Requirements for nuclear localization of the Lsm2-8p complex and competition between nuclear and cytoplasmic Lsm complexes.

Sm-like (Lsm) proteins are ubiquitous, multifunctional proteins that are involved in the processing and/or turnover of many RNAs. In eukaryotes, a hetero-heptameric complex of seven Lsm proteins (Lsm2-8) affects the processing of small stable RNAs and pre-mRNAs in the nucleus, whereas a different hetero-heptameric complex of Lsm proteins (Lsm1-7) promotes mRNA decapping and decay in the cytoplasm. These two complexes have six constituent proteins in common, yet localize to separate cellular compartments and perform apparently disparate functions. Little is known about the biogenesis of the Lsm complexes, or how they are recruited to different cellular compartments. We show that, in yeast, the nuclear accumulation of Lsm proteins depends on complex formation and that the Lsm8p subunit plays a crucial role. The nuclear localization of Lsm8p is itself most strongly influenced by Lsm2p and Lsm4p, its presumed neighbours in the Lsm2-8p complex. Furthermore, overexpression and depletion experiments imply that Lsm1p and Lsm8p act competitively with respect to the localization of the two complexes, suggesting a potential mechanism for co-regulation of nuclear and cytoplasmic RNA processing. A shift of Lsm proteins from the nucleus to the cytoplasm under stress conditions indicates that this competition is biologically significant.


Introduction
components, because mutations in yeast LSM8 are suppressed by overexpression of LSM2 or LSM4 (Pannone et al., 2001).
Lsm1-7p differs from Lsm2-8p by just one polypeptide, but is located in the cytoplasm . In S. cerevisiae, Lsm1-Lsm7 proteins and a wide range of RNA decapping and decay factors have been shown to accumulate in cytoplasmic foci, named processing or P-bodies, but only under certain conditions (Sheth and Parker, 2003;Teixeira et al., 2005). In log-phase yeast cells, P-body components, including Lsm1-7p, are spread diffusely throughout the cytoplasm, but localize to foci that increase in number and size with increased cell density (Teixeira et al., 2005). In addition, P-body formation is increased by glucose deprivation, osmotic stress and ultra-violet radiation, suggesting that they form in response to stress. In these circumstances, the transcriptome of the cell changes to cope with the new conditions, and increased mRNA degradation occurs. P-bodies appear to be sites of RNA decapping and degradation (Sheth and Parker, 2003;Teixeira et al., 2005), and they are probably also sites of nonsensemediated decay and translational repression (Bruno and Wilkinson, 2006;Sheth and Parker, 2006;Teixeira et al., 2005). Studies of lsm1⌬ yeast indicate that Lsm1p is needed for accumulation of the other Lsm proteins in P-bodies (Tharun et al., 2005), but is not required for P-body formation (Sheth and Parker, 2003).
The existence of two Lsm complexes that differ by just one member, but which have different, even apparently opposing, functions (promoting RNA stability versus degradation), is remarkable, especially because the protein sequences of Lsm1p and Lsm8p are highly similar (Salgado-Garrido et al., 1999). The different functions of the complexes might, therefore, be determined by their localization, as was suggested by Tharun et al. (Tharun et al., 2005). It is not currently known what determines the cellular localization of Lsm complexes, although it has been suggested that both the nuclear and the P-body localizations require Lsm-complex formation (Ingelfinger et al., 2002;Tharun et al., 2005;Zaric et al., 2005). In the absence of Lsm1p, nuclear levels of Lsm2p and Lsm7p are slightly elevated (Tharun et al., 2005), indicating that Lsm1p might compete with Lsm8p for complex formation.
Here, we show that sequences within Lsm8p as well as formation of a heteromeric complex are important for the nuclear accumulation of the Lsm2-8p complex. Furthermore, we investigated competition between Lsm1p and Lsm8p by overexpression and depletion of these proteins. Imbalance between these two factors affects localization of other Lsmcomplex members and, under some conditions, even shows deleterious effects on cell viability. Under normal physiological conditions, competition between Lsm1p and Lsm8p might provide a link between RNA processing events in the nucleus and mRNA degradation in the cytoplasm. We therefore investigated the effects of stress on nuclear localization of the Lsm7 and Lsm8 proteins. We observed a small shift of Lsm7p to the cytoplasm upon glucose deprivation, and a rapid and almost complete depletion of Lsm7p and Lsm8p from the nucleus after hyperosmotic shock. This effect occurred independently from Lsm1p; however, deletion of LSM1 inhibited subsequent recovery of nuclear Lsm protein levels. Taken together, our findings suggest that co-regulation of cytoplasmic and nuclear RNA processing events could be mediated through changes in sub-cellular Lsm protein levels.

Lsm localizations
Yeast strains were constructed that produce 13myc-tagged Lsm1p, Lsm7p or Lsm8p (Fig. 1A), and immunofluorescencemicroscopy results clearly show specific localization patterns for the Lsm proteins: Lsm1p was predominantly cytoplasmic (Fig. 1B, note the 'holes' in the immunofluorescence, highlighted by arrows, and the lack of colocalization of immunofluorescence with DAPI staining of nuclear DNA in the merged image), Lsm8p localized exclusively to the cell nucleus and Lsm7p was present throughout the cells. These results are consistent with the proposed existence of two Lsm complexes, a nuclear Lsm2-8p complex and a cytoplasmic Lsm1-7p complex.
Lsm proteins are actively imported through the nuclear pore To investigate the mechanism of nuclear accumulation of Lsm proteins, a nup49-313 strain (a nuclear-pore mutant that affects protein import) (Doye et al., 1994) was constructed that produces 13myc-tagged Lsm1p, Lsm7p or Lsm8p. Because this mutation causes temperature-sensitive growth, the cultures were grown at 23°C and then shifted to 37°C (restrictive temperature) for 5 hours prior to processing for microscopic analysis. Following the shift to 37°C, Lsm7-13myc displayed a reduced signal in the nuclei of the nup49-313 cells compared with wild-type cells ( Fig. 2A). This effect was clearer for Lsm8-13myc, which was no longer restricted to the nucleus in the nup49-313 cells at 37°C (Fig. 2B). To control for a nonspecific effect of the nup49-313 mutation on the integrity of the nuclear membrane, U1 snRNA localization was Journal of Cell Science 120 (24) investigated and showed no difference between wild-type and nup49-313 cells (Fig. 2C). In combination with our previous report showing that the nuclear accumulation of Lsm8p is importin ␤/Kap95p-dependent (Spiller et al., 2007), these results suggest that, although individual Lsm proteins are small (10-21 kDa), their nuclear accumulation probably depends on active import through the nuclear pores. This is in agreement with the report that the human LSM2-8 complex is actively imported into rat fibroblast nuclei (Zaric et al., 2005). In contrast to the effect of the nup49-313 mutation on Lsm protein localization, the temperature-sensitive xpo1-1 nuclear-export mutation showed no effect on the localization of Lsm1p, Lsm7p or Lsm8p at the restrictive temperature in otherwise wild-type cells (Fig. 2D). Thus, it seems that the cytoplasmic localization of Lsm1p is not a consequence of nuclear exclusion by continual active export from the nucleus, at least not through this export pathway. By contrast, the xpo1-1 mutation did show a clear effect on the localization of a control protein (NLS-NES-GFP), both under permissive and restrictive conditions ( Fig. S1 in supplementary material) (Stade et al., 1997) Nuclear localization of Lsm7p requires other Lsm proteins As the only member of the Lsm2-8p complex that is exclusively nuclear, Lsm8p might be required for nuclear uptake or retention of the Lsm2-Lsm7 proteins. To investigate this, yeast cells that produce 13myc-tagged Lsm7p and in which LSM8 was under control of a galactose-inducible promoter (P GAL1 ) were grown to log phase in galactose then switched to glucose medium for 12 hours (long enough to deplete Lsm8p but not long enough to significantly deplete U6 snRNA) (Mayes et al., 1999), and Lsm7p localization was examined. In cells depleted of Lsm8p, Lsm7p levels were decreased in the nuclei (Fig. 3A, large arrow) and increased in cytoplasmic foci (probably P-bodies; small arrows).
To test for the dependence of Lsm7p nuclear accumulation on the presence of other Lsm proteins, yeast strains were tested in which LSM3, LSM4 or LSM5 were expressed from the P GAL1 promoter (for unknown reasons it proved difficult or impossible to 13myc-tag Lsm7p in the P GAL -LSM2 strain) and these were shifted from galactose to glucose medium for 12 hours to metabolically deplete these proteins (Mayes et al., 1999), whereas lsm1⌬ and lsm6⌬ cells, which are heatsensitive, were grown in glucose at the permissive temperature of 30°C. The nuclear localization of Lsm7-13myc was unaffected by the absence of Lsm1p (Fig. 3B). Depletion of Fig. 2. Localization of the Lsm proteins in the nup49-313 nuclearimport mutant and the xpo1-1 export mutant. Cultures were grown at 23°C to log phase and then at 37°C for a further 4.5 hours. In each case, a representative cell is shown. (A) Localization of Lsm7-13myc in MPS2 (wild type, WT) and MPS12 (nup49-313) at 23°C and 37°C. (B) Localization of Lsm8-13myc in MPS3 (WT) and MPS13 (nup49-313) at 23°C and 37°C. (C) Fluorescent in situ hybridization showed that localization of U1 snRNA in nup49-313 yeast at restrictive temperature was the same as in wild-type cells. (D) Localizations of Lsm1-13myc, Lsm7-13myc and Lsm8-13myc at 37°C in the xpo1-1 mutant strains MPS13, MPS14 and MPS15, respectively, were the same as for wild-type cells. Arrows indicate 'holes' in the immunofluorescence at the positions of nuclei. Bars, 10 m.
Lsm3p, Lsm4p, Lsm5p or Lsm6p appeared to reduce the nuclear Lsm7p signal slightly, as seen by decreased colocalization of Lsm7p with the DAPI stain, with depletion of the essential Lsm4 protein having the strongest effect, as seen by the hole in the immunofluorescence (Fig. 3B, arrow). Thus, nuclear localization of Lsm7p requires the presence of Lsm8p and is more efficient when most or all of the other components of the Lsm2-8p complex are present, but it is not affected by the absence of cytoplasmic Lsm1p.

Depletion of Lsm2p or Lsm4p disrupts Lsm8p localization
Because Lsm8p is normally nuclear, a defect in its localization is more readily detected. Therefore, to confirm that complex formation is required for Lsm2-8p nuclear localization, Lsm8p localization was investigated in strains in which Lsm2p and Lsm4p, its proposed neighbours in the Lsm2-8p ring, were depleted. This assignment is based on the organization of the Sm protein complex, in which SmB (closest in structure to Lsm8p) is flanked by SmD1 and SmD3 (most similar to Lsm2p and Lsm4p, respectively) (Kambach et al., 1999), and on genetic and yeast two-hybrid interactions between LSM2, LSM4 and LSM8 (Lehner and Sanderson, 2004;Pannone et al., 2001). 13myc-tagged Lsm8p localization was examined in wild-type, P GAL -LSM2, P GAL -LSM4 and lsm6⌬ cells (Fig. 4). Following depletion of Lsm2p or Lsm4p by growth in glucose medium for 12 hours (Mayes et al., 1999), there was still some nuclear signal for Lsm8p, but there was a dramatic increase in the level of signal in the cytoplasm. By contrast, absence of Lsm6p caused no visible change in Lsm8p localization. Overall, these results demonstrate that Lsm8p by itself does not accumulate in the nucleus, because loss of either of its proposed partners in the Lsm2-8p ring results in its delocalization. However, it seems that a complete Lsm2-8p complex is not essential, because lack of Lsm6p has no effect, which might be expected because Lsm6p is a non-essential protein (Mayes et al., 1999).
Lsm7p and Lsm8p delocalization is not caused by defective splicing Depletion of Lsm2-Lsm8 proteins leads to decreased levels of U6 snRNA and an accumulation of pre-mRNA (Mayes et al., 1999). To investigate whether delocalization of Lsm7p and Lsm8p from the nucleus upon depletion of other Lsm proteins might be due to an indirect effect on pre-mRNA splicing, cells were depleted of SmD1 and localization of myc-tagged Lsm7p and Lsm8p was investigated (supplementary material Fig.  S2A). Depletion of SmD1 had no effect on nuclear localization of either of these Lsm proteins, whereas northern blot analysis  showed decreased levels of U1 snRNA and an accumulation of pre-U3 RNA (supplementary material Fig. S2B).

Lsm8p truncations affect its nuclear localization
Because Lsm8p is important for the nuclear accumulation of other Lsm proteins, we performed deletion analysis on Nterminally GFP-tagged Lsm8 protein to investigate sequences in Lsm8p that might be responsible for its nuclear localization. Plasmids encoding the GFP-Lsm8 variants (Fig. 5A) were tested Journal of Cell Science 120 (24) for their ability to support the growth of strain MPS11 (P GAL1 -LSM8) on glucose (Table 1) and for localization ( Fig. 5B). SmB, the member of the Sm protein family that is structurally most similar to Lsm8p, contains a functional nuclear-localization signal in its C-terminus (Bordonne, 2000). The C-termini of both proteins are basic in nature, containing a high number of lysine residues, which, in SmB as well as SmD1 and SmD3, are part of a nuclear-localization signal (NLS)-like motif (Bordonne, 2000). The effect of C-terminal truncations of Lsm8p on its nuclear localization was therefore tested. GFP-Lsm8-2 protein, an Lsm8 construct that lacks the extreme C-terminal 10 amino acids of Lsm8 (analogous to the lsm8-2 mutation) (Pannone et al., 1998), showed normal nuclear accumulation (Fig. 5Bi,ii), whereas Lsm8-313p, which lacks a further 14 residues at the Cterminus, was mislocalized (Fig. 5Biii). However, the Lsm8 Cterminus (aa65-109) alone, when fused to GFP, failed to accumulate in the nucleus (Lsm8C; Fig. 5Biv). Thus, unlike the C-terminus of SmBp (Bordonne, 2000), the C-terminus of Lsm8p, although apparently required for nuclear localization, is not by itself sufficient to determine nuclear localization. Although the region of Lsm8p that is missing in Lsm8-313p contains six lysine residues, simultaneous mutagenesis of all six lysines to alanine (Lsm8-6A3; Fig. 5Bv) did not significantly affect nuclear accumulation of GFP-Lsm8p, supporting the conclusion that the C-terminus of Lsm8p does not behave like a classical NLS or a functional NLS-like motif. Truncation of 11 amino acids at the N-terminus (Lsm8⌬N; Fig. 5Bvi), or BMA38a plus pMPS8 (i.e. GFP-Lsm8 produced in the presence of endogenous Lsm8p) or (viii) pGFP-N-FUS (GFP). In all cases, GFP localization was examined in live cells after growth in SD-Ura-Met (to induce expression of the GFP construct). Bar, 10 m. (C) Coimmunoprecipitation of myc-tagged Lsm7p with GFP-Lsm8p. Lsm8p-containing complexes were precipitated with anti-GFP antibodies, and Lsm7p was detected with anti-myc antibodies. (D) All the GFP-Lsm8 constructs were stably expressed, as shown by western blotting (and data not shown) using anti-GFP antibodies. deletion of residues 52-64, corresponding to the Sm2 motif that is required for Lsm-complex formation (Lsm8⌬Sm; Fig. 5Bvii), caused these mutant proteins to localize throughout the cell, similar to GFP alone (Fig. 5Bix). This latter result emphasizes the importance of complex formation for nuclear localization of Lsm8p, because the Sm motif is crucial for inter-subunit interactions within the Lsm complexes.
To determine the effects of some of these Lsm8 mutations on complex formation, tagged proteins were precipitated with anti-GFP antibodies and co-precipitation of 13myc-Lsm7 (as a representative of the other members of the Lsm2-8p complex) was analyzed by western blotting. Lsm7-13myc was coprecipitated with GFP-Lsm8-2p, albeit less efficiently than with full-length GFP-Lsm8p, whereas GFP-Lsm8⌬N and GFP-Lsm8-313 did not pull-down any Lsm7p (Fig. 5C), although the GPF-Lsm8 proteins were present in similar amounts in the respective extracts (Fig. 5D). Also, overexpression of the Lsm8⌬N and Lsm8-313 proteins (which do not by themselves support growth; Table 1) did not affect growth of cells containing wild-type Lsm8p (data not shown), a finding that is compatible with these mutant proteins being incapable of competing with wild-type Lsm8p for assembly into Lsm2-8p complexes. Thus, the nuclear accumulation of the GFP-Lsm8 (mutant) proteins correlated with their ability Fig. 6. Over-production of Lsm1p or Lsm8p has opposing effects on Lsm7p localization. (A) HA-tagged Lsm1p or Lsm8p was overproduced from plasmid pAEM80 or pAEM76, respectively, in strain MPS2 (Lsm7-13myc) grown in SDGal-Ura. Lsm7-13myc localization (red in merge) in wild type (WT; MPS2 carrying pBM125 empty vector), or with LSM1 or LSM8 overexpression (o/e LSM1 and o/e LSM8, respectively). Over-production of Lsm1p caused reduction of nuclear Lsm7p (large arrow) and its accumulation in foci (small arrows). Bar, 10 m. (B) Lsm8p overproduction does not affect Lsm1p levels. MPS1 was grown with pBM125 or pBM125-HA-LSM8 in SD-Ura (Glu) or SDGal-Ura (Gal). Total protein was separated by SDS-PAGE and the western blot was probed for Lsm1-13myc, HA-Lsm8 and ␣-Tubulin. to associate with Lsm7p, which probably reflects their incorporation into a complete Lsm2-8p complex. Furthermore, in the presence of chromosomally encoded wild-type Lsm8p, plasmid-encoded GFP-Lsm8p shows weaker nuclear accumulation (Fig. 5Bviii). This is probably due to the Lsm8 protein being in excess over other members of the Lsm2-8p complex, and indicates that GFP-Lsm8p by itself does not accumulate in the nucleus. Taken together, these results strongly support the conclusion that the Lsm8 protein needs to interact with other Lsm proteins for its nuclear accumulation.
Over-production of Lsm1p or Lsm8p has opposing effects on Lsm7p localization To investigate the effect of overproducing Lsm1p or Lsm8p, HA-tagged LSM1 or LSM8 was overexpressed from the P GAL1 promoter in yeast cells in which LSM7 was myc-tagged. Overproduction of Lsm8p (confirmed by western blot; data not shown) caused an increase in the nuclear fraction of Lsm7p compared with control cells (Fig. 6A and Fig. 3A), whereas over-production of Lsm1p had the opposite effect, namely a Journal of Cell Science 120 (24) reduced level of nuclear Lsm7p and accumulation of Lsm7p in cytoplasmic foci (Fig. 6A), similar to depletion of Lsm8p (Fig.  3A). The level of Lsm1p did not change with LSM8 overexpression compared to no overexpression, as shown by western blot analysis (Fig. 6B).
Although Lsm8p is essential for viability, the lsm8-1 mutation, which causes dramatically decreased levels of Lsm8p, is not lethal, resulting only in a weak growth phenotype (Pannone et al., 1998). Intriguingly, Pannone et al. (Pannone et al., 1998) showed that the lsm8-1 mutation is synthetic lethal with deletion of LHP1 (which encodes the yeast homolog of La, another U6 RNA-binding protein), and that the requirement for Lhp1p in an lsm8-1 strain can be suppressed by low-copy overexpression of LSM2 (Pannone et al., 2001). In contrast to the effect of LSM2 overexpression, we found that overexpression of LSM1 in lsm8-1 cells (strain MPS17) resulted in a severe slow-growth phenotype, but had only a minor effect with wildtype cells (Fig. 7A). These results further indicate that Lsm1p and Lsm8p act in an antagonistic fashion. Because the Lsm2-8p complex is required for stability of the U6 snRNA, the level of U6 was examined in these yeast strains. When LSM1 was overexpressed in the lsm8-1 strain the U6 RNA level was reduced to only 10% of the wild-type level (normalized to the level of U1 snRNA; Fig. 7B), indicating that a high level of Lsm1p interferes directly or indirectly with the function of Lsm8p (in this case Lsm8-1p). Lsm7p localization was examined in the lsm8-1/LSM1 overexpression strain and was found to be almost entirely cytoplasmic, much of it in foci, and it was undetectable in the nucleus (Fig. 7C). Thus, the effect on the level of U6 snRNA of over-producing Lsm1p was most likely a consequence of reduced nuclear accumulation of the Lsm2-8p complex.
Lsm7p and Lsm8p are de-localized upon hyperosmotic shock The existence of an apparent equilibrium between the Lsm1-7p and Lsm2-8p complexes raises the possibility that this balance might be altered in response to changing physiological conditions. Therefore, Lsm7-13myc localization was examined after glucose deprivation (galactose or YP medium) or osmotic shock (exposure to 1 M KCl). As expected, Lsm7p accumulated in P-bodies at 5-15 minutes after glucose deprivation or hyperosmotic shock (Fig. 8A). There was also an apparent reduction in nuclear Lsm7p, which was most striking following hyperosmotic shock. Hyperosmotic shock also led to quick and almost complete depletion of Lsm8p from the nucleus (Fig. 8B). To determine whether these effects were due to active export of Lsm proteins from the nucleus, their localization was examined after hyperosmotic shock in the temperature-sensitive xpo1-1 strain (Fig. 8A,B). The xpo1-1 strains showed an identical shift of Lsm7-13myc and Lsm8-13myc to the cytoplasm, indicating that these proteins are not actively exported by Xpo1p after osmotic shock. Because the half-life of Lsm7p is more than 2 hours ( Fig. 8C; tested in a P GAL1 -LSM7strain, AEMY35) (Mayes et al., 1999), the reduced nuclear Lsm7p signal within 15 minutes of stress most probably represents movement of Lsm7p from the nucleus to the cytoplasm rather than failure of newly synthesized Lsm7p to enter the nucleus.
To rule out a non-specific effect of osmotic stress on nuclear protein localization, GFP-Lhp1 localization was examined before and after exposure to 1 M KCl (Fig. 8D). GFP-Lhp1 localizes exclusively to the nucleus, and concentrates in the nucleolus in some cells. No increase in cytoplasmic localization was detected 15 minutes after exposure to 1 M KCl. It did appear to localize to a smaller, more compact area, just like the DAPI-stained nuclear DNA. This is presumably due to an effect of osmotic stress on nuclear morphology and recovers after longer periods of time. By contrast, Lsm8-GFP showed delocalization similar to Lsm8-13myc, although somewhat less severe; interestingly, some cells showed accumulation of Lsm8-GFP at the nuclear periphery (Fig. S3 in supplementary material).
Lsm delocalization does not depend on Lsm1p, whereas relocalization does Delocalization of Lsm7 and Lsm8 proteins is reversible because nuclear levels return to normal after longer periods of incubation ( Fig. 9A; Fig. S3 in supplementary material and data not shown). Recovery was more complete for lower salt concentrations and started around 30 minutes after first exposure (Fig. 9A). Exposure to 1 M sorbitol showed a similar effect on Lsm8 and Lsm7-13myc localization (data not shown). Other effects of hyperosmotic stress, including those on translation initiation, have previously been shown to occur Fig. 9. Lsm-protein delocalization upon osmotic shock is reversible and Lsm1p-independent. (A) MPS3 (Lsm8-13myc) cells grown in YPDA were fixed before and at 5, 15, 30, 60 or 120 minutes after shifting to YPDA with 0.6 M NaCl. Lsm8-13myc is shown in red; DAPI in green. (B) MRY83 (lsm1⌬ LSM8-13myc) cells grown in YPDA were fixed before and at 5, 15 or 120 minutes after shifting to YPDA with 0.6 M NaCl. Lsm8-13myc is shown in red; DAPI in green. within a similar time-frame and recovery was shown to depend on the Hog1p protein kinase (Uesono and Toh, 2002). We therefore investigated Lsm8 and Lsm7-13myc localization after hyperosmotic shock in hog1⌬ strains (Fig. S4 in supplementary material and data not shown). Both delocalization and recovery were identical to that seen for the isogenic HOG1 strains, indicating that these effects are independent of this particular protein kinase. Because P-body localization of Lsm1-7p depends on Lsm1p (Tharun et al., 2005) and osmotic shock leads to accumulation of Lsm proteins in these cytoplasmic foci, we investigated whether nuclear delocalization of Lsm proteins is dependent on Lsm1p (Fig. 9B). Surprisingly, nuclear localization of Lsm8-13myc was slightly reduced in an lsm1⌬ strain under normal growth conditions. This effect was even more apparent for GFP-Lsm8 expressed in the same strain background (data not shown). Delocalization of Lsm8-13myc from the nucleus was even stronger after hyperosmotic shock and failed to recover after up to 2 hours in YPDA with 0.6 M NaCl, whereas some (incomplete) recovery occurred when cells were shifted back to YPDA. These results might indicate that, in the lsm1⌬ strain, Lsm8p might move to the cytoplasm to replace Lsm1p.

Discussion
In this work, factors that affect the localization of the Lsm7 and Lsm8 proteins were investigated in order to try to understand what determines the nuclear localization of the Lsm2-8p complex. The results show that Lsm8p is a determinant for the nuclear accumulation of Lsm7p, although they do not clearly distinguish between nuclear import and nuclear retention. However, considering the effect of the nup49-313 nuclear-pore mutation as well the previously demonstrated dependence of Lsm8p nuclear accumulation on importin ␤ (Spiller et al., 2007), Lsm8p might function as a nuclear-import determinant for the rest of the Lsm2-8p complex. The deletion studies show that most of the Lsm8p sequence seems to be essential, including the N-terminus, the Sm domain and the C-terminus. In particular, a deletion of part of the Sm domain caused a dramatic mislocalization of Lsm8p, strongly suggesting the importance of interaction with other Lsm proteins for nuclear accumulation of Lsm8p. Unexpectedly, a relatively small N-terminal deletion outside the Sm core motif also affected complex formation. In principal, this could be due to a direct or indirect effect on complex formation or complex stability.
These results strongly suggest that Lsm8p must interact with other Lsm proteins to form a nuclear-localization signal that is unlikely to be of the basic SV40 type of NLS. Whereas depletion of Lsm2p and Lsm4p, the presumed neighbours of Lsm8p in the Lsm2-8p complex, resulted in delocalization of Lsm8p, lack of the non-essential Lsm6p had no apparent effect. By contrast, the complete Lsm2-8p complex is required for nuclear accumulation of U6 snRNA (Spiller et al., 2007). Lsm6p and Lsm7p are nonessential; thus, in the absence of Lsm6p or Lsm7p, alternative Lsm complexes must form in which there are fewer subunits or in which Lsm6p and Lsm7p are replaced by other proteins (Verdone et al., 2004). However, because U6 snRNA is unstable and mislocalized in lsm6⌬ and lsm7⌬ strains, these alternative complexes are probably less-stably associated with U6 snRNA. Thus, nuclear retention of U6 snRNA requires its stable association with a complete Lsm2-8p complex. The normal Journal of Cell Science 120 (24) occurrence of nuclear Lsm complexes that have different subunit compositions and that associate with other RNAs is possible. For example, the processing of pre-tRNAs, pre-snoRNAs and pre-rRNAs is unaffected by lack of Lsm6p or Lsm7p, but depends on Lsm2, Lsm3, Lsm4, Lsm5 and Lsm8 (Kufel et al., 2003b;Kufel et al., 2002;Kufel et al., 2003a). The proposed existence of an Lsm2-7p complex that associates with snR5 in the nucleolus (Fernandez et al., 2004) is in apparent contradiction with our finding of Lsm8p requirement for nuclear localization. It seems possible that the full Lsm2-8p complex might interact with snR5, but that the Lsm8p epitope tag might be masked in the snR5 RNP.
Our results are compatible with the observation of Zaric et al. (Zaric et al., 2005) that an RNA-free LSM2-8 complex, which had been pre-assembled from recombinant human LSM proteins and injected into the cytoplasm of rat fibroblast cells, accumulated in nuclei, whereas LSM8 alone did not. Thus, the Lsm2-8 assembly pathway might be conserved throughout eukaryotes.
Because all the Lsm proteins are small enough to diffuse into the nucleus, there might be a mechanism to retain the Lsm1-7p complex in the cytoplasm. In this scenario, if Lsm1p is present in excess, Lsm2-Lsm7 proteins will be cytoplasmic unless incorporated into the Lsm2-8p complex. This might explain why depletion of Lsm8p had the most-dramatic effect on the nuclear localization of Lsm7p, because lack of any of the other Lsm proteins probably affects formation of the cytoplasmic Lsm1-7p complex as well, thereby allowing some diffusion of free Lsm7p into the nucleus. This can also explain the strong antagonistic effect of over-producing either Lsm1p or Lsm8p, if each is competing for the same pool of cytoplasmic Lsm proteins rather than interacting with the available pools of cytoplasmic or nuclear Lsm proteins, respectively.
Although no increased nuclear accumulation of Lsm7p was observed in an lsm1 deletion strain, nuclear accumulation of Lsm7p might be limited by the level of Lsm8p. One of the major functions of Lsm2-8p is in U6 snRNP biogenesis and stability, and repression of LSM8 transcription stops cell growth (Mayes et al., 1999). However, the lsm8-1 mutant strain, which has a low level of Lsm8 protein, has only a moderately reduced U6 snRNA level and no growth defect at 30°C, suggesting that the yeast cell requires only a low level of Lsm8p for survival. This could explain why overexpression of Lsm1p does not cause a significant growth defect despite the effect on Lsm7p localization. The fact that it requires both mutation of LSM8 and overexpression of LSM1 to see a severe effect on cell growth indicates that the yeast cell can absorb large reductions in Lsm2-8p complex without significant deleterious effects. Thus, the ability to survive severe alterations in the levels of Lsm complexes in these mutant strains suggests that wild-type cells might significantly alter the equilibrium in response to various stimuli and stresses without detrimental effects.
As shown here, causing stress by hyperosmotic shock, or to a lesser extent by glucose deprivation, leads to a rapid shift of Lsm proteins from the nucleus to the cytoplasm and localization of Lsm1-7p to P-bodies. However, this delocalization depends neither on P-body formation (no effect of hog1⌬), nor on the presence or action of Lsm1-7p in these foci (no effect of lsm1⌬). By contrast, Lsm1p appears to be essential for relocalization when cells recover from hyperosmotic shock, indicating that an intact Lsm1-7p complex is required. The activity of Lsm1-7p in RNA turnover might be required for cells to efficiently reprogramme to cope with a sudden change in conditions.
Because the Lsm1 and Lsm8 proteins are rather similar in sequence, it is remarkable that they effect the different localizations of their constituent complexes. A moreextensive analysis of the mechanism of Lsm-complex localization will require a detailed examination of the roles of individual amino acids in these and other Lsm proteins, and is a focus of our ongoing investigations. In addition, there is the interesting question of why has the family of Lsm proteins evolved to form two competing complexes? The multiple functions of the Lsm proteins and their conservation throughout all organisms suggests that they evolved as general RNA/RNP chaperones, and that gene amplification produced the many Sm and Lsm proteins now found in eukaryotes, with their more specialized functions possibly being determined by their localization in the cell. Interestingly, no LSM1 gene has been identified in the genomes of Trypanosoma brucei or Trypanosoma cruzi, and RNA-silencing experiments in T. brucei indicate that Lsm8 functions in both U6 stabilization and mRNA decay, suggesting that a single Lsm protein performs the roles of Lsm1 and Lsm8 (Liu et al., 2004). Thus, it seems likely that Lsm1 and Lsm8 have evolved from a common ancestral protein by gene duplication, and developed separate intracellular locations and functions. Having two or more Lsm complexes, with overlapping composition, involved in different metabolic processes, such as pre-mRNA splicing and degradation in the nucleus and mRNA degradation in the cytoplasm, allows scope for a regulatory link between these processes. For example, by transiently varying the relative levels of each Lsm complex, nuclear RNA degradation could be reduced while cytoplasmic RNA turnover is enhanced. This would allow a quick and efficient change in genome expression in response to a sudden change in environmental conditions. Our overexpression experiments show that such effects can be artificially created, and similar effects in cells under stress show that cells are able to respond by changing sub-cellular localizations of the Lsm1-7p and Lsm2-8p complexes, thus allowing co-regulation of nuclear and cytoplasmic RNA-processing events.

Yeast media, plasmids and strains
Yeast media and manipulations were as described previously (Sherman, 1991); YPGalA is YPDA with 2% glucose replaced by 2% galactose. For overexpression in yeast and for GFP fusions, complete synthetic drop-out medium (SD) was used. A list of plasmids used is given in Table S1 in supplementary material, and yeast strains are described in Table S2 in supplementary material.

Construction of epitope-tagged proteins
Thirteen copies of coding sequence for the c-myc epitope were integrated at the 3Ј end of the LSM genes by homologous recombination in BMA38a or a mutant derivative, using PCR product amplified from pFA6a-13Myc-kanMX6 (Longtine et al., 1998) or pFA6a-13Myc-HphkanMX6 (derived from pFA6a-13Myc-kanMX6, our laboratory). Each PCR-amplified DNA contained the last 45 base pairs of Lsm coding sequence, thirteen copies of the c-myc epitope, hygromycin-or kanamycinresistance sequence, and 45 base pairs of downstream sequence. All wild-type tagged strains exhibited wild-type growth at 14, 23, 30 and 37°C.

GFP-tagged constructs
GFP-tagged genes were constructed by PCR amplification of the relevant part of LSM8, using primers containing XbaI and ClaI sites at their 5Ј ends. The PCR products were cut with XbaI and ClaI and ligated into pGFP-N-FUS or pGFP-C-FUS (Niedenthal et al., 1996). Site-directed mutagenesis was performed (Costa et al., 1996) to delete the part of the LSM8 gene encoding the N-terminal Sm motif. Details of the GFP-Lsm8p fusions are given in Table 1.

Immunofluorescence and fluorescent in situ hybridization
For immunofluorescence, yeast cells grown to logarithmic phase in liquid medium were fixed for 40 minutes in 3.7% formaldehyde and spheroplasted for 30 minutes with Lyticase. Cells were incubated with anti-myc antibody (Abcam) overnight in 5% milk, and then for 2 hours with Cy3-conjugated anti-mouse antibody (Jackson ImmunoResearch). Mounting media containing DAPI (Vectashield) was added and cells were viewed using a Leica FW400 microscope.
For in situ hybridization, yeast cells in logarithmic growth phase in liquid culture were fixed, probed with fluorescently labelled oligodeoxynucleotides, stained with DAPI and imaged as described previously (Long et al., 1995;Samarsky et al., 1998).
Imaging was performed essentially as described (Carter et al., 1993;Samarsky et al., 1998) and images were captured using LeicaFW4000 software (Scanalytics, Fairfax, VA) with a CH-250 16-bit, cooled CCD camera (Photometrics, Tucson, AZ) mounted on a Leica FW4000 fluorescence microscope (Leica). When images were restored, a three-dimensional data set, composed of 20 images separated by 200 nm in the axial direction, was acquired and deconvolved with an acquired point spread function using Leica Deblur software (Leica). Oligonucleotide probes for the U1 snRNA were labelled with a single fluorescein attached to the 5Ј end and had the sequences 5Ј-ACACCAATTTGAATTTGGGTGTCAAACTTCTCC AGGC A -GAAGAAACAAAGGGCCCCAAAAATCAGTTTAA-3Ј and 5Ј-AATCTCCGTC -AAAAACTAAAATGGCACGCTAGAGAAAAGTAGTCAAAAAGAATGCCTC -TACAAAG-3Ј.

RNA extraction and northern blotting
Total RNA was extracted (Schmitt et al., 1990) from BMA38a and lsm8-1 cells carrying either pAEM80 or an empty vector that had been grown in SDGal-Ura medium to OD 600 0.5. Purified RNA was fractionated in an 8% (19:1) denaturing acrylamide urea gel. After transfer to nitrocellulose, the membrane was probed with labelled DNA complementary to the U1 and U6 snRNAs (Cooper et al., 1995). Total RNA was similarly extracted from MPS7, MRY76 and MRY77 cells before and after growth in YPDA. The same probes for U1 and U6 snRNAs were used, as well as probes against U3A (5Ј-GGTTATGGGACTCATCA-3Ј) and scR1 (5Ј-ATC CC -GGCCGCCTCCATCAC-3Ј)