in the YB-1 C-terminus (net charge: +41 e−). Despite this limitation, mRNA flexibility can allow many YB-1 molecules to interact physically into globules (Figure 8A). DNA rigidity prevents such short-ranged bending. As a result, on isolated DNA, YB-1 cannot form multimer which would require an impossible DNA bending. On the other hand, at DNA crosses, YB-1 molecules can interact with each other at the interface between two DNA helices without mechanical constraint (Figure 8B). In agreement with this view, we show that YB-1 prefers to multimerize along supercoiled plasmids than on relaxed plasmids or linear DNA because the occurrence of crosses is significantly higher in supercoiled DNA (Figure 5B and S7).
If we now consider what could be the possible consequences of the YB-1 multimerization at DNA crosses and the ensuing alignment of DNA helices (Figure 8B), our attention then naturally turns to topoisomerase II which binds to DNA at crosses to modify supercoiled DNA topology. As observed from NRK cell extracts (Figure 7), YB-1 interferes negatively with the topoisomerase II activity, most probably by masking DNA crosses. The expression of topoisomerase II correlates with the presence of YB-1 in the nucleus which has been attributed to a putative targeting of an inverted CCAAT box in the promoter region of topoisomerase II (30). However, the role of YB-1 in transcription is challenged by recent reports (40,72), YB-1 may rather indirectly increase toposiomerase II expression level to compensate the YB-1-mediated loss of topoisomerase II activity. In addition to this, YB-1 may also participate/interfere with some DNA repair mechanisms like homologous recombination (73) through the YB-1-mediated alignment of two DNA helices (Figure 6D). Altogether, our mechanistic view of the binding of YB-1 to DNA may provide a novel view on its role in DNA repair and drug resistance of cancer cells.
Supplementary Material
Acknowledgments
We gratefully thank Dr Lyabin Dmitry and Dr Skabkin Maxim for helpful discussions on mRNA:YB-1 interactions and Dr Olga Lavrik and Dr. Maria Sukhanova for providing PARP-1 protein.
SUPPLEMENTARY DATA
Supplementary Data are available at NAR Online.
FUNDING
Institut National de la Santé et de la Recherche Médicale; Genopole®Evry and the Program on ‘Molecular and Cell Biology of the Russian Academy of Sciences; Russian Scientific Foundation [14-14-00879 to D.A.K and L.P.O, in part]; GDRI ‘From Molecular to Cellular Events in Human Pathologies’; ARC (Association pour le Recherche sur le Cancer, France). Fund for open access charge: Inserm and Université d'Evry.
Conflict of interest statement. None declared.
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