1. Introduction
All living organisms are connected by the necessity to replicate their DNA. However, the process of unwinding the parental DNA to serve as a template at replication forks is dangerous. The ssDNA generated by helicases is inherently cytotoxic; not only because it is more prone to damage, but it can also be an inappropriate target for nucleases and recombination proteins leading to loss of genetic material or gross chromosomal rearrangements [1]. Normally, the replication machinery rapidly restores this single-stranded template DNA to its more stable double-stranded form. However, replication forks are prone to stalling if they encounter obstacles that the DNA polymerase is unable to bypass, such as sites of damage or DNA sequences with complex secondary structures [2], resulting in long stretches of ssDNA remaining exposed [3]. Replication stress, therefore, represents an important mechanism that erodes the genetic integrity of organisms. Not surprisingly, replication stress has been linked to aging in budding yeast, which can likely be extrapolated to higher eukaryotes as well [4]. Furthermore, inducing replication stress in normal human fibroblasts results in pathogenic changes in copy number due to duplication or deletion events [5]. Therefore, the ability of eukaryotes to detect, stabilize and resolve stalled replication forks using the replication checkpoint represents an important safeguard for genomic stability.
The replication checkpoint response relies on a cascade of kinases that either remain localized to the stalled fork or disseminate the stress signal to distal sites resulting in the suppression of late origin firing, pausing of the cell cycle, and increasing the expression of DNA repair enzymes [6]. Overall, this checkpoint involves individual proteins and protein complexes coming together to assemble intricate supramolecular complexes triggered by stalled replication forks. For simplicity’s sake, this chapter will focus on the
Several BRCT-containing proteins are essential for the assembly of the pre-replication complex. For instance, the regulatory subunit of the Cdc7 kinase, Dbf4, contains a single BRCT domain [9, 10] and Dpb11, whose function is essential to activate pre-replication complexes, contains two BRCT pairs [8]. The Rfc1 subunit of the RFC complex, which functions in loading the sliding clamp onto ssDNA/dsDNA junctions during replication [11], also contains a BRCT domain required for DNA binding [12]. Most replication proteins containing BRCT domains are also involved in the replication checkpoint response, suggesting that BRCT domains may have fundamental roles in preserving DNA integrity. During the DNA damage response, BRCT domains are often used to recognize the site of damage, as they can bind to DNA breaks directly [13, 14] or indirectly by recognizing phosphorylated histone H2A that marks areas of damage [15-20]. In the case of replication stress, at least two first responders are recruited to the ssDNA gap at stalled forks (Figure 1). The first is the protein kinase Mec1 and its targeting subunit Ddc2 that mediates the interaction with RPA-coated ssDNA [21]. The second is the 9-1-1 clamp that encircles the DNA at the ssDNA/dsDNA junction [22]. This requires the action of a clamp loader, which is composed of Rad24 and Rfc2-5. Interestingly, this complex is the alter ego of the clamp loader RFC, which differs only in having Rfc1 instead of Rad24 [23]. In contrast to the sliding clamp, the 9-1-1 complex is held statically by protein-protein interactions at the stalled fork [24].
After the recognition of DNA damage or stalled forks, both FHA- and BRCT-containing proteins feature prominently in bridging protein–protein interactions that disseminate the stress signal (Figure 1). For instance, Dpb11 bridges the interaction between the 9-1-1 clamp and Mec1, leading to the full activation of the Mec1 kinase [24, 25]. Mec1 has many roles at the stalled fork including facilitating the activation of the next downstream kinase in the pathway, Rad53 [26]. This is accomplished after Mec1 phosphorylates Mrc1—a protein naturally associated with the stalled replisome [27]. This creates phospho-epitopes that act as beacons for the FHA domain of Rad53. Multiple copies of Rad53 are thus recruited, increasing the local concentration of this kinase, which can then be autophosphorylated
These themes are echoed in other DNA damage response pathways, where BRCT and FHA domains are known to mediate important interactions. Not surprisingly, mutations in the BRCT and FHA domains of critical damage repair proteins such as Chk2 [36], Nbs1 [37] and BRCA-1 [38, 39], lead to cancer predisposing syndromes. Why does nature rely so heavily on BRCT and FHA domains to respond to stress? The answer may seem to lie in the ability of BRCT and FHA domains to recognize phospho-epitopes, since they are an important cue during replication stress and the DNA damage response, when a number of kinases are awakened. However, their power could also lie in the plasticity of these two domains that can use multiple interaction surfaces to mediate additional interactions beyond phospho-epitope recognition. Such plasticity could, in turn, mediate the interaction network sustaining the formation of the large protein complexes required to promote genome stability in eukaryotes. Along with the well-characterized phosphate recognition ability of FHA and BRCT domains, these varied and unique alternative interaction surfaces will be considered in this chapter. Interactions occurring during the replication checkpoint will be discussed, but examples from other cellular pathways will also be included.
2. Interaction Modes of FHA Domains
An FHA domain consists of an 11-stranded β sandwich connected by loops that often contain short helical regions. The phospho-epitope binding groove is located at the apical surface of the β-sandwich, with the N- and C-termini at the opposite end of the domain. Unlike BRCT domains, that are often present in multiple copies in a single protein, FHA domains are almost always singular. Only two proteins are known to possess two FHA domains in the same polypeptide: Rad53 from
2.1. Phospho-epitope dependent interactions
FHA domains recognize phosphorylated proteins with a strict specificity for pThr-containing epitopes. The majority of interactions between FHA domains and their phosphorylated partners have been studied using short peptides including a central phosphorylated threonine [41-46]. These phospho-peptides bind to the apical surface of the FHA domain in an extended conformation using two pockets that determine their binding specificity. The β3–β4 and β4–β5 loops from the FHA domain primarily define the pThr-binding site, where a conserved arginine and serine (Arg70 and Ser85 in Rad53) provide critical contacts with the phosphate group. An extensive hydrogen-bond network mediated by non-conserved residues further stabilizes the interaction with the phosphorylated threonine. The second pocket recognizes the third residue C-terminal to the phospho-threonine (pThr+3), and is usually defined by the β6–β7 and β10–β11 loops of the FHA domain (Figure 2A and B).
A unique aspect of the pThr-binding pocket in FHA domains is its ability to distinguish between phospho-threonine and phospho-serine residues, a talent not shared by other phospho-epitope recognition modules. For instance, MH2 domains share a common ancestor with FHA domains and, yet, MH2 domains can also bind phospho-serine with high affinity [42, 47]. The difference is that the pThr-binding pocket in the FHA domain includes a well-defined hydrophobic nook that provides a docking site for the methyl moiety of the phosphorylated threonine (Figure 2C). While most residues in this nook are not conserved, the hydrophobic nature of this pocket is strictly maintained, thus providing a number of Van der Waals interactions that orient the phospho-threonine such that its phosphate moiety is locked in the most favorable geometry for the interaction with the domain [48]. Thus, the pThr pocket of an FHA domain can be thought of as a glove where only a phospho-threonine can fit (Figure 2C). Despite this rigid mode of binding, certain FHA domains can accommodate deviations. For instance, the FHA2 domain from Rad53 can bind pTyr-containing peptides with low affinity [47] and the FHA domain found in Dun1 has a unique preference for phosphorylated substrates including two pThr residues [49].
In contrast to the pThr pocket, the residues defining the pThr+3 pocket are not conserved allowing for different domains to have different target-sequence specificities. This is called the “pThr+3 rule” wherein different FHA domains have different specificities for the pThr+3 residue. While this provides a convenient way to classify FHA domains, it should be noted that the specificity of the pThr+3 pocket is not fixed. For example, the FHA1 domain from Rad53 prefers aspartic acid as the pThr+3 residue using short peptides
FHA domains often bind only weakly to pThr-containing peptides [43, 51], supporting the idea that additional contact points beyond the phospho-epitope binding site are necessary to form high avidity complexes with their partners. For example, the interaction between the FHA domain from Chk2 and the tandem BRCT repeat from BRCA-1 requires an additional hydrophobic patch on the surface of one of the FHA β-sheets. Mutating either the phosphate binding pocket or this hydrophobic patch destroys the interaction with BRCA-1 even though structurally these two sites are more than 20 Å apart [52]. Reinforcing the importance of this additional interaction surface
This long phospho-peptide does not conform to the “pThr+3” rule. Instead, binding to the FHA domain induces the formation of an α helix that nestles in a hydrophobic pocket formed by the β4–β5 and β10–β11 loops [50], underscoring the need for additional structural information using full-length phosphorylated binding partners.
2.2. Phospho-epitope independent interactions
Although FHA domains were initially identified as pThr binding domains, it has been predicted that they can also mediate phosphorylation-independent interactions. Members of the kinesin-3 family, a class of motor proteins that transport vesicles to the tips of axons in neural cells [53], contain an N-terminal FHA domain in addition to their motor domain and coiled-coil regions [53]. One member of this family, KIF13B, uses its FHA domain to transport PIP3-rich vesicles in order to facilitate axon development. This involves the formation of a tetrameric complex with CENTA1, which has been studied through X-ray crystallography [54]. This complex has two CENTA1 molecules and two kinesin molecules, with the FHA domain of each kinesin involved in two simultaneous interactions (Figure 4). The first is with the ArfGAP domain of one of the CENTA1 molecules, which contacts the FHA loops that normally recognize a pThr. However, this interaction is phosphorylation-independent because the FHA domain of KIF13B lacks the conserved residues for phospho-threonine recognition [54]. The second CENTA1 molecule in the tetramer uses its Pleckstrin Homology 1 (PH1) domain to contact a surface on the β-sandwich of the same KIF13B FHA domain. This situation is reminiscent of the interaction between Chk2 and BRCA-1, and suggests that auxiliary contacts mediated by the β-sandwich may enhance both phosphorylation dependent and independent interactions. Phosphorylation independent interactions are not exclusive to FHA domains that lack the pThr-recognition residues. Another member of the kinesin-3 family, KIF1A, has a canonical phospho-epitope binding site and, yet, is also suspected of using this pocket for a phosphorylation-independent interaction [55]. Similarly, the FHA domain of
Some bacterial proteins can also interact with the phospho-epitope binding site of an FHA domain in a phosphorylation-independent manner. Although bacteria primarily rely on histidine kinases and their associated regulatory responders for phosphorylation-dependent signaling, some also utilize eukaryotic-like Ser/Thr Protein Kinases (STPKs) [56]. Like eukaryotes, bacteria can use STPKs to respond to stress, but they also participate in other processes such as pathogenicity, thereby providing important drug targets [56]. The best characterized bacterium in this regard is
3. Interaction Modes of BRCT Domains
BRCT domains are named after the breast cancer associated protein 1 (BRCA-1) C-terminus because they were originally identified at this end of BRCA-1. However, the BRCT is an ancient domain that originates in prokaryotic NAD+ ligases where it is used to bind to DNA. Eukaryotes obtained the BRCT domain through horizontal gene transfer, and while some eukaryotic BRCT domains still retain DNA binding function, the vast majority have evolved to recognize protein partners instead [60]. BRCT domains are defined by a central four-stranded parallel β-sheet surrounded by three helices: α1 and α3 on one side, and α2 on the other of the β-sheet [61]. However, additional secondary structure elements have been described in the loop regions. There are also BRCT domains that lack elements, notably helix α2 [61]. Rap1 is the most extreme example of this, having only three strands in its central β-sheet and all helices packed against the same side of the sheet, leaving the other side exposed [62]. This unique structure is highly flexible and relatively unstable [62].
BRCT domains can occur both as single or multiple units, which usually consist of two BRCT domains and are referred to as tandem BRCT repeats. The structural diversity of BRCT domains is perhaps best illustrated by the human homologue of Dpb11 (human TopBP1), which contains eight BRCT domains that function as single, double or triple BRCT units [63-65]. Similarly to FHA domains, BRCT domains are overrepresented in DNA damage response proteins where they recognize phosphorylated targets generated during damage recognition and repair [7]. While the molecular intricacies of phospho-epitope recognition by tandem BRCT repeats have been extensively studied, phosphorylation-independent interactions mediated by BRCT tandems or the functions of single BRCT domains remain poorly characterized. Elegant proteolysis studies have shown that mutations in the BRCT tandem repeat of BRCA-1, with a causal link to early onset breast and ovarian cancer, destabilize the BRCT fold [39], suggesting that BRCT domains may work as protein scaffolds. These studies also revealed the hypersensitivity of BRCT domains to mutations, an effect that was attributed to its minimal size (95-100 amino acids) [66] and, consequently, the fact that every residue contributes to either maintaining the domain fold or mediating interactions with BRCT-binding partners [67].
3.1. Tandem BRCT Domains: The Two-Knob Hypothesis
The tandem BRCT repeat was formed through a gene duplication event, in which the binding pocket originally used to bind to the phosphate backbone of DNA evolved to recognize a phospho-epitope in a target protein [60]. Being an α/β fold, the BRCT domain has a topological switch point; a region along the C-terminal edge of the β-sheet whereupon a groove is formed in the connecting loops. Tandem BRCT repeats use the topological switch point—termed the P1 pocket—of their first BRCT domain to bind phospho-serine (pSer) residues in their interaction partners (Figure 5). Similar to FHA domains, this interaction involves the side chain of a conserved serine residue, but in BRCT domains the phosphate moiety of the pSer residue is further stabilized by the interaction with the side chain of a conserved lysine, as well as the backbone atoms from the glycine immediately following the conserved serine [68].
Similar to FHA domains, tandem BRCT repeats also subscribe to a “pSer+3 rule” to enhance phospho-epitope binding specificity [68]. However, the pSer+3-binding pocket—termed the P2 pocket—only forms in tandem BRCT repeats as it is defined by residues at the interface between the first and second BRCT domains. When two BRCT domains coalesce to define a tandem repeat, the central β-sheet of both domains adopt a parallel arrangement that defines an intervening hydrophobic three-helix bundle form by α2 from the N-terminal and α1 and α3 from the C-terminal BRCT domains (Figure 5) [69]. Helical bundles are known to facilitate molecular interactions [70] and, in the case of tandem BRCT domains, it allows for the recognition of a bulky hydrophobic residue at the pSer+3 position [68]. Indeed, the high specificity of tandem BRCT repeats for their phospho-epitopes is primarily due to the presence of the P2 pocket that imposes the need for a second knob in the phospho-epitope, thus precluding non-specific binding.
In certain tandem BRCT repeats, the P1 pocket is found in the C-terminal rather than the N-terminal BRCT, however due to the absence of the P2 pocket it is presumed that this mode of interaction is weaker than the canonical binding mode [71]. In fact, BRCT repeats containing a P1 pocket on the C-terminal BRCT are known to mediate phosphorylation-independent protein–protein interactions [72], suggesting that the binding specificity for a phospho-epitope may not be as critical. In the structure of the tandem BRCT repeats found in 53BP1 bound to the DNA-binding domain of p53 [73, 74], the inter-domain linker is critical to mediate the interaction between 53BP1 and p53. Similarly, in the structure of the
3.2. BRCT “Super-domains”: Expanding the two-knob model
The individual units in a tandem BRCT repeat are dependent on each other for structural stability due to the hydrophobicity of the α helices that define the intervening helix bundle [69]. Thus, a tandem BRCT repeat can actually be considered one single domain module, distinct from single BRCT domains. Beyond single and tandem BRCT arrangements, a number of BRCT structures over the past decade have revealed many unexpected tertiary structures formed by the combination with other functional domains. This is not only in the number of BRCT domains involved, such as the structure of the triple BRCT repeat from the human TopBP1 [76], but also in the diversity of domains that can be ensnared by a BRCT neighbor. This includes the Fibronectin Type III domain (FN3) found at the N-terminus of a tandem BRCT domain in the
The crystal structure of the FHA–BRCT–BRCT super-domain of Nbs1 emphasizes the ability of BRCT domains to build scaffolds capable of multiple interaction modes. While the two BRCT domains in Nbs1 associate to form a canonical tandem BRCT repeat with a phospho-epitope binding site, the FHA domain interacts with the hydrophobic core of the first BRCT domain leaving helices α1 and α3 exposed to the solvent (Figure 6) [78, 79]. In contrast to other BRCT domains, these two helices are amphipathic and, hence, break the theme of BRCT domains using hydrophobic three-helix bundles to build super-domains. Surprisingly, the FHA and the first BRCT domain (FHA–BRCT1) form the most stable unit of Nbs1, whereas the second BRCT (BRCT2) is quite flexible despite forming a canonical tandem repeat with the first BRCT domain [78, 79]. Given its tertiary structure, the FHA–BRCT–BRCT super-domain could bind two phospho-epitopes simultaneously, suggesting that the interactions of Nbs1 with its binding partners may be highly regulated.
The recent structure of the triple BRCT repeat in TopBP1 (BRCT0/1/2) provides another example of a BRCT super-domain deviating from the canonical three-helix bundle interface (Figure 6). In this case, neither BRCT0/1 nor BRCT1/2 associate to form canonical tandem BRCT repeats, primarily due to the unusually short inter-domain linkers that connect adjacent BRCTs [76]. Beyond connecting adjacent BRCT domains, the inter-domain linkers in some tandem BRCT repeats actively mediate protein-protein interactions [73, 74] and, in extreme cases, it is the linker rather than the BRCT domains that mediates the interaction. For example, the damage response protein XRCC4 interacts exclusively with the inter-domain linker connecting the two BRCT domains of ligase IV [80]. Collectively, these structures demonstrate that not only the BRCT repeat, but also the length and composition of the inter-domain linker joining the two domains affect the binding plasticity of BRCT repeats and their ability to form higher order structures with diverse binding specificities.
3.3. Single BRCT Domains: Is One the Loneliest Number?
The association of multiple BRCT domains with other functional domains within a single polypeptide chain is becoming a common theme found in many DNA damage response proteins. This poses the question as to whether the increased binding specificity, and hence the underlying ability to fine tune interactions during the checkpoint response, is the driving force for BRCT domains to build such complex structures. Surprisingly, the majority of eukaryotic proteins that possess BRCT domains have at least one that functions solo. The exposed α helices (α1, α2 and α3) in single BRCT domains are amphipathic, with a hydrophobic face interacting with the central β-sheet and a polar face exposed to the solvent, unlike their tandem counterparts where both faces are chiefly hydrophobic. This enhances the stability of single BRCT domains but does not shed light on their functions.
There is mounting evidence indicating that both single and tandem BRCT domains may require additional secondary structural elements to form functional units [10, 12, 81, 82]. Some of these structural elements are required for structural stability, such as the additional C-terminal α-helix in the PARP-1 BRCT [81], while others enhance function (Figure 7). An example of the latter comes from the largest subunit of the budding yeast clamp loader, Rfc1. Rfc1 has a single BRCT domain that is required for DNA-binding [12]. However, as an isolated unit, this domain is unable to recognize DNA despite having a positively charged patch positioned at the conserved P1 pocket [12]. The inclusion of an N-terminal extension recapitulates DNA binding with a KD in the nM range. The extension encompasses an additional α helix that directly contacts DNA [12]. Rather than being a structural element integrated into the BRCT fold, however, this helix is predicted to act as an auxiliary element to enhance function [12]. Based on this model, both the BRCT domain and its auxiliary helix likely bind synergistically to the DNA leading to a robust interaction (Figure 7). Similarly, the presence of an additional N-terminal helix necessary to bind DNA is also predicted in the single BRCT domain from the translesion polymerase Rev1 [12, 82]. It is conceivable that these additional structural elements play the dual role of stabilizing the BRCT fold and enhancing its function. In fact, this is the case of
4. Dbf4/Rad53: A Case Study for phosphorylation-independent BRCT and FHA Interactions
The DDK complex, formed by the association of the Cdc7 kinase and its regulatory subunit Dbf4, is required for initiating DNA replication and, hence, it is essential for the life of all eukaryotes [84]. Like many other replication proteins, DDK is also involved in the replication stress checkpoint [31-34, 85, 86]. The ability of Dbf4 to crossover into the stress response pathway is partly due to a conserved motif at the N-terminus of the protein (motif N). Based on sequence alignments, it was a matter of debate whether motif N was a bona fide BRCT domain [9, 87], however concerns were laid to rest when the crystal structure of the N-terminal region of
The interaction between the H–BRCT domain of Dbf4 and the first FHA domain of Rad53 also poses an interesting paradigm during the checkpoint response because Dbf4 and Rad53 interact in a phosphorylation independent manner using domains notable for recognizing phosphorylated epitopes. This interaction was initially proposed to depend on the recognition of a phospho-epitope in Dbf4 because a point mutation in the conserved arginine (R70A) involved in phospho-threonine recognition by FHA1 effectively abolished the interaction between the two proteins in a yeast two-hybrid experiment [31]. Yeast two-hybrid experiments conducted in the past have demonstrated that phosphorylation-dependent interactions with Rad53 can indeed be detected, likely due to the activity of endogenous kinases [89]. However, all the threonine residues located within or surrounding the H–BRCT domain of Dbf4 can be mutated without abrogating the interaction with Rad53 [10]. Several possible scenarios can explain the critical role of Arg70 in mediating the interaction with Dbf4. First, Arg70 may be part of the interaction interface despite the lack of a phospho-epitope in Dbf4. This scenario would be reminiscent of
5. Conclusion
Through the use of short phospho-peptides, the basic mechanism underlying pThr recognition by FHA domains has been elucidated. However, it is clear that full-length binding partners harboring pThr-epitopes will likely contact the FHA domain at multiple sites in addition to the pThr pocket, many of which will be unique to that particular interaction. Additionally, proteins are capable of interacting with FHA domains in a phosphorylation independent manner, using the phospho-epitope binding site as well as alternative interfaces, most often the surfaces of the β-sandwich. While phosphorylation-dependent interactions have a clear mode for turning the interaction on and off, regulation of phosphorylation-independent interactions remains unexplored. If these interactions are mediated by the phospho-epitope binding site it may simply be a matter of availability of phosphorylated binding partners that can compete with the unmodified protein. However, if the canonical phosphate binding residues are absent or the interaction takes place on an alternative surface, the mechanism for control is less clear.
BRCT domains have previously been divided in tandem repeats, which can interact with phosphorylated partners in a well-defined manner, and the enigmatic single domains. The plethora of interaction mechanisms used by single BRCT domains can seem overwhelming, but like FHA domains a common theme is now emerging. The BRCT fold may serve as a structural core upon which more complex and unique assemblies can be built. In this way, specific interaction surfaces can be created allowing for the BRCT domain to gain function. Therefore, BRCT domains can use extra secondary structural elements, either integrated into the fold as in Dbf4 or as an auxiliary element as in Rfc1, or entire domains such as in the case of Chs5 and Nbs1—or even in tandem BRCT repeats—to modulate their functions.
Functional and structural analyses of FHA and BRCT domains during the last decade have unveiled a complex repertoire of interactions mediated by these two domains. Once regarded as mere phospho-epitope binding units, we now know that they can mediate very sophisticated interactions regulated by multiple binding knobs. Further structural and functional analysis of protein complexes mediated by these two domains will delineate the common mechanisms that regulate the DNA damage response, and will extend the lessons learned from studying the replication stress pathway in yeast to a variety of stress response networks that rely on BRCT and FHA domains across all kingdoms of life.
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