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Genetics, Vol. 175, 441-452, January 2007, Copyright © 2007
doi:10.1534/genetics.106.064360
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,1
* Institut de Génétique et Microbiologie, Université Paris-Sud, UMR8621, F-91405 Orsay, France, Laboratoire Evolution, Génomes et Spéciation, Centre National de la Recherche Scientifique, FR-91198 Gif-sur-Yvette, France, Wageningen University and Research Center, Plant Research International B.V., 6700 AA Wageningen, The Netherlands and Institut Jacques Monod, Universités Paris 6 et 7, UMR7592, 75251 Paris, France
2 Corresponding author: Institut de Génétique et Microbiologie, Bât 400, Université Paris-Sud, F-91405 Orsay Cedex, France.
E-mail: marie-jose.daboussi{at}igmors.u-psud.fr
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ABSTRACT |
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 TOP ABSTRACT MATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEDGEMENTSLITERATURE CITED |
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More recently, a link between MITE families and well-characterized DNA transposons, belonging mainly to the Tc1-mariner superfamily (FESCHOTTE et al. 2002), has been established on the basis of TIRs and TSD sequence similarities, supporting the idea that MITEs are a particular type of nonautonomous class II transposons. However, the origin of these short elements is still unclear: some exhibiting extended regions of similarity with full-length elements may have originated by internal deletions; others with homology limited to the TIRs or to terminal regions may originate de novo by capture of DNA sequences between the TIRs.
The classification of MITEs within class II TEs also implies that they are mobilized by a transposase from autonomous members of their own (or a related) family by a cut-and-paste mechanism. The recent studies on a rice MITE (JIANG et al. 2003; KIKUCHI et al. 2003) confirmed the cut-and-paste mechanism and indicated that amplification could be influenced by specific (environmental or genomic) conditions (JIANG et al. 2003; SHAN et al. 2005). However, although putative autonomous partners have been proposed for several MITE families, a clear demonstration that they are indeed necessary for MITE transposition is still lacking.
In Fusarium oxysporum, numerous DNA transposon families have been identified, mainly by trapping into a target gene or sequencing of some genomic regions (DABOUSSI and LANGIN 1994; HUA-VAN et al. 2000; DABOUSSI and CAPY 2003). Autonomous members of the Tc1-mariner superfamily have been identified: Fot1 is a pogo-like element that may be present in a relatively high copy number (
100 copies), essentially full-length copies (DABOUSSI et al. 1992; MIGHELI et al. 1999); impala is a representative of the Tc1 family (ROBERTSON 2002) present in low copy number and composed of at least five different subfamilies (E, D, F, K, and P) (HUA-VAN et al. 2001a). Two of these (E and D) contain autonomous members presenting up to 20% divergence at the DNA level (HUA-VAN et al. 1998, 2001b). By sequencing genomic regions surrounding copies of the D subfamily, five elements of 200 bp were identified. These elements, called mimp, have no coding capacity but display TIRs very similar to those of impala (HUA-VAN et al. 2000). We wondered whether these short elements are mobile and, if so, whether they could be transactivated by an impala transposase. Here we show that the mimp1 family is present in a number of related species and that its distribution follows the distribution of impala. Using a phenotypic excision assay in two different species, we demonstrate that they are trans-mobilized by the impala transposase and that transposition occurs through a cut-and-paste mechanism. The functionality of the double-component system in the heterologous species F. graminearum, the genome sequence of which is available, provided the opportunity to analyze the insertion site preference of newly transposed copies. Preliminary results suggest that this system is an interesting alternative tool for gene tagging in filamentous fungi.
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MATERIALS AND METHODS |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEDGEMENTSLITERATURE CITED |
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Plasmids:
pHEO62 contains the ORF encoding the impalaE transposase (HUA-VAN et al. 1998), cloned between the gpdA promoter and the trpC terminator of Aspergillus nidulans. The entire cassette was extracted from plasmid pEO62 (LI DESTRI NICOSIA et al. 2001) as an EcoRI/HindIII fragment and cloned into plasmid pBC1004 (CARROLL et al. 1994), which permits hygromycin selection. pNm1H18 was constructed by introduction of a mimp1 element into the first intron of the niaD gene (Figure 3). This mimp1 copy corresponds to the reamplification of the mimp1.1 element (AF076624) using the HindImp primer (5'-GCCCTAAGCTTACAGTGGGGTGCAATAAGTTTG-3'). This primer anneals to the TIRs of mimp1 and impala and contains a HindIII site (underlined) at the 5'-end. PCR conditions were 1 min denaturation at 95°, followed by 30 cycles of 1 min at 94°, 1 min at 59°, and 30 sec at 72°, and then an elongation step of 10 min at 72°. The PCR product was then digested with HindIII and inserted into the HindIII site of the first intron of the niaD gene in plasmid pAN301 (MALARDIER et al. 1989), deleted from a dispensable NdeI fragment (in which a NdeI fragment located downstream of the niaD gene has been removed), resulting in the niaD::mimp1 construct.
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Revertant selection:
Spores of cotransformants were recovered by washing and filtration from a single spore culture grown on solid medium and spread at different dilutions on nitrate minimal agar medium supplemented with triton X100 (0.06%) as previously described (HUA-VAN et al. 2001b). Alternatively, plugs of each cotransformant were picked on plates of nitrate minimal agar medium. Revertants are easily detected as patches of aerial mycelium with a wild-type phenotype on a background of sparse mycelium corresponding to a niaD mutant (Figure 4).
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100 µl of glass beads (200- to 500-µm diameter, Fisher Scientific, Illirch, France), the mycelium was ground using the Fastprep101 machine (twice for 30 sec at 4000 rpm). DNA was purified by successive extractions using phenol, phenol/chloroform (1/1), and chloroform and then precipitated by adding 1/20 vol 3 M sodium acetate and 0.6 vol isopropanol. After a washing step in 70% ethanol and drying, genomic DNA was resuspended in sterile distilled water plus RNAse A at a final concentration of 1 mg/ml and incubated 1 hr at 37° for RNA digestion. Ten micrograms of genomic DNA was digested with EcoRI or XbaI, separated electrophoretically on 0.7% agarose gels, and transferred on nylon membranes, using a vacuum blotter. DNA templates were 32P-labeled using the redi primeII kit (Amersham Biosciences). Hybridizations were conducted under standard conditions (SAMBROOK et al. 1989).
Polymerase chain reaction and primer sequences:
Hybridization probes were obtained by PCR. Primers SpeE3 and SpeE5 (HUA-VAN et al. 2001a) were used to generate a PCR product corresponding to impala elements of the E subfamily, with 50 ng of genomic DNA from the FOM24 strain as a template. PCR conditions were as described in HUA-VAN et al. (2001a). The HindImp primer was used, as described above, to generate either PCR products from different genomic DNAs (see Figure 1D) or the mimp1 PCR product used as a probe. The 419-bp niaD probe was generated with primers niaCG1 (5'-CACTAGTATGTGCAGGCAAC-3') and niaCG2 (5'-TTCAGCCACTTGACACTG-3'), using the pAN301 plasmid as a template. PCR conditions were as follows: 2 min at 94°, then 30 cycles of 30 sec at 94°, 30 sec at 59°, and 2 min at 72°.
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mimp1 amplification in different strains was obtained using primer mi1 (5'-TACAGTGGGATGCAATAAGTTTGAATAC-3') located within TIRs, alone or in combination with primers SacR (5'-CTGAGGAGGGAGCTCGATCTAGCC-3') or SacF (5'-GGCTAGATCGAGCTCCCTCCTCAG-3'). A denaturation step of 3 min at 95° followed by 35 cycles of 30 sec at 95°, 30 sec at 59°, 1 min at 72°, and a final extension of 5 min at 72° was used.
Characterization of the FO5 endogenous mimp1 copy was performed using the HindImp primer alone or in combination with SacR or SacF. PCR conditions were 5 min at 95° and then 45 cycles of 1 min at 94°, 1 min at 59°, and 1 min at 72° and a final elongation step of 10 min at 72°.
Excision events were controlled by PCR on 50 ng of genomic DNA of putative revertants and of the corresponding transformants, using primers niaD144 (5'-GTTCATGCCGTGGTCGCTGC-3') and niaD754r (5'-AGTTGGGAATGTCCTCGTCG-3') under the following conditions: 4 min at 94° and then 30 cycles of 1 min at 94°, 1 min at 59°, and 2 min at 72°. The sizes of the expected PCR products are 717 bp for a transformant and 485 bp for a revertant.
Amplification of mimp1 flanking sequences:
Two approaches were used to recover mimp1 flanking sequences. For nonsequenced Fusarium strains, inverse PCR was performed. A 100-ng aliquot of genomic DNA of a given strain was digested with either one or two restriction enzymes at 37° during 30 min. The enzymes were then inactivated by incubation at 65° for 10 min. A total of 30 ng of the digested DNA was self-circularized during 30 min at room temperature using T4 DNA ligase (Biolabs) in a final volume of 10 µl. The ligase was then inactivated by incubation at 65° for 10 min. Approximately 7.5 ng of ligated DNA was used in PCR experiments with the primers Div149 (5'-GCAGGCTAAACTCCAAATAGGC-3') and Div53 (5'-GTAGCGTGGCTCAAAGAGGC-3'), which correspond to internal regions of the canonical mimp1 element and are directed toward the TIRs. The amplification program was as follows: a denaturation step of 1 min at 95° and then 1 min at 94°, 45 sec at 58°, and 4 min at 72° for 35 cycles, followed by an elongation step of 10 min at 72°.
For revertants from the F. graminearum genetic background, mimp1 flanking sequences were recovered using a modified thermal asymetric interlaced (TAIL)–PCR approach.(LIU and WHITTIER 1995). Two rounds of PCR were performed on 50 ng of genomic DNA of the revertants. In the primary PCR, the arbitrary degenerate (AD) primer AD2, 5'-AG(A/T)GNAG(A/T)ANCA(A/T)AGA-3', and the specific primer m1Div53F, 5'-GCCTCTTTGAGCCACGCTAC-3', were used with reduced-stringency and high-stringency annealing temperatures of 44° and 66°, respectively. The secondary PCR was set up on 2 µl of a 1/100 dilution of the primary PCR, using the same AD primer and Div149 (see above) as the second specific primer. The annealing temperatures were the same as for the primary PCR. PCR programs were as described in LIU and WHITTIER (1995).
Cloning of PCR products and DNA sequencing:
PCR products were directly cloned into the pGEM-T Easy vector (Promega, Madison, WI) using 3 µl of either rough or purified PCR products, following the manufacturer's instructions. Sequencing of PCR products cloned into the pGEM-T Easy vector was performed by Genome Express (Meylan, France) using an ABI Big Dye terminator kit (Perkin-Elmer, Norwalk, CT) and the universal M13/pUC sequencing primer (–20) (forward) and pR primer (5'-GGAAACAGCTATGACCATG-3'; reverse).
Sequence analysis:
Multiple alignments were performed using Clustal W (THOMPSON et al. 1994) and slightly modified at both 5'- and 3'-ends for improvement. The parsimony analysis was realized on 179nt using PAUP4.0b10 (SWOFFORD 2002) with default parameters. The bootstrap analysis comprised 100 replicates. The potential of the sequences to form stable secondary structures was analyzed with the RNAFOLD program (http:www.infobiogen.fr) using standard parameters. Searches for matches of nucleotide sequences in the current database (nonredundant GenBank) or in the F. graminearum Genome Database available at the Munich Information Center for Protein Sequences (MIPS) (http://mips.gsf.de/genre/proj/fusarium/) used the BlastN or BlastX algorithms (ALTSCHUL et al. 1997).
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RESULTS |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEDGEMENTSLITERATURE CITED |
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220 bp), the lack of coding capacity, and the presence of short terminal inverted repeats of 27 bp (Figure 1A). They have been grouped into two subfamilies (mimp1 and mimp2) on the basis of an absence of internal sequence homology. The mimp TIRs present a strong similarity with the first 27 nt of impala ends (Figure 1B), a F. oxysporum Tc1-like family organized in different subfamilies (HUA-VAN et al. 1998, 2001b). Furthermore, mimp are flanked by TA dinucleotides, as is impala, which presumably correspond to the target duplication generated upon integration. Apart from the TIRs, no obvious sequence similarities were found between mimp and impala, or between mimp and any other known repetitive element. To gain insight into the structure and the evolution of the mimp1 family, we used a PCR approach to investigate sequence and size variability of mimp1 elements in different genetic contexts belonging to the Fusarium genus. Primers located in the TIRs were first used and allowed amplification of fragments of different sizes in several strains. It was then determined that the larger ones (>220 bp) corresponded to full-length (1300 bp) or internally deleted (400–600 bp) impala (Figure 1C, top, lanes 4 and 5) while the 220-bp product was mimp1 amplicon. In contrast, the use of mimp1-specific primers (see MATERIALS AND METHODS) under the same conditions each time revealed only the expected 197-bp PCR product (Figure 1C, bottom).
In addition to the uniformity in size of the different amplified full-length copies, the mimp1 family also contains some truncated elements at either the 5'- or the 3'-end. Indeed, three truncated copies were previously identified (HUA-VAN et al. 2000). In this analysis, we obtained one other truncated copy among 18 independent inverse-PCR products recovered from different species (data not shown).
A total of 37 new mimp1 sequences were obtained either by sequencing of FOM24 genomic clones (6) or by PCR (31) for other strains, including 12 from various strains of F. oxysporum and 19 from other closely related species. The latter ones were obtained using a combination of specific internal and TIR primers. These sequences corresponded to 23 different nucleotide sequences that were aligned with the four known mimp1 sequences and a sequence retrieved from the GenBank database (AJ608703). The nucleotide differences calculated on 179 internal nucleotides (excluding the primer sequences) ranged from 0 to 20% within species as well as between species. This relatively high sequence identity has allowed us to perform a conventional phylogenetic analysis. A tree deduced from this alignment permits us to define clearly only one well-supported clade, containing sequences closely related mainly from FOM24. Others were more scattered and did not show clustering according to the species (data not shown).
Finally, the mimp1 nucleotide sequence showed a strong potential to form a stable secondary structure (see Figure 1D). Although some exceptions exist (BUREAU et al. 1996), a number of MITE elements display this property. The mimp1 predicted a 
G0 value of –87.7 kcal/mol that corresponds to the lowest values reported for other families (BUREAU and WESSLER 1994a; CASACUBERTA et al. 1998).
In conclusion, the mimp1 elements showed an inverted terminal repeated structure that was able to fold into a stable secondary structure. The family appears homogeneous in size, in contrast with most nonautonomous elements such as internally deleted impala. The sequence of the TIRs (similar to those of impala) and of the TSD indicated a relationship with the Tc1-mariner superfamily of class II transposons, a group known to be associated with numerous MITE families (FESCHOTTE et al. 2002).
Copy number and genomic representation in the Fusarium genus:
We first examined mimp1 distribution in a wide collection of strains of the Fusarium oxysporum complex (FOC), previously studied for the presence of different TEs (HUA-VAN et al. 2001a; DABOUSSI et al. 2002; CHALVET et al. 2003). This analysis was extended to different Fusarium species either phylogenetically closely related to FOC (BAAYEN et al. 2001; SKOVGAARD et al. 2003) or more distantly related.
Southern blot experiments performed on 16 FOC strains, representative of seven formae speciales and one nonpathogenic strain, revealed that all contained mimp1 elements (Figure 2; data not shown). mimp1 was also detected in the three strains from FOC-related species (Figure 2, lanes 2–4), but not in more distant species (Figure 2, lane 1; data not shown).
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The TIR similarity of mimp1 and impala elements suggests that mimp1 could use the impala transposase to move and multiply. To clarify the functional relationship between mimp1 and impala, the presence of impala, the putative autonomous partner of mimp1, was also investigated in these genomes. The membranes used to detect mimp1 were thus hybridized with an impala probe allowing the detection of the impala E subfamily (see MATERIALS AND METHODS). As observed for mimp1, the distant species appeared to be devoid of impala. In all the strains containing mimp1 elements, impala signals were observed except in FO5 (Figure 2, lane 10). Beyond the absence of impala signal, this context was already shown to lack any impala activity (HUA-VAN et al. 2001b). We attempted to explain the unique faint mimp1 hybridization signal by conducting PCR experiments. No amplification was obtained using specific TIR primers, even with extended elongation time. Using a combination of specific internal and TIR primers, only the 3' part could be amplified (data not shown), indicating that the mimp1-hybridizing band in FO5 likely corresponds to a truncated copy. Moreover, the corresponding sequence showed only one nucleotide difference with the mimp1 consensus sequence (>59 positions). The weakness of the hybridization signal in FO5 could thus reflect the truncation of this copy rather than a high sequence divergence.
Hence, mimp1 and impala seem to exhibit a similar distribution within the Fusarium genus except in the FO5 strain.
Mobilization of mimp1 by an autonomous impala element:
Given TIR and target-site similarities between mimp1 and impala, as well as the presence of mimp1 in strains containing impala elements, it was tempting to speculate that the nonautonomous mimp1 elements could be mobilized by the transposase encoded by an autonomous impala element (MIGHELI et al. 1999; HUA-VAN et al. 2001b; CHALVET et al. 2003). To test this hypothesis, we performed a phenotypic assay for excision, previously used to demonstrate transposition of different TEs (MIGHELI et al. 1999; HUA-VAN et al. 2001b; CHALVET et al. 2003). To this end, we constructed a plasmid, pNm1H18, in which a mimp1 element was inserted within the first intron of the niaD gene, leading to a nonfunctional gene (see MATERIALS AND METHODS and Figure 3). This construct was introduced in three genetic backgrounds, which contained or lacked an impala source of transposase. The strain FOM150 nia9 contains different autonomous impala copies, and this context has been already used to verify the mobility of defective impala copies (HUA-VAN et al. 2001b). Three [nia–] transformants carrying pNm1H18 yielded Nia+ revertant colonies (1–5/plate). Southern blot and PCR analyses performed on a sample of Nia+ colonies revealed that mimp1 is mobile and has been excised from niaD (data not shown). The excision events were confirmed by the presence of excision footprints at the empty sites (Table 1). The FO5 nia13 context is devoid of all types of TEs previously identified within the FO complex (MIGHELI et al. 1999; HUA-VAN et al. 2001b; CHALVET et al. 2003). From seven transformants in which pNm1H18 was introduced alone, very few Nia+ colonies were observed (<1 colony/plate). Of the three recovered, only one showed an empty site, but sequencing revealed a 5-nt deletion instead of a typical footprint of two to five additional nucleotides (Table 1); the two others still showed the mimp1 copy into the niaD intron. When plasmid pNm1H18 was introduced into the same genetic background, together with the plasmid carrying the impalaE transposase under the control of a strong promoter, we obtained 6 cotransformants, 5 of them giving numerous Nia+ colonies (5–50/plate, see Figure 4). The remaining cotransformant gave very few Nia+ colonies, none of them resulting from mimp1 excision but more likely from reversion of the endogenous nia gene, as previously observed (MIGHELI et al. 1999; HUA-VAN et al. 2001b; CHALVET et al. 2003). In the F. graminearum genetic background, similar results were observed. A total of 11 transformants carrying the pNm1H18 alone were obtained. None of them gave rise to Nia+ colonies even after 6 weeks of growth on nitrate minimal agar medium. On the contrary, among 41 cotransformants carrying the pNm1H18 plasmid, together with the pHEO62 plasmid carrying the exogenous source of impala transposase, 33 gave rise to Nia+ colonies, the number varying from 4 to 20/petri dish (data not shown).
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91% (10/11) of the revertants analyzed.
Similarly, the molecular analysis of 12 revertants derived from two independent cotransformants from the Fg820nia background was performed. Hybridization with the impE probe showed that each strain contains at least one intact copy of the construct carrying the source of transposase as shown by the presence of a 4.8-kb hybridizing XbaI fragment (Figure 5B, top). Additional bands were observed, corresponding most likely to a disrupted copy of the same plasmid. The presence of a single 1.7-kb hybridization band using the niaD probe demonstrated that all correspond to an excision event (Figure 5B, middle). Another set of 12 revertants, each derived from a different transformant, was used to examine the presence of excision footprints at the empty site. Typical excision footprints were found in all cases (Table 1). Using the mimp1 element as a probe, reinsertion was observed in 83% (10/12) of the strains analyzed. These results tend to confirm that the reinsertion frequency appears higher than that observed for impala, which is in the range of 50–75% (MIGHELI et al. 2000; HUA-VAN et al. 2001b).
Molecular analysis of mimp1 insertion sites:
Previous studies indicate that some MITE families insert preferentially into genic regions (MAO et al. 2000; ZHANG et al. 2000) and/or have a propensity to insert into each other, giving nested structures (JIANG and WESSLER 2001). In addition, for a given family, the distribution of ancient vs. recently inserted elements with respect to predicted genes can vary (SANTIAGO et al. 2002), suggesting that selection can also shape the genomic distribution of MITEs.
To obtain data on the target-site preference of mimp1 elements, the regions flanking different mimp1 elements were cloned by inverse polymerase chain reaction (IPCR) or TAIL–PCR, sequenced, and used to seek homologies in databases. For those giving a match, we calculated the distance to putative initiator ATGs or stop codons of the closest predicted genes. Two types of mimp1 insertions were considered: (i) elements originally present in the genome of formae speciales of F. oxysporum or different Fusarium species closely related to the FOC and (ii) newly inserted elements either in the FO5 or in the Fg820 backgrounds, resulting from the mobilization of the mimp1 copy by the impala E transposase, totaling 43 mimp1-insertion sites.
The four copies of mimp1 previously identified in FOM24 (mimp1.1-mimp1-4) had been found in transposon nests (HUA-VAN et al. 2000). From 18 other ancient insertions analyzed, 10 clones yielded no significant hits in the databases, 7 showed high homology with known transposable elements (Table 2), and 1 corresponded to the insertion of mimp1 in the 5'-untranslated region of a fungal gene, very close to the putative start codon (Table 2). It is interesting to note that in three cases mimp1 was found close to F. oxysporum solo-LTR Han or Han-like elements, which have a strong potential to form stable secondary structures (G0 values of –70 and –55 kcal/mol, respectively).
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DISCUSSION |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEDGEMENTSLITERATURE CITED |
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By analyzing the distribution of impala and mimp1 elements across the Fusarium genus, we observed that both are widely distributed within the FOC complex, being present in closely related species and absent in more distantly related ones. The structural analysis of the mimp1 family revealed a size homogeneity but a nucleotide divergence ranging from 0 to 20%, suggesting an old, but nevertheless recently active, element.
Overall, mimp1 presented several features of MITEs except that its copy number appears unusually low. Indeed, most MITEs families in plant and animal species are associated with a high copy number (TU 1997; SANTIAGO et al. 2002), although rare examples of MITE families with moderate copy number have also been described (HOLYOAKE and KIDWELL 2003; SAITO et al. 2005). The low copy number of mimp1 could simply reflect the low activity of impala. This element itself is usually present in low copy number. Moreover, it is the representative of a basal branch of Tc1-like elements containing few members (PLASTERK et al. 1999). On the other hand, as for all fungal genomes, the genome of F. oxysporum, estimated to be in the range of 40–50 Mb (DAVIèRE et al. 2001), is very small compared to genomes in which MITEs were found in large copy numbers. Considering that the larger the genome, the higher the number of transposable elements (KIDWELL and LISCH 2002), huge amounts of TEs are not expected. This is supported by data from recently sequenced fungal genomes and other studies that reported a moderate TE content 5–10% (DEAN et al. 2005; LOFTUS et al. 2005) with a maximum of 20% for Neurospora crassa (GALAGAN et al. 2003). Finally, although a great diversity of TEs can be found (for review see DABOUSSI and CAPY 2003), few MITE families have been identified in fungi up to now, suggesting that this kind of element is not very successful in such organisms.
Although a clear relationship between mimp1 and impala was found, the origin of mimp1 remains enigmatic. The simplest hypothesis is that mimp1 was derived from impala by internal deletion. This is the case for guest, identified as a severely deleted relic of a full-length element in N. crassa (RAMUSSEN et al. 2004). Several deletion derivatives of impala were identified (HUA-VAN et al. 2001a; this work) and could always be unambiguously related to a particular impala subfamily due to the few nucleotide differences observed. The situation for mimp1 is clearly different since no homology is detectable between mimp1 and any of the impala subfamilies, except for the TIRs, implying a high selective pressure on these sequences. A de novo formation is also possible. This model supposes that new transposons can be created following the fortuitous association of TIRs bordering a segment of genomic DNA. This scenario was proposed for the origin of Ds1 (MACRAE and CLEGG 1992) and the creation a new P element in Drosophila (TSUBOTA and HUONG 1991).
Other mimp families with elements of the same size, exhibiting impala-like TIRs but with unrelated central regions, have been identified. Their analysis may help to clarify the origin of these elements.
In this study, we provide direct evidence that impala is the autonomous partner of mimp1 since transposition of mimp1 occurs only when a source of impala transposase is provided. The use of another genetic background free of active impala elements (H. C. KISTLER, personal communication), F. graminearum, confirmed the functional relationship between mimp1 and impala. Although several MITE families could be linked to elements encoding a transposase on the basis of TIRs similarities (JIANG et al. 2003; SAITO et al. 2005) and comobilization or in vitro physical interactions between the two suspected partners (FESCHOTTE et al. 2005; SHAN et al. 2005), there are very few cases of direct evidence of the mobilization of a MITE by an autonomous candidate (REZSOHAZY et al. 1997; JIANG et al. 2003; SAITO et al. 2005). The results presented here clearly connect a fungal MITE and the transposase of a Tc1-like element. This is the first functional system reported in fungi and a new example of a Tc1/mariner-related MITE.
We also show that mimp1 transposes by a cut-and-paste mechanism. The transposition mechanism of MITEs has long remained mysterious because excision was rarely observed (WESSLER et al. 1995; WESSLER 1998). Direct evidence of excision was obtained recently with the rice element mPing (KIKUCHI et al. 2003), allowing the classification of MITEs as class II elements. Our results reinforce the fact that MITEs are capable of both excision and reinsertion.
The characteristics of impala transposition, excision/reinsertion, excision footprints, and target-site duplication are retrieved for mimp1. It is noteworthy that interesting transposition specificities appeared associated to mimp1. First, the frequency of mimp1 reinsertion, >80%, appears higher than that observed for impala. Second, one-third of the newly reinserted mimp1 elements in F. oxysporum lie <500 nt from an ORF. Even more promising results were obtained in the F. graminearum strain as more than half of the reinsertion sites were shown to be located <500 nt from an ORF. The discrepancy between the two results might be due to differences between the two genomes but may also be attributed to the poor sequence availability in F. oxysporum.
Previous studies have demonstrated that MITEs are frequently found flanking many plant genes. Tourist and Stowaway have been identified in association with >100 plant genes (BUREAU and WESSLER 1992, 1994a,b). A computer-based systematic survey reveals a predominance of MITEs in wild-type rice genes (BUREAU et al. 1996). However, the association of MITEs with genes is not uniform among the different MITE families, i.e., only 10.5% for explorer, but nearly 98% for Stowaway (MAO et al. 2000). Some MITEs were found to insert into other MITEs or adjacent to other TEs (JIANG and WESSLER 2001). This is what we observed in backgrounds containing TEs where mimp1 insertions were frequently found within or adjacent to solo-LTRs, mimp, or impala elements but not to DNA transposons such as Fot1 and Hop (DABOUSSI et al. 1992; CHALVET et al. 2003), although these elements constitute a much larger fraction of the genome. One explanation could be that mimp1 amplification preceded the amplification of the TEs now found in a high copy number. Other hypotheses include preference for self-insertions or targeting through secondary structure, as proposed by JIANG and WESSLER (2001). The fact that Han, Han-like, and mimp elements all can be folded into a stable secondary structure favors this hypothesis. The difference observed between resident and newly inserted copies may result from the differential richness of the TEs or may reflect the effect of selection on ancient insertions.
In conclusion, the identification of this mobilizing MITE system offers great prospects to tag genes in filamentous fungi. First, as for the impala system, the double component mimp1/impala is expected to function in a large range of fungal species. Second, if the higher ability to reinsert in the vicinity of genes is confirmed on a larger set of revertants, this system should represent a powerful molecular tool for the functional analysis of fungal genomes.
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ACKNOWLEDGEMENTS |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEDGEMENTSLITERATURE CITED |
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FOOTNOTES |
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LITERATURE CITED |
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TOPABSTRACTMATERIALS AND METHODSRESULTSDISCUSSIONACKNOWLEDGEMENTSLITERATURE CITED |
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ALTSCHUL, S. F., T. L. MADDEN, A. A. SCHÄFFER, J. ZHANG, Z. ZHANG et al., 1997 Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25: 3389–3402.
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