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Repeated DNA makes up a large fraction of a typical mammalian genome, and some repetitive elements are able to move within the genome (transposons and retrotransposons). DNA transposons move from one genomic location to another by a cut-and-paste mechanism. They are powerful forces of genetic change and have played a significant role in the evolution of many genomes. As genetic tools, DNA transposons can be used to introduce a piece of foreign DNA into a genome. Indeed, they have been used for transgenesis and insertional mutagenesis in different organisms, since these elements are not generally dependent on host factors to mediate their mobility. Thus, DNA transposons are useful tools to analyze the regulatory genome, study embryonic development, identify genes and pathways implicated in disease or pathogenesis of pathogens, and even contribute to gene therapy. In this review, we will describe the nature of these elements and discuss recent advances in this field of research, as well as our evolving knowledge of the DNA transposons most widely used in these studies.
Eukaryotic genomes contain an abundance of repeated DNA, and some repeated sequences are mobile. Transposable elements (TEs) are defined as DNA sequences that are able to move from one location to another in the genome. TEs have been identified in all organisms, prokaryotic and eukaryotic, and can occupy a high proportion of a species’ genome. For example, transposable elements comprise approximately 10% of several fish species, 12 % of the C. elegans genome [1, 2], 37% of the mouse genome , 45% of the human genome , and up to >80% of the genome of some plants like maize . From bacteria to humans, transposable elements have accumulated over time and continue to shape genomes through their mobilization.
The mobilization of TEs is termed transposition or retrotransposition, depending on the nature of the intermediate used for mobilization. There are several ways in which the activity of TEs can positively and negatively impact a genome; for example, TE mobilization can promote gene inactivation, modulate gene expression or induce illegitimate recombination. Thus, TEs have played a significant role in genome evolution. However, from a strictly theoretical point of view, TEs can be considered as selfish DNA or junk DNA, and the existence of these elements in a genome represents the fight between selfish DNA (to be perpetuated) and the host (to curtail their spread and its consequences).
As TEs make up a large percentage of genome volume, it is hypothesized that they have participated in changes of genome size during speciation and evolution, as reported in plants , Drosophila or primates [7-9]. The trigger(s) for TE-induced genome size increases is not clearly known, although it is thought that stress could be implicated in the amplification of TEs . TEs are able to produce various genetic alterations upon insertion as a consequence of the transposition process (insertions, excisions, duplications or translocations in the site of integration). For example, DNA transposons can inactivate or alter the expression of genes by insertion within introns, exons or regulatory regions [11-15]. In addition, TEs can participate in the reorganization of a genome by the mobilization of non-transposon DNA [16-18] or by acting as recombination substrates. This recombination would occur by homology between two sequences of a transposon located in the same or different chromosomes, which could be the origin for several types of chromosome alterations . Indeed, TEs can participate in the loss of genomic DNA by internal deletions  or other mechanisms [21, 22].
The reduction in fitness suffered by the host due to transposition ultimately affects the transposon, since host survival is critical to perpetuation of the transposon. Therefore, strategies have been developed by host and transposable elements to minimize the deleterious impact of transposition, and to reach equilibrium. For example, some transposons tend to insert in nonessential regions in the genome, such as heterochromatic regions [23-26], where insertions will likely have a minimal deleterious impact. In addition, they might be active in the germ line or embryonic stage [27-29], where most deleterious mutations can be selected against during fecundation or development, allowing only non-deleterious or mildly deleterious insertions to pass to successive generations. New insertions may also occur within an existing genomic insertion to generate an inactive transposon, or can undergo self-regulation by overproduction-inhibition (see below). On the other hand, host organisms have developed different mechanisms of defense against high rates of transposon activity, including DNA-methylation to reduce TE expression [30-33], several RNA interference mediated mechanisms  mainly in the germ line [35, 36], or through the inactivation of transposon activity by the action of specific proteins [37-39].
In some cases, transposable elements have been “domesticated” by the host to perform a specific function in the cell . A well-known example are RAG proteins, which participate in V(D)J recombination during antibody class switching, and exhibit a high similarity to DNA transposons, from which these proteins appear be derived [41-45]. Another example is the centromeric protein CENP-B, which seems to have originated from the pogo-like transposon . The analogous human mariner Himar1 element has been incorporated into the SETMAR gene, which consists of the histone H3 methylase gene and the Himar1 transposase domain. This gene is involved in the non-homologous end joining pathway of DNA repair, and has been shown to confer resistance to ionizing radiation . From a genome wide view, it has been estimated that ~25% of human promoter regions and ~4% of human exons contain sequences derived from TEs [48, 49]. Thus, we are likely underestimating the rate of domestication events in mammalian genomes.
A type of TE, RNA transposons (Class I), function via reverse transcription of an RNA intermediate (replicative mechanism) and can be further subdivided in two main groups depending on the presence of Long Terminal Repeats (LTR) flanking the retroelement main body (Fig. 11). LTR retrotransposons are similar in structure and life cycle to retroviruses, and their biology has been recently reviewed . Additionally, the biology and impact of non-LTR retrotransposons in mammalian genomes has been reviewed extensively (see , for a recent review) as well as their potential use as mutagens in genomics . Thus, no Class I TEs will be reviewed in this manuscript, although they posses some unique characteristics that may be very useful in genomics studies.
DNA transposons (Class II) generally move by a cut-and-paste mechanism in which the transposon is excised from one location and reintegrated elsewhere. Most DNA transposons move through a non-replicative mechanism, although there are exceptions (see below). DNA transposons consist of a transposase gene that is flanked by two Terminal Inverted Repeats (TIRs) (Fig. 11). The transposase recognizes these TIRs to perform the excision of the transposon DNA body, which is inserted into a new genomic location (see below for further details). Upon insertion, target site DNA is duplicated, resulting in Target Site Duplications (TSDs), which represent a unique hallmark for each DNA transposon. DNA transposons are classified into different families depending on their sequence, TIRs, and/or TSDs. The families in Subclass I are: Tc1/mariner, PIF/Harbinger, hAT, Mutator, Merlin, Transib, P, piggyBac and CACTA. Helitron and Maverick transposons belong to a different subclass (Subclass II), since they are replicated and do not perform double-strand DNA breaks during their insertion (see below).
Within both classes of TEs (Class I and II) we can find non-autonomous elements (i.e., do not encode proteins required for their mobilization), which are presumably dependent on autonomous transposons for mobility. As an example, Miniature Inverted-repeat Transposable Elements (MITEs) are short (80-500 bp) DNA transposon-like elements present in large numbers in many eukaryotes, particularly plant species [53, 54], and occasionally in bacteria [55, 56]. Although they have TIRs and are flanked by TSDs, lack transposase coding potential and are thus presumably dependent on autonomous DNA transposons for their mobilization.
In the following sections, we will describe and review several DNA transposon families, from their nature to their applications as genomic tools.
The elements from the superfamily Tc1/mariner are probably the most widely distributed family of TEs in nature, represented in such diverse taxa as rotifers, fungi, plants, fish and mammals [57-59]. Despite this fact, the vast majority harbor multiple inactivating mutations and only ten naturally occurring elements are known to be active: Tc1 and Tc3 from C. elegans [60, 61], Minos from Drosophila hydei , Mos1 from D. mauritiana [63, 64], Famar1 from European Earwig (Forficula auricularia) , Osmar5 from rice (Oryza sativa) , Fot1 and Impala from the fungus Fusarium oxysporum [67, 68], ISY100 isolated in bacteria , and Mboumar-9 from the ant Messor bouvieri . In addition, four well-characterized active Tc1/mariner transposons have been reconstructed from inactive elements: Sleeping Beauty from salmonid-type fishes , Himar1 from the Horn Fly (Hematobia irritans) , Frog Prince from the frog Rana pipiens  and Hsmar1, incorporated into the SETMAR gene, from H. sapiens [74-76].
Tc1/mariner elements are between 1 and 5 kb in length, and encode a transposase of 282 to 345 amino acids which is flanked by two TIRs that can vary between 17 to 1100 bp in length [58, 77]. The transposase proteins from different Tc1/mariner elements are not very similar in sequence, but all of them harbor two characteristic domains: an amino-terminal region containing the helix-turn-helix (HTH) motif necessary for recognition and binding of TIRs, and a carboxy-terminal domain harboring the catalytic motif constituted by three amino acids, DDD in the case of mariner-like elements, or DDE in the case of Tc1-like elements (Fig. 22). The first and second aspartate residues are separated by 92 amino acids, whereas the distance between the second and third residue is variable, between 31 and 39 amino acids in the different families from the superfamily Tc1/mariner . Other motifs harbored by the transposase are the Nuclear Localization Signal (NLS), indispensable for transposase transport through the nuclear membrane , and the WVPHEL linker motif, which might participate in the interaction between transposase monomers .
Tc1/mariner elements can be further sub-classified in seven different groups or families: maT elements (DD37D), isolated from Bombyx mori, C. elegans and C. briggsae ; DD37E elements isolated from mosquito and rotifers [59, 80]; Tc1-like elements (DD34E) isolated from insects, nematodes and vertebrates [71, 81-84]; Gambol elements (DD34E), phylogenetically distinct from the group above and isolated from mosquito ; DD39D elements isolated only in plants ; and mariner-like elements (DD34D). The mariner family is probably the most widely distributed family of transposons in nature, represented in such diverse taxa as fungi, ciliates, rotifers, insects, nematodes, plants, fish and mammals [57-59]. The phylogenetic analysis of theses elements define at least five clear sub-families: mauritiana, cecropia, mellifer/capitata, irritans and elegans/briggsae.
None of the transposition steps described above require energy (in the form of the cofactor ATP), since the necessary energy to form the phosphodiester bonds in the integration process comes from the cleavage reaction of target DNA (exergonic reaction) [87-89]. Indeed, the catalytic motif DDE/D in the transposase carries out both excision and insertion reactions during transposition. However, the DDE/D motif needs to interact with a divalent cation to perform the transposition reaction. Although the physiological ion is Mg2+, the transposase can also use the cofactor Mn2+, which seems to cause a relaxation in target site specificity. This has been seen for many transposition systems and is supported by experimental evidence that indicates that Mn2+permits more flexible DNA strand positioning in the active site than does Mg2+ [74, 90].
Consistent with these data, transposition of Tc1/mariner elements requires no proteins or cofactors other than Mg2+and the transposase itself. Indeed, elements from this superfamily are able to perform transposition in vitro, when provided the right pH and salt conditions, a donor and target DNA, Mg2+ or Mn2+, and an active transposase protein [70, 72, 91]. Therefore, this fact confirms that Tc1/mariner elements are not dependent on host factors to mediate their mobility, making them excellent tools for genomic manipulation in non-native hosts (see below). However, in some circumstances, it has been reported that the transposition efficiency can be affected by the cellular environment .
To complete a round of transposition, the DNA double strand breaks (DSBs) left behind by the Tc1/mariner transposons upon excision must be repaired by the host cellular machinery. One possible pathway of DSB repair is homologous recombination (HR), either using the homologous chromosome (or the sister chromatid) or a homologous sequence on the same chromosome as a template. In the first case, the result is the regeneration of a new copy of the transposon . In the second case, repair occurs by single-strand annealing, generating a deletion in the DNA flanking the excision site . Another possibility is to repair the DSBs through the Non-Homologous End-Joining (NHEJ) DNA repair pathway, which leads to the generation of a transposon footprint flanked by the TA duplication [94, 95]. The choice of DSB repair is likely dictated by the host, as different organisms are more prone to repair DSBs lesions through either HR or NHEJ.
Transposition is potentially deleterious to the host as well as the transposon, whose replication and propagation depend on the survival of their host. Thus, the development of ways to decrease the impact of transposition on host fitness is beneficial for both host and transposon. Some of the known strategies for transposon control are the following:
The transposase itself can act as a transposition inhibitor, as when it exceeds a threshold concentration, transposon activity is decreased. This fact has been observed in Tc1/mariner elements [96, 97], although the nature of this mechanism is not clear. It has been suggested that transposase monomers could form inactive or less active oligomers, thus decreasing the activity of the transposition process [96, 97]. When the copy number of these elements increases in the host genome, the production of transposase is also increased, and through OPI the mobilization of the transposon is reduced.
Although Tc1/mariner elements are widespread in nature, the vast majority harbor multiple inactivating mutations and only a few naturally occurring elements are known to be active (see above). It has been suggested that this is the result of selective pressure to reduce damage to the host genome . In addition, inactive elements could produce inactive transposases that would impede the transposition of active elements, by OPI or by competition with the active transposases for TIRs. As two functional transposase molecules are necessary to perform transposition, inactive transposase proteins act as dominant negative inhibitors of transposition [96, 99]. On the other hand, inactive elements with active TIRs can recruit active transposase to mediate their mobilization. This phenomenon could explain the replacement of active elements by inactive elements, which seems to have occurred in many species during the course of evolution .
As mentioned above, the host can develop different mechanisms to decrease the activity of transposons. One way used by the host to silence a Tc1/mariner element is DNA methylation, thereby preventing its transcription , or using post-transcriptional silencing mechanisms such as RNA interference [101, 102].
TEs are parasitic DNAs whose only function is to replicate and propagate themselves. When a transposon invades a new host, it must colonize the germline genome to persist in the population. Then, it will increase in copy number , and persists in the genome until, by vertical inactivation, all transposon copies become inactive and remain only as fossils. These inactive elements may even disappear by genetic drift . To escape this cycle, a transposon must invade a new species, or extends to multiple species. In other words, to ensure its survival, the transposon must pass to a new genome by Horizontal Transfer, and begin its life cycle again (Fig. 55).
As discussed previously, Tc1/mariner elements do not require specific factors from the host to perform the transposition process, and therefore are not restricted to one specific host. Indeed, many cases of horizontal transfer between different hosts have been proposed for these elements. Examples include transfer between marine crustaceans , between insects from different orders [105, 106], and even between organisms from different phyla, as divergent as human and a parasitic nematode . However, it is not known how these elements are able to invade new genomes. Potential vectors that might be implicated in this horizontal transfer are external parasites, such as mites, which seems to be the vehicle for the horizontal transfer of P elements in Drosophila , or internal parasites such as viruses .
Sleeping Beauty (SB) is the Tc1/mariner element most widely used as a genetic tool. It is a synthetic transposable element reconstructed from defective copies of eight salmon species by reverse engineering . SB is active in species ranging from protozoa to vertebrates, including frogs, fish, mice, rats or humans . The hyperactive version of SB, SB100X, exhibits approximately a 100-fold increase in efficiency when compared to the first generation of SB transposase, facilitating robust stable gene transfer in vertebrates . Therefore, SB represents a promising system for gene transfer in vertebrates (somatic and germ line), embryonic stem cells, and many other cultured cell lines [110, 111].
The SB transposon system, similar to other DNA transposons, consists of two components (Fig. 66): the SB transposon vector, which contains the gene to be mobilized flanked by SB TIRs, and the SB transposase expression vector, which is the transposase mRNA or an expression plasmid. The SB transposase expression vector contains the SB transposase open reading frame (ORF) between a strong promoter (ubiquitous or cell-type restricted) and a poly(A) signal. To achieve transposition of SB, the two components of the system are introduced in the host (transfection in cell cultures, injection into fertilized eggs, injection in live animals, etc.) where insertion takes places. The SB system has been tested in several fish species, the frog Xenopus, rat, mouse and in cultured human cell lines [110, 112-114].
In humans, the SB transposon system was initially used in human T cells, resulting in stable gene transfer and expression of the reporter gene . The novel hyperactive SB100X has been tested in primary human CD34-positive hematopoietic stem cells, resulting in stable gene expression . Furthermore, transgenic mice have been generated by co-injecting the SB transposon vector with the SB transposase mRNA into fertilized oocytes, some of which gave rise to transgenic offspring . Additionally, SB has also been used in functional genetic screens in mammals for the identification of genes implicated in diseases such as cancer. SB is used to induce insertional mutagenesis, and candidate genes identified through the analysis of insertion sites in tumors vs control tissues (in gain of function studies [115, 116], reviewed in ).
Although Sleeping Beauty is currently the most promising gene transfer system for vertebrate cells within the Tc1/mariner superfamily, other transposons from this family have been used as genomic tools as well. Frog Prince was reconstructed from the Northern Leopard frog, Rana pipiens, and is characterized by the presence of 214 bp-long TIRs flanking the transposase gene (which harbors a DD34E catalytic domain, see above). Frog Prince shows preference for intronic insertions, and is very efficient in gene trapping experiments conducted in tissue culture cells . Furthermore, Frog Prince has been tested in zebrafish embryos and other cultured vertebrate cell lines . Similarly, the transposon Minos, isolated from Drosophila hydei, is 1.8 kb in length, has 254 bp-long TIRs and a two-exon transposase gene (60 bp-long intron) with the catalytic domain DD34D. This transposon has preference for genes, inserting mostly into introns, and has been tested in cultured human cells , mouse tissues  and the sea squirt Ciona intestinalis . Another example is Himar1 (also with a DD34D transposase), reconstructed from Haematobia irritans, which has been used in screens to identify genes implicated in bacterial pathogenicity by insertional mutagenesis [121-123], and in cultured human cells . In addition, there are other Tc1/mariner transposons that are active, but have not been tested in cells yet; for example, Mboumar-9, a new naturally active mariner transposon from ant, which shows robust efficiency of transposition in vitro .
piggyBac is a DNA transposon identified in the genome of the Cabbage Looper moth (Trichoplusia ni). Much of its biology is shared with Tc1/mariner elements, including transposition mechanism, control, and life cycle. Related piggyBac transposable elements have been found in plants, fungi and animals, including humans , although they are probably inactive due to mutation. piggyBac is 2.4 kb in length, contains 13 bp TIRs, and additional 19 bp internal inverted repeats located asymmetrically with respect to the ends . Its target insertion site is TTAA and it harbors a single ORF (1.8 kb) that encodes a functional transposase, although the DNA-binding domain and catalytic core have not yet been defined. The transposase from piggyBac has been optimized to generate a more active transposition system . This transposon has been used in such diverse organisms as protozoa, planaria, insects and mammals, including human cells [128-132].
piggyBac represents a versatile gene-trap vector for transgenesis in insects, being the most widely used transposon system for germline transformation in these organisms (dipteran, hymenopteran, coleopteran and lepidopteran species). It is an important tool to generate modified insects carrying lethality or sterility genes by transgenesis for plague control and thus pest control [133-135]. In mammals, the piggyBac system has been used for different applications, such as germline or somatic mutagenesis and gene therapy. It has been used to mediate gene transfer in human cells  and recently to generate transgene-free induced pluripotent (iPS) stem cells from mouse cells .
DNA transposons from the superfamily hAT (hobo/Ac/Tam3) have been isolated in eukaryotes, are 2.5 to 5 kb in length, and encode a transposase harboring a catalytic DDE motif and a DNA binding domain BED zinc finger (named after Drosophila proteins DEAF and DREF) [136, 137]. In hobo/Ac/Tam3 transposons, the transposase gene is flanked by TIRs of 5 to 27 bp in length, and the TSDs of these elements consist of heterogenic sequences of 8 bp in length. A member from this family widely used as a genetic tool is Tol2, which was the first active autonomous transposon isolated in vertebrate species [138, 139]. This element was identified in Medaka fish (Oryzias latipes) where it had generated a mutation in the tyrosinase gene, resulting in albino mutant fish. Tol2 is 4.7 kb in length and consists of two TIRs of variable length flanking the transposase gene which is made up of four exons . It has also been engineered for improved efficiency to facilitate its use as a tool for enhancer trap screens in vertebrates to identify genes implicated in different functions and pathways [141-143]. Tol2 can have a cargo capacity of more than 10 kb [144, 145], and its integration preference is not clear, although similarly to other hAT elements, it could have preference for 5’ regions of genes . This system has been used in different vertebrates such as zebrafish and Xenopus, chicken embryos, and cultured vertebrate cells, including human stem cells [141, 147-149].
In the following section, we will discuss the most useful characteristics of each DNA transposon as well as their known limitations.
There are many ways to manipulate an organism’s genome (somatic or germline), and viral delivery systems applied in gene therapy have several disadvantages when compared to transposon vectors. For example, viral vectors may induce a destructive immune response [150, 151], their production is difficult and expensive [152, 153], they prefer to integrate within 5’UTR regions of genes which may induce oncogenesis [150, 154, 155], and they have a relatively limited cargo capacity (less than 8 kb in lentivirus, retrovirus or adeno-associated viral vectors) , among others. In contrast, transposon systems are inexpensive and easier to purify, and are non-inmunogenic [156-158]. In addition, they permit elimination of the transgene and, in some cases such as piggyBac, can be excised without leaving notable genetic alterations . Unfortunately, relative to viral systems, DNA transposons are less efficient for gene transfer. However, the efficiencies of newly developed transposon systems such as piggyBac and SB100X are comparable to those of viruses [110, 127]. In addition, with a DNA transposon system as SB, almost 70% of the integrations occur in intergenic regions; they do not exhibit targeting of the 5’ region of genes as occurs with viruses [159, 160].
Among the characteristics that distinguish DNA transposon systems as biotechnical tools, we highlight:
Transposon insertion efficiency can vary depending on the size of the gene to be transferred. Tc1/mariner elements are notably affected by this factor, since an increase in cargo size decreases the efficiency of transposition in cultured cells . In contrast, piggyBac or Tol2 transposons are more tolerant in their capacity for cargo. In piggyBac, when the cargo approaches 9 kb the efficiency decreases in pronucleus-injected mice , and in Tol2 the efficiency begins to drop off only when the cargo is higher than 10 kb . To overcome this limitation in the SB system, a “sandwich SB vector” has been designed, which consists of two complete SB transposons flanking the gene to be mobilized, increasing the number of SB binding sites and thereby improving the efficiency of transposition for transgenes longer than 10 kb .
Integration site preference is an important consideration when choosing a transposon system for a given application. For example, piggyBac has preference for transcription units, with insertions primarily targeting introns . On the other hand, SB prefers heterochromatin over actively transcribed genes [26, 159], and when it does insert into genes, it prefers intronic sequences. Finally, superfamily hAT members like Tol2 seem prone to insert within 5’ regions of genes . The integration site preference is likely dictated by the transposase protein, and SB as well as other Tc1/mariner elements seem to have structural preferences with regards to their integration site [164, 165]. On the other hand, piggyBac inserts in its target TTAA without any other apparent requirements [166, 167]. Thus, depending on the study, both SB and piggyBac can be useful systems. In the case of mutagenesis screens, it is preferable for the transposon to insert into genes, whereas gene therapy protocols require a system with less affinity for insertion within genes and, in general, low-risk chromosomal regions. However, integration within heterochromatin (as observed for SB, ) has the disadvantage of typically producing low levels of transgene expression .
In functional genomic studies, it is often desirable to inactive genes by insertional mutagenesis by transposons. If the transposon insertion takes place within an intron, splicing would likely render such an insertion irrelevant. To avoid this situation, a splice acceptor followed by the reporter gene and a poly(A) tail may be included in the transposon. In this way, splicing is altered, leading to the fusion of the trapped gene and reporter gene downstream (Fig. 77). Thus, the trapped gene remains inactivated and the reporter gene is expressed. In sum, for insertional mutagenesis studies, both Tol2 and piggyBac are superior to SB, while for gene therapy SB is theoretically more secure than either Tol2 or piggyBac transposon systems.
Like others Tc1/mariner elements, SB tends to insert in the vicinity of the donor locus. This phenomenon is known as Local Hopping and seems to be a property of the Tc1/mariner family, as well as other DNA transposons including P elements or Ac elements. For example, SB shows a much larger local transposition interval (5-15 Mb) than P elements (100 kb). Differences in the range of Local Hopping have been observed for the same transposon, depending on host species and chromosomal location of the donor site [169-172]. In some cases, this phenomenon could be exploited to produce insertions in a limited chromosomal region. In the opposite case, when it is necessary to extend the mutagenesis region, a solution could be to establish several donor loci. In contrast, recent reports have indicated less Local Hopping for piggyBac , although further studies are required to truly determine its Local Hopping constrains.
The Overproduction Inhibition (OPI) phenomenon, as described previously, consists of decreasing transposition due to high transposase concentration. This phenomenon appears in Tc1/mariner elements and is variable depending on the transposon from this family [96, 163], whereas in piggyBac and Tol2 the OPI has not yet been described [132, 141]. In fact, this is the main limitation of the SB system. Using piggyBac, it is also possible to use a transposase-transposon vector, which results in a 2-fold higher activity in human cells relative to protocols in which the transposon and transposase plasmids are transfected separately. Therefore, OPI represents a disadvantage for gene transfer in Tc1/mariner elements, but not for transposons from others families such as piggyBac and hAT. However, the mechanism responsible for OPI is not clearly understood.
DNA transposon systems represent an important alternative to viral systems for gene therapy studies, and they have several advantageous properties that make them very promising tools for a wide variety of genomic studies (Table 11).
If we compare the characteristics of the most frequently used DNA transposon systems, SB and piggyBac, we believe that piggyBac has some advantages over SB, such as its high efficiency of insertion, the lack of OPI, non-local hopping, and a relatively high tolerance for cargo size (9-14 kb)  (Table 11). In contrast, SB undergoes OPI, local hopping and its efficiency of insertion decreases as a function of transgene length. However, the new hyperactive SB version, SB100X, seems to have a higher efficiency of insertion than piggyBac , unlike previous SB versions . Another advantage of piggyBac is that it does not leave “footprint” upon excision, unlike DNA transposons such as Tc1/mariner elements. The “footprint” of SB is TAG(T/A)CTA, whereas the piggyBac target site is repaired to the original sequence , which allows removal of the inserted transposon leaving the genome without any sequence alteration, a very important characteristic for applications in gene therapy. For example, piggyBac has been used to generate iPS cells, and later the reprogramming factors have been removed from the genome of iPS cells by re-expressing the transposase .
Taking into consideration the virtues and disadvantages of current DNA transposons for genomics studies, the hypothetical “perfect” transposon system would be: a high-efficiency system comparable with that of viral vectors or higher, that does not manifest OPI, that lacks local hopping (although in some cases this could be useful), with a high capacity for cargo, that leaves no-footprint upon insertion, and that induces the lowest possible level of mutations and chromosomal rearrangements. Among some other characteristics to consider, the preference of insertion site could be variable depending on the goal of the study. If the purpose is insertional mutagenesis for a screen of gene function, it would be necessary that the transposon has a preference for insertion into genes, as do piggyBac and likely Tol2. However, in gene therapy protocols it is essential that the insertion occurs outside genes, as with SB, to avoid deleterious mutations or chromosomal alterations that could originate during integration–excision events.
At present, the transposon system that encompasses more of these characteristics is piggyBac, follow by SB. Although Tol2 is similar to piggyBac in most aspects, the mobilization of piggyBac seems to be more efficient . SB and piggyBac have been tested successfully in mammalian genomes, including humans, to carry out transgenesis and functional genomics studies. Therefore, by virtue of their natural characteristics acquired over the course of their evolution as genetic parasites or selfish DNA, DNA transposons constitute a promising tool to perform important advances in functional genomics studies, gene therapy approaches, and for the generation of animal models with Knock-Out in each gene contained in its genome. Many of the useful characteristics of DNA transposons have been improved, and efforts have been made to overcome their inherent disadvantages. Further research, however, is required to obtain a perfect transposon system. Despite potential limitations inherent to their “free life” in host genomes, among them the propensity to generate mutations or chromosomal rearrangements, we should emphasize that these characteristics have been an important catalyst for genomic variability, which ultimately represents the raw material of evolution. Although repeated DNA and TEs are sometimes considered junk DNA, they have and will continue to prove useful in many biotechnical applications, and will remain a motor for the evolution of species.
We thank J.L.G.-P. lab members and colleagues at the Andalusian Stem Cell Bank for helpful discussions and comments to the manuscript. Research in J.L.G.-P. lab is supported by ISCIII-CSJA (EMER07/056), by a Marie Curie IRG action (FP7-PEOPLE-2007-4-3-IRG), by a Miguel Servet Contract (CP07/00065,ISCIII), by CICE (P09-CTS-4980) and Proyectos en Salud (PI-002) from Junta de Andalucia, and through the Spanish Ministry of Health (FIS PI08171).