Emergence of novel domains in proteins
© Toll-Riera and Alba; licensee BioMed Central Ltd. 2013
Received: 28 November 2012
Accepted: 31 January 2013
Published: 20 February 2013
Proteins are composed of a combination of discrete, well-defined, sequence domains, associated with specific functions that have arisen at different times during evolutionary history. The emergence of novel domains is related to protein functional diversification and adaptation. But currently little is known about how novel domains arise and how they subsequently evolve.
To gain insights into the impact of recently emerged domains in protein evolution we have identified all human young protein domains that have emerged in approximately the past 550 million years. We have classified them into vertebrate-specific and mammalian-specific groups, and compared them to older domains. We have found 426 different annotated young domains, totalling 995 domain occurrences, which represent about 12.3% of all human domains. We have observed that 61.3% of them arose in newly formed genes, while the remaining 38.7% are found combined with older domains, and have very likely emerged in the context of a previously existing protein. Young domains are preferentially located at the N-terminus of the protein, indicating that, at least in vertebrates, novel functional sequences often emerge there. Furthermore, young domains show significantly higher non-synonymous to synonymous substitution rates than older domains using human and mouse orthologous sequence comparisons. This is also true when we compare young and old domains located in the same protein, suggesting that recently arisen domains tend to evolve in a less constrained manner than older domains.
We conclude that proteins tend to gain domains over time, becoming progressively longer. We show that many proteins are made of domains of different age, and that the fastest evolving parts correspond to the domains that have been acquired more recently.
Proteins are organized in discrete functional modules called domains [1–3]. Domains are considered independent evolutionary units that have specific functions, fold independently and can combine with other domains in different modular arrangements [3–5]. They have an average length of approximately 120 amino acids  and, while short proteins typically contain only one domain, long proteins are usually composed of several domains . Even though most domains have an ancient origin , few domain combinations are shared between the three domains of life [3, 8]. This indicates extensive reuse of domains during evolution. Proteins can acquire additional domains over time through several mechanisms, including gene fusion, exon extension, exon recombination, intron recombination and retrotransposition [4, 9]. Of these, gene fusion has been proposed to be the most important mechanisms in metazoan proteins .
Domains that originated in particular lineages are of special interest in helping understand the molecular basis of lineage-specific adaptations [2, 5, 7, 11]. The age of domains can be dated with more precision than that of individual sequences. We can take advantage of the specific patterns of amino acid conservation displayed by each domain type and use sequence profiles or hidden markov models (HMMs) to identify homologues in distant species . Using domain-specific HMMs, Pal and Guda estimated about 40% of human domains had originated in the metazoan or a more recent phylogenetic node . They also found that about 3% of domains corresponded to primate- or human-specific sequences, illustrating the fact that novel domains are continuously formed. The phylogenetic distribution of Pfam domains has also been recently used to date the age of complete proteins from a given species in ProteinHistorian, a dedicated server for the analysis of protein origin .
One well-characterized example of lineage-specific domain is the Kruppel-associated box (KRAB), found in several vertebrate species but greatly expanded in mammals. This domain combines with the Zn-finger motif, which is an older domain, and confers strong transcriptional repressor activity to the protein . There is evidence that recently evolved domains are enriched in low-complexity sequences , and tend to be more structurally disordered , than older domains. An example of a recently formed low-complexity domain is the cornifin domain in the mammalian-specific small proline rich protein (SPRP) family. The repeats in this domain mediate the formation of a thick layer of cross-linked proteins in keratinocytes and thus play a fundamental role in the formation of the skin .
In spite of the fact that recently emerged domains are likely to play key roles in the evolution of new protein functions, we still know very little about them. For example it is not known which fraction of young domains is located in newly evolved genes, or which fraction is formed in the context of older - previously existing - genes. Recently originated genes have special characteristics: they are poorly annotated [17, 18], they tend to be shorter than average [19, 20] and they evolve particularly rapidly [19, 21–23]. However, there has been no study to date that compares the evolutionary properties of domains of different age. To address these questions we use domain genome-wide data from human and mouse, and to a lesser extent from Drosophila.
Identification of recently evolved domains
Domains in mammalian proteins classified by age
About 12.3% of the domain types only had homologues in species separated from human in the approximately past 550 million years (Mammalian or Vertebrate), suggesting that they had originated relatively recently (Table 1). We obtained a similar number of domains classified in different age groups with varying stringencies in the domain-specific HMM searches (Additional file 1: Table S2), indicating that the results are robust to different HMM search conditions.
List of the most abundant domains in each age group
7 transmembrane receptor (rhodopsin family)
Protein kinase domain
Zinc finger, C2H2 type
RNA recognition motif
Zinc finger, C3HC4 type
Immunoglobulin I-set domain
S-100/ICaBP type calcium binding domain
Small cytokines (intecrine/chemokine), interleukin-8 like
Mammalian taste receptor protein
Protein of unknown function
Transcription elongation factor A
Intracellular adhesion molecule, N-terminal domain
Cornifin (SPRR) family
Domains classified as Mammalian were generally found in a single human protein (and its mammalian orthologues). However, some domains were present in paralogues. One example is the Transcription elongation factor A domain (TF_A/BEX domain), present in a family of transcription factor genes located on chromosome X and which include TCEAL7, a putative tumour suppressor gene, which negatively regulates NF-kappaB mediated pathways .
Gain of recently evolved domains
Evolutionary properties of human proteins of different age
Proteins with domains
Proteins without domains
Analysis of the domain content of proteins of different age showed that the majority of young domains have formed in the context of a newly evolved gene. This was true for 50 of the 63 different Mammalian domain types (79.4%) and 234 of the 363 Vertebrate domain types (64.4%). In the remaining cases the younger domain could be found combined with one or more older domains (13 Mammalian and 129 Vertebrate domain types), reflecting either domain fusion events or the emergence of novel domains in existing older proteins.
Rapid evolution of young domains independently of protein context
One example of a protein containing domains of different age is the human progesterone receptor. This protein contains three Pfam domains, an intracellular domain named ‘progesterone receptor’, which is activated by the steroid hormone progesterone, a Zn finger domain, and an extracellular ligand-binding domain. The first domain is vertebrate-specific, and has a dN/dS of 0.2, whereas the other two domains, which are older, have dN/dS values of 0.001 and 0.023, respectively. This illustrates the patterns observed in many proteins, in which the younger parts are evolving much more rapidly. This and other examples are shown in Additional file 1: Figure S6. A complete list of annotated proteins with Old and Vertebrate domains is provided in Additional file 2.
Domains typically cover the majority of a protein sequence and play a crucial role in protein evolution. The way different domains combine, and the mechanisms of domain gain in proteins, have been thoroughly studied [1, 3–6, 9, 11, 31]. Other works have described the existence of domains of different age and the relationship of recently evolved domains with lineage-specific innovations [2, 7, 11]. Here we have focused on the evolutionary properties of young domains to better understand which is their impact on the evolution of the complete proteome. We have found that about two thirds of the young (vertebrate- or mammalian-specific) domains are located in newly evolved genes and the rest arose in already existing proteins. Young domains are preferentially found at the proteins ends, more often at the N-terminus than at the C-terminus, although the reasons for this latter bias are yet unclear. The addition of young domains to already existing proteins is likely to contribute to an increase in protein sequence length over time. We have also discovered that younger domains tend to evolve significantly faster than older domains, even when located in the same protein.
Among young domains, we have been able to identify many less mammalian-specific (Mammalian) domains than vertebrate-specific (Vertebrate) domains (63 versus 363). This is not surprising given that the number of Mammalian proteins is about one third the number of Vertebrate proteins. In addition, the percentage of Mammalian proteins with annotated domains is less than half the corresponding percentage of Vertebrate proteins. As the length of the two periods considered is not very different, this very likely reflects strong under-annotation of mammalian-specific sequences in the databases, both in relation to the number of expressed genes and to the number of functional domains in the encoded proteins. In line with this, Capra and colleagues found that younger proteins in yeast were less well covered by Pfam domains than average .
Proteins lacking annotated domains show a slight tendency to be longer and evolve more rapidly than proteins containing annotated domains (Table 3). The same characteristics have been previously attributed to proteins with low-complexity regions (LCRs), which undergo continuous repeat expansions and are associated with high mutational dynamics . Therefore, one possible explanation of the data in Table 3 is differences in LCR content . We confirm such differences: the average fraction of the protein covered by LCRs is 11.76 for proteins without domains and 9.34 for proteins with domains (median 8.58 and 6.4, respectively, Kolmogorov-Smirnov test p < 10-5). In addition, the underrepresentation of domains in younger proteins is consistent with the previous finding that younger proteins are enriched in LCRs . In conclusion, a large part of the variation in length and evolutionary rate is probably related to differences in LCR content. However, we cannot completely rule out the possibility that some proteins lacking annotated domains have escaped domain detection due to very fast sequence divergence.
We identify 330 proteins in which Vertebrate and Old domains combine. The fraction of Vertebrate domains that belong to Pfam clans (groups of evolutionary related domains) is much smaller for Vertebrate domains than for Old domains (14% vs 59%), emphasizing the recent origin of most Vertebrate domains. In general, novel domains in proteins can be gained by several mechanisms, such as gene fusion, exon extension, recombination and retro-transposition [4, 9, 33]. It has been hypothesised that domain architecture in all branches of life tends to gain in complexity over time, with a preponderance of fusion events over other types of rearrangements [10, 34]. We have observed that Vertebrate domains tend to exist in a single configuration, showing a strong dependence for a given Old domain (or combination of Old domains). In contrast, Old domains from these proteins can also be found in proteins that lack any Vertebrate domain. This provides strong evidence for protein extension as the main mechanism of gain of newly evolved domains in existing proteins (Figure 1). This may be mediated by different mechanisms such as the cooption of adjacent non-coding sequences (exon extension), expansion of repetitive sequences by slippage  or insertion of sequences derived from retrotransposons . The gain of new domains in existing proteins, together with the finding that old proteins contain more domains than younger ones (Table 3), is consistent with a scenario in which proteins tend to become more complex over time with regards to the number of different functional domains they contain.
Newly evolved domains are predominantly gained at the N-terminus and, to a lesser extent, at the C-terminus. Diverse authors have found that both domain gain and loss are more frequent at the protein termini than at the protein central region [10, 33, 36, 37]. This may be expected given that the protein ends tend to be more flexible, charged and located at the protein surface than other regions . However, a strong bias towards the N-terminus has not been documented previously, perhaps because it is a special feature of recently evolved domains.
Younger proteins have been found to evolve more rapidly than older proteins in a variety of organisms, including bacteria , Drosophila, mammals , yeast  and primates . Here we have demonstrated that this age-related effect also applies to protein domains, with younger domains showing higher non-synonymous to synonymous substitution rate ratios (dN/dS) than older ones (Figure 3). In addition, we observe a similar relationship in Drosophila domains of different age (Additional file 1: Figure S7 and Table S8), indicating that the observed property is likely to be universal. Therefore younger domains can diverge much more rapidly than older ones, probably mainly due to relaxed selective constraints, as shown to be the case for recently arisen complete coding sequences . It is remarkable that young domains found in otherwise highly conserved proteins (containing Old domains) also evolve very rapidly, further stressing the importance that the time elapsed since a protein sequence originated has on its evolutionary rate.
This work highlights the importance of recently evolved domains in the ongoing evolution of proteins. It shows that proteins should be considered heterogeneous entities in which sequences formed at different times maintain their characteristic evolutionary signatures. The expected future characterization of a larger number of lineage-specific proteins and their functional domains will help shed more light on the early stages of domain evolution.
The identification of protein domains of recent evolutionary origin is crucial to understand species and lineage-specific adaptations, but these domains are still poorly characterized. In order to fill this gap we have compared the evolutionary properties of human protein domains of different age: mammalian-specific, vertebrate-specific and older. We have found that when domains of different age combine in the same protein the younger domain tends to evolve much faster than the older domain, reinforcing the idea that the time elapsed since a sequence originated largely determines its current evolutionary rate.
Protein domain identification
We obtained 15,630 one-to-one orthologous human and mouse genes using version 56 of Ensembl . We took the protein corresponding to the longest coding transcript for each gene as representative, as defined in Ensembl. We used Hmmpfam (HMMER 2.3.2)  to identify all known protein domains in the human and mouse proteins with an E-value cut-off of 10-5. We employed the Pfam_ls (version 23) library, which contains 10,340 hidden markov models derived from Pfam domains . We used an in-house Perl program to parse the Hmmpfam results and to assign the domains to the proteins. We identified 3,482 different domains in 14,784 human proteins with 1:1 orthologs in mouse. The results are available from Additional file 3.
Determination of the age of protein domains
To classify human domains into age groups we used the following classes: mammals (Mus musculus, Rattus norvegicus, Bos Taurus), non-mammalian vertebrates (Danio rerio, Gallus gallus, Takifugu rubripes, Xenopus tropicalis), other metazoans (Anopheles gambiae, Caenorhabditis elegans, Ciona intestinalis, Drosophila melanogaster) and other eukaryotes (Arabidopsis thaliana, Oryza sativa, Saccharomyces cerevisiae, Schizosaccharomyces pombe). We assigned an age group to each domain following the rank of species in which a domain was found, allowing for secondary losses. For example if a human domain was found in at least one mammalian species but in none of the other vertebrate, metazoan or eukaryotic species it was classified as Mammalian. We classified 2,294 different human domains as Eukarya, 745 as Metazoan, 369 as Vertebrate and 65 as Mammalian. The Eukarya and Metazoan groups were both considered Old (older than 550 million years) and merged into a single class (Tables 1 and 2). Using less stringent E-value cut-offs we obtained similar results in the classification of domains (Additional file 1: Table S2).
Determination of the age of proteins
We defined the phylogenetic age of a protein as equal to the oldest domain it contained. We obtained 11,039 proteins classified as Old, 473 as Vertebrate and 62 as Mammalian (Table 3). The dataset contained 3,088 proteins that did not have any domain. For these proteins we used BLASTP sequence similarity searches against the genomes listed before to classify them in phylogenetic age groups (E-value < 10-4) . Following this procedure we obtained 1,816 proteins classified as Old, 851 as Vertebrate and 358 as Mammalian (Table 3).
Estimation of evolutionary rates
We aligned orthologous amino acid sequences using T-coffee . To make sure that we were aligning orthologous domains, we focused on orthologues for which the domain structure was completely conserved between human and mouse, which resulted in alignments of 18,193 orthologous domain pairs. Subsequently, we obtained nucleotide coding sequence alignments based on the T-coffee protein alignments using an in-house Perl program.
For each pairwise human and mouse alignment, we estimated the number of non-synonymous substitutions per non-synonymous site (dN), the number of synonymous substitutions per synonymous site (dS), and the dN/dS ratio. We used the maximum likelihood approach implemented in the codeml program of the PAML software package .
Domains shorter than 60 amino acids or with a dN > 0.5 or dS > 2 were discarded to ensure robustness in the evolutionary rate estimation. After the filtering process we obtained 12,647 different human domains with dN and dS data. We observed that Eukarya and Metazoan showed a very similar dN/dS distribution and for this reason we considered them as a single group (Old) in all analyses presented here.
Comparisons of evolutionary rates from pairs of domains located in the same protein
We compared the non-synonymous to synonymous substitution rates (dN/dS) of pairs of Old and Vertebrate domains located in the same protein (330 proteins). We computed the difference in dN/dS of the Vertebrate domain minus the dN/dS of the Old domain and divided it by the higher dN/dS of the two. To determine if the difference in the estimated number of non-synonymous substitutions to synonymous substitutions was statistically different between Old and Vertebrate domains we applied a binomial test comparing the total number of non-synonymous substitutions and synonymous substitutions between the two age groups.
Distribution of domains located in the same protein
We assigned each pair of domain types Vertebrate-Old in the 330 proteins (see section above) to one of the following classes: 1. Vertebrate domain dependence on a given Old domain: when the Old domain, but not the Vertebrate domain, could be found in a different domain configuration (243 proteins, 115 Vertebrate domain types); 2. Vertebrate and Old domain dependence on each other: when neither the Old domain nor the Vertebrate domain could be found in a different configuration (16 proteins, 13 Vertebrate domain types); 3. Domain fusion: when both the Old and the Vertebrate domain could be found in a different domain configuration (40 proteins, 10 Vertebrate domain types); 4. Complex: when there were more than two domains in a protein and the different Old-Vertebrate pairs showed a different behaviour (31 proteins). Cases in 1 and 2 were considered to be compatible with the gain of a Vertebrate domain into an existing older protein (259 proteins). No cases where found of “Old domain dependence on a given Vertebrate domain”.
Statistical tests and graphics
The R statistical software package  was used to perform all statistical tests and generate graphics.
We would like to thank Nicolás Bellora and the Evolutionary Genomics Group members for fruitful discussions over the course of this work. We are also grateful to Steve Laurie for text revision. We received financial support from Ministerio de Educación (FPU to M.T.-R.), Ministerio de Innovación y Tecnología grant BIO2009-08160, Ministerio de Economía y Competitividad grant BFU2012-36820, and Institució Catalana de Recerca i Estudis Avançats (ICREA contract to M.M.A.).
- Chothia C, Gough J, Vogel C, Teichmann SA: Evolution of the protein repertoire. Science. 2003, 300 (5626): 1701-1703. 10.1126/science.1085371.PubMedView ArticleGoogle Scholar
- Muller A, MacCallum RM, Sternberg MJ: Structural characterization of the human proteome. Genome Res. 2002, 12 (11): 1625-1641. 10.1101/gr.221202.PubMed CentralPubMedView ArticleGoogle Scholar
- Vogel C, Bashton M, Kerrison ND, Chothia C, Teichmann SA: Structure, function and evolution of multidomain proteins. Curr Opin Struct Biol. 2004, 14 (2): 208-216. 10.1016/j.sbi.2004.03.011.PubMedView ArticleGoogle Scholar
- Ekman D, Bjorklund AK, Frey-Skott J, Elofsson A: Multi-domain proteins in the three kingdoms of life: orphan domains and other unassigned regions. J Mol Biol. 2005, 348 (1): 231-243. 10.1016/j.jmb.2005.02.007.PubMedView ArticleGoogle Scholar
- Moore AD, Bjorklund AK, Ekman D, Bornberg-Bauer E, Elofsson A: Arrangements in the modular evolution of proteins. Trends Biochem Sci. 2008, 33 (9): 444-451. 10.1016/j.tibs.2008.05.008.PubMedView ArticleGoogle Scholar
- Buljan M, Bateman A: The evolution of protein domain families. Biochem Soc Trans. 2009, 37 (Pt 4): 751-755.PubMedView ArticleGoogle Scholar
- Pal LR, Guda C: Tracing the origin of functional and conserved domains in the human proteome: implications for protein evolution at the modular level. BMC Evol Biol. 2006, 6: 91-10.1186/1471-2148-6-91.PubMed CentralPubMedView ArticleGoogle Scholar
- Apic G, Gough J, Teichmann SA: An insight into domain combinations. Bioinformatics. 2001, 17 (Suppl 1): S83-S89. 10.1093/bioinformatics/17.suppl_1.S83.PubMedView ArticleGoogle Scholar
- Marsh JA, Teichmann SA: How do proteins gain new domains?. Genome Biol. 2010, 11 (7): 126-10.1186/gb-2010-11-7-126.PubMed CentralPubMedView ArticleGoogle Scholar
- Buljan M, Frankish A, Bateman A: Quantifying the mechanisms of domain gain in animal proteins. Genome Biol. 2010, 11 (7): R74-10.1186/gb-2010-11-7-r74.PubMed CentralPubMedView ArticleGoogle Scholar
- Moore AD, Bornberg-Bauer E: The dynamics and evolutionary potential of domain loss and emergence. Mol Biol Evol. 2012, 29 (2): 787-796. 10.1093/molbev/msr250.PubMed CentralPubMedView ArticleGoogle Scholar
- Eddy SR: Profile hidden Markov models. Bioinformatics. 1998, 14 (9): 755-763. 10.1093/bioinformatics/14.9.755.PubMedView ArticleGoogle Scholar
- Capra JA, Williams AG, Pollard KS: ProteinHistorian: tools for the comparative analysis of eukaryote protein origin. PLoS Comput Biol. 2012, 8 (6): e1002567-10.1371/journal.pcbi.1002567.PubMed CentralPubMedView ArticleGoogle Scholar
- Margolin JF, Friedman JR, Meyer WK, Vissing H, Thiesen HJ, Rauscher FJ: Kruppel-associated boxes are potent transcriptional repression domains. Proc Natl Acad Sci U S A. 1994, 91 (10): 4509-4513. 10.1073/pnas.91.10.4509.PubMed CentralPubMedView ArticleGoogle Scholar
- Toll-Riera M, Rado-Trilla N, Martys F, Alba MM: Role of low-complexity sequences in the formation of novel protein coding sequences. Mol Biol Evol. 2012, 29 (3): 883-886. 10.1093/molbev/msr263.PubMedView ArticleGoogle Scholar
- Gibbs S, Fijneman R, Wiegant J, van Kessel AG, van De Putte P, Backendorf C: Molecular characterization and evolution of the SPRR family of keratinocyte differentiation markers encoding small proline-rich proteins. Genomics. 1993, 16 (3): 630-637. 10.1006/geno.1993.1240.PubMedView ArticleGoogle Scholar
- Capra JA, Pollard KS, Singh M: Novel genes exhibit distinct patterns of function acquisition and network integration. Genome Biol. 2010, 11 (12): R127-10.1186/gb-2010-11-12-r127.PubMed CentralPubMedView ArticleGoogle Scholar
- Tautz D, Domazet-Loso T: The evolutionary origin of orphan genes. Nat Rev Genet. 2011, 12 (10): 692-702. 10.1038/nrg3053.PubMedView ArticleGoogle Scholar
- Domazet-Loso T, Tautz D: An evolutionary analysis of orphan genes in Drosophila. Genome Res. 2003, 13 (10): 2213-2219. 10.1101/gr.1311003.PubMed CentralPubMedView ArticleGoogle Scholar
- Toll-Riera M, Bosch N, Bellora N, Castelo R, Armengol L, Estivill X, Alba MM: Origin of primate orphan genes: a comparative genomics approach. Mol Biol Evol. 2009, 26 (3): 603-612.PubMedView ArticleGoogle Scholar
- Alba MM, Castresana J: Inverse relationship between evolutionary rate and age of mammalian genes. Mol Biol Evol. 2005, 22 (3): 598-606.PubMedView ArticleGoogle Scholar
- Cai JJ, Woo PC, Lau SK, Smith DK, Yuen KY: Accelerated evolutionary rate may be responsible for the emergence of lineage-specific genes in ascomycota. J Mol Evol. 2006, 63 (1): 1-11. 10.1007/s00239-004-0372-5.PubMedView ArticleGoogle Scholar
- Cai JJ, Petrov DA: Relaxed purifying selection and possibly high rate of adaptation in primate lineage-specific genes. Genome Biol Evol. 2010, 2: 393-409. 10.1093/gbe/evq019.PubMed CentralPubMedView ArticleGoogle Scholar
- Hubbard TJ, Aken BL, Ayling S, Ballester B, Beal K, Bragin E, Brent S, Chen Y, Clapham P, Clarke L: Ensembl 2009. Nucleic Acids Res. 2009, 37 (Database issue): D690-D697.PubMed CentralPubMedView ArticleGoogle Scholar
- Punta M, Coggill PC, Eberhardt RY, Mistry J, Tate J, Boursnell C, Pang N, Forslund K, Ceric G, Clements J: The Pfam protein families database. Nucleic Acids Res. 2012, 40 (Database issue): D290-D301.PubMed CentralPubMedView ArticleGoogle Scholar
- Williams AJ, Blacklow SC, Collins T: The zinc finger-associated SCAN box is a conserved oligomerization domain. Mol Cell Biol. 1999, 19 (12): 8526-8535.PubMed CentralPubMedView ArticleGoogle Scholar
- Emerson RO, Thomas JH: Gypsy and the birth of the SCAN domain. J Virol. 2011, 85 (22): 12043-12052. 10.1128/JVI.00867-11.PubMed CentralPubMedView ArticleGoogle Scholar
- Castresana J, Guigo R, Alba MM: Clustering of genes coding for DNA binding proteins in a region of atypical evolution of the human genome. J Mol Evol. 2004, 59 (1): 72-79.PubMedView ArticleGoogle Scholar
- Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W: Initial sequencing and analysis of the human genome. Nature. 2001, 409 (6822): 860-921. 10.1038/35057062.PubMedView ArticleGoogle Scholar
- Rattan R, Narita K, Chien J, Maguire JL, Shridhar R, Giri S, Shridhar V: TCEAL7, a putative tumor suppressor gene, negatively regulates NF-kappaB pathway. Oncogene. 2010, 29 (9): 1362-1373. 10.1038/onc.2009.431.PubMedView ArticleGoogle Scholar
- Ekman D, Bjorklund AK, Elofsson A: Quantification of the elevated rate of domain rearrangements in metazoa. J Mol Biol. 2007, 372 (5): 1337-1348. 10.1016/j.jmb.2007.06.022.PubMedView ArticleGoogle Scholar
- Laurie S, Toll-Riera M, Rado-Trilla N, Alba MM: Sequence shortening in the rodent ancestor. Genome Res. 2012, 22 (3): 478-485. 10.1101/gr.121897.111.PubMed CentralPubMedView ArticleGoogle Scholar
- Bjorklund AK, Ekman D, Light S, Frey-Skott J, Elofsson A: Domain rearrangements in protein evolution. J Mol Biol. 2005, 353 (4): 911-923. 10.1016/j.jmb.2005.08.067.PubMedView ArticleGoogle Scholar
- Fong JH, Geer LY, Panchenko AR, Bryant SH: Modeling the evolution of protein domain architectures using maximum parsimony. J Mol Biol. 2007, 366 (1): 307-315. 10.1016/j.jmb.2006.11.017.PubMed CentralPubMedView ArticleGoogle Scholar
- Frenkel ZM, Trifonov EN: Origin and evolution of genes and genomes. Crucial role of triplet expansions. J Biomol Struct Dyn. 2012, 30 (2): 201-210. 10.1080/07391102.2012.677771.PubMedView ArticleGoogle Scholar
- Vibranovski MD, Sakabe NJ, de Oliveira RS, de Souza SJ: Signs of ancient and modern exon-shuffling are correlated to the distribution of ancient and modern domains along proteins. J Mol Evol. 2005, 61 (3): 341-350. 10.1007/s00239-004-0318-y.PubMedView ArticleGoogle Scholar
- Weiner J, Beaussart F, Bornberg-Bauer E: Domain deletions and substitutions in the modular protein evolution. FEBS J. 2006, 273 (9): 2037-2047. 10.1111/j.1742-4658.2006.05220.x.PubMedView ArticleGoogle Scholar
- Daubin V, Ochman H: Bacterial genomes as new gene homes: the genealogy of ORFans in E. coli. Genome Res. 2004, 14 (6): 1036-1042. 10.1101/gr.2231904.PubMed CentralPubMedView ArticleGoogle Scholar
- Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997, 25 (17): 3389-3402. 10.1093/nar/25.17.3389.PubMed CentralPubMedView ArticleGoogle Scholar
- Notredame C, Higgins DG, Heringa J: T-Coffee: a novel method for fast and accurate multiple sequence alignment. J Mol Biol. 2000, 302 (1): 205-217. 10.1006/jmbi.2000.4042.PubMedView ArticleGoogle Scholar
- Yang Z: PAML 4: phylogenetic analysis by maximum likelihood. Mol Biol Evol. 2007, 24 (8): 1586-1591. 10.1093/molbev/msm088.PubMedView ArticleGoogle Scholar
- R: A languange and environment for statistical computing. 2007, Vienna (Austria): R fundation for statistical computingGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.