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Dramatic chromosome motion is a characteristic of mid-prophase of meiosis observed across broadly divergent eukaryotic phyla. Although the specific mechanisms of motions vary among organisms studied thus far, the outcome is similar in all cases: vigorous back-and-forth movement (as fast as ~1μm/sec for budding yeast), led by chromosome ends (or near-end regions), and directed by cytoskeletal components through direct association through the nuclear envelope. The exact role(s) of movements remains unknown, although an idea gaining currency is that movement serves as a stringency factor, eliminating unwanted inter-chromosomal associations or entanglements that have arisen as part of the homolog pairing process and, potentially, unwanted associations of chromatin with the nuclear envelope. Turbulent chromosome movements observed during bipolar orientation of chromosomes for segregation could also serve similar roles during mitosis. Recent advances shed light on the contribution of protein complexes involved in the meiotic movements in chromosome dynamics during the mitotic program.
Meiosis is the process by which a diploid cell gives rise to the haploid gamete cells required by sexual reproduction. A key feature of this process is the occurrence of two successive rounds of chromosome segregation, first of homologous maternal and paternal chromosomes (‘homologs’) and then of sister chromatids, as during mitosis. The existence and mechanics of the first division require the prior execution of a series of carefully regulated events including recognition, juxtaposition and intimate synapsis of homologs all along their lengths. Part way through this process, chromosomes initiate dramatic dynamic movements (Box 1; supplementary movie 1). Molecular studies are now revealing that these movements involve direct associations of chromosome ends, or near-end regions, with cytoskeletal motion-generating machineries by means of linkages that span the nuclear envelope (NE). Issues of interest raised by these findings include: the role(s) of such movements for the meiotic process, the basis for their temporal regulation, their detailed mechanism(s), and the possibility of functional and mechanistic analogies with general processes common to all types of cells. Also of interest are the chromosome reorganizations that precede these dynamic active mid-prophase events, including changes in the associations of heterochromatic regions and early stages of homolog pairing, the basis for which is still mysterious. Here, we review characteristics of movements accompanying the different phases of prophase and the mechanisms of zygotene/pachytene motion, and the interplay between the different components of the system. Understanding the potential roles of motion, as well as potential mitotic implications, are currently under investigation.
The first evidence that meiotic prophase chromosomes are experiencing rotational movements during the formation of synapsis came from rat spermatocytes . Time-lapse phase-contrast observation of zygotene and pachytene spermatocytes revealed oscillatory movements of both nuclei and chromosomes, the latter also exhibiting more complex tri-dimensional trajectories. The importance and potential widespread existence of similar movements across eukaryotic phyla emerged twenty years later from a very different organism, Schizosaccharomyces pombe. The group of Yasushi Hiraoka described during the zygotene and early pachytene stage of meiotic prophase dynamic and rapid (~5 μm/min) movements along the length of the cell of the telomeres clustered at the SPB (reviewed in ; ). Such phenomena explained the characteristic “horse-tail” shape of the nucleus previously observed in snapshots of fission yeast meiotic prophase. This observation open the way to a large number of studies deciphering the precise mechanisms of meiotic chromosomes movements, and analyzing the molecular role of motion (see text). Cytoplasmic microtubules play a key role in the S. pombe movements, as they exert a pulling force on the SPB, thus on the clustered telomeres [20; 31]. The force is generated by the minus-end directed motor protein dynein Dhc1 that binds to the cell cortex and whose uneven distribution may account for the back and forth redirection of motion of microtubules along the length of the cell (Figure 1b). In their original paper, Chikashige et al. proposed that motion led by clustered telomeres could be necessary to facilitate pairing by reducing the dimensionality of the search and maybe helping to resolve interlocks . Recent results indeed revealed an role for fission yeast nuclear oscillation in promoting chromosome pairing (; further discussion in text).
The central event of meiotic prophase is pairing (and accompanying recombination) of homologs, which involves the stable, close juxtaposition of chromosomes that, in most species, have entered this stage unpaired. The earliest stages of this process are not well understood and likely involve interactions of telomeres/centromeres and between homologous interstitial regions through recombination-independent processes (reviewed in [3-5]; discussed below). Once recombination begins, at the G2/prophase transition, pairing becomes obvious. In many organisms, including plants, animals and filamentous fungi, chromosome axes are first brought close together along their lengths to a separation of ~400 nm, through the actions of axis-associated recombination complexes that then form the links that span the two axes. In a next stage, axes become closely associated at ~100 nm (‘synapsed’) through the synaptonemal complex (SC), a close-packed array of transverse filaments, plus other components . These steps occur during specific stages of meiotic prophase as originally defined by light microscopy: coalignment occurs during leptotene, when chromosomes are ‘threadlike’; SC formation underlies zygotene, when chromosomes are closely and obviously paired in some regions; and pachytene is the stage when SC extends along the full length of all chromosomes (Box 2). These events are all tightly integrated, temporally, spatially and functionally, with a highly regulated series of meiotic recombination events [7-12].
Figure I (a) shows classically fixed and stained chromosomes of rye (Secale cereale) showing leptotene (“threadlike”), zygotene (partial coming-together, i.e. synapsis) and pachytene (full synapsis). (courtesy of D. Zickler). (b) The seven pairs of chromosomes from the filamentous fungus Sordaria macrospora illuminated along their structural axes by Spo76-GFP (courtesy of D. Zickler; ; bar = 5μm). From left to right: midleptotene – homolog axes coaligned at ~400 nm and no bouquet; late leptotene – coaligned axes with loose bouquet; zygotene – partial synapsis with loose bouquet (chromosome ends are indicated by red lines); pachytene – full synapsis: early with tight bouquet (left) and late with ends dispersed around the nuclear periphery (right). (c) Bouquet stage in Salamander [adapted with permission from 85], with Sordaria nucleus from (b) shown at lower right for size comparison (bar: 10 μm). (d) Bombyx silkworm oocyte: zygotene nucleus with bouquet (left) and pachytene nucleus with full synapsis and ends dispersed (right) [reproduced with permission from 86; NV nuclear vacuole; N nucleolus]. (e) Telomere positions in meiosis of the budding yeast S. cerevisiae [reproduced from 26; bar ~2μm]. Trajectories of Rap1-GFP telomere foci recorded at a frame rate of 0.5 sec over 7 minutes superimposed over a nucleus of the corresponding stage. Perinuclear telomere foci in vegetative nuclei exhibit relatively constrained movements along the NE. Leptotene: telomeres move around the nucleus; zygotene bouquet: a subset of telomeres appears confined within a subregion of the NE; Pachytene: dynamic dispersal of telomeres around the NE. Note that yeast has 16 pairs of chromosomes, implying that the bouquet contains 64 individual telomeres and 32 pairs of telomeres.
In certain organisms, pairing and recombination are not accompanied by SC formation (e.g. the fission yeast Schizosaccharomyces pombe), whereas in others, such as male Drosophila melanogaster, pairing and stable homolog association occur in the absence of recombination (see for instance ). Nonetheless, irrespective of the details, homologous chromosomes must come together in space and generate intimate, stable interactions, and in such a way that they are not topologically entangled with unrelated chromosomes .
Two related types of chromosome movement are superimposed on the later stages of the pairing process, during the periods when chromosomes are synapsing and synapsed. First, three-dimensional reorganization of chromosome ends, which dynamically cluster into the so-called ‘bouquet configuration’ at zygotene and then decluster back to a dispersed configuration at pachytene (Box 2; [4, 15-18]); and, second, global chromosome motions, which initiate at zygotene and persist into pachytene. The existence of such movements was initially revealed by light-microscopy studies of living meiotic cells from rat spermatocytes [1; Figure 1a]. With the advent of time-lapse fluorescence microscopy, movies of living S. pombe cells revealed dynamic back-and-forth nuclear deformations at the corresponding stage ([2, 19, 20]; Figure 1b). Most recently, analogous motions have been described in budding yeast Saccharomyces cerevisiae (Figure 1c; [21-25]) and in the nematode Caenorhabditis elegans (A. Dernburg cited in ). In budding yeast, a bias in the global distribution of telomeres-led chromosomal movements could account for bouquet clustering and declustering [22, 26].
Within this general commonality, programmatic diversity among different organisms again occurs. In most organisms, telomeres in the bouquet configuration are mostly colocalized in a general region of the NE surrounding the microtubule organizing center (MTOC). Clustering density can vary from ‘tight’ to loose plus intermediate states. The loose configuration may sometimes precede the tight configuration (e.g. ; see Box 2 Fig. Ib). Alternatively, in time-lapse analysis of living S. cerevisiae cells, the two configurations dynamically interconvert: rapid telomere movements lead to transient colocalization and dynamic local clustering/declustering within the vicinity of the spindle-pole body (SPB, the yeast MTOC; ; see Box 2 Fig. Ie). However, in S. pombe, telomeres remain tightly clustered to the SPB for the entire length of prophase [reviewed in 2]. Also, in C. elegans, clustering at the NE is mediated by specific subtelomeric regions, rather than telomeres per se as in other organisms [reviewed in 4, 28].
This review focuses on the programmed motions that initiate during meiotic mid-prophase. It should be noted, however, that interesting dynamic changes also occur prior to this (relatively late) point in the program. Most dramatically, chromosomes exit the preceding mitosis in a ‘Rabl’ configuration, with centromeres clustered together as a consequence of being brought to the corresponding pole of the mitotic spindle and, usually (although not in many fungi and basidiomycetes), free of the nuclear envelope [15, 17, 18]. Thus, bouquet formation is preceded by both loss of the Rabl configuration and association of telomeres to the NE. In addition, centromeres in particular, or heterochromatic regions in general, appear to cluster and decluster dynamically during the early prophase of most organisms, suggesting an important role that remains unclear [reviewed in 29].
The mechanisms responsible for dynamic zygotene/pachytene chromosome movements are now elucidated, or largely so, in a handful of organisms. In all cases described so far, forces appear to be generated via cytoskeleton elements and are exerted on NE-localized chromosome ends via specialized complexes that span the NE (below). Correspondingly, in some cases, force-mediated NE deformations are seen to accompany chromosomal motion. However, the molecular mechanisms by which these effects are implemented are different in different organisms.
In fission yeast, and more recently in budding yeast, the mechanisms responsible for these movements have been partially deciphered. In S. pombe, telomeres cluster together on the NE at the SPB, and these ensembles move back and forth within the cell through direct association with cytoplasmic microtubules that run tangentially to the nuclear periphery and with microtubule-associated dynein motor protein complexes playing a central role [Figure 1bii; 2, 30]. The observed motions can be explained by dynamic redistribution of dynein motors from the ‘leading’ side of the SPB complex to the ‘trailing’ side, as directed by microtubule length and mechanical load . In S. cerevisiae, unpaired and paired telomeres become associated transiently through the NE, to nucleus-hugging actin cables that are continuous with the actin cytoskeleton [see notably 23; see also 21, 26, 22]. In this case, the telomere–actin associations seem to be passive, with actin-tethered chromosome ends moving because of the dynamic tread-milling of the underlying actin cable per se rather than as a cargo being transported along the cable by a motor protein [Figure 1cii; 22]. Interestingly, budding yeast uses an analogous mechanism for retrograde transport of mitochondria from the bud tip to the mother cell tip , suggesting that meiotic chromosome movement systems could have evolved from processes used more generally for cytoplasmic transport of vesicles and/or the nucleus itself (see below).
Information for other systems is just beginning to emerge. In C. elegans, microtubule-associated dynein seems to play a role [A. Dernburg cited in 4; 33]. By contrast, in some plants, complete depolymerization of cytoplasmic microtubules by the chemicals vinblastine and amiprophos-methyl does not disrupt telomere clustering in rye anthers, although addition of colchicine at a concentration too low to depolymerize microtubules, does. This result points to a non-cytoplasmic-microtubule mechanism for movement in this organism  – for example potentially by means of actin or an alternative cytoskeleton element. Finally, for mammalian meiosis, the nature of the force-generating mechanism is thus far unknown.
The NE–cytoskeleton associations involved in these dynamic chromosomal movements involve the same types of proteins used by non-meiotic cells to link the nuclear envelope directly to the global cytoskeleton, where the resulting associations anchor, move and position the nucleus within the cell [reviewed in 34-37]. Typically, such processes involve proteins of the SUN (for: S. pombe Sad1 and Caenorhabditis elegans Unc-84 proteins ) and KASH (for: Klarsicht/ANC-1/Syne-1 homology ) domain families. These two types of proteins locate within the inner and outer nuclear membrane of the NE, respectively, and interact physically with each other in the lumen, thereby directly connecting the involved NE regions with the cytoskeleton networks [35, 37]. The precise structures of the interaction and the stoichiometries of the proteins involved remain unknown . Notably: how do the relatively small (<35 aa) C-terminal domain of the KASH protein interact with the SUN protein in the perinuclear space, and also whether both KASH and SUN proteins are needed so that the telomere/NE attachment appears mature? These molecules provide not only molecular connections but structural reinforcement such that the forces generated by movement of the nucleus do not (usually) rupture the association sites.
During meiosis, the SUN domain protein Mps3 in S. cerevisiae [23, 40], Sun1 and Sun2 in rodents [41, 42], Sun-1 in C. elegans  and Sad1 in S. pombe  are all implicated in meiotic telomere–NE attachment. In S. pombe, additional components of telomere–NE–cytoskeleton complexes are now characterized, with Bqt1 and Bqt2 connecting telomeres to Sad1, which itself connects to the KASH domain protein Kms1, which in turn interacts with the dynein light chain Dlc1 [43-46]. In S. cerevisiae, no KASH domain protein has been identified thus far as playing a role with Mps3, but the putative tail-anchored membrane protein Csm4 is a good candidate for playing a similar role [22-25]. Furthermore, at the chromosomal level, the meiosis-specific telomere-binding protein Ndj1 has been shown to tether telomeres to the NE during meiosis by means of interactions with Mps3 [40, 23; Figure 2]. In addition, Mps3 is also involved in the Sir4–Esc1 pathway of telomere recruitment to the nuclear membrane during vegetative growth . In mammals, while the motion-generating system has not been identified, Sun1 and Sun2 are inner nuclear membrane (INM) components of meiosis-specific telomere–NE attachments and presumably are thus, by analogy, involved [41, 42]. In C. elegans, the KASH domain protein Zyg-1 interacts with Sun-1 to link chromosomes to microtubules .
Two aspects of the mid-prophase motion phenomenon remain poorly understood in all systems. First, SUN-domain proteins relocate during meiotic prophase, from other locations (principally the vicinity of the SPB in yeast mitotic cells, the centrosome in C. elegans and a more homogeneous rim in mammalian somatic cells) to chromosome extremities [33, 42, 48]. The temporal and spatial signals for this relocalization remain unclear . Second, what are the signals that activate the sequential events and the motion itself? Importantly, in budding yeast, this signal must act after telomere–NE association, which is complete prior to onset of zygotene motion. An obvious possibility is regulatory activation of the association between telomere–NE ensembles and actin cables, either directly or through effects on SUN-domain protein localization, similar to the anchoring of dynein to the cortex by a meiosis-specific gene product .
Since the first description of the bouquet stage in the early 20th century [see 17], the primary rationale for its existence was thought to be to promote the coming-together of homologous chromosomes. Indeed, association and alignments of homologs in the bouquet prior to the onset of pairing could reduce the dimensionality and distances involved in homology searching. Modern studies have shown that homolog pairing can be aberrant (although never completely abrogated) in the presence of mutations impairing chromosome movement [e.g. 50, 51] or in mutants likely defective in such movement  and, conversely, ectopic recombination frequencies increase in correlation with closeness to telomeres [52, 53]. Nonetheless, significant challenges to this original idea are beginning to emerge, pointing to alternative or additional roles. Most importantly, in several cases, bouquet formation appears to occur too late in the pairing process to be the primary mediator of homology searching [reviewed in 17; see Box 2b]. Furthermore, in budding yeast, dynamic movement begins exactly at zygotene, i.e. concomitant with SC formation and thus well into the recombination process, when stable strand exchange intermediates are already formed between homologous interacting DNAs [7, 21-23]. Additionally, in both fission yeast and budding yeast, mutations conferring disruption of telomere motion have only relatively modest effects on either recombination or pairing [24, 25, 46, 54]. Finally, in the three organisms studied, the movements of mid-prophase chromosomes have a back-and-forth character (rotationally within rat spermatocytes nuclei, longitudinally in S. pombe, and circum-nuclear in S. cerevisiae), which does not have the effect of ‘stirring’ chromosomes (Figure 1). Indeed, different chromosomes tend to move coordinately either because their telomeres are stably colocalized (S. pombe) or because of other types of connections (S. cerevisiae). For these reasons, we want to focus more on the possibility that the crucial functional effect is chromosome movement, including but not limited to movement into and out of the bouquet configuration, rather than the existence of a bouquet configuration per se.
One proposal suggests that that motion would resolve topological entanglements among chromosomes that impede completion of recombination and juxtapositioning of homologs [8, 22, 24]. Topological ‘interlockings’ are seen at the zygotene stage and undergo resolution during the pachytene stage in several organisms, with strong indications that there is a specific mechanism for their resolution during those stages . Furthermore, a back-and-forth motion could be highly appropriate to ‘get the kinks out’ of a set of chromosomes that are in the final stages of pairing and synapsis. In accord with such a possibility, a maize mutation that disrupts formation of the bouquet configuration, and thus potentially chromosome movement, results in accumulation of prophase interlocks [pam1; 56].
Movements could also help to free chromosomes from interconnections of other kinds. In budding yeast, at pachytene, motion led by one chromosome end causes other, unrelated, chromosomes to move coordinately [Figure 1ci], implying the existence either of direct nonspecific interchromosomal links and/or parallel independent association of multiple ends to a particular patch of NE substructure . Such connections must ultimately be eliminated if homologs are to segregate cleanly from one another, independent of other chromosomes at meiosis I; mid-prophase movement could help to accomplish this task. Indeed, colocalization of telomeres (or, in C. elegans, potentially analogous ‘pairing centers’; ) in a polarized configuration might specifically promote inappropriate connections that must be resolved by the dynamic motions of telomere redistribution during bouquet exit. Similarly, it has been suggested that chromosome movement might eliminate ectopic recombination in which a sequence at one position interacts with an homologous position located at a non-corresponding position on another chromosome [16, 22, 23, 52, 53, 57, 58]. In accord with this possibility, abrogation of motion confers a slight increase in ectopic recombination in budding yeast [for discussion, see 23]; however, in fission yeast, while abrogation of telomere clustering significantly increases ectopic recombination, mutation induced abrogation of motion does not [57, 58]. Similarly, motion might help to disrupt nonhomologous associations between centromeres that often precede their homologous association (reviewed in ). Another potential role for motion could be to abrogate the local associations that occur between chromatin and the NE or nuclear pore complexes that have been recently revealed to modulate transcription [59-61] or DNA repair [62-64]. Overall, dynamic programmed movements could be a way to free chromosomes from all inappropriate or leftover interconnections and associations they might have been acquired. In summary: dynamic chromosome movements could well serve as a ‘stringency factor’ to eliminate unwanted (and thus presumably weaker) connections so that chromosomes can be fully and intimately synapsed along their lengths by the end of pachytene. Cytological studies (such as screening for interlocks by visualizing axis components) and genetics and chromosomal dynamics analysis of mutants of the members involved in the telomere–NE–cytoskeleton complexes should provide further insights on the actual role of motion.
It would be interesting to know whether telomere- (or centromere- or pairing-center-) directed homolog pairing comprises a ‘primordial’ mechanism that preceded evolution of recombination-mediated pairing or whether recombinational mechanisms that had evolved for mitotic double-strand break repair were the original pairing process. The need for a mechanical stringency factor would be a central requirement of both scenarios.
Situations where telomere dynamics are abrogated by mutation or by drug(s) are characterized by variable delays and/or defects in recombination, assayed genetically or physically and/or in recombination-mediated pairing, manifested as juxtaposition of fluorescently tagged loci at corresponding positions on homologs [24, 25, 56-58]. The fact that these delays and defects do not impair totally the progression of meiosis has led to the suggestion that motion could be required for completion of interhomolog interactions. One specific hypothesis is that telomere clustering plays a supporting role in accelerating the rate of recombinational progression [reviewed in 16]. A second hypothesis is that motion is required to mechanically promote steps of recombination . Since resolution of the recombination intermediates single end invasion and double Holiday junction does not require motion , these steps would be early post-double strand breaks recombination steps. However, mutation-induced delays could be indirect regulatory checkpoints effects that delay recombination progression. For example, mutations of the NE/telomeric ensembles could disorganize those complexes thus generating a checkpoint response. By this model, regulatory delays would reflect defects in basic telomere biology irrespective of any effects on chromosome motion . Alternatively, or in addition, these delays could be triggered by primary defects in eliminating unwanted connections. For example, interlocking of chromosomes will tend to preclude completion of recombinational interactions in the affected region, and the presence of such, even one or a few, stalled recombinational interactions could trigger a checkpoint surveillance response, which in turn would confer broader defects and delays on a nucleus-wide basis.
The notion that vigorous movements serve to eliminate unwanted connections can be extended also to the prometaphase/metaphase stages, in mitotic as well as meiotic cells. During these periods, chromosomes undergo dramatic back-and-forth movements directed by kinetochore–microtubule associations as part of the process by which sisters (or homologs) become oriented to opposite poles . Indeed, nonspecific physical connections are frequently observed for late-stage mitotic chromosomes, particularly but not exclusively at their ends ; conversely, the somatic pairing that is robust throughout most of the cell cycle in Drosophila is partially disrupted during the segregation process in euchromatic regions .
Roles for motion other than for chromosome dynamics have also been suggested. In higher plants, nuclear pores cluster to the same regions as telomeres during the bouquet stage [reviewed in 17], leading to the suggestion that this configuration might promote direct loading of newly synthesized proteins onto chromosome ends [D. Zickler, pers. commun.]. Also, stretching forces transmitted through the cytoskeleton to the nuclear membrane of mouse fibroblasts appear to activate stretch-sensitive channels within the membrane that lead to transient elevation of nuclear [Ca2+], presumably through its release from the endoplasmic reticulum . Perhaps the NE deformations that accompany meiotic chromosome movement play an analogous role at that stage.
All of the components involved in meiotic chromosome movements are in direct mechanical linkage. In this regard, it is interesting that budding yeast pachytene chromosomes are semi-flexible objects having flexural persistence lengths (i.e. the distance over which the correlation between the direction of two vectors tangent to the polymer is lost) comparable to those of actin filaments . Also in budding yeast , visualization of a fluorescently tagged nuclear pore component reveals that the NE undergoes a cone-like deformation at the point of end-directed chromosome movement, implying that pulling encounters resistance from the envelope substructure and proteins of the inner and outer membranes [Figure 1ciii, pink line]. Occasionally small thin projections are also observed, implying that this substructure occasionally ruptures, leading to formation of a membrane tubes [Figure 1ciii, green line]. Additionally, the chromosomes are not simply free in solution; instead they sit in a crowded environment and are likely engaged in non-specific interconnections with other objects from the nucleoplasm that, in addition, might be connected to one another (see above). Thus, chromosomes are expected to resist telomere-led movement, and there are hints to this effect. For example, in budding yeast, force exerted on the end of one chromosome results in coordinate movements of other nearby chromosomes, perhaps through inter-chromosomal linkages; however, occasional membrane tubes also contain a chromosome, and, when that occurs, the orphaned chromosome is always small. As small chromosomes are less likely to be involved in linkages with other chromosomes, this finding points to a constraining role of such linkages.
The zygotene/pachytene period of chromosome movement could therefore provide an interesting system not only for studying the mechanical capacities of the motion-generating system but, concomitantly, the properties of the nucleus and the partitioning of mechanical load between the NE and the underlying chromosomes. For a whole mammalian nucleus, the primary force-bearing component can be the chromatin (for instance in human stem cells) and/or the lamina of the NE (for instance in human epithelial cells) [69, 70]. During meiosis, chromatin is more compact during zygotene (when motion is biased toward the bouquet tendency) and more expanded during pachytene (when chromosome ends disperse throughout the nuclear periphery). We have suggested that this change in chromatin state also produces an overall change in whole chromosome stiffness (persistence length) that could be important for driving the transition from the zygotene telomere-clustering state to the pachytene state where telomeres are dispersed. It would be interesting to know whether changes in chromatin state confer changes in the deformability of the NE [e.g. 69] that are also seen during this transition. Similarly, it would be interesting to know whether the force required to move a chromosome varies over time in relation to these effects.
Two recent findings highlight the potential of bridging members from nuclear envelope proteins to play new and unsuspected roles in chromatin metabolism and organization in non-meiotic cells. First, the SUN–KASH complex couples the microtubule network and heterochromatin/centromeric regions in interphase S. pombe cells . Similarly, in S. cerevisiae, the N-terminal domain of the SUN-protein Mps3 is required for telomere tethering to the nuclear periphery in vegetative cycling cells . Second, in budding yeast, a DNA double-strand break whose repair is impaired or delayed is recruited to the nuclear periphery, where it associates with Mps3 [64; see also 72, 73]. The involvement of Mps3, and the consequences of what could be a secondary response to persistent unrepaired breaks remain, however, poorly understood.
It should also be recalled that disruption of actin polymerization is required for movement of an interphase chromosomal site activated for transcription away from the NE . More generally, actin plays important roles in transcription-related phenomena. While the present consensus suggests that a pool of nuclear actin monomers plays important roles within this compartment [74-78], it is conceivable that future work will reveal a role for cytoplasmic actin, as well as nuclear actin, in some of the described phenomena or others. In particular, identification of SUN–KASH linkages between cytoplasm and NE, plus appreciation that certain diseases, such as muscular dystrophy or cardiomyopathy , are attributable to defects in lamin structure, have triggered multiple lines of investigation into whether/how mechanical forces, potentially even transduced directly from the cell surface, could influence the NE and its linked chromosomal regions [e.g. 69, 80-83].
Clearly, fully understanding of the important role(s) that dynamic motor-mediated chromosome movements play in meiosis is an outstanding goal (Box 3). Understanding these molecular mechanisms will also shed light on the dynamic phenomena observed during the basic mitotic cell cycle.
We thank D. Zickler for allowing reproduction of unpublished pictures in Box 2 Fig. I, panels a and b, and Y. Hiraoka, M. Parvinen, and H. Scherthan for allowing reproduction of their work. This work was supported by a grant to N.K. (NIH RO1 GM-044794 and GM 025326).
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