Engineered bacterial hydrophobic oligopeptide repeats in a synthetic yeast prion, [REP-PSI+]

The yeast translation termination factor Sup35p, by aggregating as the [PSI+] prion, enables ribosomes to read-through stop codons, thus expanding the diversity of the Saccharomyces cerevisiae proteome. Yeast prions are functional amyloids that replicate by templating their conformation on native protein molecules, then assembling as large aggregates and fibers. Prions propagate epigenetically from mother to daughter cells by fragmentation of such assemblies. In the N-terminal prion-forming domain, Sup35p has glutamine/asparagine-rich oligopeptide repeats (OPRs), which enable propagation through chaperone-elicited shearing. We have engineered chimeras by replacing the polar OPRs in Sup35p by up to five repeats of a hydrophobic amyloidogenic sequence from the synthetic bacterial prionoid RepA-WH1. The resulting hybrid, [REP-PSI+], (i) was functional in a stop codon read-through assay in S. cerevisiae; (ii) generates weak phenotypic variants upon both its expression or transformation into [psi-] cells; (iii) these variants correlated with high molecular weight aggregates resistant to SDS during electrophoresis; and (iv) according to fluorescence microscopy, the fusion of the prion domains from the engineered chimeras to the reporter protein mCherry generated perivacuolar aggregate foci in yeast cells. All these are signatures of bona fide yeast prions. As assessed through biophysical approaches, the chimeras assembled as oligomers rather than as the fibers characteristic of [PSI+]. These results suggest that it is the balance between polar and hydrophobic residues in OPRs what determines prion conformational dynamics. In addition, our findings illustrate the feasibility of enabling new propagation traits in yeast prions by engineering OPRs with heterologous amyloidogenic sequence repeats.


Introduction
Modularity is a basic principle of organization in proteins and their assemblies. In the case of the aggregation-prone amyloidogenic proteins, modularity comes from the existence of sequence stretches that become the β-strand building blocks in cross-β sheets (reviewed in Eisenberg and Jucker, 2012). Such stretches can either have hydrophobic or polar average residue compositions, but usually not both at the same time, thus posing constrains to homotypic interactions, which require chemically compatible side chains to cross-aggregate. Polar glutamine/asparagine (Q/N)-rich amyloidogenic sequences are a hallmark of prion domains in yeast (Alberti et al., 2009;reviewed in Liebman and Chernoff, 2012), in which cross-seeding has been well characterized, e.g., for the Rnq1p/[PIN + ] prion nucleating the aggregation of Sup35p/[PSI + ] (Vitrenko et al., 2007;Sharma and Liebman, 2013). In the translation releasing factor Sup35p, its prionforming domain (N) includes up to five and a half oligopeptide repeats (OPRs; Figure 1A; reviewed in Tessier and Lindquist, 2009). OPRs, while still assembled in the amyloid fibers, have been proposed to be the targets for the disaggregase chaperone Hsp104p (Chernoff et al., 1995) that, with the aid of Hsp70 chaperones Ssa1-4p (Shorter and Lindquist, 2008;Winkler et al., 2012), generate [PSI + ] propagons, i.e., oligomeric primordia that are readily diffusible to the progeny (Cox et al., 2003;Derdowski et al., 2010). The modularity of Sup35p OPRs has allowed their partial or total replacement by heterologous sequences, such as the octapeptide repeats in the mammalian prion protein PrP (Parham et al., 2001;Dong et al., 2007;Tank et al., 2007), while keeping the resulting chimeras their original function as epigenetic determinants of reading-through stop codons in yeast. With the accumulated knowledge on Sup35p/[PSI + ], this is probably the most suitable model system to address the molecular determinants of the prion condition in proteins (Sabate et al., 2015).
RepA, the DNA replication protein of the Pseudomonas plasmid pPS10, is one of the members best characterized of a protein family spread across a large group of plasmids from Gram-negative bacteria (reviewed in Giraldo and Fernández-Tresguerres, 2004). Soluble RepA dimers, which function as transcriptional self-repressors of the repA gene, undergo a large conformational change upon binding to specific DNA sequences from the plasmid replication origin, resulting in their dissociation into replication-competent RepA monomers (Díaz-López et al., 2003. Such structural change consists in an increase in β-sheet at the expense of the α-helical secondary structure component and affects WH1, the most Nterminal of the two 'winged-helix' domains in RepA, which is transformed from a dimerization domain into a secondary DNA binding module, ancillary to the main DNA recognition determinant, C-terminal WH2 (Giraldo et al., 1998(Giraldo et al., , 2003. RepA monomers are aggregation-prone and, once a replication round is completed, the resulting plasmid copies are held together through interactions between RepA monomers bound to the replication origins of the two plasmid molecules, thus inhibiting further replication rounds (Gasset-Rosa et al., 2008a). Such complex interplay between transcriptional repression and DNA replication initiation/inhibition, focused further research on the molecular basis for the ligand (DNA)modulated balance between RepA solubility and functional aggregation. In RepA-WH1, a single hydrophobic sequence stretch partially folded as a α-helix changes its conformation, upon transient binding to specific DNA sequences, to assemble as a β-strand in amyloid fibers (Giraldo, 2007;Gasset-Rosa et al., 2008b). The RepA-WH1 domain, when expressed in Escherichia coli as a metastable fusion to the fluorescent protein mCherry, behaves as a synthetic prionoid, i.e., an amyloidogenic protein lacking infectivity (Aguzzi, 2009).
Unlike prions in yeast, RepA-WH1 triggers a sort of intracellular amyloid 'proteinopathy' in its host (Fernández-Tresguerres et al., 2010), where the 'vertical' propagation (i.e., from mother cell to daughter cells) and the conformational selection of 'strains' of the prionoid are dependent on the Hsp70 chaperone DnaK, rather than on the Hsp104 ortholog ClpB . A recent electron microscopy reconstruction of the RepA-WH1 fibers, as templated in vitro on soluble molecules of the protein by amyloid seeds preformed in vivo, showed that the fibers are composed of intertwined amyloid tubules built by distorted protein monomers (Torreira et al., 2015).
Since the amyloidogenic sequence stretch in RepA-WH1 has clearly distinct features to those naturally found in yeast prions, -i.e., a single hydrophobic amyloidogenic stretch in a properly folded domain, rather than multiple repeats with polar residue composition in the frame of an intrinsically disordered tailthe bacterial prionoid is a suitable source of radically heterologous sequences to explore their ability to supplant the OPRs in Sup35p/[PSI + ]. We report here that chimeras between Sup35p and at least three repeats of the hydrophobic amyloidogenic stretch in RepA-WH1 constitute novel functional prions in yeast that we have named [REP-PSI + ]. Furthermore, [REP-PSI + ] can cross-seed the propagation of [PSI + ], but generating [PSI + ] WH1 , a new strain with very low mitotic stability (i.e., epigenetically unstable), as expected for a weak prion with severe limitations on the generation of propagons. These findings validate the possibility of tailoring yeast epigenetics by engineering aggregationprone hydrophobic amyloidogenic repeats within prion-forming domains.

Plasmid Constructs
Substitution of Sup35p-OPRs by Tandem Repeats of the Amyloidogenic Stretch in RepA-WH1 (WH1-R1-5) The reporter plasmid pUKC1620 (Parham et al., 2001;Von der Haar et al., 2007), harboring a WT copy of the SUP35 gene with its natural promoter, was used as template for PCR-amplification (Pfu DNApol) of N R6-sup35 using primers with BamHI (3 to the promoter) and EcoRV (annealing after the 5th repeat) ends. After digestion with those enzymes, the product replaced the BamHI-EcoRV N-SUP35 fragment in the original plasmid, leading to pUKC_R5. On this vector, WH1-R1 was inserted through PCR, including the reverse primer (5 -CGAGgatatcCG ATCAAAGACACAGCGCATAGCACTAGATTGAATTGCTGC TGAT), after the EcoRV site (lowercase), the complement of the sequence coding for the nine core amino-acid residues (LVLCAVSLI) in WH1(A31V) (bold; Giraldo, 2007). WH1-R2 was built in a similar way, but the reverse primer had that sequence repeated twice with a TCC/Gly spacer. For pUKC_R0, a construction lacking the five natural OPRs in Sup35p, the PstI site previous to the first OPR in the parental plasmid was mutated to EcoRV (QuikChange kit, Stratagene), followed by digestion with this enzyme and in-frame religation of the vector. WH1-R1-3 were built (B) The R0 + WH1-R1-5 chimeras. Sup35p OPRs were totally replaced by 1-5 tandem repeats of the hydrophobic amyloidogenic stretch in the RepA-WH1 variant A31V (arrow; Giraldo, 2007). The heterologous sequences were engineered to fold as zigzag β-arcades (reviewed in Kajava et al., 2010), in which turns were made by inserting a Gly residue between the natural Asp (blue) C-and Arg (red) 'gatekeeper' N-ends from contiguous WH1 repeats. β-strand packing (faces of strands in black, backs in gray) would be guided by interdigitation of chemically compatible side chains. β-arcades from distinct protein monomers would stack through main-chain hydrogen bonds into a parallel superpleated β-structure, as proposed for Sup35p/[PSI + ] (reviewed in Kajava et al., 2010). In the resulting fiber, the engineered repeats should have to accommodate as a hydrophobic spine within an otherwise polar Q/N-rich axis. (C) The amyloidogenicity profiles (red plots) for the distinct chimeric N-domains, as estimated by the AGGRESCAN (left column; Conchillo-Solé et al., 2007) and WALTZ (right;Maurer-Stroh et al., 2010) algorithms, suggest that the synthetic peptide arrays assemble as amyloids. Horizontal lines: blue, aggregation hot spot threshold; green, sequence average. by annealing the pre-phosphorylated (T4-PNK) oligos 5 -GGCCGCCTAGTGCTATGCGCTGTGTCTTTGATCGAT/5 -GCATAGCACTAGGCGGCCATCGATCAAAGACACAGC (complementary sequences in bold) followed by filling of the ends (Klenow DNApol) and self-ligation, a step that generated an extra terminal half repeat. Each repeat in the concatemers includes the natural C-terminal Asp and N-terminal Arg found in the RepA-WH1 amyloidogenic stretch (Giraldo, 2007) plus a linker Gly. Upon ligation of the concatemers mix at the EcoRV site in pUKC_R0 and transformation into E. coli, DNA sequencing identified clones with up to three RepA-WH1 repeats. Since WH1-R4-5 were recalcitrant to be obtained through such approach, a fragment including three RepA-WH1 repeats was made through chemical synthesis (ATG:biosynthetics, Germany) and inserted into pUKC_R1-2, in which EcoRV had been regenerated by site directed mutagenesis, to give pUKC_R4-5.

Plasmids for Protein Expression in Yeast under the pGAL1 Promoter
The full-length WH1(Rn)-SUP35 chimeras were inserted into the pYeF2 vector (Cullin and Minvielle-Sebastia, 1994) after amplification by PCR, using as templates the pUKC series (see above) and primers having BamHI and NotI ends. These chimeras carried a C-terminal hemagglutinin (HA)-tag from the vector. For fluorescence microscopy observation, fusions were made between the NM-domains from the chimeras and the monomeric red fluorescent protein mCherry at their C-termini. With this purpose, each NM-domain was amplified by PCR on the pUKC plasmids, with oligonucleotides carrying BamHI and BspEI ends, and then ligated with a BspEI (5 )-NotI (3 ) mCherry fragment, amplified using as template pWH1(A31V)-mRFP (Fernández-Tresguerres et al., 2010). The BamHI-NotI fragments were then cloned into pYeF2 as above.

Epigenetic Assay for Yeast Colony Color
The pUKCs derivatives (encoding the different chimeric alleles) were electroporated in a [PSI + ] [PIN + ] strain (see above) that initially carried pYK810, a plasmid bearing a copy of SUP35 (Von der Haar et al., 2007). For displacing the resident pYK810, thus assuring that the incoming pUCKs were the only source of Sup35p (or its chimeras with the WH1 repeats), colonies growing in SD-His were replicated on the same medium containing 0.1% 5-FOA, thus counter-selecting for cells that carried pYK810 (URA3). Colonies were then plated on 1 /4 YPD and SD-adenine. For full development of color in colonies, agar plates were incubated for ≥72 h at 30 • C and then transferred to 4 • C for 24 h before photographic documentation.

Aggregate Extraction and Sedimentation Assay
Two hundred ml cultures of yeast carrying the full-length protein chimeras cloned into pYeF2s (see above) were grown overnight in selective medium (SD-Ura) with glucose. Then cultures were diluted to OD 600 = 0.07 in SD-Ura, but with 2% raffinose and 0.1% glucose, and grown to OD 600 = 0.2, when protein expression was induced by adding 2% galactose and further incubated until OD 600 = 2. Cells were then harvested and resuspended in 500 μl of 25 mM Tris . HCl pH 6.8, 250 mM NaCl, 5 mM EDTA, 10% glycerol (plus protease inhibitors; Roche). Lysis was then carried-out with glass beads (Lysing matrix C) in a MP FastPrep-24 homogenizer (five cycles, level 5, for 30 s at 4 • C). Cell debris was removed by a low-speed sedimentation step (600 × g, 3 min). Two hundred microliter of the resulting whole cell extracts were ultracentrifuged at 50,000 rpm (100,000 × g), for 15 min at 4 • C (Beckman Optima Max-XP, TLA100 rotor). Supernatants were collected and pellets were resuspended in 200 μl of the lysis solution. Proteins in equivalent volumes of supernatant and pellet fractions were analyzed by SDS-PAGE (10% polyacrylamide; 30 μg/lane) plus Western-blotting, using an anti-HA antibody (Roche, 1:1,000) and chemiluminescence detection (ECL2; Pierce).

Visualization of Aggregates by Fluorescence Microscopy
Overexpression of the NM-mCherry Chimeras pYeF2s encoding the chimeras were transformed into the YJT28 strain and protein expression was carried out as described above. Culture aliquots were taken along 22 h for live cell observation.

Fluorescence Microscopy
It was performed with a Nikon Eclipse 90i microscope, equipped with CFI PLAN APO VC (NA 1.40) oil immersion objective and a Hamamatsu ORCA-R 2 CCD camera. A red filter with excitation 543/22 and emission 593/40 was used. Differential interference contrast (DIC) images were also captured.

Analytical Ultracentrifugation
NM-mCherry chimeras were dialyzed in 0.1 M Na 2 SO 4 , 20 mM Na 2 HPO 4 pH 6, 5 mM 2-mercaptoethanol. Four hundred microliter of each sample were diluted to 0.8, 0.2, and 0.08 mg/ml and then centrifuged for 5 min at 13,000 rpm, 4 • C. The clarified supernatants were studied by sedimentation velocity. Centrifugation was carried out in a Beckman-Coulter XLI analytical ultracentrifuge, at 48,000 rpm and 20 • C, measuring absorbance at 280 nm. Sedimentation coefficient distributions, c(s), were determined, with a confidence level of 0.68, using the SEDFIT 14.1 software (Schuck, 2000).

Results
Engineering Chimeras between the Amyloidogenic Stretch in RepA-WH1 and [PSI + ] Structural modeling of the amyloid fibers assembled by the Ndomains of yeast prion proteins suggests that their basic building block might be a β-arch (reviewed in Kajava et al., 2010), in which adjacent Q/N-rich stretches would assemble as β-strands interdigitated through compatible side chains, while the intervening sequence would form a turn. If multiple stretches were present, as in Sup35p OPRs, β-arches would be further folded as β-arcades. The stacking of β-arcades from distinct protein monomers, stabilized through parallel main-chain hydrogen bonding, would result in a parallel superpleated β-structure (reviewed in Kajava et al., 2010). With a β-arcade based model in mind, we used a plasmid reporter system (Parham et al., 2001) in which all the OPRs in Sup35p were replaced by up to five tandem repeats of the hydrophobic amyloidogenic stretch found in the bacterial prionoid RepA-WH1 (Giraldo, 2007; WH1-R1-5; Figure 1).

RepA-WH1 + Sup35p Chimeras are Functional in Yeast
The engineered chimeras were expressed in yeast from the SUP35 promoter in a centromeric plasmid, and tested in an epigenetic red-white colony color assay (Figure 2): upon Sup35p aggregation as [PSI + ], the reporter ade1-14 allele, including a premature amber stop codon, is read-through by the ribosomes allowing for the synthesis of adenine, thus giving white color colonies on rich, unselective medium. Otherwise, soluble Sup35p efficiently terminates translation resulting in red [psi − ] colonies by accumulation of the adenine precursor metabolite 5 -P-ribosyl-5-aminoimidazole (reviewed in Tessier and Lindquist, 2009). In the absence of endogenous Sup35p-WT, achieved in [PSI + ] cells upon displacement of a resident SUP35 plasmid by vectors encoding the chimeras, five of the native OPRs fused to two chimeric RepA-WH1 repeats (R5 + WH1-R2) were sufficient to yield a [PSI + ]-like prion phenotype. However, with just one bacterial repeat (R5 + WH1-R1) the phenotype of this chimera was even weaker (more intense red color) than the R5 parental, suggesting that the insertion of a single hydrophobic stretch in the Q/N-repeats destabilized their assembly as amyloid. Interestingly, in the absence of any OPRs all the constructs including RepA-WH1 repeats (R0 + WH1-R1-5) gave a nearly WT phenotype, indicating that, in these chimeras, amyloids were successfully built with little interference between the RepA-WH1 and the Sup35p moieties (Figure 2A). In adeninedeficient media, all chimeras supported yeast growth, i.e., they read-through ade1-14 thus restoring a functional pathway for adenine synthesis, albeit R5 + WH1-R1 led again to a poor phenotype ( Figure 2B). When, after several passages through liquid rich medium, yeast carrying the chimeras were plated on 1 /4 YPD agar ( Figure 2C) red sectored colonies appeared if the number of WH1 peptide repeats was ≤2, indicating that these were unstable chimeric prions. The chimeric prions including ≥3 WH1 repeats, which we termed [REP-PSI + ], exhibited two clearly different phenotypes, namely white and pink colonies (Figure 2D, top). To explore the mitotic stability of both phenotypes, single colonies of each kind were subcultured and plated again on 1 /4 YPD. White colonies showed a remarkable stability (frequency of conversion to red ≈10 −6 , matching that described for [PSI + ]; as reviewed in Liebman and Chernoff, 2012; Figure 2D, left), whereas light pink colonies were very unstable, giving rise with high frequencies to dark pink (≈2 × 10 −1 ) and red (≈10 −2 ), or reverting to white (≈3 × 10 −3 ), colonies (Figure 2D, right). Tentatively, the white phenotype was associated to a strong prion variant, s[REP-PSI + ], the two pink tones to weak prion variants, w1 and w2[REP-PSI + ] (light or dark pink, respectively), and the red colonies to cured (i.e., having lost the prion phenotype) [rep-psi − ].

[REP-PSI + ] Prion is Infectious and Templates on Sup35p a New Weak, Unstable Variant, [PSI + ] WH1
Yeast spheroplasts can be transformed with prion particles, either assembled in vitro or extracted from cultured cells (Tanaka, 2010). Spheroplasts prepared from red colonies, thus expressing either Sup35p-WT or the WH1-R3-5 chimeras in their non-prion form ([psi − ] or [rep-psi − ], respectively), were transformed with protein extracts from cells also carrying the chimeras but grown from white colonies, thus with a [REP-PSI + ] phenotype. When the epigenetic phenotype of the transformants was assayed (Figure 3A), all colonies showed the white or the light pink stop codon read-through phenotype characteristic of the incoming prion aggregates (Sup35p-WT or the chimeras, respectively). The demonstration of the 'infectivity' of the R0 + WH1-R3-5 chimeras through the transformation of their aggregated forms qualifies [REP-PSI + ] as a new synthetic yeast prion. However, after serial sub-culturing without selective pressure, in those clones expressing Sup35p-WT and cross-transformed with the WH1-R3-5 [REP-PSI + ] chimeras, besides the pink phenotype of the incoming aggregates, red [psi − ] colonies appeared frequently ( Figure 3B). These results indicated that the WH1-R3-5 chimeras can template their conformation on Sup35p-WT to generate a new very weak prion strain (or ensemble of weak strains) that we have named [PSI + ] WH 1 .

[REP-PSI + ] Prion Assembles Amyloids Larger than [PSI + ]
Biochemical analysis of the solubility of the engineered chimeric proteins, performed upon their overexpression from the GAL1 promoter, showed that constructs R0 + WH1-R3-5 aggregated massively, whereas R0 + WH1-R1-2 were proteolytically more unstable (Figure 4A). Regarding the extra, higher mobility band observed in the SDS-PAGE of the whole cellular lysates for R0 + WH1-R1, including a single WH1 hydrophobic repeat in the context of the Sup35p Q/N-rich sequences might generate instability in the natural beta-arcades built by the prion, which will thus become proteolysis-prone. Following this speculation, that higher mobility band would correspond to molecules of the chimera that have lost the bit N-terminal to the single engineered WH1 repeat. The R0 + WH1-R1-2 chimeras were further degraded during the manipulation of the cell lysates for ultracentrifugation analysis, in spite of performing the experiment at low temperature and supplying the samples with protease inhibitors. Semi-denaturing detergent agarose gel electrophoresis (SDD-AGE), a technique for the detection of amyloid aggregates in a broad range of sizes (Bagriantsev et al., 2006), was carried out by immediately running in the gel the WCL fractions under conditions that should denature proteases, thus reducing degradation of the R0 + WH1-R1-2 chimeras to a minimum. SDD-AGE revealed (Figure 4B) that the chimeras form two populations of aggregates according to their electrophoretic mobilities. The species with higher molecular weights were evident in R0 + WH1-R1-5, showing sizes in direct correlation with the increasing number of RepA-WH1 repeats, but were barely detectable for Sup35p-WT, R0 or the construct carrying R5 + WH1-R2. This result points to the construction of a distinct type of assembly by the chimeras in which the hydrophobic repeats have completely replaced the Q/N-OPRs. The presence of very high molecular weight species in SDD-AGE has been described in [PSI + ] variants resistant to Hsp104 chaperonepromoted shearing, thus resulting in weak prion phenotypes with low mitotic stabilities (Derdowski et al., 2010;Alexandrov et al., 2012).

RepA-WH1 Repeats in [REP-PSI + ] Alter the Structure of the Amyloids Assembled by the NM-Domains
The results above pointed to a singular structural arrangement in [REP-PSI + ] for the hydrophobic RepA-WH1 OPRs within the flanking polar Q/N-rich sequences, which remained unaltered from the Sup35p N-domain. The N and M domains (Figure 1A) in the [REP-PSI + ] chimeras were then fused to the monomeric red fluorescent protein mCherry and expressed in E. coli. Those expressed at sufficiently high levels were purified and their assembly morphologies (Figure 5A), average secondary structure compositions (Figure 5B), and association states ( Figure 5C) were physically analyzed. NM-mCherry and NM-R0-mCherry controls were able to assemble into fibers under standard conditions (Giraldo, 2007;Fernández-Tresguerres et al., 2010; Figure 5A). However, NM-mCherry fusions carrying WH1-R2 or WH1-R4 did not form fibers, but irregular oligomers whose average sizes (≤10 and ≈25 nm, respectively), directly correlated with the number of hydrophobic repeats. Such oligomers were compatible with the smaller aggregates detected by means of SDD-AGE for the [REP-PSI + ] chimeras ( Figure 4B).
Circular dichroism (CD) analysis of the purified proteins ( Figure 5B) indicated a net increase in β-sheet structure (broad band at ≈220 nm) for NM-R2/4-mCherry compared with NM-mCherry, whereas NM-R0-mCherry spectrum resembled the spectra of Q/N-rich peptides when forming coiled-coils (redshifted band at >225 nm; Fiumara et al., 2010). Since sedimentation velocity experiments ( Figure 5C) showed that purified NM-R0-mCherry was a monomer (s = 2.3 S), such coiled-coil should be intramolecular. On the contrary, poly-dispersed aggregation was evident as multiple peaks with increasing sedimentation coefficients for NM-R2/4-mCherry and the WT control NM-mCherry. These in vitro experiments indicated that the chimeric [REP-PSI + ] prions, carrying hydrophobic OPRs of bacterial origin, assemble as amyloid oligomers rather than fibers, as Sup35p/[PSI + ] does.

[REP-PSI + ] Prion Aggregates as Perivacuolar Foci In Vivo
The NM-mCherry fusion proteins were then expressed in yeast from a Gal-inducible plasmid ( Figure 5D). When the N domain carried the Sup35p wild-type sequence, the characteristic ringlike aggregates appeared in the cytoplasm (Tyedmers et al., 2010), whereas if it lacked all the OPRs (NM-R0-mCherry) fluorescence labeling was found diffused. If the constructs included the N domain of the distinct [REP-PSI + ] chimeras, aggregation appeared as multiple dots/foci whose sizes increased with the number of RepA-WH1 repeats. They were disposed around the vacuole (IPOD compartment), as previously described for mature NM-GFP amyloids (Tyedmers et al., 2010). Interestingly, the fraction of yeast cells expressing the NM-R2-mCherry chimera was significantly reduced, and the lysis of many cells became evident. It has been proposed that the cellular toxicity of hydrophobic amyloidogenic peptides is linked to their ability to assemble as oligomeric pores upon insertion into lipid bilayers (reviewed in Butterfield and Lashuel, 2010). It might be the case that NM-R2-mCherry, lacking the ability to further assemble into a stable parallel superpleated β-structure (Figure 1B), would have a preference for membrane targeting.

Discussion
In this work, we have generated chimeras (Figure 1) by replacing the polar OPRs in Sup35p with tandem repeats of the hydrophobic amyloidogenic stretch found in the bacterial prionoid RepA-WH1 (Giraldo, 2007;Gasset-Rosa et al., 2008a. The resulting synthetic [REP-PSI + ] prions are functional in yeast, generating both a strong [PSI + ]-like phenotype and various weak phenotypes (Figures 2 and 3), which are compatible with a cloud of prions strains (Bateman and Wickner, 2013). These chimeric prions assemble themselves in vitro as discrete size particles (Figure 5), which probably would suffice to act as competent propagons in vivo.
Our results suggest that cross-seeding of [REP-PSI + ] through conformational templating, since the wild-type OPRs were absent from the chimeras, must be exerted by the flanking Q/Nrich sequences in the N-terminal domain that come from Sup35p-WT. This is compatible with findings showing that mutants including hydrophobic and/or aromatic residues at the N-terminus (residues 1-40) of Sup35p enhance [PSI + ] nucleation, whereas aromatic side-chains at the OPRs promote chaperone-mediated propagation (Toombs et al., 2010(Toombs et al., , 2011Alexandrov et al., 2012;Gonzalez-Nelson et al., 2014;MacLea et al., 2015). It is noteworthy that such studies were performed by RepA-WH1 repeats drive the assembly of the NM-mCherry proteins into particles whose sizes increase with the number or repeats. (B) Circular dicroism (CD) spectra of the purified, preassembled NM-mCherry proteins (15 μM) showed an increase in β-sheet structure (broad minima at ≈220 nm) for the R0 + WH1-R2/4 chimeras. (C) Sedimentation velocity experiments were performed in an analytical ultracentrifuge with the same purified NM-mCherry proteins (10 μM) studied in (A,B). The analyses indicate poly-dispersed aggregation for the chimeras (i.e., multi-peaked profiles), with a direct correlation between the number of RepA-WH1 repeats and the sedimentation coefficient values/number of peaks. However, the profiles for the R0 + WH1-R2/4 chimeras were simpler than that for the NM-Sup35 fusion, reflecting the ability of the latter to assemble fibers (A). (D) Epifluorescence microscopy imaging of yeast cells expressing the chimeric NM-mCherry fusions. Exposure times: 200 ms (Sup35-WT, R0, R0 + WH1-R1), 600 ms (R5 + WH1-R2, R0 + WH1-R3-5), and 2 s (R0 + WH1-R2). ND filter: 1 /4. Left: superposition of the DIC and fluorescence images. Chimeras carrying R0 + WH1-R3-5 form foci (arrows) whose sizes increase with the number of WH1 repeats, whereas WH1-R1 is dispersed through the cytoplasm and R0 + WH1-R2 is cytotoxic (cell lysis). The fraction of cells expressing the chimeras (i.e., those fluorescence-labeled) is indicated (%); 200-400 cells of each type were counted. mutating a single OPR out of five in Sup35p, yielding constructs somehow analogous to our unstable R5 + WH1-R1-2 chimeras, whereas in this work we have built a complete assembly made of up to five hydrophobic repeats (R0 + WH1-R1-5). According to the results discussed here, there seems to be in [REP-PSI + ] a minimum threshold of three hydrophobic WH1 repeats in order to build a hydrophobic spine in the β-arcades sufficiently stable to surpass the control exerted by the surrounding natural polar sequences on prion nucleation and propagation. Thus, the engineered superpleated β-structure in [REP-PSI + ] seems to behave as an orthogonal synthetic module functional in prion propagation, in the sense proposed by Toombs et al. (2012). It has also been described that point mutations replacing polar Q/Y residues by charged Lys in OPRs positions confronted in the β-arcades, thus leading to electrostatic repulsion, result in new prion variants, [PSI + ] M1−M5 , some of which are unstable, and template on Sup35p-WT a non-epigenetically heritable conformation (Bondarev et al., 2013(Bondarev et al., , 2014. The 'prion no more' mutant G58D, which affects the second OPR (R2) in Sup35p, can be incorporated in WT aggregates, leading to increased frequency of fragmentation, thus compensating for deficiencies in propagation of weak [PSI + ] variants but curing, as dominant-negative, strong prion variants (DiSalvo et al., 2011;Verges et al., 2011). We have shown here that even more extensive engineering of the OPRs can give way to a new prion, [REP-PSI + ], that templates on Sup35p a new weak variant, [PSI + ] WH1 . Conversely, during the initial expression of the WH1-R1-5 chimeras from plasmids, the [PSI + ] prion resident in the yeast cells, before the displacement of its encoding (SUP35) vector, could influence through templating the compatibility and selection of the distinct [REP-PSI + ] variants described in this work. Cross-seeded aggregation between distinct RepA-WH1 variants has also been reported in bacteria (Molina-García and Giraldo, 2014). The possible contribution of the [PSI + ]-ancillary prion Rnq1p/[PIN + ] (Sharma and Liebman, 2013) to [REP-PSI + ] nucleation will require further studies.
Interestingly, the R0 + WH1-R3-5 chimeras build oligomers rather than fibers, as Sup35p does: most probably, having a large hydrophobic beta-arcade inserted in the polar Q/N-rich prion domain will impose a hindrance to the assembly of long, structurally regular fibers. Similarly, the natural, non-Q/N-rich prion [GAR + ] (Brown and Lindquist, 2009), which has recently been described to overcome glucose catabolite repression in Saccharomyces cerevisiae and other yeast (Jarosz et al., 2014), does not assemble as fibers but as oligomeric aggregates, as described here for the [REP-PSI + ] chimeras. In yeast, under normal conditions, binding of Ssa1p (an Hsp70 chaperone) to Sup35p targets Hsp104p to [PSI + ] aggregates for the generation of prion seeds (Winkler et al., 2012). Sup35p alleles defective in OPRs generate prions, such as [PSI + ] 22/69 (Borchsenius et al., 2001), that also build large aggregates behaving as unstable, weak prion variants (Tanaka et al., 2006;Derdowski et al., 2010). When the Q/N-rich OPRs in S. cerevisiae Sup35p were replaced by heterologous non-Q/N sequences from other yeast species, the propagation of the resulting chimeric prion became independent on Hsp104p (Crist et al., 2003). The region between the OPRs and the initial residues in the medium (M) domain is the target recognized by Hsp104p in the Sup35p amyloids (Frederick et al., 2014). Besides this, the intermolecular contacts characteristic of weak [PSI + ] variants exhibit an increased dependence on Hsp70s for Hsp104p-driven shearing, compared with those found in strong variants (DeSantis and Shorter, 2012). The propagation of [GAR + ] is independent of the activity of the Hsp104 disaggregase, probably because the oligomeric nature of this prion allows for diffusion-driven propagation, but this becomes strictly dependent on Hsp70 (Brown and Lindquist, 2009;Jarosz et al., 2014). Interestingly, the bacterial Hsp104p orthologue, ClpB, does not contribute either to the propagation of the RepA-WH1 prionoid in E. coli, a function relying mainly on the Hsp70 chaperone DnaK . DnaK conformationally selects for an amyloid variant of RepA-WH1 with reduced toxicity and generates relatively small oligomeric particles, readily diffusible to the progeny . In the case of [REP-PSI + ], the contribution of chaperones to its propagation in yeast remains to be explored.
Heterologous model systems have made fundamental contributions to the understanding of prion propagation. The expression of the yeast prion [PSI + ] in bacteria has revealed that Sup35p aggregates as inclusion bodies which retain the ability to nucleate distinct strains (Garrity et al., 2010;Espargaró et al., 2012), and that, as in its original host, it still needs nucleation by [PIN + ] (Garrity et al., 2010) and depends on Hsp104 for propagation (Yuan et al., 2014). In addition, [PSI + ] has also been propagated in mammalian cells in culture, exhibiting the hallmarks of cytoplasmic inheritance (Krammer et al., 2009;Hofmann et al., 2013). The synthetic [REP-PSI + ] prion, by expanding the repertoire of [PSI + ] variants and rewiring amyloidogenic parts of Sup35p with alien, non-Q/N-rich sequences of bacterial origin, is a proof of concept for the feasibility of generating new phenotypic traits in prions. Engineering the consortium between [REP-PSI + ] and its possible chaperone modulators will surely enable new trends in yeast epigenetics.