Circular permutation in proteins

Schematic representation of a circular permutation in two proteins. The first protein (outer circle) has the sequence a-b-c. After the permutation the second protein (inner circle) has the sequence c-a-b. The letters N and C indicate the location of the amino- and carboxy-termini of the protein sequences and how their positions change relative to each other.

A circular permutation is a relationship between proteins whereby the proteins have a changed order of amino acids in their peptide sequence. The result is a protein structure with different connectivity, but overall similar three-dimensional (3D) shape. In 1979, the first pair of circularly permuted proteins – concanavalin A and lectin – were discovered; over 2000 such proteins are now known.

Circular permutation can occur as the result of evolutionary events, posttranslational modifications, or artificially engineered mutations. The two main models proposed to explain the evolution of circularly permuted proteins are permutation by duplication and fission and fusion. Permutation by duplication occurs when a gene undergoes duplication to form a tandem repeat, before redundant sections of the protein are removed; this relationship is found between saposin and swaposin. Fission and fusion occurs when partial proteins fuse to form a single polypeptide, such as in nicotinamide nucleotide transhydrogenases.

Circular permutations are routinely engineered in the laboratory to improve their catalytic activity or thermostability, or to investigate properties of the original protein.

Traditional algorithms for sequence alignment and structure alignment are not able to detect circular permutations between proteins. New non-linear approaches have been developed that overcome this and are able to detect topology-independent similarities.

History

Two proteins that are related by a circular permutation. Concanavalin A (left), from the Protein Data Bank (PDB: 3cna​), and peanut lectin (right), from PDB: 2pel​, which is homologous to favin. The termini of the proteins are highlighted by blue and green spheres, and the sequence of residues is indicated by the gradient from blue (N-terminus) to green (C-terminus). The 3D fold of the two proteins is highly similar; however, the N- and C- termini are located on different positions of the protein.[1]

In 1979, Bruce Cunningham and his colleagues discovered the first instance of a circularly permuted protein in nature.[1] After determining the peptide sequence of the lectin protein favin, they noticed its similarity to a known protein – concanavalin A – except that the ends were circularly permuted. Later work confirmed the circular permutation between the pair[2] and showed that concanavalin A is permuted post-translationally[3] through cleavage and an unusual protein ligation.[4]

After the discovery of a natural circularly permuted protein, researchers looked for a way to emulate this process. In 1983, David Goldenberg and Thomas Creighton were able to create a circularly permuted version of a protein by chemically ligating the termini to create a cyclic protein, then introducing new termini elsewhere using trypsin.[5] In 1989, Karolin Luger and her colleagues introduced a genetic method for making circular permutations by carefully fragmenting and ligating DNA.[6] This method allowed for permutations to be introduced at arbitrary sites.[6]

Despite the early discovery of post-translational circular permutations and the suggestion of a possible genetic mechanism for evolving circular permutants, it was not until 1995 that the first circularly permuted pair of genes were discovered. Saposins are a class of proteins involved in sphingolipid catabolism and antigen presentation of lipids in humans. Chris Ponting and Robert Russell identified a circularly permuted version of a saposin inserted into plant aspartic proteinase, which they nicknamed swaposin.[7] Saposin and swaposin were the first known case of two natural genes related by a circular permutation.[7]

Hundreds of examples of protein pairs related by a circular permutation were subsequently discovered in nature or produced in the laboratory. As of February 2012, the Circular Permutation Database[8] contains 2,238 circularly permuted protein pairs with known structures, and many more are known without structures.[9] The CyBase database collects proteins that are cyclic, some of which are permuted variants of cyclic wild-type proteins.[10] SISYPHUS is a database that contains a collection of hand-curated manual alignments of proteins with non-trivial relationships, several of which have circular permutations.[11]

Evolution

There are two main models that are currently being used to explain the evolution of circularly permuted proteins: permutation by duplication and fission and fusion. The two models have compelling examples supporting them, but the relative contribution of each model in evolution is still under debate.[12] Other, less common, mechanisms have been proposed, such as "cut and paste"[13] or "exon shuffling".[14]

Permutation by duplication

The permutation by duplication mechanism for producing a circular permutation. First, a gene 1-2-3 is duplicated to form 1-2-3-1-2-3. Next, a start codon is introduced before the first domain 2 and a stop codon after the second domain 1, removing redundant sections and resulting in a circularly permuted gene 2-3-1.

The earliest model proposed for the evolution of circular permutations is the permutation by duplication mechanism.[1] In this model, a precursor gene first undergoes a duplication and fusion to form a large tandem repeat. Next, start and stop codons are introduced at corresponding locations in the duplicated gene, removing redundant sections of the protein.

One surprising prediction of the permutation by duplication mechanism is that intermediate permutations can occur. For instance, the duplicated version of the protein should still be functional, since otherwise evolution would quickly select against such proteins. Likewise, partially duplicated intermediates where only one terminus was truncated should be functional. Such intermediates have been extensively documented in protein families such as DNA methyltransferases.[15]

Saposin and swaposin

Suggested relationship between saposin and swaposin. They could have evolved from a similar gene.[7] Both consist of four alpha helices with the order of helices being permuted relative to each other.

An example for permutation by duplication is the relationship between saposin and swaposin. Saposins are highly conserved glycoproteins, approximately 80 amino acid residues long and forming a four alpha helical structure. They have a nearly identical placement of cysteine residues and glycosylation sites. The cDNA sequence that codes for saposin is called prosaposin. It is a precursor for four cleavage products, the saposins A, B, C, and D. The four saposin domains most likely arose from two tandem duplications of an ancestral gene.[16] This repeat suggests a mechanism for the evolution of the relationship with the plant-specific insert (PSI). The PSI is a domain exclusively found in plants, consisting of approximately 100 residues and found in plant aspartic proteases.[17] It belongs to the saposin-like protein family (SAPLIP) and has the N- and C- termini "swapped", such that the order of helices is 3-4-1-2 compared with saposin, thus leading to the name "swaposin".[7][18]

Fission and fusion

The fission and fusion mechanism of circular permutation. Two separate genes arise (potentially from the fission of a single gene). If the genes fuse together in different orders in two orthologues, a circular permutation occurs.

Another model for the evolution of circular permutations is the fission and fusion model. The process starts with two partial proteins. These may represent two independent polypeptides (such as two parts of a heterodimer), or may have originally been halves of a single protein that underwent a fission event to become two polypeptides.

The two proteins can later fuse together to form a single polypeptide. Regardless of which protein comes first, this fusion protein may show similar function. Thus, if a fusion between two proteins occurs twice in evolution (either between paralogues within the same species or between orthologues in different species) but in a different order, the resulting fusion proteins will be related by a circular permutation.

Evidence for a particular protein having evolved by a fission and fusion mechanism can be provided by observing the halves of the permutation as independent polypeptides in related species, or by demonstrating experimentally that the two halves can function as separate polypeptides.[19]

Transhydrogenases

Transhydrogenases in various organisms can be found in three different domain arrangements. In cattle, the three domains are arranged sequentially. In the bacteria E. coli, Rb. capsulatus, and R. rubrum, the transhydrogenase consists of two or three subunits. Finally, transhydrogenase from the protist E. tenella consists of a single subunit that is circularly permuted relative to cattle transhydrogenase.[20]

An example for the fission and fusion mechanism can be found in nicotinamide nucleotide transhydrogenases.[20] These are membrane-bound enzymes that catalyze the transfer of a hydride ion between NAD(H) and NADP(H) in a reaction that is coupled to transmembrane proton translocation. They consist of three major functional units (I, II, and III) that can be found in different arrangement in bacteria, protozoa, and higher eukaryotes. Phylogenetic analysis suggests that the three groups of domain arrangements were acquired and fused independently.[12]

Other processes that can lead to circular permutations

Post-translational modification

The two evolutionary models mentioned above describe ways in which genes may be circularly permuted, resulting in a circularly permuted mRNA after transcription. Proteins can also be circularly permuted via post-translational modification, without permuting the underlying gene. Circular permutations can happen spontaneously through autocatalysis, as in the case of concanavalin A.[4] Alternately, permutation may require restriction enzymes and ligases.[5]

The role of circular permutations in protein engineering

Many proteins have their termini located close together in 3D space.[21][22] Because of this, it is often possible to design circular permutations of proteins. Today, circular permutations are generated routinely in the lab using standard genetics techniques.[6] Although some permutation sites prevent the protein from folding correctly, many permutants have been created with nearly identical structure and function to the original protein.

The motivation for creating a circular permutant of a protein can vary. Scientists may want to improve some property of the protein, such as:

Alternately, scientists may be interested in properties of the original protein, such as:

Algorithmic detection of circular permutations

Many sequence alignment and protein structure alignment algorithms have been developed assuming linear data representations and as such are not able to detect circular permutations between proteins.[34] Two examples of frequently used methods that have problems correctly aligning proteins related by circular permutation are dynamic programming and many hidden Markov models.[34] As an alternative to these, a number of algorithms are built on top of non-linear approaches and are able to detect topology-independent similarities, or employ modifications allowing them to circumvent the limitations of dynamic programming.[34][35] The table below is a collection of such methods.

The algorithms are classified according to the type of input they require. Sequence-based algorithms require only the sequence of two proteins in order to create an alignment.[36] Sequence methods are generally fast and suitable for searching whole genomes for circularly permuted pairs of proteins.[36] Structure-based methods require 3D structures of both proteins being considered.[37] They are often slower than sequence-based methods, but are able to detect circular permutations between distantly related proteins with low sequence similarity.[37] Some structural methods are topology independent, meaning that they are also able to detect more complex rearrangements than circular permutation.[38]

NAME Type Description Author Year Availability Reference
FBPLOT Sequence Draws dot plots of suboptimal sequence alignments Zuker 1991 [39]
Bachar et al. Structure, topology independent Uses geometric hashing for the topology independent comparison of proteins Bachar et al. 1993 [35]
Uliel at al SequenceFirst suggestion of how a sequence comparison algorithm for the detection of circular permutations can work Uliel et al. 1999 [36]
SHEBA Structure Uses SHEBA algorithm to create structural alignments for various permutation points, while iteratively improving the cut point. Jung & Lee 2001 [14]
Multiprot Structure, Topology independent Calculates a sequence order independent multiple protein structure alignment Shatsky 2004 server, download [38]
RASPODOM Sequence Modified Needleman & Wunsch sequence comparison algorithm Weiner et al. 2005 server [34]
CPSARST Structure Describes protein structures as one-dimensional text strings by using a Ramachandran sequential transformation (RST) algorithm. Detects circular permutations through a duplication of the sequence representation and "double filter-and-refine" strategy. Lo, Lyu 2008 server [40]
GANGSTA + Structure Works in two stages: Stage one identifies coarse alignments based on secondary structure elements. Stage two refines the alignment on residue level and extends into loop regions. Schmidt-Goenner et al. 2009 server, download [41]
SANA Structure Detect initial aligned fragment pairs (AFPs). Build network of possible AFPs. Use random-mate algorithm to connect components to a graph. Wang et al. 2010 download [42]
CE-CP Structure Built on top of the combinatorial extension algorithm. Duplicates atoms before alignment, truncates results after alignment Bliven et al. 2015 server, download [43]

References

open access logo This article incorporates content from PLoS Computational Biology that is available under the terms of the Creative Commons Attribution 2.5 License.

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  2. ↑ Einspahr, H.; Parks, E. H.; Suguna, K.; Subramanian, E.; Suddath, F. L. (1986). "The crystal structure of pea lectin at 3.0-Å resolution". The Journal of Biological Chemistry 261 (35): 16518–16527. PMID 3782132.
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Further reading

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