Introduction
Transposable elements (TEs), mobile segments of genetic material, were first discovered by McClintock [1]. Since then, they have been identified in a variety of eukaryotes [2]. Recent genome sequencing projects have consistently shown that TEs make up ~50% of primate genomes, while coding DNA occupies only ~2% of the genomes [3-5]. TEs are generally divided into two categories, DNA transposons and retrotransposons (Fig. 1), based on their manner of mobilization. DNA transposons move using a cut-and-paste mechanism [6]. In contrast, retrotransposons move in a copy-and-paste fashion by duplicating the element into a new genomic location via an RNA intermediate [7]. Thus, retrotransposons increase their copy number more rapidly than DNA transposons.
Retrotranspons include short interspersed element (SINE), long interspersed element (LINE), and human endogenous retrovirus (HERV). Alu and short interspersed element/variable number of tandem repeats/Alu (SVA) elements are primate-specific retrotransposons, and their full-length is 300 bp and 2 kb, respectively. The Alu element is the most successful SINE in terms of its copy number; ~1.2 million Alu copies exist in the human genome. LINE is ~6 kb in length, and thus, it is much longer than the SINEs. This element has two open reading frames encoding enzymatic machineries essential for the propagation of the three elements; the Alu element depends on reverse transcriptase of LINE for making their dispersed copies in the host genome [8]. In contrast to SINE and LINE, which do not have long terminal repeats (LTRs), the full-length HERV (~10 kb) has two LTRs, and three genes-gag, pol, and env-are located between them [8, 9].
Studies on active TEs have suggested that the elements could alter gene expression by providing cis-regulatory elements, such as promoters, enhancers, and transcription factor binding sites [10]. Through these mechanisms, altered transcriptional activity could lead to dysfunctional and abnormal proteins. Through de novo TE insertion within a gene, TEs could alter a gene product, which could be either harmful or beneficial to its host genome [11, 12]. In cases where an inserted TE causes a harmful effect on its host genome, the TE is likely to go to inactivation and fossilization by evolutionary accumulation of mutations and silencing effects [13].
Since the divergence of the human and chimpanzee, ~6 million years ago, many TEs have propagated in each genome. Among them are the Alu, L1, SVA, and HERV-K (HML-2) elements. During the past 6 million years, 5,530 Alu, 1,835 L1, 864 SVA, and 113 HERV-K (HML-2) elements are estimated to have been newly inserted in the human genome (Table 1) [8, 14, 15]. These elements could act as an agent causing human-specific genomic rearrangements via de novo TE insertions, TE insertion-mediated deletions, and homologous recombination events [12, 16-19]. Furthermore, some of the recent integrated TEs are capable of producing new copies in the human genome. These de novo TE insertions have the potential to cause a genomic difference among human populations and even human individuals, which could be related to human phenotypes and diseases [20].
In this review, we describe species-specific TEs and discuss how they affect their host genomes, focusing on illustrating the mechanisms that they utilize with examples. Taken together, we suggest that TEs, often called 'junk' DNA, in fact have many functions and play a significant and dynamic role in primate genomic evolution.
TEs Recently Inserted into the Human Genome
Comparative genomics allows us to investigate species-specific TEs. Through a combinational method of computational data mining and experimental verification, species-specific TEs have been well studied in various primate genomes, including human, chimpanzee, and rhesus macaque. During the past 6 million years, more than 10,000 human-specific TEs were newly inserted in the human [21]. The majority of the identified elements belong to Alu, L1, and SVA retrotransposons. These elements have contributed to the genomic difference between human and non-human primates through insertion and post-insertion recombination between the elements [8, 22].
Alu elements are most ubiquitous in the human genome. A master gene model has been generally accepted to explain the amplification of Alu elements. In the model, only limited numbers of hyperactive "source" or "master" genes are able to produce a high number of Alu copies over evolutionary time. One of the previous studies about the AluYb subfamily, one of the most active Alu subfamilies in the human genome, found that the copy number of AluYb elements is very different between human and non-human primates; a high copy number of AluYb elements exists in the human, but a very small number of the elements exists in non-human primates [23]. The oldest AluYb element resides at its orthologous position in all hominid primate genomes, demonstrating that the AluYb subfamily emerged 18 to 25 million years ago. Then, after approximately 20 million years of retrotranspositional quiescence, a major expansion of the subfamily occurred only in the human genome within the past several million years. To explain their successful proliferation in the human genome, a new model, "stealth driver," was introduced. In this model, a high copy of the Alu elements could be driven at least in part by "stealth driver" elements, which maintain low retrotransposition activity over extended periods of time. Although this element has low retrotransposition activity, they have the potential to produce short-lived hyperactive copies responsible for the remarkable expansion of AluYb elements within the human genome [24].
L1 is another successful element, occupying ~17% of the human genome. The copy number of Alu elements is much higher than that of L1 (Alu, ~1.2 million copies; L1, ~520,000 copies). Nonetheless, Alu elements are responsible for ~11% of the human genome, because the Alu element is much shorter than L1 (Alu average length, 300 bp; full-length of LINE, 6 kb) [25]. Through characterization of sequence diversity of chimpanzee-specific L1 subfamilies as compared to their human-specific counterparts, it was concluded that L1s experienced different evolutionary fates between humans and chimpanzees within the past ~6 million years. Although the species-specific L1 copy numbers were on the same order in the two species (1,800 human-specific L1s vs. 1,200 chimpanzee-specific L1s), the number of retrotransposition-competent elements was much higher in the human genome than in the chimpanzee genome. The species-specific L1s were grouped into several L1 subfamilies. All human L1 subfamilies belonged to a single lineage, but two distinct L1 lineages were identified in the chimpanzee genome [15].
SVA is shared only in human and apes. Fewer than 1,000 copy numbers were detected in orangutan (~15 million years ago), and no SVA detected in Old World monkeys indicating SVA is a hominid-specific element. Like Alu elements, SVA elements retrotranspose to another locus in trans by using reverse-transcriptase encoded by L1s [8]. Due to the limited mobilization and short evolutionary time, the copy number of SVA is very small compared to Alu and L1 elements [15, 26, 27]. There are six SVA subfamilies (SVA_A to SVA_F) in the human genome. The older, SVA_A to SVA_D, evolved in a single lineage, whereas human-specific SVA_E and SVA_F were derived independently from their ancestral sequences. The copy number of SVA was estimated throughout the primate genomes of human, chimpanzee, and gorilla, and there was no significant difference among them. The two elements, Alu and L1, showed a huge expansion at a specific evolutionary time along the primate lineage, but SVA still did not show any burst in its copy number [26, 27].
Genomic Rearrangements by TEs
The comparison of human and chimpanzee genomic sequences showed that the two genomes have a much higher sequence identity than we expected [3, 4]. In spite of the sequence similarity, TEs have remarkably generated genomic differences between the two species since their divergence [22]. Many studies have suggested that a number of TEs are still active to retrotranspose and have the potential to cause genomic variations as a major driver [12, 16-19, 28]. In reality, TEs have rearranged human and non-human primate genomes through various mechanisms, such as de novo TE insertion, TE insertion-mediated deletion, and homologous recombination between them (Fig. 2) [29]. These genomic changes caused by TEs have increased the genomic difference between human and non-human primates, and some of the human-specific genomic rearrangements caused human diseases [28, 34].
Advanced sequencing technology, including next-generation sequencing, and combined computational analyses have accelerated the studies on the dynamics of TE mobilization [35]. In reality, human-specific TEs have been continuously investigated, and the majority of them are Alu, L1, and SVA elements [8, 14]. The relationship between human brain evolution and Alu elements was studied. Since the divergence of the human and chimpanzee lineages, the human brain has rapidly changed in terms of mass [36]. It is not an exaggeration to say that Alu elements are in part responsible for the human brain mass. Interestingly, de novo
Alu insertions have been identified in many human brain genes that are related to neuronal functions and neurological disorders [37]. The inserted Alu elements belong to AluYa5, AluYb8, and AluYc1, which are human-specific Alu subfamilies [37].
Approximately 1,800 human-specific L1s were identified in the human genome [15]. They belonged to two different subfamilies, pre-Ta and Ta; Ta is subdivided into Ta-0 and Ta-1 by diagnostic nucleotides [38]. Among hominid-specific SVA subfamilies, SVA_E and SVA_F are only detected in the human genome, but the other four subfamilies, SVA_A, SVA_B, SVA_C, and SVA_D, are shared in human and other apes, including chimpanzee and gorilla [26]. HERV appeared in the primate genome through germ-line infection [30]. There are approximately 98,000 HERVs in the human genome. Full-length HERVs are ~10 kb in length, but most of the HERVS existing in the human are defective due to truncation and accumulation of mutations during primate evolution [39]. Among various HERV subfamilies, HERV-K (HML2) is the youngest element in the human genome [8, 40]; 113 human-specific HERV-Ks were identified in the human genome, and among them, there were 15 and 98 full-length HERV-Ks and solitary LTRs, respectively [39]. These de novo TE insertions showed polymorphisms among human populations and even human individuals [31, 39, 41, 42]. Therefore, they have the potential to be used as a genetic marker for racial identification [31, 41, 42].
De novo TE insertions contribute to the genome expansion. Actually, some of them somewhat decreased their host genomes involving the insertion-mediated deletion of host genome sequences [32, 33]. Through comparative genomic analyses, 50 L1 insertion-mediated deletion events were found in the human and chimpanzee genomes [18]. The sizes of the deleted sequences were variable, and in sum, ~18 kb and ~15 kb of sequences were removed from the human and chimpanzee genomes, respectively. Based on the result, it was estimated that L1 insertions may have deleted up to 7.5 Mb of target genomic sequences during the primate radiation. Alu insertions were also involved in the genomic deletions at its insertion target regions through Alu retrotransposition-mediated deletion. A total of 33 deletion events responsible for a ~9,000-bp deletion in human and chimpanzee genomes were identified. It was suggested that Alu retrotransposition may have contributed to over 3,000 deletion events, leading to a ~900-kb deletion during primate evolution [17]. Additionally, 13 SVA insertion-mediated deletions (SIMDs) were also identified in the human genome, and they deleted 30,785 bp of the human genome compared with the chimpanzee genome (Table 1). Among the 13 SIMDs, 9 were associated with the SVA_D subfamily, occupying the largest portion of SVAs, which suggests that SIMD frequency is directly correlated to the copy number of SVA elements. Furthermore, one of the deletion events occurred in the tMDC II gene associated with sperm-egg binding prior to fertilization [43, 44].
After TE insertions into the host genome, they could generate genomic variations through unequal homologous recombination events between them [17, 19, 43]. The copy number of TEs is closely related to the frequency of the recombination between them. Thus, compared to other TEs, Alu and L1 elements have a high probability of generating genomic structural variations due to their ubiquity. In reality, 492 Alu recombination-mediated deletions (ARMDs) were identified in the human genome, and they deleted ~400 kb of human genomic sequences (Table 1). About 60% of the deletion events were related to known or predicted genes, including three that deleted functional exons. Thus, the ARMD process has produced a considerable portion of the genomic and phenotypic variations between humans and chimpanzees since the divergence of the two species [16]. The recombination between L1 elements has also deleted human genome sequences. Seventy-three L1 recombination-associated deletions (L1RADs) were identified in the human genome [45]. The sizes of the deletion events range from 56 to 64,113 bp, and ~450 kb of human genomic sequence was deleted through this L1RAD process (Table 1). Thus, the L1RAD event has deleted 25 times as much human genomic sequence as the L1 insertion-mediated deletion event [18, 45].
Genomic Instability Generated by TEs
The TEs inserted in intra- and inter-genic regions could alter cellular gene expression, increasing genomic instability [9]. About a decade ago, gene regulation by TEs was studied only in specific genes through experimental validation. However, genome-wide analyses of gene regulation by TEs were recently conducted due to the developed high-throughput technologies. The findings showed that TEs have many regulatory sequences, such as promoters, enhancers, polyadenylation signals, and cryptic splicing donor (5') and acceptor (3') sites, by which the transcript architecture of nearby genes can be altered [10, 46, 47].
When TEs insert into the intronic region of genes, they could create a new exon by offering splicing sites, and this process is called "exonization" [48]. This mechanism is related to exon variations, such as cassette exons and intron retention in exons, increasing mRNA instability [49]. The TEs residing upstream of any gene could act as an alternative promoter, leading to new alternative transcripts with a new transcriptional start site [10]. Some TEs carry bidirectional promoters with transcription factor binding sites. For example, LTR and L1 have sense promoters initiating their transcription and antisense promoters having the potential to initiate the transcription of other genes in the opposite direction [50, 51]. There is a microRNA gene cluster in human chromosome 19 (C19MC), over 100 kb in length. This cluster consists of the duplication of a core cassette, including a minus-strand Alu element. The cluster grew successfully during primate evolution, and the Alu element promotes microRNA expression by RNA polymerase III [52]. TEs not only initiate transcription but also terminate it by offering a polyadenylation signal. A full-length L1 contains 19 polyadenylation signals that could cause premature mRNA truncation [53]. The genes that contain TEs in their genic region have a tendency to produce various transcript forms, causing transcriptome diversity [10].
The orientation of TEs could be a factor affecting gene expression, which is well described by a "head-on collision" hypothesis. During DNA replication, DNA polymerase collides with RNA polymerase transcription complexes moving in the opposite direction to the movement of the DNA polymerase. It was observed that the collision slows down the DNA replication [54]. In cases where active TE exists in the opposite direction to its nearby genes, an RNA polymerase transcription complex transcribing the TE could encounter any of the RNA polymerase transcription complexes transcribing nearby genes, which could reduce the expression of the gene [54, 55]. In reality, transcription of the E-globin gene is repressed by an Alu element that has been inserted in the opposite direction to the gene [56]. On the other hand, TEs inserting in the same direction to its nearby genes show no effect on the expression of the genes [55].
Histone modification plays an important role in gene transcriptional regulation, and through this process, the host genome could regulate the activation of TEs [57, 58]. In reality, most TEs are accompanied by repressive histone modifications (e.g., H3K9me2 and H3K27me3), which cause the formation of heterochromatin. Conversely, TEs could affect the expression of host genes through histone modifications [59, 60]. The level of histone modifications was calculated in all families of human TEs, and older TE families carried more histone modifications than younger families. Interestingly, TEs proximal to genes carry more histone modifications than the ones that are distal to genes, which suggests that some epigenetic modifications of TEs may serve to regulate the expression of host genes [61].
DNA methylation is a strict silencing mechanism, and the host genome could use this process to repress the activation of TEs [61]. In general, DNA methylation occurs in a CpG dinucleotide. Because Alu and SVA elements have a high degree of CpG dinucleotides, they are vulnerable to methylation [26, 62]. It was observed that TEs regain their activity to mobilize and regulate the expression of host genes when the silencing effect becomes slackened with increasing genomic instability. In addition, the demethylation of TEs is associated with human diseases, commonly in cancer [63-65].
miRNAs, one of the most active factors regulating gene expression, could be derived from TEs. Fifty-five genes derived from TEs were identified in the human genome, and their characterization showed that TE-derived miRNAs could potentially regulate the complex and dynamics of human genes [66].
Conclusions
TEs have shown a variety of impacts on their host genomes. In this review, we describe HERV, Alu, L1, and SVA elements, which are thought to still be active in the human genome. A number of research studies related to TEs have shed new light on their amplification mechanisms and their function in primate genomes. Furthermore, recent research of TEs in the rhesus macaque genome provides a glimpse into their diversity and strong influence on the overall differences in genomic architecture between the Old World monkey (e.g., rhesus macaque) and hominid (e.g., human and ape) lineages [67]. The occurrence of de novo TE insertions, TE insertion-mediated deletions, and post-insertion recombination between TEs within the human and chimpanzee lineages has caused genetic alteration, lineage-specific genomic rearrangements, and phenotypic variations, further contributing to the divergence of humans and chimpanzees. As a whole, this review calls into question whether TEs should be considered "junk" DNA at all. Rather, TEs represent a potent evolutionary force associated with genomic fluidity in their host genomes.
PDF Links
PubReader
ePub Link
XML Download
Full text via DOI
Full text via PMC
Download Citation
Print
