- Research article
- Open Access
Immobility, inheritance and plasticity of shape of the yeast nucleus
BMC Cell Biology volume 8, Article number: 47 (2007)
Since S. cerevisiae undergoes closed mitosis, the nuclear envelope of the daughter nucleus is continuous with that of the maternal nucleus at anaphase. Nevertheless, several constitutents of the maternal nucleus are not present in the daughter nucleus. The present study aims to identify proteins which impact the shape of the yeast nucleus and to learn whether modifications of shape are passed on to the next mitotic generation. The Esc1p protein of S. cerevisiae localizes to the periphery of the nucleoplasm, can anchor chromatin, and has been implicated in targeted silencing both at telomeres and at HMR.
Upon increased Esc1p expression, cell division continues and dramatic elaborations of the nuclear envelope extend into the cytoplasm. These "esc apades" include nuclear pores and associate with the nucleolus, but exclude chromatin. Escapades are not inherited by daughter nuclei. This exclusion reflects their relative immobility, which we document in studies of prezygotes. Moreover, excess Esc1p affects the levels of multiple transcripts, not all of which originate at telomere-proximal loci. Unlike Esc1p and the colocalizing protein, Mlp1p, overexpression of selected proteins of the inner nuclear membrane is toxic.
Esc1p is the first non-membrane protein of the nuclear periphery which – like proteins of the nuclear lamina of higher eukaryotes – can modify the shape of the yeast nucleus. The elaborations of the nuclear envelope ("escapades") which appear upon induction of excess Esc1p are not inherited during mitotic growth. The lack of inheritance of such components could help sustain cell growth when parental nuclei have acquired potentially deleterious characteristics.
The position, shape, size and orientation of organelles varies among differentiated cells, thereby allowing distinct cell types to be recognized. The approximately spherical nucleus itself generally is near the center of the cell and in yeasts the spindle pole body (SPB) provides a landmark at one pole of the nucleus, thereby allowing one to witness changes of nuclear orientation during the cell cycle [1, 2]. Related to these observations is the question of whether all portions of the nuclear envelope (NE) are necessarily inherited by the daughter nucleus at mitosis – an issue which bears directly on the ability of cells to cope with the impact of damage or change accrued during a single generation. The present investigation shows that a novel landmark of the perimeter of the yeast nucleus is not inherited.
The nuclear lamina in higher eukaryotic cells governs nuclear morphology and serves as a scaffold for the organization of the nucleoplasm, where it anchors heterochromatin and can affect both DNA replication and transcription. The best-characterized proteins of the lamina are the intermediate filament lamins, which self-associate via coiled-coil domains, generating a compact meshwork at the nuclear periphery .
Alterations in the structure, organization, and composition of the nuclear lamina are likely to account for aberrant shapes of the nuclei of malignant cells, as well as the distinct nuclear morphology of neutrophils. Moreover, the increased titer of mutant lamins can have major consequences for the shape and integrity of the nuclear surface [3–6]. Lamin orthologs are absent from yeast, and it is not known whether a structural or functional equivalent of the lamina exists in S. cerevisiae. When higher eukaryotic lamin B1 or its receptor is expressed in S. cerevisiae, these proteins concentrate at the periphery of the nucleoplasm .
Several non-membrane proteins that normally localize to the periphery of the nucleoplasm in yeast possess coiled-coil domains (Esc1p, Mlp1/2p, Sir4p, Smc5/6p) [8–11]. Esc1p (Establishes Silent Chromatin), contains three equally spaced coiled-coil domains, can function as an anchor for chromatin, interacts with Rap1p and Sir4p, promotes targeted silencing at telomeres and HMR, is needed for proper organization of the "nuclear baskets" of nuclear pores, and promotes nuclear retention of unspliced transcripts [8, 12, 13]. Esc1p is larger than lamins (187 vs 70 kDa) and lacks the C-terminal isoprenylated CAAX motif present in A and B-type lamins.
The present study demonstrates that accumulation of Esc1p at the nuclear periphery causes dramatic modifications of the nuclear envelope. These modifications are structurally distinct from those which have been reported in a screen of deletion strains  or upon deletion of an ER/NE membrane phosphatase [15–17], mutation of components of the nuclear pore complex , proteins which function in the early secretory path [19, 20], or Acc1p, which reduces very long-chain fatty acids . Interestingly, the titer of Esc1p affects levels of several transcripts, only some of which originate from telomere-proximal loci. The structural abnormalities of the NE which are caused by Esc1p are not passed on to daughter cells, showing that inheritance of components of the nuclear perimeter can be selective.
To learn whether the composition of the nuclear periphery influences nuclear shape, and to extend previous observations on Esc1p , we have induced synthesis of GFP-tagged Esc1p in S. cerevisiae. After 3–5 hrs we observe the progressive elaboration of fin- and ring-like "esc apades" that extend from the surface of > 80% of nuclei. ~6% of nuclei also have bright patches of GFP-Esc1p at the nuclear periphery. After overnight induction, rings and patches predominate (Fig. 1A). Similar observations have been made with both haploid and diploid strains. Equivalent observations have also been made with untagged Esc1p, in which case we visualize a GFP-tagged ER membrane protein to define the perimeter of the nucleus (Fig. 1B). Judging from estimates of transcript levels presented below, the titer of Esc1p could increase as much as 20–30x over controls upon overnight induction.
Images of cells which express Nup49p-GFP (Fig. 1C) show that escapades include nuclear pores (Fig. 1C). Ultrastructural examination also detects nuclear pores in the escapades and demonstrates that escapades are double-membrane sheets (rather than tubules) of constant width (Fig. 1D). Since escapades are limited by two layers of NE it is reasonable that – in cells expressing GFP-Esc or ER membrane proteins – their fluorescent intensity can exceed that of the rest of the NE (Fig. 1A/B). Time-lapse observations show that the position and contour of most escapades remains essentially constant for tens of minutes; however the fin-like structures occasionally fuse back to the nucleus and generate rings (Fig. 1E). Examination of cells which express a tagged histone (Htb2p-mRFP) as well as GFP-Ec1p shows that escapades include little or no chromatin (Fig 1F).
To learn whether excess of other proteins of the nuclear periphery causes similar changes, we have compared the impact of excess Esc1p to that of the non-membrane protein, Mlp1p [See Additional file 1] which colocalizes with Esc1p [9, 22], the tail-anchored inner membrane protein, Prm3p  [See Additional file 2], and the integral membrane proteins of the inner membrane, Heh1p and Heh2p  [See Additional files 3 and 4]. Excess Mlp1p is known to distribute throughout the nucleoplasm . As shown, Mlp1p has no obvious effect and Prm3p causes changes of the NE roughly comparable to those caused by Esc1p. By contrast, the Heh proteins are much more perturbing, with Heh1p not even leaving the quasi-spherical shape of the chromatin mass intact. Induction of either Esc1p or Mlp1p allows continued growth, while induction of Heh1p, Heh2p, or Prm3p is toxic (not shown). We therefore have not pursued these membrane proteins further.
Relation of Escapades to Intranuclear Structures
In cells which express the nucleolar marker, Sik1p-mRFP, and can be induced to express GFP-Esc1p, systematic examination of through-focal series after 5 hr induction shows that > 90% of escapades contact the perimeter of the nucleus at or immediately adjacent to the nucleolus (Fig. 2A, and see Additional file 5). The nucleolus is not however present within the escapades themselves. The yeast spindle pole body (SPB) is embedded in the NE at a position which is usually opposite the nucleolus [25, 26]. Consistent with the observed nucleolar association, the localization of escapades and karmellae does not coincide with the tagged SPB protein, Spc42p (Fig. 2B and see Additional file 6). Systematic counting of through-focal series of cells which exhibit escapades shows that only ~10% of the tagged SPBs contact escapades. Another modification of the NE, the "karmellae" which result from overexpression of HMG-CoA reductase, also associates with the nucleolus  and avoids the SPB (Fig. 2C). A third instance of association with the nucleolus is that of the "flares" which appear upon deletion of the ER/NE membrane proteins, Nem1p or Spo7p. In this case, the flares define a pocket which encloses the nucleolus .
Since centromeres are close to the SPB during most of the cell cycle , we also studied their relation to escapades, using cells which express lac operator arrays integrated near a centromere and GFP-tagged lac repressor. No obvious association is seen between this centromere and escapades (Fig. 2D and see Additional file 7). Equivalent experiments to localize a telomere again show no obvious association (Fig. 2E and see Additional file 8). In both cases, systematic counting of through-focal series of cells which exhibit escapades shows that only ~10–12% of the tagged loci contact escapades. A functional GFP-tagged form of the telomere-associated protein, Rap1p, which binds Esc1p , also is not detected outside the chromatin mass, as would be expected if it were in escapades (Fig. 2F and see Additional file 9). This is also the case for Sir4p .
Formation of Escapades-Relation to Cytoplasmic Structures
Following the separation of sister chromatids at the onset of anaphase, the nucleus of the mother cell quickly extends into the bud, generating a dumbbell-shaped structure with a narrow bridge of NE connecting the two nuclei . Fission of the bridge leaves protruding membrane remnants that are normally resorbed by the two resulting nuclei. Escapades superficially resemble these remnants and therefore might be derived from them. Nevertheless, time-lapse microscopy of cells which exit mitosis shows that GFP-Esc1p-positive remnants are efficiently resorbed, as in control cells (see below). Moreover, cells treated with α-factor (3 hr, 1 μg/ml) [See Additional file 10] or hydroxyurea (3 hr, 0.1 M) [See Additional file 11] can generate escapades when Esc1p expression is induced in the absence of cell cycle progression.
The formation of escapades does not appear to depend on the integrity of the tubulin or actin cytoskeleton, judging from experiments in which they are induced in the presence of doses of nocodazole or latrunculin A which effectively depolymerize the corresponding cytoskeletal structures [See Additional files 12 and 13].
Like the surface of the yeast nucleus , escapades are intimately associated with vacuoles, as detected with the membrane dye, FM4-64 (Fig. 3A). Live-cell imaging reveals that escapades can originate at or near the nucleus-vacuole junction (NVJ), prior to extending along the surface of the vacuole (Fig. 3B). Nevertheless, small ring-like escapades and patches of Esc1p can be induced in pep3-Δ cells which lack conventional vacuoles  (Fig. 3C).
Inheritance of Escapades
The distribution of escapades was examined as cells pass through anaphase. Intriguingly, they are excluded from > 95% of daughter nuclei (Fig. 4/Table 1). The asymmetric distribution is especially conspicuous in a mob1-77 mutant which makes it possible to maintain cells in late anaphase for hours (Table 1) .
Why are Escapades not Present in Daughter Nuclei ?
Escapades could be actively retained by the maternal nucleus, excluded from the daughter nucleus, or could simply not be able to diffuse in the plane of the membrane. Since septin filaments at the bud neck can restrict transfer of proteins between mother and bud [32–35], we have examined inheritance in strains that carry mutations in septin subunits and disorganize the septin collar at the restrictive temperature (cdc3-3, cdc10-1). In these mutants, escapade exclusion from daughter nuclei is again seen (Table 1). Karmellae are also restricted to the mother in wt and in septin mutants (not shown). Consistent with the suggestion that there is no structural impasse at the bud neck, most escapades which remain in the mother do not accumulate at the neck. Moreover, electron microscopic examination shows that a significant space separates the outer nuclear membrane from the inner aspect of the plasma membrane at the bud neck during anaphase .
To evaluate the maternal retention model, we have studied the distribution of escapades in cells for which nuclear division does not require traversal of the bud neck. For this purpose, we have disrupted actin filament integrity with latrunculin A, which allows the spindle to deviate from the mother/bud axis, with the result that nuclear division can occur entirely within the maternal cytoplasm. Strikingly, escapades are restricted to a single nucleus in such binucleates (Fig. 5). This finding led us to investigate whether association with the vacuole could account for maternal retention; however, escapades are overwhelmingly retained in a pep3Δ strain (Table 1).
To inquire whether escapades and karmellae are intrinsically immobile, we have examined the constancy of their position when the nucleus with which they associate fuses with a conventional nucleus during karyogamy. As shown in Fig. 6, they show no tendency to migrate into the trans nucleus over a period of time greater than that required for anaphase. Nevertheless, tagged nuclear pores are able to access the trans nucleus [37, 38]. Note the rapid transit of GFP-Esc1p to the trans nucleus. At least at this level of expression, it has considerable mobility.
Despite dramatic changes in nuclear shape, cells that express excess Esc1p or GFP-Esc1p are not seriously growth impaired in liquid culture or on solid media. Furthermore, they show a distribution of DNA content comparable to wt, and can mate (not shown and Figure 6). The maternal restriction of escapades may direct most physiological consequences of their presence to the mother and thereby contribute to the lack of a major growth phenotype, as each cell division produces progeny which initially lack escapades.
It is therefore of interest that a differential effect at the level of cell cycle progression is evident. Normally, when a mother cell gives rise to a daughter, the mother will rebud quickly, while daughters must grow to a critical size before budding . By contrast, when pre-induced GFP-Esc1p-expressing cells are observed, the bud interval is slowed in mothers (possibly due to interference by the escapades themselves) and accelerated in daughters. As a result, the difference in timing of budding between mothers and daughters is reduced by more than 50% (Fig. 7). The net impact of these events could account for the modest reduction of relative growth rate which can best be detected in mixed cultures in which isogenic wt and GFP-Esc1p-expressing cells are both present. Pure cultures of cells which can be induced to express GFP-Esc1p remain fluoresecent for days of culture in galactose medium, while addition of an equal number of wild type cells prior to culture is followed by a gradual and progressive reduction in the proportion of fluorescent cells.
To further investigate the consequences of excess Esc1p, we initiated microarray analysis of poly(A)+ mRNAs of a pair of isogenic strains grown in galactose medium, only one of which allows Esc1p induction from a GAL1 promoter (Table 2). Upon overnight growth in galactose medium, there is a ~20–30x increase in the signal corresponding to ESC1 mRNA and only 48 other changes which exceed 1.8x fold. Both positive and negative changes are seen. Considering that GFP-Esc1p concentrates at the extreme periphery of the nucleoplasm along with telomeres, it is of interest that both the increases and decreases (> 1.8 fold) are enriched within 40 kb of telomeres, i.e. even though this region accounts for only ~4.1% of the length of the average yeast chromosome, it accounts for ~30% of these changes. Nevertheless, ~70% of the changes are not in this region. No notable changes in mRNA levels were seen for genes whose products associate with Esc1p, such as RAP1 and SIR4. Since deletion of ESC1 does not obviously affect nuclear morphology [See Additional file 14], we have not investigated corresponding transcriptional changes.
The morphology of organelles is intimately related to their function and deviation from normal morphology can have profound physiological consequences. It is thus plausible that NE shape alterations contribute to events which cause cellular malfunction in disease.
Nevertheless, radical changes of the composition of the nuclear periphery can be compatible with cell survival, as in a variety of yeast deletion strains lacking transmembrane proteins which localize to the NE and ER (Nem1p, Spo7p, Ssh1p), nucleoplasmic proteins (Thp1p), or nucleoporins (Seh1p) [14, 17]. None of these proteins normally are restricted to the periphery of the nucleoplasm itself.
Interestingly, the shape of the nucleus is not affected by deletion of Esc1p or deletion of two other proteins which normally localize to the periphery of the nucleoplasm, Mlp1p and Mlp2p [9, 22, 40]. Moreover, the growth of nem1-Δ, seh1-Δ, spo7-Δ, ssh1-Δ and thp1-Δ  is not obviously affected by overexpression of Esc1p (not shown).
Mutations in nuclear lamina constituents, most notably lamin A and C, cause a diverse spectrum of diseases, the laminopathies. Laminopathies caused by excess pre-lamin A at the nuclear periphery are characterized by bleb-like expansions of the nuclear surface [41–44]. The dependence of the shape of the yeast nucleus on both nuclear membrane proteins and proteins that concentrate at the periphery of the nucleoplasm is reminiscent of a distinct laminopathy (Emery-Dreyfuss Muscular Dystrophy), which can result from either mutation of the inner nuclear membrane protein, emerin, or mutation of lamin A [45, 46]. Moreover, overexpression of a GFP-tagged form of the inner membrane protein, Prm3p, distorts the shape of the NE in much the same fashion as Esc1p, and excess Heh1p and Heh2p  grossly distort the NE and chromatin mass, while Mlp1p induction has no obvious impact. These differential effects may signify that the Heh proteins have a high affinity for chromatin, that Esc1p and Prm3p are more closely linked to the inner nuclear membrane per se than to chromatin, and that Mlp1p is relatively independent.
The characteristic structure of escapades and distribution of excess GFP-Esc1p are compatible with the hypothesis that excess Esc1p forces enlargement of the NE due to end-to-end association of the protein, that chromatin has an intrinsic coherence which tends to preserve a roughly globular shape, and that the inner aspect of the NE (or perhaps Esc1p itself) can also self-associate laterally (Fig. 8). Indeed, although there has never been an experimentally accessible model for investigation of this latter issue, the NE of malignant cells – like escapades – is frequently characterized by focal self-apposition of the lamina and/or the nucleoplasmic surface of the inner nuclear membrane [47, 48].
There is no reason to expect that Esc1p is fully comparable to higher eukaryotic lamins. For example, unlike lamins, tagged Esc1p (or Mlp1p) expressed from its own promoter does not completely encircle the nucleus, being absent from beneath the nucleolus [13, 40]. Moreover, the observation of rapid diffusion of GFP-Esc1p upon karyogamy shows that at least the overexpressed protein is mobile.
The transcriptional consequences of overexpressing Esc1p emphasize the importance of this protein (or escapades themselves) for gene expression. Since both negative and positive changes are seen, Esc1p appears to be a complex regulator, not only an enhancer of silencing. In this regard, it resembles many transcriptional regulators including Rap1p . It is also notable that ~70% of the changes which we detect occur at loci which are further than 40 kb from telomeres (which concentrate at the periphery). In addition to their intrinsic interest, these microarray data provide a possible prototype against which to evaluate the transcriptional characteristics of laminopathies, which presumably account for their cell type-specific effects.
Daughter cells differ from mothers in several regards [50, 51]. Escapades are not transferred to daughter cells, apparently due to their immobility. These structures – and karmellae – are thus part of a "lagging" domain of the nuclear perimeter. The nucleolus may also be part of this domain, judging from its association with escapades and karmellae, as well as the observation that it is one of the last nuclear components to reach the bud during anaphase [52, 53]. Extra rDNA circles  and ARS plasmids  are also retained.
This study demonstrates the extreme structural plasticity of the yeast nucleus and shows that the unusual "escapades" which can be generated are essentially immobile and therefore are not inherited. Their lack of inheritance provides a striking example of the exclusion of epigenetic change. Such mechanisms – coupled with equivalent normalization of phenotype at the molecular level – are likely to sustain cell identity through mitosis. Higher eukaryotic cells may cope with such issues by extensive disassembly and reassembly of the NE during mitosis, which could provide an opportunity to avoid incorporation of structurally aberrant components.
Yeast Strains and Plasmids
Yeast strains and plasmids used in this study are listed in Table 3 and Table 4. The GFP-tagged form of Esc1p which we employ is known to complement the plasmid partitioning defect of esc1Δ . Strains were constructed using standard methods for transformation, mating, and sporulation. To place ESC1 transcription under control of a galactose-inducible promoter, we used the plasmid, pFA6A-pGAL1 , as template to generate PCR products which could be targeted upstream of ESC1. Plasmid pMET25-GFP-ESC1 was constructed by PCR sub-cloning of the full length Esc1p coding sequence from plasmid pEDA129 , into pGFP-N-FUS . Restriction endonuclease sites, SpeI and XhoI, present in the polylinker, were utilized such that the ESC1 ORF is in-frame down-stream of GFP and expression is driven by the methionine-repressible MET25 promoter and terminated by the CYC1 terminator. Recombinant clones were identified by restriction endonuclease analysis and DNA sequencing of the 5' cloning junction to verify orientation and reading frame. The level of expression observed in transformed strains cultured under inducing conditions was sufficient to generate NE alterations.
Media and Supplements
Cells were grown in complete synthetic medium or the appropriate dropout medium supplemented with 2% D-glucose, D-raffinose or D-galactose. Generally strains were maintained in mid-log phase in raffinose medium and were induced by addition of galactose. All incubations were at room temperature except when ts conditional strains needed to be shifted to 37°C. As required, media were supplemented with: 200 μM latrunculin A (Sigma) diluted from a 20 mM stock in DMSO, 5 μg/ml α-factor (Sigma) diluted from a 5 mg/ml stock in sterile water, 0.1 M hydroxyurea (Sigma) diluted from a 1 M stock in sterile water, 15 μg/ml nocodazole (Sigma) diluted from a 3 mg/ml stock in DMSO, or 40 μM FM4-64 (Molecular Probes) diluted from a 2 mM stock in DMSO.
GAL-GFP-Esc1p strain ATY2102 and isogenic wild-type ATY2501 were grown overnight to mid-log phase in galactose-containing synthetic medium at room temperature. Total RNA was purified from duplicate 1 ml samples by mechanical disruption with 0.2 micron glass beads in an equal volume of hot acid phenol and used for biotinylated cRNA synthesis according to Affymetrix protocols at the Case Cancer Center Gene Expression Array Facility. Replicate samples were hybridized to Affymetrix GeneChip yeast genome Y98 arrays. Scanned chip images were analyzed with the Affymetrix GeneChip Operating Software (GCOS) using the MAS 5.1 algorithm for fold-change calculations. The results were tabulated with Microsoft Access and annotated using NETAFFX (Affymetrix) and Genespring (Silicon Genetics) software packages. In the tabulation in Table 2, the average values for GFP-Esc1p-overexpressing cells are divided by the averaged data for control cells.
GAL-GFP-Esc1p strain ATY2102 and isogenic wild-type strain ATY2501 were pre-induced in galactose media for 3 hrs at 23°C, washed and examined on agarose pads in glucose medium over 5 hr, during which time fluorescent escapades remained visible. DIC images captured every 10 min allowed measurement of the timing of bud initiation for each cell in four replicate experiments. Time measurements were all relative to the emergence of the first bud by each mother cell, M1. For example, the mother's bud interval, M2-M1 measures the delay prior to the appearance of the second bud on the mother. Correspondingly, D-M1 measures the interval prior to the appearance of the first bud on the daughter.
The time difference of budding between mothers and daughters is referred to as the budding differential and is calculated as: (D-M2 = bud differential) where D is the time at which a bud appears in the daughter cell and M2 is the time at which a second bud appears in the mother cell.
Epifluorescent, phase time-lapse, and DIC microscopy were performed on a Leica DMLB microscope equipped with a SPOT camera (Diagnostic Instruments Inc.) and the SPOT Advanced software package. Confocal microscopy for live cell Z-stack and time-lapse imaging were performed on either a Zeiss LSM510 or a Leica AOBS. Volocity (Improvision) and Metamorph (Molecular Devises) software packages were utilized for image analysis and generation of time-lapse movie sequences. Other z-stack images were collected with a DeltaVision microscope and deconvolved before inspection. For quantitation of association of escapades with various structures, through-focal series were examined systematically and the distribution of nucleoli, etc. was counted in greater than 100 cells.
Vacuole membrane staining with the vital dye FM4-64 was conducted according to  with the following modifications. Briefly, log phase galactose-induced cultures were concentrated by centrifugation and resuspended at OD600 = 1 in glucose-containing medium supplemented with 40 μM FM4-64. The cells were then incubated at 30°C with shaking for 30–60 minutes, followed by extensive washing to remove excess dye. Stained vacuoles were imaged at 546 nm with a Zeiss LSM510 confocal microscope.
For time-lapse microscopy, dilute cultures were briefly centrifuged and 2 μl aliquots from the pellet were applied to the middle of 1.5% Agarose pads prepared on microscope slides in glucose- or galactose-containing culture medium, as appropriate. Samples were overlayed with a coverslip and sealed with vaseline before examination.
To learn whether escapades or karmellae are free to move in the plane of the NE, we have crossed cells which express these structures with cells of the opposite mating type and then observed the structure of the nucleus during and after nuclear fusion. For this purpose, pairs of cells grown overnight in galactose-containing medium were mixed, sedimented, and applied to an agarose pad in glucose-containing complete synthetic medium (as above). After approximately 2 hrs, they were observed.
Transmission electron microscopy was performed on samples prepared from cultures grown to mid-log phase at 30°C. Samples were fixed in 2% glutaraldehyde followed by secondary fixation/staining in 4% potassium permanganate and uranyl acetate en bloc. Samples were dehydrated, embedded in Spurr resin, stained with lead citrate and uranyl acetate and examined in a JEOL 1200CX EM.
Jaspersen SL, Winey M: The budding yeast spindle pole body: structure, duplication, and function. Annu Rev Cell Dev Biol. 2004, 20: 1-28. 10.1146/annurev.cellbio.20.022003.114106.
Loidl J: Chromosomes of the budding yeast Saccharomyces cerevisiae. Int Rev Cytol. 2003, 222: 141-196.
Gruenbaum Y, Margalit A, Goldman RD, Shumaker DK, Wilson KL: The nuclear lamina comes of age. Nat Rev Mol Cell Biol. 2005, 6 (1): 21-31. 10.1038/nrm1550.
Best S, Salvati F, Kallo J, Garner C, Height S, Thein SL, Rees DC: Lamin B-receptor mutations in Pelger-Huet anomaly. Br J Haematol. 2003, 123 (3): 542-544. 10.1046/j.1365-2141.2003.04621.x.
Davido T, Getzenberg RH: Nuclear matrix proteins as cancer markers. J Cell Biochem Suppl. 2000, 136-141. 10.1002/1097-4644(2000)79:35+<136::AID-JCB1137>3.0.CO;2-E. Suppl 35
Yabuki M, Miyake T, Doi Y, Fujiwara T, Hamazaki K, Yoshioka T, Horton AA, Utsumi K: Role of nuclear lamins in nuclear segmentation of human neutrophils. Physiol Chem Phys Med NMR. 1999, 31 (2): 77-84.
Smith S, Blobel G: Colocalization of vertebrate lamin B and lamin B receptor (LBR) in nuclear envelopes and in LBR-induced membrane stacks of the yeast Saccharomyces cerevisiae. Proc Natl Acad Sci USA. 1994, 91 (21): 10124-10128. 10.1073/pnas.91.21.10124.
Andrulis ED, Zappulla DC, Ansari A, Perrod S, Laiosa CV, Gartenberg MR, Sternglanz R: Esc1, a nuclear periphery protein required for Sir4-based plasmid anchoring and partitioning. Mol Cell Biol. 2002, 22 (23): 8292-8301. 10.1128/MCB.22.23.8292-8301.2002.
Kolling R, Nguyen T, Chen EY, Botstein D: A new yeast gene with a myosin-like heptad repeat structure. Mol Gen Genet. 1993, 237 (3): 359-369.
Moretti P, Freeman K, Coodly L, Shore D: Evidence that a complex of SIR proteins interacts with the silencer and telomere-binding protein RAP1. Genes Dev. 1994, 8 (19): 2257-2269. 10.1101/gad.8.19.2257.
Zhao X, Blobel G: A SUMO ligase is part of a nuclear multiprotein complex that affects DNA repair and chromosomal organization. Proc Natl Acad Sci USA. 2005, 102 (13): 4777-4782. 10.1073/pnas.0500537102.
Lewis A, Felberbaum R, Hochstrasser M: A nuclear envelope protein linking nuclear pore basket assembly, SUMO protease regulation, and mRNA surveillance. J Cell Biol. 2007, 178 (5): 813-827. 10.1083/jcb.200702154.
Taddei A, Hediger F, Neumann FR, Bauer C, Gasser SM: Separation of silencing from perinuclear anchoring functions in yeast Ku80, Sir4 and Esc1 proteins. Embo J. 2004, 23 (6): 1301-1312. 10.1038/sj.emboj.7600144.
Teixeira MT, Dujon B, Fabre E: Genome-wide nuclear morphology screen identifies novel genes involved in nuclear architecture and gene-silencing in Saccharomyces cerevisiae. J Mol Biol. 2002, 321 (4): 551-561. 10.1016/S0022-2836(02)00652-6.
Campbell JL, Lorenz A, Witkin KL, Hays T, Loidl J, Cohen-Fix O: Yeast nuclear envelope subdomains with distinct abilities to resist membrane expansion. Mol Biol Cell. 2006, 17 (4): 1768-1778. 10.1091/mbc.E05-09-0839.
Santos-Rosa H, Leung J, Grimsey N, Peak-Chew S, Siniossoglou S: The yeast lipin Smp2 couples phospholipid biosynthesis to nuclear membrane growth. Embo J. 2005, 24 (11): 1931-1941. 10.1038/sj.emboj.7600672.
Siniossoglou S, Santos-Rosa H, Rappsilber J, Mann M, Hurt E: A novel complex of membrane proteins required for formation of a spherical nucleus. Embo J. 1998, 17 (22): 6449-6464. 10.1093/emboj/17.22.6449.
Fabre E, Hurt E: Yeast genetics to dissect the nuclear pore complex and nucleocytoplasmic trafficking. Annu Rev Genet. 1997, 31: 277-313. 10.1146/annurev.genet.31.1.277.
Kimata Y, Lim CR, Kiriyama T, Nara A, Hirata A, Kohno K: Mutation of the yeast epsilon-COP gene ANU2 causes abnormal nuclear morphology and defects in intracellular vesicular transport. Cell Struct Funct. 1999, 24 (4): 197-208. 10.1247/csf.24.197.
Matynia A, Salus SS, Sazer S: Three proteins required for early steps in the protein secretory pathway also affect nuclear envelope structure and cell cycle progression in fission yeast. J Cell Sci. 2002, 115 (Pt 2): 421-431.
Schneiter R, Hitomi M, Ivessa AS, Fasch EV, Kohlwein SD, Tartakoff AM: A yeast acetyl coenzyme A carboxylase mutant links very-long-chain fatty acid synthesis to the structure and function of the nuclear membrane-pore complex. Mol Cell Biol. 1996, 16 (12): 7161-7172.
Strambio-de-Castillia C, Blobel G, Rout MP: Proteins connecting the nuclear pore complex with the nuclear interior. J Cell Biol. 1999, 144 (5): 839-855. 10.1083/jcb.144.5.839.
Beilharz T, Egan B, Silver PA, Hofmann K, Lithgow T: Bipartite signals mediate subcellular targeting of tail-anchored membrane proteins in Saccharomyces cerevisiae. J Biol Chem. 2003, 278 (10): 8219-8223. 10.1074/jbc.M212725200.
King MC, Lusk CP, Blobel G: Karyopherin-mediated import of integral inner nuclear membrane proteins. Nature. 2006, 442 (7106): 1003-1007. 10.1038/nature05075.
Bystricky K, Laroche T, van Houwe G, Blaszczyk M, Gasser SM: Chromosome looping in yeast: telomere pairing and coordinated movement reflect anchoring efficiency and territorial organization. J Cell Biol. 2005, 168 (3): 375-387. 10.1083/jcb.200409091.
Yang CH, Lambie EJ, Hardin J, Craft J, Snyder M: Higher order structure is present in the yeast nucleus: autoantibody probes demonstrate that the nucleolus lies opposite the spindle pole body. Chromosoma. 1989, 98 (2): 123-128. 10.1007/BF00291048.
Wright R, Basson M, D'Ari L, Rine J: Increased amounts of HMG-CoA reductase induce "karmellae": a proliferation of stacked membrane pairs surrounding the yeast nucleus. J Cell Biol. 1988, 107 (1): 101-114. 10.1083/jcb.107.1.101.
Nasmyth K: Segregating sister genomes: the molecular biology of chromosome separation. Science. 2002, 297 (5581): 559-565. 10.1126/science.1074757.
Pan X, Roberts P, Chen Y, Kvam E, Shulga N, Huang K, Lemmon S, Goldfarb DS: Nucleus-vacuole junctions in Saccharomyces cerevisiae are formed through the direct interaction of Vac8p with Nvj1p. Mol Biol Cell. 2000, 11 (7): 2445-2457.
Preston RA, Manolson MF, Becherer K, Weidenhammer E, Kirkpatrick D, Wright R, Jones EW: Isolation and characterization of PEP3, a gene required for vacuolar biogenesis in Saccharomyces cerevisiae. Mol Cell Biol. 1991, 11 (12): 5801-5812.
Luca FC, Mody M, Kurischko C, Roof DM, Giddings TH, Winey M: Saccharomyces cerevisiae Mob1p is required for cytokinesis and mitotic exit. Mol Cell Biol. 2001, 21 (20): 6972-6983. 10.1128/MCB.21.20.6972-6983.2001.
Faty M, Fink M, Barral Y: Septins: a ring to part mother and daughter. Curr Genet. 2002, 41 (3): 123-131. 10.1007/s00294-002-0304-0.
Longtine MS, Bi E: Regulation of septin organization and function in yeast. Trends Cell Biol. 2003, 13 (8): 403-409. 10.1016/S0962-8924(03)00151-X.
Luedeke C, Frei SB, Sbalzarini I, Schwarz H, Spang A, Barral Y: Septin-dependent compartmentalization of the endoplasmic reticulum during yeast polarized growth. J Cell Biol. 2005, 169 (6): 897-908. 10.1083/jcb.200412143.
Takizawa PA, DeRisi JL, Wilhelm JE, Vale RD: Plasma membrane compartmentalization in yeast by messenger RNA transport and a septin diffusion barrier. Science. 2000, 290 (5490): 341-344. 10.1126/science.290.5490.341.
Byers B, Goetsch L: Behavior of spindles and spindle plaques in the cell cycle and conjugation of Saccharomyces cerevisiae. J Bacteriol. 1975, 124 (1): 511-523.
Belgareh N, Doye V: Dynamics of nuclear pore distribution in nucleoporin mutant yeast cells. J Cell Biol. 1997, 136 (4): 747-759. 10.1083/jcb.136.4.747.
Bucci M, Wente SR: In vivo dynamics of nuclear pore complexes in yeast. J Cell Biol. 1997, 136 (6): 1185-1199. 10.1083/jcb.136.6.1185.
Hartwell LH, Unger MW: Unequal division in Saccharomyces cerevisiae and its implications for the control of cell division. J Cell Biol. 1977, 75 (2 Pt 1): 422-435. 10.1083/jcb.75.2.422.
Galy V, Gadal O, Fromont-Racine M, Romano A, Jacquier A, Nehrbass U: Nuclear retention of unspliced mRNAs in yeast is mediated by perinuclear Mlp1. Cell. 2004, 116 (1): 63-73. 10.1016/S0092-8674(03)01026-2.
Goldman RD, Shumaker DK, Erdos MR, Eriksson M, Goldman AE, Gordon LB, Gruenbaum Y, Khuon S, Mendez M, Varga R: Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome. Proc Natl Acad Sci USA. 2004, 101 (24): 8963-8968. 10.1073/pnas.0402943101.
Mounkes L, Kozlov S, Burke B, Stewart CL: The laminopathies: nuclear structure meets disease. Curr Opin Genet Dev. 2003, 13 (3): 223-230. 10.1016/S0959-437X(03)00058-3.
Pollex RL, Hegele RA: Hutchinson-Gilford progeria syndrome. Clin Genet. 2004, 66 (5): 375-381. 10.1111/j.1399-0004.2004.00315.x.
Worman HJ, Courvalin JC: How do mutations in lamins A and C cause disease?. J Clin Invest. 2004, 113 (3): 349-351. 10.1172/JCI200420832.
Fairley EA, Kendrick-Jones J, Ellis JA: The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane. J Cell Sci. 1999, 112 (Pt 15): 2571-2582.
Morris GE: The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy. Trends Mol Med. 2001, 7 (12): 572-577. 10.1016/S1471-4914(01)02128-1.
Stein GS, Montecino M, van Wijnen AJ, Stein JL, Lian JB: Nuclear structure-gene expression interrelationships: implications for aberrant gene expression in cancer. Cancer Res. 2000, 60 (8): 2067-2076.
Zink D, Fischer AH, Nickerson JA: Nuclear structure in cancer cells. Nat Rev Cancer. 2004, 4 (9): 677-687. 10.1038/nrc1430.
Pina B, Fernandez-Larrea J, Garcia-Reyero N, Idrissi FZ: The different (sur)faces of Rap1p. Mol Genet Genomics. 2003, 268 (6): 791-798.
Colman-Lerner A, Chin TE, Brent R: Yeast Cbk1 and Mob2 activate daughter-specific genetic programs to induce asymmetric cell fates. Cell. 2001, 107 (6): 739-750. 10.1016/S0092-8674(01)00596-7.
Sinclair D, Mills K, Guarente L: Aging in Saccharomyces cerevisiae. Annu Rev Microbiol. 1998, 52: 533-560. 10.1146/annurev.micro.52.1.533.
Fuchs J, Loidl J: Behaviour of nucleolus organizing regions (NORs) and nucleoli during mitotic and meiotic divisions in budding yeast. Chromosome Res. 2004, 12 (5): 427-438. 10.1023/B:CHRO.0000034726.05374.db.
Torres-Rosell J, Machin F, Jarmuz A, Aragon L: Nucleolar segregation lags behind the rest of the genome and requires Cdc14p activation by the FEAR network. Cell Cycle. 2004, 3 (4): 496-502.
Sinclair DA, Guarente L: Extrachromosomal rDNA circles – a cause of aging in yeast. Cell. 1997, 91 (7): 1033-1042. 10.1016/S0092-8674(00)80493-6.
Murray AW, Szostak JW: Pedigree analysis of plasmid segregation in yeast. Cell. 1983, 34 (3): 961-970. 10.1016/0092-8674(83)90553-6.
Longtine MS, McKenzie A, Demarini DJ, Shah NG, Wach A, Brachat A, Philippsen P, Pringle JR: Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae. Yeast. 1998, 14 (10): 953-961. 10.1002/(SICI)1097-0061(199807)14:10<953::AID-YEA293>3.0.CO;2-U.
Niedenthal RK, Riles L, Johnston M, Hegemann JH: Green fluorescent protein as a marker for gene expression and subcellular localization in budding yeast. Yeast. 1996, 12 (8): 773-786. 10.1002/(SICI)1097-0061(19960630)12:8<773::AID-YEA972>3.0.CO;2-L.
Vida TA, Emr SD: A new vital stain for visualizing vacuolar membrane dynamics and endocytosis in yeast. J Cell Biol. 1995, 128 (5): 779-792. 10.1083/jcb.128.5.779.
Wiederkehr A, Du Y, Pypaert M, Ferro-Novick S, Novick P: Sec3p is needed for the spatial regulation of secretion and for the inheritance of the cortical endoplasmic reticulum. Mol Biol Cell. 2003, 14 (12): 4770-4782. 10.1091/mbc.E03-04-0229.
Adams IR, Kilmartin JV: Localization of core spindle pole body (SPB) components during SPB duplication in Saccharomyces cerevisiae. J Cell Biol. 1999, 145 (4): 809-823. 10.1083/jcb.145.4.809.
Hampton RY, Koning A, Wright R, Rine J: In vivo examination of membrane protein localization and degradation with green fluorescent protein. Proc Natl Acad Sci USA. 1996, 93 (2): 828-833. 10.1073/pnas.93.2.828.
Huh WK, Falvo JV, Gerke LC, Carroll AS, Howson RW, Weissman JS, O'Shea EK: Global analysis of protein localization in budding yeast. Nature. 2003, 425 (6959): 686-691. 10.1038/nature02026.
Heun P, Laroche T, Shimada K, Furrer P, Gasser SM: Chromosome dynamics in the yeast interphase nucleus. Science. 2001, 294 (5549): 2181-2186. 10.1126/science.1065366.
Luca FC, Winey M: MOB1, an essential yeast gene required for completion of mitosis and maintenance of ploidy. Mol Biol Cell. 1998, 9 (1): 29-46.
Tsankov AM, Brown CR, Yu MC, Win MZ, Silver PA, Casolari JM: Communication between levels of transcriptional control improves robustness and adaptivity. Molecular systems biology. 2006, 2: 65-10.1038/msb4100106.
E. Bi, G. Blobel, V. Doye, J. Drazba, E. Fabre, S. Gasser, D. Goldfarb, J. Haber, M. Hitomi, W.-K. Huh, E. Jones, J. Kilmartin, M. Lam, J. Lithgow, M. Luca, P. Lusk, A.G. Matera, D. MacDonald, D. Meyer, F. Najm, D. Narendra, T. Rapoport, M. Rout, K. Runge, D. Shore, R. Sternglanz, P. Tiedrez, E. Townsley, A. Vasanji, K. Weis, H. Worman, R. Wright, D. Wu and Y. Zhang. Confocal Microscopy Core Facility in the Comprehensive Cancer Center of CWRU/UHC (P30 CA43703-12). T.H. was supported by an NIH training grant: "Normal and Abnormal Development" T32-HD7104. A.T.'s contribution was supported by institutional resources.
TH conducted most of the experiments as part of his doctoral work.
EA, who made the first observations of deformation of the nuclear envelope/nucleus upon Esc1p induction, provided frequent advice.
AT made the initial observations on escapade induction in this laboratory, coordinated the study, and wrote most of the manuscript.
All authors read and approved the text.
Electronic supplementary material
Additional file 1: Impact of excess Mlp1p. Cells expressing the ER/NE membrane protein, Sec61p-GFP (ATY3255), or Htb2p-mRFP (ATY3256) were induced to overexpress Mlp1p for 5 hr by addition of galactose. Note the conventional distribution of GFP signal at the NE and throughout the peripheral ER (left panel) as well as the roughly spherical chromatin mass (right panel). (TIFF 682 KB)
Additional file 2: Impact of excess Prm3p. Htb2p-mRFP-expressing cells were induced to overexpress GFP-Prm3p for 5 hr by transfer to methionine-free medium (ATY3244). Note the appearance of GFP-positive ring-like structures and a fin at the margin of the nucleus. (TIFF 211 KB)
Additional file 3: Impact of excess Heh1. Htb2p-mRFP-expressing cells were induced galactose to overexpress Heh1p-GFP for 5 hr by addition of 2% (ATY3245). The red and green images have been separated for clarity. Note the massive change of organization of both chromatin and the GFP signal, which often encircles the chromatin. (TIFF 276 KB)
Additional file 4: Impact of excess Heh2p. Htb2p-mRFP-expressing cells were induced to overexpress Heh2p-GFP for 5 hr by addition of 2% galactose (ATY3246). The red and green images have been separated for clarity. Note the massive change of organization of both chromatin and the GFP signal, which generally encircles the chromatin. (TIFF 231 KB)
Additional file 5: Spatial relation of escapades to the nucleolus. Cells expressing the nucleolar marker, Sik1p-mRFP, were induced to express GFP-Esc1p for 5 hr by addition of 2% galactose (ATY3258). Systematic examination of through-focal series detects association of escapades and Sik1p-mRFP in > 90% of cells which have escapades. Nevertheless, in a given section the extent of association often appears only modest. (TIFF 651 KB)
Additional file 6: Spatial relation of escapades to the spindle pole body. Overview comparison of the localization of GFP-tagged Esc1p and the spindle pole body, in a strain (ATY3276) which expresses Spc42p-mRFP and has been induced by addition of 2% galactose for 5 hr. Systematic examination of through-focal series detects association in ~10% of cells which have escapades. (TIFF 569 KB)
Additional file 7: Spatial relation of escapades to a centromere. Overview comparison of the localization of GFP-tagged Esc1p and a centromere, in a strain (ATY2098) which expresses a GFP-lac repressor fusion, an insertion of lac operator arrays near CENIV and Nup49p-GFP. It has been induced by addition of 2% galactose for 5 hr. Systematic examination of through-focal series detects association in ~10% of cells which have escapades. (TIFF 706 KB)
Additional file 8: Spatial relation of escapades to a telomere. Overview comparison of the localization of GFP-tagged escapades and a telomere, in a strain (ATY2097) which expresses a GFP-lac repressor fusion, an insertion of lac operator arrays near telomere XIVL and Nup49p-GFP. It has been induced by addition of 2% galactose for 5 hr. Systematic examination of through-focal series detects association in ~10% of cells which have escapades. (TIFF 702 KB)
Additional file 9: Spatial relation of escapades to Rap1p. Overview localization of Rap 1-GFP in a strain (ATY3275) which expresses Htb2p-mRFP and allows galactose induction of untagged Esc1p. It was induced by addition of 2% galactose for 5 hr. Note that the labeled foci often are at the periphery of the chromatin mass, but – unlike escapades – do not extend centrifugally toward the cytoplasm. (TIFF 699 KB)
Additional file 10: Induction of escapades in cells treated with mating factor. GFP-Esc1p was induced by addition of 2% galactose for 5 hr in cells which had already been treated with 5 μg/ml α-factor for 2 hr (ATY2101). Note that the appearance of escapades is comparable to that illustrated in Figure 1A. (TIFF 730 KB)
Additional file 11: Induction of escapades in cells treated with hydroxyurea. GFP-Esc1p was induced by addition of 2% galactose for 5 hr in cells which had already been treated with 0.1 M hydroxyurea for 2 hr (ATY2101). Note that the appearance of escapades is comparable to that illustrated in Figure 1A. (TIFF 698 KB)
Additional file 12: Induction of escapades in cells treated with nocodazole. GFP-Esc1p was induced by addition of 2% galactose for 5 hr in cells which had already been treated with 15 μg/ml nocodazole 2 hr (ATY2101). Note that the appearance of escapades is comparable to that illustrated in Figure 1A. (TIFF 709 KB)
Additional file 13: Induction of escapades in cells treated with latrunculin A. GFP-Esc1p was induced by addition of 2% galactose for 5 hr in cells which had already been treated with 200 μg/ml latrunculin A 2 hr (ATY2101). Note that the appearance of escapades is comparable to that illustrated in Figure 1A. (TIFF 692 KB)
Additional file 14: Nuclear shape in the absence of Esc1p. The contour of the NE was defined in cells which lack Esc1p by monitoring the distribution of Sec63p-GFP in a corresponding deletion strain (ATY3278). (TIFF 113 KB)
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Hattier, T., Andrulis, E.D. & Tartakoff, A.M. Immobility, inheritance and plasticity of shape of the yeast nucleus. BMC Cell Biol 8, 47 (2007). https://doi.org/10.1186/1471-2121-8-47
- Daughter Nucleus
- Nuclear Periphery
- Nuclear Lamina
- Spindle Pole Body