Total sequence decomposition distinguishes functional modules, "molegos" in apurinic/apyrimidinic endonucleases
© Schein et al; licensee BioMed Central Ltd. 2002
Received: 8 May 2002
Accepted: 25 November 2002
Published: 25 November 2002
Total sequence decomposition, using the web-based MASIA tool, identifies areas of conservation in aligned protein sequences. By structurally annotating these motifs, the sequence can be parsed into individual building blocks, molecular legos ("molegos"), that can eventually be related to function. Here, the approach is applied to the apurinic/apyrimidinic endonuclease (APE) DNA repair proteins, essential enzymes that have been highly conserved throughout evolution. The APEs, DNase-1 and inositol 5'-polyphosphate phosphatases (IPP) form a superfamily that catalyze metal ion based phosphorolysis, but recognize different substrates.
MASIA decomposition of APE yielded 12 sequence motifs, 10 of which are also structurally conserved within the family and are designated as molegos. The 12 motifs include all the residues known to be essential for DNA cleavage by APE. Five of these molegos are sequentially and structurally conserved in DNase-1 and the IPP family. Correcting the sequence alignment to match the residues at the ends of two of the molegos that are absolutely conserved in each of the three families greatly improved the local structural alignment of APEs, DNase-1 and synaptojanin. Comparing substrate/product binding of molegos common to DNase-1 showed that those distinctive for APEs are not directly involved in cleavage, but establish protein-DNA interactions 3' to the abasic site. These additional bonds enhance both specific binding to damaged DNA and the processivity of APE1.
A modular approach can improve structurally predictive alignments of homologous proteins with low sequence identity and reveal residues peripheral to the traditional "active site" that control the specificity of enzymatic activity.
Genomic cloning has revealed that most of the enzyme families essential for maintaining cell growth have been conserved throughout evolution . However, mammalian enzymes with different functional activity may have evolved by combining elements from several bacterial ancestral genes. Even small proteins may contain several individual domains that link them to different superfamilies . While many endonucleases share a common active site that is highly conserved across many subfamilies, identifying residues that control substrate specificity requires sophisticated analysis that combines both sequence conservation and structural data [3–5].
In this paper we distinguish, using a word-based "molego" approach, structural elements that control substrate specificity. We postulate here that elements conserved in all the members of related protein families dictate common structures and also common "functions", i.e., individual steps in a complex reaction. Areas that affect substrate specificity will be less conserved in the superfamily than they are in subfamilies of enzymes that catalyze specific activities. We have chosen to illustrate this approach using the multifunctional family of DNA repair proteins, the apurinic/apyrimidinic endonucleases (APEs), which have a clearly defined bacterial ancestor, E. coli exonuclease III (ExoIII), and are distantly related to several enzymes with varying substrate specificity.
APEs are essential for mammalian cell growth and bacterial survival in the presence of ionizing radiation and DNA mutagens . They initiate repair of an abasic DNA site by cleaving the phosphodiester backbone 5' of the phosphodeoxyribose. This generates the necessary 3' hydroxyl group for DNA polymerases (pol β, δ or ε, in eukaryotes) to insert the correct nucleotide in later steps in the base excision repair pathway (BER-pathway) [7, 8]. Recent crystal structures of huAPE1 complexed with DNA containing an abasic site [9–11], combined with sequence analysis and site-directed mutagenesis, have defined the residues that participate in metal ion based cleavage of the phosphate backbone of the DNA [12–17].
Mutations that greatly diminish the enzymatic activity of huAPE1 do not affect, and may even increase binding to damaged DNA, while non-specific DNA binding remains low [16, 18]. Further, mutations that have little effect on APE activity in vitro prevent complementation of DNA repair deficient E. coli. As seen with other DNA repair enzymes , specificity determining residues, as yet unidentified for APEs, must be distinct from those involved in phosphorolysis.
To better assess which residues determine specificity, we assume that functions unique to APEs will be determined by motifs that are not conserved in a similar fashion in families with a different activity spectrum of functions. Besides cleaving the phosphate backbone, to achieve specificity APEs must coordinate a series of functions, including: interaction with target DNA in a series of small, possibly repetitive steps (scanning), locating damage sites, establishing the transition state complex, completing the cleavage, re-adjusting the charge status within the active site, and regulating release of product after interaction with the next enzyme in the BER pathway [20–25]. A finer breakdown of these functions can be achieved at the molecular level once all the residues in the reaction mechanism are known. APEs also have RNase H, 3'-exonuclease, and 3'-phosphodiester activities that are particularly high in the bacterial members of the family [26, 13].
Our web-based MASIA program  was used to rapidly decompose the sequences of APEs and related protein families into motifs, areas of significant conservation in members of identical function, which could then be correlated structurally using data from crystal structures. Having determined that 12 motifs were common to all APE1's, we compared the structure of the subset of these that occurred in both DNase 1 and synaptojanin, a member of the IPP family. These shared motifs had a similar 3D structure in representatives of these functionally diverse families, and we therefore called these motifs "molegos" (molecular legos). We then demonstrated that the shared molegos served a similar role in substrate binding by comparing the DNA binding profile of huAPE1 with that for the less specific enzyme DNase 1. The molegos present in both enzymes interact with target DNA in a similar fashion, while residues in molegos distinctive for APE1 control specificity by binding primarily to the bases around the apurinic site. Matching of molegos, guided by the degree of conservation of individual residues across the three families, allowed a better alignment of the individual secondary structure elements among the proteins than DALI achieved. This word based, sequence (motif) to structure (molego) to function method has clear implications for genomic analysis and template based homology modeling, as well as immediate application in recognizing specificity determinants in proteins that share active sites common to many enzymes .
Total sequence decomposition of human Ape1 with MASIA
Motifs characteristic of the APE family.
The 12 motifs, which account for about half of the protein, are bridged by areas that vary in the different members of the APE family. These connecting regions may account for the differing activities of the bacterial and mammalian proteins. The longest molego, 7, was broken down into two areas, with the contiguous region labeled 7a. The first 7 residues of the 7a area molego are quite similar in the bacterial and mammalian APE. However, the end is differently conserved in eukaryotes. The endonuclease activity of DNase 1 is reduced many fold by integrating this loop from E. coli exonuclease III, but the mutant cleaves at abasic sites in DNA with low efficiency . Thus additional residues in the APEs control specificity while still allowing a reasonable rate of phosphorolytic cleavage.
Finding APE molegos in the DNase 1 superfamily
Aligning sequences according to MASIA motif analysis improves the correlation between structures.
Common molegos form a similar active site in two distant relatives
The 12 conserved molegos form the β-barrel core of huAPE1. The completely conserved residues of huAPE1 concentrate, for the most part, at one end of this framework to form the metal ion binding active site (Figure 4). This core is also common to DNase 1 and synaptojanin(an IPP family member), which share the functions of metal ion based cleavage of a phosphate backbone. The shared molegos define an active site architecture conserved in all three proteins, including the orientation of the substrate toward the metal binding site.
Molegos define functional areas common to DNase 1 and APE1
The contact plots of APE1 and DNase1 with their respective substrates (Figure 6) documents that the similar molegos in the proteins serve similar functions. The N-terminal 100 residues of both proteins, including molegos 1 and 2, bind 5' of the cleavage site and to the 3' end of the opposite DNA strand. Molegos 7, 11 and 12 bind to one base 5' and the next base 3' of the cleavage site in both proteins. Overall, the pattern of protein contacts to the cleavage site, the area 5' of the cleavage site, and the 3' end of the opposite strand are common to both proteins, suggesting that the functions of forming the substrate complex and the actual phosphorolysis are similar in both proteins.
While the length of the DNA in both cases is similar, DNase 1 clearly has less binding to bases opposite and 3' of the cleavage site. The extensive contacts that APE1 makes to these positions are mediated by molegos it does not share with DNase 1. Molegos 6, 7a and 10 all have residues within hydrogen bonding distance of the three basepairs 3' of the AP-site. This redundancy of binding to the 3' side is unique to APE, as is its strong binding to the DNA opposite the abasic site.
The importance of such bonds for activity was shown in other work, where huAPE1's binding to the DNA backbone is only inhibited by ethylation of the phosphates two and three positions 3' to an abasic site . Mutation of R177A, at the end of Molego 6, that binds to this region and to the bases opposite the AP-site had enhanced activity , while mutations at W280 (Molego 11) and F266 (Molego 10)  reduce activity and, in the latter case, substrate selectivity.
In work from this group that will be described separately, we used this analysis to generate mutants of APE1 with altered activity. An alanine substitution mutant, N226A, of a conserved residue at the end of molego 7a that forms a hydrogen bond with the second phosphate group downstream of the abasic site, had enhanced APE activity but increased Km and Kd values, similar to an alanine mutant of R177, which binds to the same site, reported previously . A combination of the two mutants, N226A and R177A, substantially reduced the ability of APE1 to bind to DNA containing an abasic site (Izumi et al., in preparation). Thus, molegos can effectively guide the redesign of enzymes to alter specificity.
Molegos to improve structural alignment
Previously, a "lego® block" approach described for organic synthesis [36–38] was used to describe the reshuffling of large sections of plant genomes  and as a rational method to build novel protein structures in the lab [36, 40]. Here we demonstrate that the concept is also useful to define the structural and functional role of conserved amino acids. Combining the MASIA decomposition approach to sequence analysis (Figure 1 and Tables 1 and 2) with data from crystal structures and site directed mutagenesis (Figure 2,3,4,5,6,7) showed that molegos can indicate areas of the protein that control individual functions that contribute to enzymatic activity and improve alignments for template based modeling of homologues with low identity (Table 2 and Figure 7). Most of the MASIA-motifs were near the DNA, metal ions, or both in the co-crystal structures of huAPE1.
Further, functional roles could be assigned to motifs based on their occurrence in related protein families. The similarity of the 3D structures of these motifs in three distantly related proteins and even their modes of binding substrate (Table 2, Figs. 2,3,4,5,6,7) imply that these molegos will be found in even more distantly related proteins. Several molegos can contribute to the same interacting surface and can thus define domains that are not linearly located in the protein sequence. The combined structural/sequence definition allows much more flexibility in defining a functional element than is possible with purely sequence based approaches such as PROSITE .
Is the specificity of APE determined by binding 3' to an abasic site?
Crystal structure data, coupled with molego analysis, outlined the areas of APE1 that distinguish its mode of DNA binding from the less specific DNase 1. Contact maps (Figure 6) illustrate how the conserved motifs direct DNA binding in the distributive (i.e., rapidly releasing substrate/product), relatively non-specific DNase1 as opposed to the processive, highly specific huAPE1. Both enzymes cleave only one DNA strand in a duplex and bacterial Xth cleaves ssDNA containing an abasic site . The additional contacts huAPE1, compared to DNase 1 (Figure 6), makes 3' to the damage site and to the opposite strand lower its turnover rate and its potential to cleave normal DNA. The residues contacting the region 3' to the abasic site come from three different uniquely conserved areas of APEs (molegos 6,7a, 10) as well as 11, a molego that is similar to that in DNase-1. These observations, coupled with DNA ethylation data , indicates that 3' binding is a key element in specific recognition by APEs.
This is confirmed by site directed mutagenesis studies. Of the four protein areas that bind to the DNA 3' of the abasic site, mutating F266 (molego 10) or W280 (middle of molego 11) decreases APE activity . The F266 mutation is particularly interesting, as the mutants at this position had reduced substrate specificity and enhanced 3'-exonuclease activity. However, an R177A mutant had enhanced APE activity , as do mutations at N226 (Izumi et al., in preparation). Combining these mutations however greatly decreases substrate binding (Izumi et al., in preparation). The 3' approach to the DNA  and the wide area covered by the protein on both sides of the abasic site  are both consistent with the need to hold the product until the correct polymerase moves in 5' to 3' to complete the repair . This implies that the mammalian enzyme has evolved to be processive, to facilitate more efficient functioning of the overall BER pathway, and may not be optimized for simple catalysis. Processivity is an important facit of the activity of enzymes that function in complex pathways . Reduced processivity may explain, for example, the repair deficits in Xeroderma pigmentosum (XPA) cells . Our molego approach provides a basis for exploring the role of segments of the protein in its functions, rather than relying only on data from missense mutations.
Using molegos to detect structural and functional homologues
We have demonstrated here the derivation and uses of molegos for analyzing the specificity of enzymes, based on those derived from the APE family. The methodology can be used to complement searches with programs such as PSIBLAST and PROSITE  to detect distantly related functional or structural homologues in sequences revealed by genome sequencing. PSIBLAST searches often reveal areas of local similarity in proteins that have no significant overall sequence identity. Molego analysis could be useful to analyze the significance of such findings. The combined sequence and structure definition makes molegos more flexible for defining shared protein elements than methods such as PROSITE that require a strict one-dimensional definition. An improved motif definition method, based on physical property similarity , which has been incorporated into our MASIA tool] also promises to enhance the usefulness of the method. This may eventually lead to a method to find functional relationships between proteins with even lower overall sequence similarity.
Another potential area for applying the molego approach is in homology modeling. Molegos may prove useful in to check alignments for template based modeling of homologues with low identity (Table 2 and Figure 7), if the "anchoring" residues are conserved in sequence or property across the members of both subfamilies. Our molego approach is closest in principle to that of the ROSETTA program  whereby the latter seeks only to connect structure, not function, to a sequence element. We are currently testing the usefulness of the molego approach in modeling in the CASP5 competition.
The MASIA program can parse sequences into discrete blocks of significant conservation. The motifs identified in the APE family could be structurally annotated using crystal data to derive molegos, words in the protein sequence that correlate with structural elements. These molegos could in turn be functionally annotated by comparing the DNA binding profile of APE1 with that of the less specific nuclease DNase 1. This analysis indicated that residues binding 3' to the site of phosphorolytic cleavage control the substrate specificity of APE1. These results indicate that molegos can provide a useful basis for identifying specificity determining regions in enzymes with similar active sites but different activity spectra [46, 28, 3]. Site directed mutagenesis based on these results can define the function of the unique elements of the APEs, and aid in the design of enzymes with altered specificity.
Materials and Methods
A BLAST http://www.ncbi.nlm.nih.gov/BLAST/ search of the "non-redundant" protein database using the whole sequence of human APE1 yielded over 100 related sequences. Some sequence entries represented the same protein, called by different names or isolated in different screens, including many entries for huAPE1,Drosophila Rrp 1 protein (~40% identical to the mammalian APE1 in the C-terminal third of the protein), Xth from E. coli, and counterparts of this and exodeoxyribonuclease (exo A) sequences from many bacteria, which are about 25% identical to mammalian APE1. The mammalian sequences are highly conserved, with only 6 non-conservative residue variations between the human and murine sequences, 5 of which occur in the apparently unstructured N-terminus. Several proteins with more distant relationship to APE1, such as mammalian and yeast APEIIs, and the CRC protein from Pseudomonas, which has no APE activity  were in the BLAST list, but were not used for this analysis. To derive functional motifs, the BLAST list was culled to 37 unique sequences with identity ranging from 25% to 98%. These were aligned using the default parameters of CLUSTALW [49, 50]http://www2.ebi.ac.uk/clustalw/. Sequences were the APE1 protein from human, bovine, monkey, rat murine, Arabidopsis thaliana (Mouse-ear cress) Dictyostelium discoideum (Slime mold), Schizosaccharomyces pombe (Fission yeast), Caenorhabditis elegans, Saccharomyces cerevisiae (Baker's yeast), Thermoplasma acidophilum, Neisseria meningitidis. Methanobacterium thermoautotrophicum, Leishmania major, Trypanosoma cruzi, Coxiella burnetii; the Rrp1 protein of Drosophilia; exonuclease III from E. coli, Bacillus subtilis, Mycobacterium tuberculosis, Haemophilus influenzae, Salmonella typhimurium, Helicobacter pylori, Rickettsia prowazekii, Archaeoglobus fulgidus, Actinobacillus actinomycetemcomitans, Streptomyces coelicolor, Synechocystis sp. PCC 6803, Haemophilus influenzae; Exonuclease A from Steptococcus pneumonia, Treponema pallidum, Borrelia burgdorferi. Plasmodium falciparum. Different set conditions and sequence lists were tested in CLUSTALW for their effect on alignment and subsequent motif definition with MASIA. Areas peripheral to the endonuclease domain, such as the 50 amino acid mammalian and the 428 residue Drosophila Rrp-1 N-terminal regions were eliminated to improve the consensus.
Identification of motifs using MASIA
Motifs were identified in the aligned sequences using the MASIA consensus macro http://www.scsb.utmb.edu/masia/masia.html. Motifs start when at least 3 of 4 consecutive positions are more than 40% conserved according to the dominant criterion , and extend until at least 2 positions in a row are less than 40% conserved. To allow for mistakes in the alignment of all the sequences, essential residues are those >90% conserved by MASIA criteria over all sequences in the alignment.
Genomic cross-networking with PSIBLAST
A PSIBLAST search, using huAPE1 as the founder sequence, with an e-value of 0.1 per iteration, did not converge after 6 iterations, but few new sequences were added in the last 2 cycles. Searches with an e-value of 0.01/iteration had similar results, but members of several families were not included until later cycles. Members of the DNase 1, LINE-1 repeats, inositol 5'-polyphosphate phosphatase, Nocturnin, CCR4, cytolethal distending toxin, neutral sphingomyelin phosphodiesterase, and amino acid methyltransferase families were found with expectation values of 10-4 or less to be significantly similar to APE1. To determine the presence of motifs in these relatives, a CLUSTALW alignment of at least 5 representatives of a protein family was prepared and analyzed with MASIA for significant areas of conservation. In some cases, alignments taken from literature references (e.g., for IPPs ) were used to confirm MASIA results. The motifs common to these families were compared with the APE motifs of Table 1. Criteria for inclusion (presence of motif) included conservation of residues >90% conserved (side chains shown in blue in the tables) and patterns of polarity (as determined with a macro included in the MASIA packet as a user specified feature).
Molego building and comparison
The drawings of "molego blocks" and structures (Figures 2,3,4 and 7), contact plots of protein/DNA (Figures 5,6), and calculation of the RMSD between similar segments (Table 2) were done with MOLMOL http://www.mol.biol.ethz.ch/wuthrich/software/molmol/. The RMSD values in Table 1 were calculated using SwissPDB viewer and the "fit selected residues" option.
We thank our coworkers Venkatarajan Mathura, Sankar Mitra, and Ovidiu Ivanciuc for helpful discussions. Funding for this project was provided by grants from the Department of Energy (DE-FG03-00ER63041), the Texas Higher Education Coordinating Board (ARP 004952-0084-1999) and the John Sealy Memorial Endowment Fund (2535-01).
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