Evolution of cellular innate immune genes in response to viral threats represents a rich area of study for understanding complex events that shape mammalian genomes. One of these genes, TRIM5, is a retroviral restriction factor that mediates a post-entry block to infection. Previous studies on the genomic cluster that contains TRIM5 identified different patterns of gene amplification and the independent birth of CypA gene fusions in various primate species. However, the evolution of Trim5 in the largest order of mammals, Rodentia, remains poorly characterized. Here, we present an expansive phylogenetic and genomic analysis of the Trim5 cluster in rodents. Our findings reveal substantial evolutionary changes including gene amplifications, rearrangements, loss and fusion. We describe the first independent evolution of TrimCyp fusion genes in rodents. We show that the TrimCyp gene found in some Peromyscus species was acquired about 2 million years ago. When ectopically expressed, the P. maniculatus TRIMCyp shows anti-retroviral activity that is reversed by cyclosporine, but it does not activate Nf-κB or AP-1 promoters, unlike the primate TRIMCyps. These results describe a complex pattern of differential gene amplification in the Trim5 cluster of rodents and identify the first functional TrimCyp fusion gene outside of primates and tree shrews.
Throughout millions of years of evolutionary history, retroviruses have adapted to living in concert with their hosts. This co-evolution has led to the co-option of cellular proteins used to aid viral replication as well as the emergence of innate immune factors produced by the host to antagonize viral infection. Over the past several decades, studies on retroviral replication have identified various genes that act to restrict infection by a variety of retroviruses1,2,3. One of the most well studied retroviral restriction factors is encoded by the gene TRIM5, a member of the Tripartite Motif (TRIM) gene family4,5. The TRIM family of genes produces proteins with three main domains: RING (R), B-Box (B) and Coiled Coil (CC) with a variable fourth domain6,7. Some members of this family, including TRIM5, encode a fourth domain called B30.2 or SPRY7. The TRIM family of genes has been shown to have a variety of functions in the cell, including innate immunity, autophagy, apoptosis and cellular differentiation5,7,8,9,10.
While the retroviral restriction by the longest isoform of TRIM5, TRIM5α, was originally discovered in rhesus macaques4, later studies found TRIM5α mediated inhibition of various retroviruses to be widespread among mammals5,11,12,13,14. Several studies on the mechanism of retroviral restriction by TRIM5 suggest that the incoming retroviral capsid lattice is recognized by the SPRY domain of TRIM5 following multimerization4,5,15,16,17. This leads to the proteasome dependent degradation of the viral capsid before reverse transcription can be completed16,17,18. In addition to its function as a direct retroviral antagonist, it has also been shown that TRIM5 can act as a pattern recognition receptor of the retroviral capsid structure and activate innate immune signaling through interactions with NF-κB and AP-119.
Not long after the initial discovery of TRIM5 as a retroviral restriction factor, it was demonstrated that the restriction of HIV-1 infection in owl monkey cells is caused by the expression of an unusual fusion protein made up of the N-terminal R-B-CC domains of TRIM5 and a cyclophilin A (CypA) domain at the C-terminus20,21. Further analysis of the owl monkey genome sequence revealed the presence of a retrotransposed, intronless CypA gene between exons 7 and 8 of the TRIM5 gene in this species20. The resulting fusion protein, called TRIMCyp, was shown to be a potent inhibitor of HIV-1 with the CypA domain replacing the capsid binding function of the SPRY domain found in TRIM520,21. A few years after this discovery, an independently evolved TRIMCyp fusion gene, with a distinct retroviral restriction capacity was identified in some species of the genus Macaca22,23,24,25,26. This convergently evolved macaque TRIMCyp results from insertion of a retrotransposed CypA gene downstream of the TRIM5 exon 822,23,24. A third, more ancient but currently inactive TRIMCyp fusion gene was identified in Old World monkeys and gibbons, called TRIMCypA327. More recently, the independent genesis of a TrimCyp fusion gene was discovered in the genome of Tupaia belangeri (Northern tree shrew)28. This TrimCyp contains an early stop codon in the retrotransposed CypA domain and does not have an antagonistic effect on any of the exogenous retroviruses tested28.
Previous studies on the cluster of Trim genes containing Trim5 in various mammals identified differential expansions of the Trim genes, likely generated via gene duplication11,29. The two species of rodents that were examined, mouse and rat, were found to have at least 8 and 3 copies of the genes belonging to the Trim5 clade, respectively. In this study, we set out to produce a more comprehensive analysis of the evolution of the Trim5 locus in the order Rodentia. Our genomic and phylogenetic analyses identified the presence of lineage specific gene duplications, losses and a variety of genomic organizational structures in the rodent Trim5 cluster. Our findings also revealed the independent evolution of a TrimCyp fusion gene in at least two rodent lineages. We confirmed the presence of TrimCyp in both RNA and DNA of multiple species belonging to the genus Peromyscus indicating a minimum insertion time of approximately 2 million years, and showed that CypA was acquired by Peromyscus species through retrotransposition into the Trim5 locus30,31. Our findings also show that the TRIMCyp of P. maniculatus has antiviral activity against HIV-1 in a dose-dependent manner when ectopically expressed, but unlike the primate TRIMCyp fusion genes, it does not activate NF-κB or AP-1 promoters, genes involved in innate immune responses. Collectively, these results document a complex history of genomic remodeling of the rodent Trim5 cluster and produce evidence of the independent genesis of TrimCyp fusion genes in the order Rodentia, all of which may reflect evolving responses to novel retroviral challenges.
Genomic organization of the rodent Trim5 locus
The Trim5 cluster of genes in rodents contains members of three distinct Trim genes: Trim6, Trim34 and Trim5. Trim5 includes two additional monophyletic groups designated Trim12 and Trim30. A previous description of the genomic organization of this cluster in rodents compared the then available rat and mouse genomes29. At the present time, there are 22 assembled and annotated rodent genomes in the NCBI database, containing at least two species from each of four of the five rodent suborders. To produce a more comprehensive picture of the genomic organization in the rodent Trim5 cluster, we utilized the BLAST tool on the NCBI website32,33 to search these 22 annotated genomes for the coding sequences (CDS) of the mouse Trim12c, Trim6 or Trim34a genes (Table 1). We excluded seven genomes from our analysis as the Trim5-like genes were split between different scaffolds or large sequencing gaps precluded an accurate picture of the genomic organization. Fifteen of the 22 genomes contained Trim6 and Trim5-like genes in the same scaffold or chromosome with no large or problematic sequence gaps. As shown in Fig. 1, 14 of the 15 analyzed genomes contained Trim6 and Trim34 genes in this cluster, as was previously described for the reference genomes of mouse and rat29. Twelve of the 15 genomes analyzed also contained several copies of Trim5-like genes as annotated by NCBI’s gene and mRNA prediction algorithms (Fig. 1 and Supplementary Table S1). Olfr (olfactory receptor) genes flank this Trim cluster in all species and occasionally are found within this cluster (Fig. 1). To describe the evolutionary relationship between the Trim genes in this locus, we generated separate phylogenetic trees using the aligned CDS of the Trim genes corresponding to either the R-B-CC (Fig. 2, Supplementary Fig. S1A, Supplementary Data S1 and Supplementary Data S3) or SPRY (Fig. 3, Supplementary Fig. S1B, Supplementary Data S2 and S4) domains. These results revealed the paralogous expansion of genes belonging to the Trim5 clade in most of the rodent species we analyzed (Fig. 1). We used our phylogenetic analysis and the mouse and rat genome nomenclatures34 to name the Trim5 paralogs in each of the species we analyzed (Fig. 1). Notably, our phylogenetic analysis of the genes belonging to the Trim5 clade revealed the clustering of the paralogs from the same species rather than orthologs with the same gene designation based on existing nomenclature (Figs 2, 3). This suggests that either similar paralogous expansions occurred in this locus in different lineages or that gene conversion events after speciation homogenized the sequences resulting in species specific clustering of the Trim5 paralogs. This phenomenon was observed both for newly identified and named Trim5 genes as well as previously recognized genes such as Trim30c.
The genomic organization of the Trim5 cluster showed similar patterns for species belonging to the suborders Myomorpha and Scuridae; in most species, Trim6 and Trim34 genes were upstream of at least one copy of a gene belonging to the Trim5 clade in an antisense orientation relative to Trim6 and Trim34 (Fig. 1). Most members of the suborder Hystricomorpha differ from other rodents in that there are one or more copies of the Trim5 clade of genes located between Trim6 and Trim34 (Fig. 1). Also, most Hystricomorpha species lacked the sequence coding for the SPRY domain in the Trim5 paralogs found in this locus, with the exception of a sequence coding for a partial SPRY domain found in the genome of chinchilla (Fig. 1). Moreover, in two species in the suborder Castorimorpha, we observed a pattern different from the other suborders; Dipodomys ordii genome lacks a Trim34 gene altogether, and the Castor canadensis genome only contains a partial/pseudo Trim5 gene (Fig. 1). It is important to note that in the currently available assembly of Castor canadensis this cluster is found in a genomic locus that is not in a region of conserved synteny with the other species. Thus, we cannot rule out the possibility of a mistake in the assembly of this genome.
The previous analysis of the mouse and rat Trim5 genes revealed the presence of two distinct monophyletic groups in this clade: Trim12 and Trim3029. Our results show that this phylogenetic grouping only exists in the species belonging to the families Cricetidae and Muridae (Fig. 2). Moreover, genomes we analyzed from the species belonging to these two families show a recurring pattern with a similar genomic organization in this locus; single Trim6 and Trim34 genes followed by a single gene belonging to the Trim12 clade. Each species also contains at least one Trim30 gene while the only species that contains multiple Trim12 and Trim34 clade genes is Mus musculus. Notably, some members of the family Cricetidae, including Cricetulus griseus, Microtus ochrogaster (Fig. 1) and Mesocricetus aureus (data not shown), also contain Trim30-like genes upstream of Trim6 separated by Olfr and ubiquilin genes (Fig. 1).
Evolution of multiple TrimCyp fusion genes in rodents
Our genomic database analysis of the rodent Trim5 cluster revealed the presence of an intronless CypA sequence in or near a Trim5 gene in at least three species; Microtus ochrogaster, Peromyscus maniculatus and Octodon degus. In both P. maniculatus and O. degus, CypA is annotated as part of a predicted TrimCyp fusion gene/mRNA, while in the genome of M. ochrogaster, CypA in this locus is not identified in the NCBI annotation and is not clearly located within a Trim5 gene (Fig. 1). Since each of these CypA insertions are in different positions in this locus they are independent insertions. Comparison of the TrimCyp fusion genes of P. maniculatus and O. degus to those previously identified in primates and tree shrews revealed a similar pattern in the location of the CypA insertion (Fig. 4). Despite arising independently in distant lineages, these CypA insertions are downstream of Exon7 (or Exon 6 in the case of O. degus) and upstream, downstream or inside of Exon 8 (Fig. 4). The resulting pattern substitutes the SPRY domain retroviral core binding function in TRIM5 with that of CypA as found in various primate TRIMCyps15,16. The CypA insertion in P. maniculatus is similar to what was previously reported in macaques22,23,24, where the CypA sequence is inserted downstream of Exon 8 of a Trim5-like gene where it leads to the alternatively spliced product, TrimCyp (Fig. 4). Notably, in contrast to what was observed in other lineages, in the TrimCyp fusion gene of O. degus, exon 7 and exon 8 of Trim5 are absent and the CypA insertion is located about 4 kb downstream of exon 6 (Fig. 4). These multiple independent acquisitions of TrimCyp fusion genes in the order Rodentia are the first identified outside the primate and tree shrew lineage.
Independent genesis of a TrimCyp fusion gene in the genus Peromyscus
To investigate the evolution and function of TrimCyp fusion gene in the genus Peromyscus, we isolated DNA and RNA from four species belonging to this genus; P. maniculatus, P. polionotus, P. leucopus and P. californicus. Genomic DNA sequencing confirmed the presence of CypA in the Trim5 locus in the genome of P. maniculatus (Fig. 5). Notably, the sequence of both CypA and the intronic region between CypA and Exon 8 of Trim30d was identical to the sequence in the assembled genome of this species, confirming the accuracy of this sequenced segment in this particular genome assembly. The sequence of CypA in the Trim5 cluster of P. maniculatus and the immediate surrounding region is shown in Fig. 5. Similar to what was observed in other lineages20,22,27,28, this CypA insertion bears the hallmarks of a LINE-1 mediated retrotransposition: It is an intronless copy of CypA that is surrounded by target site duplications of 15 bp and contains a 3′ poly A sequence (Fig. 5).
To test for the presence of TrimCyp in the four Peromyscus species in our possession, we designed two sets of primers to amplify the sequence between exon 8 of Trim30d and CypA (Fig. 6a). This region was successfully amplified in P. maniculatus, P. polionotus and P. leucopus, but no PCR product was obtained for P. californicus (Fig. 6a). To confirm the absence of a retrotransposed CypA gene in the Trim5 cluster of P. californicus, we designed primers from the intronic region surrounding the inserted CypA gene (Fig. 6b). We generated PCR products of ~2100 base pairs (bp) for P. maniculatus, P. polionotus and P. leucopus while P. californicus produced a smaller PCR product of ~ 1400 bp consistent with the absence of CypA in this region of the P. californicus genome (Fig. 6b). These findings indicate that P. californicus lacks this specific Trim5-associated retrotransposed CypA sequence. The varying PCR band intensities between different species and primer sets are likely due to mismatches between the genomic sequence and the primers, which were designed using the genomic sequence of P. maniculatus. However, the sequences of the PCR products are consistent with the conclusion that among the Peromyscus species tested, only P. californicus lacks the retrotransposed CypA sequence in this genomic location. Comparison of the genomic region immediately surrounding CypA in P. californicus and P. maniculatus is shown in Supplementary Fig. S2. Next, we tested the presence of TrimCyp and TrimSPRY transcriptional isoforms of Trim30d in the Peromyscus species. Consistent with the results obtained using the genomic DNA, TrimCyp cDNA was successfully amplified in P. maniculatus, P. polionotus and P. leucopus, but no PCR product was obtained for P. californicus (Supplementary Fig. S3A). Notably, P. maniculatus, P. polionotus and P. leucopus also express a Trim30d isoform with a SPRY domain coding sequence at the C-terminal end (Supplementary Fig. S3B). Identity of these isoforms were confirmed by sequencing. In addition, sequencing revealed that the retrotransposed CypA gene in this region from both P. polionotus and P. leucopus contains premature stop codons in CypA at different locations (Supplementary Fig. S4). The phylogenetic tree of these four species reveals that P. maniculatus, P. leucopus and P. polionotus are evolutionarily closer to each other than they are to P. californicus (Fig. 6c). These results indicate that the CypA retrotransposition into the Trim5 cluster of the genus Peromyscus likely happened in the most recent common ancestor of P. maniculatus, P. leucopus and P. polionotus, with a minimum insertion time of approximately 2 million years30,31.
Functional analysis of the Peromyscus TrimCyp
Independently evolved TrimCyp fusion genes were discovered in different primate lineages in large part due to their ability to restrict various retroviruses20,22. To evaluate the potential retroviral antagonism of the TRIMCyp fusion protein we found in P. maniculatus, we generated C-terminal V5-tagged constructs of the P. maniculatus Trim30d ORF with either a CypA (peroTRIMCyp) or a SPRY domain (peroTRIMSPRY) at the C-terminus. As a positive control we used a C-terminal V5-tagged owl monkey TrimCyp (omTRIMCyp) construct. We ectopically expressed these constructs in HEK293T cells at different dosages (Fig. 7a). omTRIMCyp expression led to a strong inhibition of VSV-G pseudotyped, single cycle HIV-1 (Fig. 7c) as previously reported19,20. This inhibition was more prominent with higher doses of omTRIMCyp, while also statistically significant at each dose (Fig. 7b). We observed a more modest and dose-dependent inhibition of HIV-1 by peroTRIMCyp (Fig. 7b). At the highest dose, peroTRIMCyp expression resulted in a statistically significant, 60% inhibition of HIV-1 infectivity (Fig. 7b). Notably this restriction was reversed by the addition of cyclosporine prior to infection, as has been reported for primate TRIMCyps (Supplementary Fig. S5)20,22,23,24. In contrast, we did not observe any inhibition of HIV-1 in cells ectopically expressing peroTRIMSPRY (Fig. 7b). Since peroTRIMCyp and peroTRIMSPRY share the same R-B-CC domains, the difference we observed in HIV-1 restriction by these proteins is likely due to the variation in the capacity of these proteins to interact with HIV-1’s capsid lattice. This possibility is supported by the fact that an alignment of the amino acid sequence of CypA from peroTRIMCyp and omTRIMCyp reveals almost 90% identity, while the sequence of the SPRY domain is less than 40% identical between peroTRIMSPRY and the antiretroviral rhesus TRIM5α (Supplementary Fig. S6). We also tested for antagonism of a rodent retrovirus; Moloney murine leukemia virus (MoMLV), by omTRIMCyp, peroTRIMCyp and peroTRIMSPRY (Fig. 7c). Ectopic expression of different doses of omTRIMCyp, peroTRIMCyp or peroTRIMSPRY did not inhibit infection by VSV-G pseudotyped MoMLV in HEK293 cells. These findings duplicate the known antiviral profile of omTRIMCyp20 and indicate that the TRIMCyp fusion protein of P. maniculatus has the capacity to antagonize at least one retrovirus, HIV-1.
Previous studies showed that the TRIMCyp fusion protein of owl monkey can act as a pattern recognition receptor of the incoming retroviral capsid lattice and promote innate immune signaling19,35. To investigate the ability of peroTRIMCyp to similarly induce innate immune signaling, we tested the effects of ectopic expression of omTRIMCyp and peroTRIMCyp on transcriptional luciferase reporter constructs with Nf-κB or AP-1 response elements in HEK293T cells. Similar to what was previously observed19,35, omTRIMCyp overexpression led to a robust induction of both Nf-κB and AP-1 promoter activities in a dose-dependent manner (Fig. 8a,b). In contrast, ectopic expression of peroTRIMCyp had no effect on either Nf-κB or AP-1 driven luciferase reporter expression (Fig. 8a,b). These results indicate that, unlike omTRIMCyp, overexpression of peroTRIMCyp does not activate Nf-κB or AP-1 promoters.
Our genomic and phylogenetic analyses of the Trim5 cluster identify two major and recurrent types of genomic alterations of the rodent Trim5 cluster (Fig. 1). These evolutionary events include differential gene duplications and the acquisition and retention of CypA fusions that can have antiretroviral functions. Paralogous expansion of a gene or a gene family can have a variety of effects including increased gene expression levels or gain of a new function36. In the case of rodent Trim5, such gene duplications have produced Trim5 loci in different lineages that differ in the number and organization of Trim genes. Evolutionary modification of Trim5 genes also include multiple TRIMCyp fusions in primates and also in tree shrews, and here we show that rodents make similar use of the same evolutionary mechanism to produce antiviral genes. This type of convergent evolution in different taxa may reflect responses to similar environmental challenges, especially increases in endogenous or exogenous retroviral activity. The fact that the products of these parallel gene amplification and fusion events are fixed in different lineages supports their having a positive effect on species fitness.
Notably, the Trim gene amplification in the Trim5 cluster of the rodent species we examined is limited to Trim5, while Trim6 and Trim34 tend to remain single copy genes. Olfr genes, the largest known gene family in mammals37, flank both sides of the Trim5 cluster and inserted into the Trim5 cluster in some species (Fig. 1). In addition, multiple copies of the members of the ubiquilin gene family are found in this locus38 (Fig. 1). The paralogous expansion of multiple unrelated gene families in the same genomic locus suggests that recombination driven expansion of one gene family may have facilitated the expansion of the others. Thus, it is possible that in various rodent lineages the Trim5 clade of genes may have been expanded due to their genomic proximity to the Olfr and ubiquilin genes and these duplicated genes may have been fixed in the genome due to selection pressure from unknown retroviruses.
In several members of the family Cricetidae we found one or more copies of the genes belonging to the Trim5 clade far upstream of Trim6, separated by multiple copies of olfactory receptors and ubiquilin genes (Fig. 1). Unexpectedly, the paralogous genes from the same species clustered together in the phylogenetic trees rather than with their orthologs (Figs 2, 3). This finding indicates that either these expansions happened in a common ancestor of these species followed by gene conversion events after speciation or that comparable duplications happened independently in various lineages. Our analysis of the genomic assembly of these species also suggests that the duplicated Trim30 genes that are far upstream remained intact and not pseudogenized throughout the evolution of this lineage. This implies that some manner of selection pressure was exerted on these genes either by exposure to various retrovirus challenges over millions of years or they have retained the cellular function of the original Trim5 gene.
In this study, we also describe the first chimeric TrimCyp fusion genes outside of primates and tree shrews20,22,23,24,26,28. Our genome analyses identified TrimCyp fusion genes in three rodent lineages, three species in the genus Peromyscus, the species O. degus and M. ochrogaster. The CypA insertion found in the Trim5 cluster of all of these lineages seem to be the result of a LINE-1 mediated retrotransposition of CypA close to the 3′ end of a Trim5-like gene (Fig. 5 and data not shown). The TrimCyp gene we discovered in the Trim5 cluster of M. ochrogaster differs from what we found in other rodent lineages in that this CypA gene is located about 10 kb away from the end of the exon 8 of the Trim30c gene of M. ochrogaster (Fig. 1). While we do not know if a fusion protein is made, a similar CypA retrotransposition was previously identified more than 10 kb away from the TRIM5 gene in old world monkeys and gibbons27. That study identified an alternatively spliced TrimCyp in several species27. Even though NCBI’s annotation algorithm did not include CypA in the Trim5 cluster of M. ochrogaster as part of a TrimCyp gene, it is possible that this represents another independent evolution of a TrimCyp gene in the order Rodentia. In the genus Peromyscus, the CypA insertion into the Trim5 locus is found in the same orthologous location in three species, P. maniculatus, P. leucopus and P. polionotus, suggesting that the retrotransposition event happened in an ancient common ancestor. The fact that we were unable to find a CypA sequence in this location in the genome of P. californicus indicates that either the CypA retrotransposition happened only after these species diverged, or that the CypA sequence was lost in P. californicus.
Previous studies identified at least 5 independent retrotranspositions of CypA into the TRIM5 locus in primates20,22,27,28 as well as a pseudogenized TrimCyp fusion gene in fish genomes39. Moreover, a preliminary BLAST search of the annotated mammalian genomes housed in the NCBI database using the ORF of P. maniculatus TrimCyp as a probe revealed the presence of another TrimCyp fusion gene in the species Sorex araneus (European shrew) (data not shown). Combined with the three independent CypA insertions we found in rodents, these findings suggest that periodic selective pressures likely acted on these species leading to the fixation of the CypA sequence in the Trim5 locus.
Our results also revealed that the ectopic expression of the TRIMCyp fusion protein from P. maniculatus had an inhibitory effect on HIV-1, while the splice variant TRIMSPRY containing the same R-B-CC domains had no effect (Fig. 7b). Both CypA and SPRY domains of this TRIM5 variant seem to have been maintained in multiple species in the genus Peromyscus for at least 2–5 million years30,31. Moreover, the genomic sequence of P. maniculatus reveals the presence of several other Trim5-like genes in this region (Fig. 1). Since we found that both TRIMCyp and TRIMSPRY transcriptional isoforms are made, we cannot conclude whether one capsid recognizing domain is selected over the other in these species. It is possible that TRIMCyp isoform had a selective advantage over the TRIMSPRY isoform in a common ancestor millions of years ago based on its ability to antagonize unknown, ancient retroviruses, leading to its fixation in this lineage. Moreover, it is possible that TRIMCyp and TRIMSPRY isoforms antagonized different unknown retroviruses throughout the evolution of these species, since both isoforms remain intact.
While none of the laboratory mouse TRIM5-like proteins were previously shown to inhibit infection by any of the exogenous retroviruses tested, one previous study demonstrated that replacing the SPRY domain of mouse TRIM5 paralogs with a primate CypA led to the recognition and inhibition of the incoming HIV-1 by Trim12 but not by Trim30 variants40. Notably, this retroviral restriction function was correlated with the ability of these Trim12 and Trim30 genes to activate the innate immune promoters such as NfκB and AP-140. In contrast to these findings, we found that peroTRIMCyp expression did not activate Nf-κB or AP-1 promoters even though it had an inhibitory effect on HIV-1 infection (Figs 7, 8). It was recently shown that TRIMCyp from northern pig-tailed macaque (npmTRIMCyp), similarly does not activate Nf-κB signaling and only has a minor effect on AP-1 promoter activity35. Similar to our results for peroTRIMCyp, npmTRIMCyp was also shown to have a restrictive effect on some retroviruses but not others35. These findings suggest that the correlation between the retroviral restriction and the innate immune activation function of TRIMCyp fusion genes is likely more complicated than currently modelled or hypothesized. We also cannot rule out the possibility that peroTRIMCyp may activate other signaling pathways.
While our functional analysis focused on the TrimCyp fusion gene found in the genus Peromyscus, further analysis of the TrimCyp gene we discovered in O. degus may shed light on the function and independent evolution of this novel fusion gene. Our BLAST search of the current assembly of O. degus in the NCBI database failed to identify any SPRY sequences near any of the Trim5 paralogs in this cluster (Fig. 1). The absence of Trim5-associated SPRY domain was also observed in the genome of Cavia porcellus (guinea pig) (Fig. 1). It is important to note that we cannot rule out the possibility that the lack of detection of a Trim5 encoded SPRY domain in this locus of the genomes of guinea pig and degu may be due to errors in these genome assemblies.
This study provides an extensive genomic and phylogenetic analysis of the paralogous cluster that contains the innate immune antiretroviral gene Trim5 in rodents. Our results show that this locus has been remodeled through multiple recurrent evolutionary mechanisms in various taxa belonging to the order Rodentia, mechanisms that involved selective gene duplications and conservation of fusions resulting from CypA retrotransposition. We identify, for the first time, the multiple independent evolution of TrimCyp fusion genes in the largest order of mammals, Rodentia, at least one of which is antiviral.
Materials and Methods
Reagents and plasmids
HEK293T cells were obtained from ATCC (Manassas, VA). GP2-293 packaging cells were purchased from Clontech (Mountain View, CA). The following cells were obtained from Coriell (Camden, NJ); P. leucopus skin fibroblasts (Catalog No: AG22618), P. californicus skin fibroblasts (Catalog No: AG22620), P. polionotus lung fibroblasts (Catalog No: AG22348), P. maniculatus kidney cells (Catalog No: AG20716). Each cell line was grown in DMEM (Thermo Fisher, Waltham, MA) supplemented with 10% fetal bovine serum, 1% penicillin and 100 µg/mL streptomycin. Owl monkey prostate tissue was kindly provided by Dr. Boris Skopets (National Institutes of Health, Bethesda, MD). This study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health and the procedure to produce the owl monkey fibroblast culture was in accordance with the guidelines of the Committee of the Care and Use of Laboratory Animals under the NIAID-approved animal study protocol LMM5, which was approved by the Institutional Animal Care and Use Committee (IACUC). All experiments were approved by IACUC and conducted following the relevant guidelines and regulations.
The following plasmids were obtained from Promega (Madison, WI): pRL-TK, pGL4.32[luc2P/NF-κB-RE/Hygro], and pGL4.44[luc2P/AP1 RE/Hygro]. pEF6 – V5 TOPO and PCR 2.1 TOPO plasmids were purchased from Thermo Fisher (Waltham, MA). The pVSV-G plasmid was obtained from Clontech (Mountain View, CA). pBR HIV NL4.3 nef-IRES-Renilla Δenv plasmid was previously described41 and was a kind gift from Dr. Sumit Chanda (SBP Discovery, La Jolla, CA). pCL-MFG-LacZ was obtained from Novus Bio (San Diego, CA). Anti-V5 monoclonal mouse antibody was purchased from Thermo Fisher (Waltham, MA) (Catalog No: R960-25). Anti-Beta-actin rabbit polyclonal antibody was purchased from Sigma-Aldrich (St. Louis, MO) (Catalog No: A5060). Rabbit anti-mouse-HRP and goat anti-rabbit-HRP secondary antibodies were obtained from Southern Biotech (Birmingham, AL).
PCR and sequencing
PCRs for genomic DNA samples were performed using Amplitaq Gold (Thermo Fisher) with the following program: 95 °C for 3 min; 35 cycles of 95 °C for 30 s, 54 °C for 30 s, and 72 °C for 150 s; and 72 °C for 5 min. Primers used to screen for the presence of CypA downstream of a Trim30d gene in the genomic DNA of the Peromyscus species are shown in Supplementary Table S2. The primers designated 4 F and 4 R were used for sequencing the retrotransposed CypA that is part of the TrimCyp gene in the genomic DNA of the various Peromyscus species (Supplementary Table S2).
Reverse transcription (RT)–PCR for total RNA samples was performed using Superscript III one step RT-PCR kit (Thermo Fisher) with the following program: 55 °C for 30 min; 95 °C for 3 min; 35 cycles of 95 °C for 30 s, 55 °C for 30 s, and 72 °C for 150 s; and 72 °C for 5 min. The primers designated 5 F and 5 R were used to amplify TrimCyp cDNA from the Peromyscus species (Supplementary Table S2). PCR and RT-PCR products were analyzed by 1% agarose gel electrophoresis and cloned into the PCR 2.1 TOPO (Thermo Fisher) plasmid before sequencing. Gel images were acquired using GENE FLASH (Syngene, Frederick, MD).
DNA and RNA isolation
Genomic DNA was isolated from the Peromyscus cells using PureLink Genomic DNA Mini Kit (Thermo Fisher), according to the manufacturer’s instructions. Total RNA was isolated from Peromyscus cells and owl monkey prostate tissue using PureLink RNA Mini Kit (Thermo Fisher), following the manufacturer’s instructions.
Plasmid construction for cDNA expression
TOPO cloning strategy was used for the construction of the V5-tagged pEF6 expression plasmids. To this end, total RNA from the relevant species was subjected to RT–PCR using Superscript III One Step RT-PCR kit (Thermo Fisher) with the following primers (Supplementary Table S2): for omTRIMCyp, 6 F and 6 R; for peroTrimCyp, 7 F and 7 R. peroTrimSPRY that encodes for the same R-B-CC domain as peroTrimCyp was initially amplified using the primers 8 F and 8 R. This PCR product was then used as a template for amplification of the peroTrimSPRY CDS using the primers 8 F and 9 R. PCR products were gel extracted using QIAquick gel extraction kit (QIAGEN, Germantown, MD) and cloned into pEF6-V5 TOPO plasmid (Thermo Scientific) following the manufacturer’s instructions. This plasmid contains a C-terminal V5 tag. cDNAs were cloned in frame with the V5 tag. All plasmids were sequenced.
Genomic database search of the Trim5 locus in rodent species
CDS of Trim12c (NM_001146007), Trim34a (NM_030684) or Trim6 (NM_001013616) from the mouse reference assembly were used as probes in the initial BLAST searches of 22 annotated rodent genome assemblies housed in the NCBI database (Table 1)32,33. BLASTn searches were conducted using the following parameters: gap costs, 5 and 2 (existence and extension); match/mismatch scores, + 2/−3; repeat masking filter turned off; expect threshold, 10−20. Genomes that showed multiple BLAST hits at different scaffolds/chromosomes as well as those that contained large sequencing gaps in the specific region of the scaffold/chromosome encompassing the Trim5 cluster were excluded from further analysis. Predicted mRNA from each annotated gene in the predicted Trim5 cluster that contained one or more BLAST hits was extracted to be used in sequence alignments (Supplementary Table S1).
Sequence alignment and phylogenetics
Alignments of the CDS regions of the annotated Trim5, Trim6 and Trim34 clade of genes were done using MUSCLE as implemented in Geneious 10.0.9 using the default settings42,43. Manual adjustments were made to the alignments to remove any large indels that appeared in more than a few genes. For each gene, part of the ORF coding for the R-B-CC domains were aligned separately from the part that encodes for the SPRY domains. Predicted pseudogenes were extracted from each relevant genome using either the BLAST aligned regions or annotated RNAs as a guide. Phylogenetic grouping of pseudogenes was determined by aligning them with a subset of Trim6, Trim34 and Trim5 clade genes. Relevant regions of the CDS of human TRIM22 (NM_006074) was used in the alignments to root the phylogenetic trees. Maximum likelihood phylogenetic trees were generated using RAxML with the General Time Reversible + G + I model with 500 bootstraps for branch support44.
HEK293T cells were grown in a 12 well plate as 200,000 cells/well and transfected with 50, 150 or 500 ng of either of the following plasmids; pEF6 – omTRIMCyp – V5, pEF6 – peroTRIMCyp – V5, pEF6 – peroTRIMSPRY – V5 or pEF6 – empty. Transfections were done using Fugene HD (Promega, Madison, WI), according to the manufacturer’s instructions. 2 days after the transfections, cells were counted, and 500,000 cells were lysed using RIPA buffer (Thermo Fisher) and lysates were sonicated using Q700 sonicator (QSonica, Newtown, CT). Equal amounts of lysates were loaded to a 4–12% Bis Tris polyacrylamide gel, and immunoblotting was performed on a nitrocellulose membrane after the transfer. Images of the immunoblots were produced using ChemiDoc MP imaging system (Bio-Rad, Hercules, CA).
Virus production and infection assays
For the production of VSV-G pseudotyped, single cycle HIV-1 with Renilla luciferase reporter (HIV-RenLuc), HEK293T cells were seeded at 60% confluency in 60 mm dishes and transfected with 10 ug of pBR HIV NL4.3 nef-IRES-Renilla Δenv and 2 ug of pVSV-G plasmids using Fugene HD. 3 days after transfection, supernatant was collected and filtered through 0.45 µM filters (Millipore, Burlington, MA). For the production of VSV-G pseudotyped, LacZ reporter expressing Moloney murine leukemia virus (MLV-LacZ), GP2-293 cells were seeded at 60% confluency in 60 mm dishes and transfected with 10 ug of pCL-MFG-LacZ and 2 ug of pVSV-G plasmids using Fugene HD. 3 days post-transfection, supernatant was collected and filtered through 0.45 µM filters (Millipore).
For viral infectivity tests, HEK293T cells were transfected with 50, 150 or 500 ng of either one of the following plasmids; pEF6-empty, pEF6-omTRIMCyp, pEF6-peroTRIMCyp, pEF6-peroTRIMSPRY. 2 days later, transfected cells were counted and plated to a 96 well white bottom assay plate (Corning Costar, New York, NY) as 10000 cells/well for infection with 5 uL of filtered supernatant containing either HIV-RenLuc or MLV-LacZ. 5 µM of cyclosporine (Sigma-Aldrich) was added to the relevant wells one hour prior to infection for the infection rescue assay, while the control wells received the equivalent volume of dimethyl sulfoxide. The drugs were removed one day later. Three days post infection Renilla luciferase or LacZ reporter expression was detected using Renilla-Glo (HIV-1) or Beta-Glo (MoMLV) assay systems (Promega), respectively, according to the manufacturer’s instructions.
Dual-luciferase transfection assay
HEK293T cells were co-transfected in a 12-well plate with 10, 25 or 50 ng of either of the following plasmids pEF6-empty, pEF6-omTRIMCyp, pEF6-peroTRIMCyp together with 100 ng of either pGL4.32[luc2P/NF-κB-RE/Hygro] or pGL4.44[luc2P/AP1-RE/Hygro] using Fugene HD (Promega), according to the manufacturer’s instructions. 20 ng of pRL-TK was added to each transfection to control for transfection efficiency. 48 hours post transfection, cells were collected, and luciferase reporter activities were measured using Dual-Glo luciferase assay system (Promega).
The unpaired student’s t test was utilized to calculate statistical significance as implemented in GraphPad Prism (version 7.0).
All data generated or analyzed during this study are included in this published article and its supplementary information files. The Partial genomic DNA sequence surrounding the retrotransposed CypA gene and the complete CDS of the TrimCyp and TrimSPRY isoforms of the Trim30d gene from Peromyscus species are available in Genbank under accession numbers MK585560 to MK585565 and MN078251 to MN078253
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This study was supported by the Intramural Research Program of the National Institute of Allergy and Infectious Diseases, Bethesda, MD.
The authors declare no competing interests.
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Boso, G., Shaffer, E., Liu, Q. et al. Evolution of the rodent Trim5 cluster is marked by divergent paralogous expansions and independent acquisitions of TrimCyp fusions. Sci Rep 9, 11263 (2019) doi:10.1038/s41598-019-47720-5
Nature Microbiology (2019)