Dynamic as well as stable protein interactions contribute to genome function and maintenance
The cell nucleus is responsible for the storage, expression, propagation, and maintenance of the genetic material it contains. Highly organized macromolecular complexes are required for these processes to occur faithfully in an extremely crowded nuclear environment. In addition to chromosome territories, the nucleus is characterized by the presence of nuclear substructures, such as the nuclear envelope, the nucleolus, and other nuclear bodies. Other smaller structural entities assemble on chromatin in response to required functions including RNA transcription, DNA replication, and DNA repair. Experiments in living cells over the last decade have revealed that many DNA binding proteins have very short residence times on chromatin. These observations have led to a model in which the assembly of nuclear macromolecular complexes is based on the transient binding of their components. While indeed most nuclear proteins are highly dynamic, we found after an extensive survey of the FRAP literature that an important subset of nuclear proteins shows either very slow turnover or complete immobility. These examples provide compelling evidence for the establishment of stable protein complexes in the nucleus over significant fractions of the cell cycle. Stable interactions in the nucleus may, therefore, contribute to the maintenance of genome integrity. Based on our compilation of FRAP data, we propose an extension of the existing model for nuclear organization which now incorporates stable interactions. Our new “induced stability” model suggests that self-organization, self-assembly, and assisted assembly contribute to nuclear architecture and function.
KeywordsNucleus Fluorescence microscopy FRAP Multi-protein complex Chromatin binding Dynamics Residence time Induced stability Assisted assembly Self-assembly Self-organization
C-AMP response element binding protein (CREB) binding protein
Continuous fluorescence photobleaching
Fluorescence fluctuation microscopy
Fluorescence lifetime imaging
Fluorescence loss in photobleaching
Fluorescence recovery after photobleaching
Förster resonance energy transfer
Fluorescence correlation spectroscopy
Green fluorescent protein
Homologous to A-kinase anchoring protein 95
Heat shock factor
Inverse fluorescence recovery after photobleaching
Lamin B receptor
Multiparameter fluorescence lifetime image spectroscopy
Nucleotide excision repair
- PcG proteins
Polycomb group proteins
Proliferating cell nuclear antigen
Raster image correlation spectroscopy
Small ribonucleoprotein particle
Single particle tracking
Structure and function in the nucleus
The most prominent subnuclear domains include the nucleolus, the perinucleolar compartment, speckles, paraspeckles, Cajal bodies, and promyelocytic leukemia (PML) bodies (Figs. 1 and 2). In addition, a variety of other nuclear bodies have been identified such as PcG bodies, Gemini bodies (Gems), the OPT domain, cleavage bodies, and the SAM68 nuclear body (Spector 2001; Handwerger and Gall 2006). Subnuclear structures are macromolecular complexes that consist of membrane-less accumulations of specific sets of functionally related molecules. For example, components of the ribosome biogenesis pathway are predominantly confined to the nucleolus. First thought to be exclusively devoted to the synthesis of ribosomal RNA and assembly of ribosomal subunits, it has become clear that the nucleolus serves a variety of additional functions, including regulation of mitosis, cell-cycle progression, proliferation, and various stress responses (Raska et al. 2006; Sirri et al. 2008).
The biochemical function(s) of the other subnuclear domains are less clear or unknown. PML bodies attract a selected set of nuclear proteins which are functionally quiet promiscuous. Therefore, PML bodies have been implicated in the regulation of diverse cellular functions, such as the induction of apoptosis and cellular senescence, inhibition of proliferation, maintenance of genomic stability, and antiviral responses (Bernardi and Pandolfi 2007). PML bodies are positionally stable structures at which controlled molecular traffic and posttranslational modifications may regulate the activity of specific proteins throughout the genome and the epigenome in response to various cellular stresses (Bernardi and Pandolfi 2007; Torok et al. 2009). Speckles, also referred to as interchromatin granule clusters, are enriched in pre-mRNA splicing factors. At the microscopic level, speckles appear as irregular, punctate domains varying in size and shape (Fig. 2). They are considered to be the main sites for storage, assembly, and/or recycling of the essential spliceosome components (Lamond and Spector 2003). Because highly transcribed genes are found in the periphery of speckles and also other subnuclear domains, they may also serve to efficiently integrate and regulate mRNA transcription and mRNA processing machineries (Zhao et al. 2009). Cajal bodies (CBs) are involved in the biogenesis of several classes of small ribonucleoprotein particles (snRNPs) as well as their modification (Gall 2000; Matera et al. 2009). Resembling the speckles/gene association mentioned above, CBs associate specifically with histone and snRNA genes. This colocalization is transcription-dependent, requires expression of snRNA coding regions, and is probably based on an energy-driven motor activity in the nucleus (Frey and Matera 2001; Dundr et al. 2007).
Fluorescence fluctuation microscopy
FFM allowed for the first time to not only visualize protein dynamics and chromatin interactions but also to quantitatively determine biophysical properties of proteins in the nucleus of intact cells (Erdel et al. 2010, this volume). FFM approaches include time-lapse microscopy (Heun et al. 2001), fluorescence redistribution after photobleaching (FRAP, FLIP, iFRAP, etc.) (Bancaud et al. 2009; van Royen and Houtsmuller 2010; this volume), fluorescence correlation spectroscopy (FCS) (Haustein and Schwille 2003), CP (Wachsmuth et al. 2003), raster image correlation spectroscopy (RICS) (Digman and Gratton 2009), SPT (Levi and Gratton 2008), FRET and FLIM (Wallrabe and Periasamy 2005), and MFIS (Weidtkamp-Peters et al. 2009). Figure 4 highlights some of these techniques demonstrating their potential to study nuclear protein dynamics.
Dynamic and stable interactions contribute to the assembly and maintenance of subnuclear compartments
Most nucleosomes are stable for long periods of time
FRAP analyses of GFP-tagged core histones have shown that far more than 50% of H2A, H2B, H3, and H4 are stably incorporated into chromatin and do not exchange with soluble pools (ESM 1; Kimura and Cook 2001; Gautier et al. 2004). These observations are consistent with the idea of a structural foundation of genome architecture and maintenance based on stable nucleosome arrays. The transiently incorporated sub-fraction of core histones is most likely attributable to chromatin remodeling events associated with transcription, replication or repair. All four core histones are present in the same nucleosome, yet their stabilities vary. H3 and H4 are loaded into nucleosomes during DNA replication, after which >80% remains permanently bound (Kimura and Cook 2001). In contrast, ∼50% of H2A and H2B exhibit substantial turnover (Kimura and Cook 2001; Gautier et al. 2004), compatible with the assembly properties of nucleosomes in vitro and in vivo (Annunziato 2005). While the immobile fractions might be associated with heterochromatin, the stability of the central H3 and H4 coupled with the lability of the outer H2A and H2B suggest simple ways of maintaining epigenetic marks (Kimura and Cook 2001). This is consistent with many posttranslational modifications found at the N-terminal ends of H3 and H4 providing long-term memories (Margueron and Reinberg 2010).
Genome maintenance relies on hyper-stable protein complexes at the centromere
Cell division is a highly dynamic process in which the chromosomes are segregated in a coordinated fashion. The centromere is the genetic locus required for precise and accurate chromosome segregation and provides a platform on which the kinetochore multiprotein complex assembles (Przewloka and Glover 2009). Accurate chromosome segregation is essential for cell survival and genome maintenance. Aberrant mitotic segregation can result in aneuploidy, cell death, or cancer (Kops et al. 2005). Intuitively and confirmed by FRAP data, stable chromatin–protein and protein–protein interactions are required during mitosis when sister chromatids are pulled along microtubules into daughter cells (ESM 1). However, the kinetochore/centromere complex could in principle disassemble completely during interphase, since a stable epigenetic mark such as a unique histone modification would be sufficient to transmit centromere identity through interphase. Shortly before mitosis starts, the epigenetic mark would be used as a landing platform for cell cycle-regulated factors that initiate de novo kinetochore assembly. This, however, is not the case as FRAP of centromeric proteins performed at any time during cell cycle show that at least Cenp-A and Cenp-I (ESM 1) stay ably associated with centromeres for the complete cell cycle (Hemmerich et al. 2008; Hellwig et al. 2008).
Because there is absolutely no dynamic exchange of Cenp-A between centromeres and freely diffusible nucleoplasmic pools, the question arises how the binding sites created by centromere replication are occupied. This issue has been addressed by FRAP experiments which clearly showed that Cenp-A is assembled during the G1 phase of the cell cycle via a “loading only” mechanism (Hemmerich et al. 2008): while the first FRAP experiment showed fluorescence recovery, a subsequent FRAP showed no recovery of CENP-A indicating an undetectably small off-rate. This shows that CENP-A is “loaded only,” without exchange at its binding sites. Interestingly, Cenp-A is incorporated via the “loading only” mechanism exclusively in early G1 (Hemmerich et al. 2008) corroborating earlier SNAP-tagging results (Jansen et al. 2007). The epigenetic marking of the centromere is believed to be conveyed by Cenp-A, because it is required for the association of probably all other kinetochore proteins (Buscaino et al. 2010) and because of its sustained presence at centromeres without dynamic exchange (Hemmerich et al. 2008; ESM 1). Although Cenp-A and Cenp-I are stably bound, many rapidly exchanging centromere components have also been identified (ESM 1). Taken together, the identification by FRAP of proteins which bind to the centromeres with dynamic exchange but also without dynamic exchange for longer than one cell cycle clearly indicates that in addition to organization and self-assembly, also heredity mechanisms contribute to centromere structure and function and hence genome maintenance.
A fraction of stably bound cohesin glues sister chromatids together
Sister chromatid cohesion after replication is mediated by the multiprotein complex cohesin which acts as a topological linker (Wong 2010). Gerlich et al. (2006) performed FRAP analyses identifying two distinct binding modes of cohesin to chromatin during the cell cycle. One pool of cohesin dynamically exchanged on and off chromatin throughout the entire interphase, moving through the nucleus by diffusion. This pool was absent in metaphase. About one third of the subunits SA1 and Scc1 are stably fixed to chromosomes after replication with a residence time of 6 to 7 h (ESM 1). This pool persisted until just before chromosome segregation (Gerlich et al. 2006). These analyses provided the first experimental evidence in living cells for a permanent and stable link between sister-chromatids. This stable link may functionally contribute to homologous recombination repair of DNA double-strand breaks during the G2 phase of the cell cycle.
HA95 and lamin A immobility in the nucleoplasm is consistent with the idea of a stable nuclear matrix
The existence of a nuclear matrix was proposed by Zbarskii and Debov (1948) based on their observation that high-salt extractions of purified nuclei produced microscopically visible lattice-like residual structures. These observations were confirmed in the Berezney lab using similar extraction protocols (Berezney and Coffey 1974). The lack of direct, particularly in vivo evidence, however, raised considerable skepticism about the existence of a stable nuclear structure (Pederson 2000). Homologous to A-kinase anchoring protein 95 (HA95) is a nuclear protein harboring two zinc fingers and a putative nuclear localization signal (Ørstavik et al. 2000). HA95 binds to chromatin and the nuclear lamina network where it has a role in anchoring nuclear membranes and lamins to chromatin in interphase and in releasing membranes from chromatin at mitosis. Astonishingly, bleaching experiments revealed no detectable recovery of the diffusely localized GFP-tagged HA95 in the nucleus of living 293 T fibroblasts (Martins et al. 2000). Roughly one quarter of the nuclear pool of lamin A resides outside the nuclear lamina and distributes as a diffuse veil throughout the nucleoplasm (Moir et al. 2000). FRAP analysis of the nucleoplasmic GFP-lamin A pool revealed a recovery halftime of more than 3 h, clearly indicating a stable lamin-containing structure in living cells (Moir et al. 2000). Although overexpression artifacts of the GFP fusion proteins cannot be ruled out, the immobile properties of HA95 and lamin A in the cell nucleus provide compelling evidence for the existence of a nuclear matrix in living cells. It has been suggested that HA95 provides a stable platform at the chromatin/interchromatin interface that could regulate nuclear envelope–chromatin interactions during the cell cycle (Martins et al. 2003). Recent evidence suggests that HA95 is also functionally involved in pre-mRNA splicing (Kvissel et al. 2007). Thus, HA95 could also serve as a stable platform on chromatin, linking RNA transcription with RNA processing. It will be essential to analyze if nuclear stability and particular nuclear functions are affected in HA95-depleted cells.
Constitutive heterochromatin: more stable than initially thought?
The main function of constitutive heterochromatin is to serve as a kinetochore attachment site in mitosis, where its particular chromatin structure is thought to ensure chromosome segregation. Pericentric heterochromatin also plays important roles in organizing transcription-repressive compartments of the nucleus and to ensure regulation of particular genes (Probst and Almouzni 2008). Constitutive heterochromatin is characterized by three repressive epigenetic marks: tri-methylation of H3-K9, mono-methylation of H3-K27, and tri-methylation of H4-K20. The histone methyltransferases Suv39H1/2 and Suv420H1/2 play crucial roles in the initial steps of constitutive heterochromatin formation in mammals. Mice deficient for the Suv enzyme family members display impaired pericentric heterochromatin function leading to chromosome missegregation and increase of sister-chromatid exchange. H3-K9me3 marks placed by Suv39H activities stabilize heterochromatin protein 1 (HP1) binding to heterochromatin. HP1 proteins self-oligomerize and interact with both Suv39H and Suv420H (Fodor et al. 2010).
According to its structural function, heterochromatin had been perceived as a relatively densely packed, rigid, and inert region. Surprisingly, however, FRAP had demonstrated that GFP-tagged HP1 isoforms display dynamic binding properties, suggesting that heterochromatin is a dynamic and plastic domain, in which access to the underlying DNA would not necessarily be prevented (Cheutin et al. 2003; Festenstein et al. 2003; Schmiedeberg et al. 2004). In contrast to HP1, Suv39H1 consists of both a mobile and an immobile population in heterochromatin where ∼30% of molecules do not exchange over a time period of 7 min (ESM 1; Krouwels et al. 2005). The tight association of Suv39H1 with chromatin is obviously a more common feature because a large fraction of Suv420H2 is also tightly bound at pericentric heterochromatin (ESM 1). FRAP analyses has revealed that more than 90% of GFP-tagged Suv420H2 is immobile at these domains over several minutes (Souza et al. 2009). It is, therefore, possible that the residence times of Suv39H1 and Suv420H2 in heterochromatin are even in the hours range, indicating that these enzymes may, in addition to their catalytic activity, also serve a structural role in chromatin and act as a stable interaction platform for other heterochromatin proteins. Further structural support for heterochromatin architecture may also be provided by the heterochromatin-binding protein Ki-67 which, by FRAP, also shows a cell cycle dependent turnover in heterochromatin (ESM 1; Saiwaki et al. 2005). While Ki-67 dynamically binds to mitotic chromatin, it becomes very tightly bound to peri-nucleolar heterochromatin during G1 phase. Approximately 60% of GFP-Ki-67 is immobile over 10 min during FRAP analyses in interphase cells (Saiwaki et al. 2005). These data suggest that Ki-67 may have very long residence times on chromatin.
Some transcription factors can become stably bound to chromatin: pRB, E2F, Mdm2, VHL, TFIIH, HSF, and Gal4
Most of the time, transcription factors diffuse throughout the cell nucleus, encounter gene promoters in a random fashion, and bind to them for a very short time (Misteli 2001b). This, however, does not hold for all situations.
pRB and E2F
The retinoblastoma protein (pRB) is a key cell-cycle protein that regulates the critical G1-S phase transition through interaction with E2F family members. The latter are cell-cycle transcription factors that repress transcription of genes required for G1-S checkpoint transition. pRB activity is regulated through networks sensing intracellular and extracellular signals which block or permit phosphorylation (inactivation) of the Rb protein (Poznic 2009). Quite unexpectedly, in bleaching experiments, fluorescence recovery of active (hypophosphorylated) GFP-RB and E2F is minimal (Angus et al. 2003). This behavior is in stark contrast to the mobility of most other transcription factors which are usually highly mobile (ESM 1). Only after inactivation by phosphorylation, pRB and E2F become highly mobile in chromatin. The regulation of the affinity of pRB to chromatin may constitute a new mechanism of transcriptional control.
Mdm2 and VHL
Complete immobilization, in this case within the nucleolus, was also observed for the ubiquitin ligases Mdm2 and VHL in FRAP experiments (ESM 1; Mekhail et al. 2005). Upon an activation stimulus, the nucleolus rapidly releases these enzymes from static detention, thereby restoring their high mobility profiles. These observations provide strong evidence that cells have evolved mechanisms to regulate molecular networks by reversibly switching proteins between mobile and static states (Mekhail et al. 2005).
In tissue-derived primary cells such as post-mitotic neurons, hepatocytes, and cardiac myocytes, the transcription factor TFIIH is effectively immobilized on the chromatin for hours during transcription, whereas in proliferative cells, it has the same highly dynamic behavior as in cultured cells (Giglia-Mari et al. 2009). It was proposed that static chromatin binding of TFIIH may be established during differentiation- and cell lineage-specific transcriptional programs. Interestingly, stable chromatin binding was not irreversible in the post-mitotic cells because induction of local DNA lesions remobilized TFIIH, probably based on its requirement in DNA repair (Giglia-Mari et al. 2009).
In Drosophila salivary glands, the heat shock factor (HSF; the transcription activator of hsp70) trimerizes and translocates from the nucleoplasm to chromosomal loci after heat shock (Yao et al. 2006). FRAP experiments showed a rapid exchange of HSF at chromosomal loci under non-heat shock conditions (t1/2 = 15 s) but a very slow exchange after heat shock (t1/2 > 6 min). Five minutes after the FRAP bleach pulse, ∼50% of HSF was still immobilized on chromatin. The unbound pool of HSF was found by FCS to diffuse freely, indicating that this pool was not able to compete for chromatin binding (Yao et al. 2006).
Nalley and colleagues developed a new variant of the chromatin immunoprecipitation assay that allowed a direct time-resolved observation of exchange between the transcription factor Gal4 and its DNA binding site on native promoters in yeast (Nalley et al. 2006). The assay revealed that after transcriptional activation, the Gal4–promoter complex was highly stable with a half-life of approximately 1 h. Again, this stability was established although unbound, competition–competent Gal4 molecules were present in excess amounts. During immobilization on its promoter, expression of the reporter gene occurred indicating that Gal4 functions via long-lived complexes with promoters during transcriptional induction (Nalley et al. 2006).
The nuclear envelope contains large pools of immobile proteins
Proteins of the nuclear lamina interconnect chromosomes with the nuclear envelope. The lamina harbors specific integral proteins including the lamin B receptor (LBR), lamina-associated polypeptides (LAPs), emerin, nurim, and MAN1. LBR, LAPs, and emerin bind to lamins A/C and B in vitro while LBR and LAP2b also bind chromatin via interactions with HP1 and the small DNA-binding protein BAF (Mekhail and Moazed 2010). Thus, a highly interconnected protein network provides multiple anchoring sites between chromatin and the nuclear envelope. Many of these proteins have meanwhile been subjected to FRAP analyses revealing stable incorporation of most of them into the nuclear lamina (ESM 1). Although mathematical modeling has not been employed yet, the extremely long recovery halftimes (i.e., more than 3 h for lamin B, Moir et al. 2000) of nuclear lamina constituents suggest residence times in the hours range. This is particularly true for the nuclear pore complexes, some components of which persist for long periods of time (residence times up to 70 h) within well-defined spatial regions without dynamic exchange (ESM 1; Rabut et al. 2004). Because the nucleus also undergoes dramatic morphological changes, a completely static nuclear lamina is not beneficial. Transitions between a stable and a flexible lamina might be regulated by small pools of the dynamically exchanging lamina constituents (ESM 1). Posttranslational modifications may serve as an additional mechanism to alter nuclear lamina stiffness.
Nuclear bodies contain stable components
FRAP analysis of subnuclear domains has revealed that most of their component parts rapidly exchange with nucleoplasmic pools with residence times in the seconds range (Misteli 2007; Matera et al. 2009). As a consequence, it was thought that these structures are determined by the ratio of on-rate versus off-rate of their constituents (Misteli 2008). This assembly mechanism is certainly true for speckles and nucleoli (ESM 1), which usually form in response to particular functions (splicing factor assembly and rRNA synthesis, respectively). However, FRAP experiments and mathematical modeling have revealed residence times of up to 1 h for Cajal and PML body components (ESM 1).
There are six nuclear isoforms of the PML protein in human cells from which PML V showed an extremely long residence time (48 min) (ESM 1). All other isoforms show substantially faster exchange, although they share the same nuclear body-binding domains with PML V (Weidtkamp-Peters et al. 2008). When analyzed in nuclei devoid of any endogenous PML protein (PML−/− MEFs), fractions of PML II becomes completely immobile within nuclear bodies and the residence time of PML IV is extended to 1.5 h (Brand et al. 2010). These observations indicate that probably all PML isoforms have the potential to build a stable scaffold within nuclear bodies, and that during evolution PML V was selected to execute this function (Weidtkamp-Peters et al. 2008). In Cajal bodies, p80 coiling was identified as the component with the longest residence time both, in human cells (Dundr et al. 2004) and in Xenopus germinal vesicles (Handwerger et al. 2003; Deryusheva and Gall 2004). These data indicate that the architecture of PML bodies and Cajal bodies may be primarily dictated by protein interactions forming stable scaffolds (Handwerger et al. 2003; Deryusheva and Gall 2004; Brand et al. 2010). On the other hand, their functionality certainly involves stochastic encounter of specific, fast exchanging components (Dundr et al. 2004; Weidtkamp-Peters et al. 2008).
Replication and repair factories contain a few stable components
RNA transcription sites and DNA repair foci have been visualized in mammalian cells, and initial FRAP studies indicated that they are stochastically assembled de novo in each round of transcription or repair from freely diffusible components (ESM 1; Houtsmuller et al. 1999; Dundr et al. 2002). DNA repair factor recruitment dynamics point towards diffusion-based DNA lesion recognition by individual components or small subcomplexes as the primary mode of DNA repair, instead of the recruitment of large preassembled holoenzymes (Luijsterburg et al. 2007; Dinant et al. 2009). Nevertheless, FRAP analyses also indicate that some replication and repair factors can reside on chromatin for extended periods of time (ESM 1). Data for ERCC1 for example suggest that this component is assembled at sites of DNA damage with other constituents of the nucleotide excision repair (NER) machinery into immobile holocomplexes during one repair event with a mean residence time of 4 min which is the estimated time of a single repair event (Luijsterburg et al. 2010). Furthermore, strip-FRAP on globally irradiated cells showed incomplete recovery of DDB2 for several hours after 16 J/m2 UV exposure, indicative of a significant immobile fraction over a period of hours at damaged chromatin (Luijsterburg et al. 2007). Twenty-four hours after exposure, most UV-induced lesions have been removed by NER, suggesting full release of bound molecules when repair is completed. The UV-induced immobilization was also shown for the NER proteins TFIIH, XPA, and ERCC1-XPF but was not observed for RAD52 group proteins (ESM 1; Houtsmuller et al. 1999; Essers et al. 2002; Politi et al. 2005). In UV-treated cells, the fraction of lesion-bound XPA molecules increases to maximally 35%, and the increase is directly proportional to the DNA damage load. The immobile pool of XPA at damaged chromatin remains over a period of 2 to 4 h post-UV exposure (Rademakers et al. 2003). While cells in living tissues may never experience DNA damage loads comparable to the cell culture studies, the immobilization of DNA repair factors ERCC1, XPA, and DDB1 on chromatin suggests that stable protein scaffolds may functionally contribute to DNA repair pathways.
Proliferating cell nuclear antigen (PCNA) is a further example of stable chromatin attachment. FRAP revealed elevated residence times for this factor at sites of DNA replication and repair (Sporbert et al. 2002; Solomon et al. 2004a, b; Mortusewicz et al. 2006; ESM 1). As a consequence, it was proposed that PCNA does not “bring” other factors to sites of replication or repair. Instead, PCNA appears to act as a stationary loading platform that is reused over multiple DNA synthesis or repair cycles with PCNA-binding proteins associating transiently and subsequently dissociating rather than being part of one stable, multifunctional, processive replication machinery (Mortusewicz et al. 2008).
An extension of models for the assembly of macromolecular structures in the nucleus: the “induced stability” model
The revised model is based on initial rapid binding and unbinding of proteins on DNA. Subsequent formation of dimers or multimers or interactions with additional DNA-binding proteins can induce an increase in the overall residence time of the complex on chromatin (Fig. 6). A similar effect may be realized by cooperative binding of several DNA-binding domains within the same protein, as recently demonstrated for linker histones (Stasevich et al. 2010). The more stable protein/chromatin complex may now serve as a platform for further binding partners. As the complex “grows,” the binding partners may increase their residence time on chromatin through multiplication of binding contacts. Chaperones may support the addition/incorporation of specific components as has been shown for the centromere complex (Foltz et al. 2009; Shuaib et al. 2010) or nucleosome (dis)assembly (De Koning et al. 2007; Park and Luger 2008a, b). Complex-induced alterations in chromatin structure may also contribute to increased stability (not shown in the model). All components, including the initial proteins, may exchange with short residence times at the stable core (Fig. 6a), as in chemical self-organizing systems (Aniansson and Wall 1974; Diekmann 1979). This model describes active transcription, replication, and repair complexes but also heterochromatin, cohesin, telomere, and centromere assembly.
An analogous model may also hold for the assembly of macromolecular protein complexes in the interchromatin space. A protein with homo-oligomerization properties, or interactions between different proteins, can lead to the assembly into small scaffolds onto which additional binding partners or further scaffolding proteins may attach (Fig. 6). The accumulation of additional binding partners may lead to larger, more stable scaffolds. These larger structures could acquire functional properties by transient retention of a specific set of nuclear proteins. As above, a subpopulation of scaffold components may exchange rapidly at the macromolecular structure depending on number and strength of binding events upon contact (Fig. 6). This model likely holds for the assembly of PML nuclear bodies, Cajal bodies, snRNPs, speckles, pre-nucleolar bodies, and the nuclear envelope including nuclear pore complexes. Chaperones may also be involved in the assembly process. For example, the survival of motor neurons complex can act as a chaperone for the assembly of snRNPs (Battle et al. 2006), although in vitro U1-snRNPs self-assemble (Hamm et al. 1987). Unlike Cajal bodies where most, if not all components are part of a large interaction network capable of Cajal body induction (Kaiser et al. 2008), formation of PML nuclear bodies require PML protein since typical PML body components are disperse in PML-negative cells (Ishov et al. 1999). Even quantitative expression of Sp100 failed to recruit PML body components to Sp100 nuclear bodies in PML-negative cells (Schwanitz and Hemmerich, unpublished observations).
Self-assembly, self-organization, and assisted assembly in the nucleus
Are the slowly recovering FRAPs for some nuclear components evidence for self-assembled nuclear structures? Self-assembly and self-organization are the main driving forces to create living systems from single molecules (Kirschner et al. 2000; Fraden and Kamien 2000; Gabora 2006; Pelesko 2007; Karsenti 2008). With respect to nuclear organization and function, self-organization was proposed to be the major underlying mechanism (Misteli 2001a, b, 2009; Matera et al. 2009; Rajapakse et al. 2010). Self-assembly and self-organization are often used interchangeably and sometimes in association. In current literature, the boundary between these two mechanisms is rather elusive and elastic (Bensaude-Vincent 2009).
Evidence for self-assembly of nuclear structures
Self-assembled nuclear structure
Xenopus cell free extract
Biochemically purified comonents
Ruiz-Carrillo et al. 1979
Xenopus cell free extract
Leforestier et al. 2001
Xenopus cell free extract
Lohka and Masui 1983
Xenopus cell free extract
CHO cell free extracts
Burke and Gerace 1986
Nuclear pore complex
Xenopus cell free extract
Nuclear pore complex
Bacterially expressed components
Lutzmann et al. 2002
Xenopus cell free extract
Replication factor C
Uhlmann et al. 1996
Gestaut et al. 2010
Westermann et al. 2005
Bacterially expressed components
Kline et al. 2006
Xenopus cell free extract
Hamm et al. 1987
Harborth et al. 1999
Xenopus cell free extract
Bell et al. 1992
Kentsis et al. 2002
Self-organization requires a situation far away from thermodynamic equilibrium in a steady state and is possible only in open systems with an external energy source (Gerhart and Kirschner 1997; Toussaint and Schneider 1998; John and Bär 2005; Halley and Winkler 2008). Self-organization may also be regarded as “dynamic self-assembly” (Pelesko 2007). Self-organizing complexes and self-assembly processes can also be controlled efficiently either by posttranslational modifications or by chaperone action. The assembly of NuMa scaffolds in the nucleoplasm for example is tightly controlled by phosphorylation (Saredi et al. 1997). Similarly, nuclear lamina self-assembly is regulated by phosphorylation and methylation of lamins (Gerace and Blobel 1980; Chelsky et al. 1989). SUMO-attachment to PML (which harbors three SUMOylation sites) is a requirement for PML nuclear body assembly (Ishov et al. 1999; Duprez et al. 1999; Shen et al. 2006), and the number of SUMO modifications regulates the residence time of PML molecules at nuclear bodies, ranging from seconds to hours (Weidtkamp-Peters et al. 2008; Brand et al. 2010). Gradients are used in a number of biological systems to transmit spatial information over a range of distances. Intracellular gradients utilize intrinsic auto-regulatory feedback loops and diffusion to establish regions of activity, for example within the mitotic cytosol (reviewed in Fuller 2010). These intracellular gradients bear several hallmarks of self-organizing biological systems that designate spatial information during pattern formation. Since self-organized systems are dynamic, FRAP of their components might be expected to yield fast recoveries. However, our model for nuclear assembly discussed in the preceding section proposes that initially dynamic assemblies can become more stable over time or during specific phases of the cell cycle, yielding eventually slower FRAP recoveries for some components. Thus, slow FRAP recoveries could also arise from self-organization or a mixture of self-organization and self-assembly.
In biological systems, it is obviously very difficult to clearly separate self-assembly from self-organization. In vitro, self-assembly and self-organization can act in concert to create functional large molecule aggregates (Cuccia et al. 2002; Drain 2002). For example, purified DNA can be assembled in the test tube into structures that closely resemble cell nuclei. By combining naked DNA, cytosol, and light membrane fractions from Xenopus egg extracts, complete nuclei can be formed, including nuclear membranes with pore complexes, and these reconstituted nuclei are capable of normal nuclear processes (Laskey and Leno 1990; Cross and Powers 2008). The assembled nuclei are morphologically indistinguishable from normal eukaryotic nuclei. Nuclear assembly involves discrete intermediate steps, including nucleosome assembly, scaffold assembly, and nuclear envelope assembly, indicating that during reconstitution nuclear organization is assembled one level at a time (Newport 1987). The nuclear envelope contains functional, self-assembled nuclear pore complexes (Sheehan et al. 1988). After envelope assembly, these artificial nuclei are even capable of DNA replication (Newport 1987). Notably, nuclear lamina and envelope assembly in vitro do not require energy (Burke and Gerace 1986), a hallmark of the self-assembly process. The inherent ability of a primitive genome to induce its own inclusion in a membrane has even led to a model of the origin of eukaryotic cells solely based on self-assembly mechanisms (de Roos 2006).
Potential assembly mechanisms in living cells
Nuclear pore complex
DNA Replication sites
DNA Repair sites
PML nuclear bodies
Chromatin-binding proteins are highly dynamic; they roam the nucleus in an energy-independent manner in search for high-affinity binding sites, and their residence times on chromatin are typically in the order of several seconds. This dynamic behavior is thought to play a major role in generating combinatorial protein complexes on chromatin which provide a mechanism to fine-regulate transcription, chromatin organization, and genomic plasticity (Misteli 2001a, b, 2008). By analyzing FRAP data of about 264 nuclear proteins, we identified nuclear factors that do not follow this rule of highly transient interactions, instead some of them exhibit residence times in the hours range (Fig. 5). Thus, although dynamic transient interactions are a general and important property of nuclear proteins, they are not universal. Stable complexes may arise from dynamic ones through a mechanism we coined “induced stability.” The demonstration in living cells of two proteins (HA95 and lamin B) which are almost completely immobile throughout the nucleoplasm may even reanimate research into the nuclear matrix. In particular cases, helper proteins support correct complex assembly, a phenomenon we have termed “assisted assembly.” The idea of immobile nuclear entities in the nucleus was already put forward by Bazett-Jones and colleagues in 2001 (Hendzel et al. 2001). The combined action of self-assembly and self-organization processes may lead to nuclear structures which are stable for hours. It should be considered in the future that stable interactions also contribute to the outcome of physiological cues impacting on nuclear structure and function. Therefore, “immobile populations” inferred from FRAP experiments should be studied in more detail. More examples of stable nuclear protein networks may surface as the community continues to perform fluorescence fluctuation microscopy on hitherto unexplored nuclear components.
Research in the labs of PH and SD are supported by the DFG and the BMBF. We would like to thank Karolin Klement and Sandra Münch for FISH images of chromosome territory 1 and anti-telomere immunfluorescence data, respectively. We apologize to all researchers whose FRAP data on nuclear proteins were not considered in this paper but strongly encourage them to communicate their data to us in order to complete and extend the FRAP data table on nuclear proteins started here (ESM 1).
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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