Skip to content

Advertisement

BMC Bioinformatics

Methodology Article
Open Access

MDAT- Aligning multiple domain arrangements

  • Carsten Kemena1Email author,
  • Tristan Bitard-Feildel1 and
  • Erich Bornberg-Bauer1
BMC Bioinformatics201516:19

https://doi.org/10.1186/s12859-014-0442-7

©  Kemena et al.; licensee BioMed Central. 2015

Received: 1 October 2014

Accepted: 3 December 2014

Published: 28 January 2015

Abstract

Background

Proteins are composed of domains, protein segments that fold independently from the rest of the protein and have a specific function. During evolution the arrangement of domains can change: domains are gained, lost or their order is rearranged. To facilitate the analysis of these changes we propose the use of multiple domain alignments.

Results

We developed an alignment program, called MDAT, which aligns multiple domain arrangements. MDAT extends earlier programs which perform pairwise alignments of domain arrangements. MDAT uses a domain similarity matrix to score domain pairs and aligns the domain arrangements using a consistency supported progressive alignment method.

Conclusion

MDAT will be useful for analysing changes in domain arrangements within and between protein families and will thus provide valuable insights into the evolution of proteins and their domains. MDAT is coded in C++, and the source code is freely available for download at http://www.bornberglab.org/pages/mdat.

Keywords

Domain arrangementMultiple alignment

Background

Proteins are composed of domains, i.e. amino acid segments which have a specific function and/or a structure, fold independently from the rest of the protein and are evolutionary well conserved [1-3]. Domains are units of evolution, they influence the function of a protein, and can be selected for as a whole [1,4]. The number of known domains is relatively small: currently around 15,000 domains are listed in the Pfam database [5]. About 65-70% of the known proteins contain at least one known domain [6]. However, the number of known arrangements, the combination of domains in a protein, is much higher and steadily and rapidly increasing with more genomes being sequenced [7]. These arrangements evolve over time as domains can be lost, new ones gained and domains are reordered, mostly by gene fusion and terminal domain losses. Typically, rearrangements occur at a rate of tens to hundreds over a span of one million years [8]. Accordingly, rearrangements are more frequent than loss and gain of whole genes, but substantially rarer than changes at the level of amino acids.

Several studies have shown the importance of changes in domain arrangements during evolution. New arrangements can be produced by shuffling of existing domains. These new arrangements played, for example, an important role during the evolution of vertebrates where they are involved in vertebrate specific structures like the cartilage [9]. In addition, it has been proposed that the usage of domains may facilitate convergent evolution. For example it has been shown that netrin and secreted frizzled-related proteins have several independent evolutionary origins [10]. Furthermore, it was proposed that a repository of reusable domains allows for a faster adaptation in plants [8], since a high number of new domains and arrangements in plants are involved in stress and adaption related functions. Changes in domain arrangements are less likely to occur than changes at the amino acid level and are therefore suitable traits for the reconstruction of phylogenies. Accordingly, domain occurrence has been used to calculate large scale phylogenetic trees [11]. Besides these large scale approaches it can be useful to investigate domain arrangements of a single protein family. It has been shown, for example, that the domain arrangements in virulence genes in Plasmodium falciparum are probably the result of a trade-off between optimizing within-host fitness and minimizing between-host immune selection pressure [12]. Also, the evolution of Cry toxins is strongly affected by reordering the arrangement of their constituting domains and these rearrangements are important for the virulence of several bacteria [13].

The best currently available methods to study domain arrangements are classical multiple sequence alignment (MSA) methods, for example T-Coffee [14] or Clustal Omega [15]. However, these alignment methods usually do not explicitely take domain arrangements into account and therefore do not incorporate any restriction concerning their alignment. Exceptions are Dialign-Pfam [16] and Cobalt [17] that use domain information to restrict the sequence alignments. Still, none of the existing methods produce a real multiple domain alignment (MDA). An MDA aligns multiple domain arrangements to find the best arrangement of domains using an objective function, similar to the traditional MSA that arranges amino acids and nucleotides.

There are several advantages in using MDAs instead of MSAs. Due to the much shorter arrangement length compared to the primary sequence, an MDA can be calculated faster and with lower memory requirements, which is especially an advantage with large datasets. Another advantage is that a domain arrangement is more conserved than the underlying amino acid sequence. It is therefore possible to produce meaningful MDAs when the amino acid sequences are already too divergent to be compared. Furthermore, it is easier to visually examine the resulting alignments, due to the smaller number of characters.

Since domain arrangement similarity and differences can provide insights into functional similarity and changes between proteins (see above) we present an algorithm which helps to compute an MDA and facilitate the analysis of domain arrangements of different proteins. In this paper, we present MDAT (Multiple Domain Alignment Tool), a program that takes multiple domain arrangements and aligns them. It uses a domain similarity matrix reflecting the similarity between all pairs of domains in the Pfam database. Using a combination of the RADS [18] algorithm and the MSA consistency approach described in T-Coffee [14] an MDA is calculated. The main goal of RADS is to compare and evaluate domain arrangements and to weight differences between domain arrangements. In addition, the resulting MDA can then serve as a backbone structure for the construction of an MSA.

Results and discussion

Domain similarity matrix

The Pfam database provides some rough information on domain homology (the “clans”) based on a range of various information evaluated manually [19,20]. Unfortunately, this information cannot be used in an alignment program as clan information is binary only. Therefore, one cannot use clan information reliably to distinguish which domains to match if several possibilities to align a set of domains exits. Another drawback of using clans is that currently only about one third of the almost 15,000 domains in Pfam are associated to a clan. To avoid these drawbacks, we decided to calculate the domain similarity matrix. Figure 1 displays the distribution of match probabilities for each domain pair and how this value relates to being in the same clan or not.
Figure 1
Figure 1

Domain similarity score distribution. The scores were calculated by HHsearch, for all pairwise alignment scores of Pfam-A domains (version 27). The values have been divided into two groups depending on whether the two domains belonging to the same clan or not (different or no clan). Values of self alignments are not included.

As expected, most domain pairs have a low probability of being a true positive match. It is interesting to note that a high number of domain pairs coming from the same clan have a very low probability of being a true match and that at least some domain pairs from different clans or without clan assignment have a high probability of being a true match.

MDA

We use the BAliBASE3 [21] benchmark, which was originally developed for evaluating MSAs, to evaluate the MDAT algorithm. On average 95% of the domain pairs found in the BAliBASE3 benchmark (see Methods) are also found in the test alignments produced by MDAT. Furthermore, the MDAT algorithm is the fastest of all compared methods, even when including the additional step of calculating an MSA from the MDA (see last row in Table 1). An actual example of an MDA is shown in Figure 2. The 90 sequences from the IPR021012 family (Down syndrome cell adhesion molecule, C-Terminal) have been aligned using MDAT after Pfam domain annotation. 27 different domain arrangements based on 6 different domains have been identified. The resulting alignment contains 27 different architectures showing conserved domains, repeat events as well as rare domains in this family.
Figure 2
Figure 2

Example MDA: The IPR021012 family, consisting of 90 sequences is shown. All segments contain the Dscam domain. The pfam_scan script has been used to perform the domain annotation. The first column depicts the reference arrangement ID, and the second the number of times this arrangement has been encountered.

Table 1

Results of running 3 different methods on the BaliBase3 benchmarks

 

Set

MDA

MDA (MSA)

Mafft

Clustal omega

 

RV11

-

47.78

52.91

59.01

 

RV12

-

83.61

89.30

90.60

 

RV20

-

80.49

89.31

90.21

SP

RV30

-

67.42

82.50

86.24

 

RV40

-

77.14

87.79

90.17

 

RV50

-

65.65

84.90

86.20

 

Total

-

71.78

81.36

84.00

 

RV11

-

24.13

25.76

35.76

 

RV12

-

65.02

74.93

78.86

 

RV20

-

22.51

31.56

44.95

TC

RV30

-

19.03

42.47

57.50

 

RV40

-

33.57

47.98

57.90

 

RV50

-

18.56

49.62

53.25

 

Total

-

33.09

45.82

55.44

Time (s)

Total

10.37

31.75

92.82

438.08

SP denotes the sum of pairs score, TC the column score. The running times of MDAT includes time for constructing the MDA but not the time for running the domain annotation. The MDAT row shows the time for constructing the MDA only, while MDAT (MSA) shows the time for calculating the MDA with subsequent MSA construction.

MDA2MSA

An example for the advantage of using domains in the construction of alignments can be seen in Figure 3. The upper alignment was constructed using MDAT, the lower one using the MAFFT program. Due to the benefits of domain information, MDAT was able to align all five Fer2 domains together, while MAFFT only aligned 4 of them. Moreover, these domains are not kept as unit but split up into parts that are stretched along the whole alignment. Another example can be viewed in Additional file 1.
Figure 3
Figure 3

Example of an MDA based sequence alignment: An MSA of seven sequences from the BAliBASE3 benchmark with annotated domains is shown. The upper alignment has been generated using MDAT, the bottom one using MAFFT. Due to the incorporation of domain information MDAT is able to align all 5 occurring Fer2 domains correctly together, MAFFT only aligns 4 of the domains and stretches them very widely.

The use of domains as anchor-points can strongly reduce the memory usage and running time. Table 1 shows the results of running MAFFT, Clustal Omega and MDAT algorithms on BAliBASE3. MDAT is three times faster than MAFFT and about 9 times faster when calculating only the MDA. The increased speed comes at the cost of accuracy. A combination of different reasons can explain the loss in accuracy. Domain annotations are not perfect and wrongly annotated domains or discrepancies in the boundaries may influence the resulting alignment. Furthermore, an error in the MDA can have a large influence on the resulting MSA as whole regions can no longer be aligned, a problem that all anchor based methods have in common. Additionally, we use a simple implementation of the Gotoh algorithm [22] to perform the sequence alignment; more complex techniques, such as HMMs as used for example in Clustal Omega [15], might provide better results.

Conclusion

We show that using MDAs themselves has its merits. MDAs can be used to visualize in a simple way the similarity between domain arrangements. Just like any alignment program, MDAT is not able to handle inversions. However, due to the low number of domains in a protein, inversions can be easily detected in a graphical view, which in not possible at the amino acid level. Furthermore, we demonstrate that an MDA is a good starting point for a multiple sequence alignment. It is particularly useful as guidance for the MSA, because it strongly increases the speed with which a multiple sequence alignment is calculated. Currently, the resulting MSAs from MDAT are not as accurate as traditional sequence alignments, however, due to the short calculation time, we are able to handle larger data sets. For many analyses, such as genome projects, the detection of domains is an essential part of the standard annotation procedure. Therefore, domain annotation is often readily available.

Methods

Scoring domain matches

Contrary to amino acids, no scoring matrix currently exists to handle domain matches. Therefore, we calculated a domain similarity matrix (DSM) for Pfam-A domains that stores a similarity value for each domain pair. The entries of the DSM are calculated using the HHsearch [23] program. Every HMM model of a domain in Pfam is aligned with every other HMM model in Pfam resulting in 148312 alignment pairs. As recommended [23], we used the probability of a true positive match as a similarity score and not the e-value. A true positive match value corresponds to the probability that the two models compared belong to homologous sequences or if the sequence alignment supports a good structural alignment. Contrary to the standard BLOSUM [24] and PAM [25] matrices, the DSM contains only positive values between 0 and 100. The huge majority of entries in the DSM are values below 1, corresponding to domain pairs without similarity. Accordingly, these values do not need to be stored and can therefore be removed from the matrix without loss of information, thus reducing the actual size of the DSM.

MDA construction

The MDA is constructed in several steps and is based on the RADS [18] pairwise and the T-Coffee [14] consistency aligner.
  1. 1.

    Domain collapsing: Given a set of domain arrangements, the first step of the MDA construction is to collapse identical domain arrangements into a single one. A set of identical domain arrangements is from here on represented with a single arrangement. The length of a domain in this representative arrangement is defined as the average of the domains it contains. A change in tandem domain repeats is the most frequently occurring domain rearrangement event [4]. Tandem repeats are very similar and their correct alignment on the domain level difficult to achieve. We therefore collapse successive repeats of the same domain into a single one as previously proposed [26]. This facilitates the alignment process that can be easily confused by a high number of near identical domain matches introduced by repeat copies.

     
  2. 2.

    Library construction: In the next step the RADS algorithm, a dynamic programming algorithm, is used to produce alignments between all pairs of arrangements. RADS has been extended to use the DSM to score a match of two domains instead of a fixed value. The matches identified in this alignment are then stored in a library.

     
  3. 3.

    Library extension: The matches from the library are rescored according to the algorithm described in T-Coffee. The reweighting has the purpose to increase the score of a match that is supported by matches in a third sequence: If domain α in arrangement X and domain β in arrangement Y are matching, then the score of the match α−β is increased if there are arrangements Z with domain γ that is matching α as well as β.

     
  4. 4.

    Alignment calculation: Using these scores a normal progressive alignment, as first described by Higgins and Sharp [27], is performed.

     
  5. 5.

    Refinement: The last step of the algorithm is a simple refinement step. Blocks of domains are shifted to other columns if this increases the number of identical domains in a column.

     

MDA2MSA

An MDA can be used to guide the MSA alignment process. MDAT uses a similar approach to the one described in Dialign-Pfam. Blocks of domains are used as anchor points to limit the search space and thereby increasing the speed of the alignment calculation. Furthermore, using the MDA as an anchor, guarantees that the correct domains are aligned with each other (see Results and discussion). Unlike Dialign-Pfam, MDAT uses a completely automatic approach and because we use the MDA as guide, the anchors do not need to be of a single domain type. The MDA is used as a backbone for the MSA construction. This process can be divided into two major steps. In the first step, sequences with identical domain arrangements are aligned, in the second the alignments of the first step are aligned with each other. This two-step process is shown in Figure 4.
Figure 4
Figure 4

Workflow of the MDA2MSA algorithm. Step 1: Sequences with identical domain arrangements (a) are split according to domain boundaries (b). Then each part is separately aligned (c) and finally all parts are merged back together (d) into a single alignment. Step 2: The MDA (a) is used as a guide. The sequences are split into parts according to the MDA (b). Cuts are performed at the borders of aligned domains resulting in 5 parts. Each pair of sequence segments can now be aligned separately. In case unaligned domains occur in the MDA (part 3), the dynamic programming algorithm is changed such that it maintains the order of domains (c). The striped area represents the area that is not calculated because the MDA forbids the alignment of the two domains.

First alignment step: All sequences that are represented by the same domain arrangement are aligned first. The sequences are split at domain boundaries and each pair of segments is aligned separately, thus allowing easy parallelization of this step. Domain segments are aligned using a banded alignment approach as previously described in the Pecan genome aligner [28].

Second alignment step: Following a guide tree constructed from the domain architecture similarity, the alignment profiles computed in the first step are progressively aligned with each other. At each node in the tree, two profiles are aligned that are based on different domain architectures. Similar to the first step, sequences can be split at domain boundaries. However, this is only possible at domains that are aligned with each other. The sequence segments between two aligned domains cannot be simply aligned in a global fashion, because there may be non-aligned domains which should not be aligned on the sequence level either (see Figure 4). In this case, the corresponding area in the dynamic programming matrix is declared forbidden. The alignment algorithm does not pass through these areas that are forbidden by the MDA and thus avoids violating the order of the domains as defined by the columns of the MDA.

Benchmarking

Currently no reference benchmark exists for the evaluation of MDAs. Therefore, we use the BAliBASE3 [21] benchmark that was originally developed for MSAs. To be able to evaluate an MDA, we annotated the sequences included in BAliBASE3 with Pfam domains using pfam_scan [5] in combination with the HMMER3 [29] program. Since BAliBASE3 is a set of reference sequence alignments it is possible that more than one domain is aligned to another one, conflicting with the alignment definition that a domain is aligned only to a single other domain. We define two domain as being aligned to each other if at least three quarters of both domains are aligned with each other. For this benchmark the repeat-collapsing has been turned off to allow a comparison of the MDA with the pairs extracted from BAliBASE3.

To check the performance of the MDA2MSA algorithm, MDAT has been run on the BAliBASE3 benchmark and has been compared to two other alignment methods MAFFT (v6.940b) [30] and Clustal Omega (v1.2) [15].

Declarations

Acknowledgements

We would like to thank Elias Dohmen for helpful suggestions to improve the manuscript. CK was funded by DFG grant BO2544/4-1. We acknowledge support by Deutsche Forschungsgemeinschaft and Open Access Publication Fund of University of Muenster. EBB ORCID ID is http://orcid.org/0000-0002-1826-3576.

Authors’ Affiliations

(1)
Institute for Evolution and Biodiversity, University of Münster, Münster, Germany

References

  1. Moore AD, Björklund AK, Ekman D, Bornberg-Bauer E, Elofsson A. Arrangements in the modular evolution of proteins. Trends Biochem Sci. 2008; 33(9):444–51.View ArticlePubMedGoogle Scholar
  2. Marsh JA, Teichmann SA. How do proteins gain new domains?Genome Biol. 2010; 11(7):126.View ArticlePubMedPubMed CentralGoogle Scholar
  3. Forslund K, Sonnhammer ELL. Evolution of protein domain architectures. Methods Mol Biol. 2012; 856:187–216.View ArticlePubMedGoogle Scholar
  4. Bornberg-Bauer E, Albà M M. Dynamics and adaptive benefits of modular protein evolution. Curr Opin Struct Biol. 2013; 23(3):459–66.View ArticlePubMedGoogle Scholar
  5. Punta M, Coggill PC, Eberhardt RY, Mistry J, Tate JG, Boursnell C, et al. The Pfam protein families database. Nucleic Acids Res. 2012; 40(Database-Issue):290–301.View ArticleGoogle Scholar
  6. Ekman D, Björklund AK, Frey-Skött J, Elofsson A. Multi-domain proteins in the three kingdoms of life: orphan domains and other unassigned regions. J Mol Biol. 2005; 348(1):231–43.View ArticlePubMedGoogle Scholar
  7. Levitt M. Nature of the protein universe. Proc Natl Acad Sci U S A. 2009; 106(27):11079–84.View ArticlePubMedPubMed CentralGoogle Scholar
  8. Kersting AR, Bornberg-Bauer E, Moore AD, Grath S. Dynamics and adaptive benefits of protein domain emergence and arrangements during plant genome evolution. Genome Biol Evol. 2012; 4(3):316–29.View ArticlePubMedPubMed CentralGoogle Scholar
  9. Kawashima T, Kawashima S, Tanaka C, Murai M, Yoneda M, Putnam NH, et al. Domain shuffling and the evolution of vertebrates. Genome Res. 2009; 19(8):1393–403.View ArticlePubMedPubMed CentralGoogle Scholar
  10. Leclère L, Rentzsch F. Repeated evolution of identical domain architecture in metazoan netrin domain-containing proteins. Genome Biol Evol. 2012; 4(9):883–99.View ArticlePubMedPubMed CentralGoogle Scholar
  11. Fang H, Oates ME, Pethica RB, Greenwood JM, Sardar AJ, Rackham OJL, et al. A daily-updated tree of (sequenced) life as a reference for genome research. Sci Rep. 2013; 3:2015.PubMedGoogle Scholar
  12. Buckee CO, Recker M. Evolution of the multi-domain structures of virulence genes in the human malaria parasite, Plasmodium falciparum. PLoS Comput Biol. 2012; 8(4):1002451.View ArticleGoogle Scholar
  13. de Maagd RA, Bravo A, Berry C, Crickmore N, Schnepf HE. Structure, diversity, and evolution of protein toxins from spore-forming entomopathogenic bacteria. Annu Rev Genet. 2003; 37:409–33.View ArticlePubMedGoogle Scholar
  14. Notredame C, Higgins DG, Heringa J. T-Coffee: a novel method for fast and accurate multiple sequence alignment. J Mol Biol. 2000; 302(2):205–17.View ArticlePubMedGoogle Scholar
  15. Sievers F, Wilm A, Dineen D, Gibson TJ, Karplus K, Li W, et al. Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega. Mol Syst Biol. 2011; 7:539.View ArticlePubMedPubMed CentralGoogle Scholar
  16. Ait LA, Yamak Z, Morgenstern B. DIALIGN at GOBICS–multiple sequence alignment using various sources of external information. Nucleic Acids Res. 2013; 41:W3-7.View ArticlePubMedPubMed CentralGoogle Scholar
  17. Papadopoulos JS, Agarwala R. COBALT: constraint-based alignment tool for multiple protein sequences. Bioinformatics. 2007; 23(9):1073–79.View ArticlePubMedGoogle Scholar
  18. Terrapon N, Weiner J, Grath S, Moore AD, Bornberg-Bauer E. Rapid similarity search of proteins using alignments of domain arrangements. Bioinformatics. 2014; 30(2):274–81.View ArticlePubMedGoogle Scholar
  19. Finn RD, Mistry J, Schuster-Böckler B, Griffiths-Jones S, Hollich V, Lassmann T, et al. Pfam: clans, web tools and services. Nucleic Acids Res. 2006; 34:247–51.View ArticleGoogle Scholar
  20. Finn RD, Tate J, Mistry J, Coggill PC, Sammut SJ, Hotz H-R, et al. The Pfam protein families database. Nucleic Acids Res. 2008; 36(Database issue):281–8.Google Scholar
  21. Thompson JD, Koehl P, Ripp R, Poch O. BAliBASE 3.0: latest Developments of the Multiple Sequence Alignment Benchmark. Proteins. 2005; 61(1):127–36.View ArticlePubMedGoogle Scholar
  22. Gotoh O. Significant improvement in accuracy of multiple protein sequence alignments by iterative refinement as assessed by reference to structural alignments. J Mol Biol. 1996; 264(4):823–38.View ArticlePubMedGoogle Scholar
  23. Söding J. Protein homology detection by HMM-HMM comparison. Bioinformatics. 2005; 21(7):951–60.View ArticlePubMedGoogle Scholar
  24. Henikoff S, Henikoff JG. Amino acid substitution matrices from protein blocks. Proc Natl Acad Sci U S A. 1992; 89(22):10915–9.View ArticlePubMedPubMed CentralGoogle Scholar
  25. Dayhoff MOSRM, Orcutt BC. A model of evolutionary change in proteins. Atlas Protein Sequence Struct. 1978; 5:345–52.Google Scholar
  26. Geer LY, Domrachev M, Lipman DJ, Bryant SH. CDART: protein homology by domain architecture. Genome Res. 2002; 12(10):1619–23.View ArticlePubMedPubMed CentralGoogle Scholar
  27. Higgins DG, Sharp PM. CLUSTAL: a package for performing multiple sequence alignment on a microcomputer. Gene. 1988; 73(1):237–44.View ArticlePubMedGoogle Scholar
  28. Paten B, Herrero J, Beal K, Birney E. Sequence progressive alignment, a framework for practical large-scale probabilistic consistency alignment. Bioinformatics. 2008; 25(3):259–91.Google Scholar
  29. Eddy SR. Accelerated profile HMM searches. PLoS Comput Biol. 2011; 7(10):1002195.View ArticleGoogle Scholar
  30. Katoh K, Kuma K, Toh H, Miyata T. MAFFT version 5: improvement in accuracy of multiple sequence alignment. Nucleic Acids Res. 2005; 33(2):511–8.View ArticlePubMedPubMed CentralGoogle Scholar

Copyright

© Kemena et al.; licensee BioMed Central. 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement

BMC Bioinformatics

ISSN: 1471-2105

Contact us