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  • 1
    Electronic Resource
    Electronic Resource
    Ancient and Recent Horizontal Invasions of Drosophilids by P Elements (2000)
    Springer
    Journal of molecular evolution 51 (2000), S. 577-586 
    Details
    ISSN: 1432-1432
    Keywords: Key words:P element — Transposon evolution — Horizontal transfer —Drosophila—Scaptomyza—Lordiphosa
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. P elements of two different subfamilies designated as M- and O-type are thought to have invaded host species in the Drosophila obscura group via horizontal transmission from external sources. Sequence comparisons with P elements isolated from other species suggested that the horizontal invasion by the O-type must have been a rather recent event, whereas the M-type invasion should have occurred in the more distant past. To trace the phylogenetic history of O-type elements, additional taxa were screened for the presence of O- and M-type elements using type-specific PCR primers. The phylogeny deduced from the sequence data of a 927-bp section (14 taxa) indicate that O-type elements have undergone longer periods of regular vertical transmission in the lineages of the saltans and willistoni groups of Drosophila. However, starting from a species of the D. willistoni group they were transmitted horizontally into other lineages. First the lineage of the D. affinis subgroup was infected, and finally, in a more recent wave of horizontal spread, species of three different genera were invaded by O-type elements from the D. affinis lineage: Scaptomyza, Lordiphosa, and the sibling species D. bifasciata/D. imaii of the Drosophila obscura subgroup. The O-type elements isolated from these taxa are almost identical (sequence divergence 〈1%). In contrast, no such striking similarities are observed among M-type elements. Nevertheless, the sequence phylogeny of M-type elements is also not in accordance with the phylogeny of their host species, suggesting earlier horizontal transfer events. The results imply that P elements cross species barriers more frequently than previously thought but require a particular genomic environment and thus seem to be confined to a rather narrow spectrum of host species. Consequently, different P element types acquired by successive horizontal transmission events often coexist within the same genome.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s002390010121
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  • 2
    Electronic Resource
    Electronic Resource
    P-related sequences inDrosophila bifasciata: A molecular clue to the understanding of P-element evolution in the genusDrosophila (1990)
    Springer
    Journal of molecular evolution 31 (1990), S. 478-484 
    Details
    ISSN: 1432-1432
    Keywords: P-element evolution ; Drosophila bifasciata ; Recent invasion hypothesis ; Horizontal gene transfer ; Sequence divergence ; Substitution rate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Two P-elements (bif1 and bif2) were isolated from a genomic library ofDrosophila bifasciata. Both elements are internally deleted and have lost the coding capacity for a functional transposase. One of the elements (bif2) contains an insert consisting of a repetitive sequence. The terminal inverted repeats and the segments necessary for passive mobility are well conserved. Element bif2 has retained rudiments of the coding sequence of exon 0 and exon 3, but the reading frame is destroyed by insertions and deletions. The comparison of theD. bifasciata P-elements with P-elements ofDrosophila melanogaster andDrosophila nebulosa reveals that the two latter sequences are more similar to each other than either of them is to theD. bifasciata elements. This finding contradicts the phylogenetic relationship of the species and can be taken as an indirect but unequivocal evidence for recent horizontal gene transfer from a relative ofD. nebulosa to the gene pool ofD. melanogaster. The P-elements ofD. bifasciata are phylogenetically ancient and have evolved independently for about 50 million years. A higher substitution rate at the third codon position as well as a predominance of conservative replacements at the amino acid level indicates that the P-elements ofD. bifasciata have been under selective constraint over a long period and that immobilization has occurred only recently.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02102074
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  • 3
    Electronic Resource
    Electronic Resource
    Transcription and Splicing Patterns of M- and O-Type P Elements in Drosophila bifasciata, D. helvetica, and Scaptomyza pallida (1998)
    Springer
    Journal of molecular evolution 46 (1998), S. 542-551 
    Details
    ISSN: 1432-1432
    Keywords: Key words:Drosophila—Scaptomyza—P element — RT-PCR — Expression — Splicing pattern
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. RT-PCR was applied to analyze the splicing patterns of P-element-derived mRNAs in Drosophila bifasciata, D. helvetica, and Scaptomyza pallida. D. melanogaster was used as a control. The experiments revealed that P elements are transcribed in all species investigated. However, there are differences in the splicing patterns of IVS3, which has to be removed in order to produce transposase mRNA instead of repressor mRNA. These differences are observed among species as well as between the P element subfamilies, the M and the O type, which coexist in the genomes of D. bifasciata and S. pallida. In D. helvetica M-type transposase mRNA was found in the germline and repressor mRNA in the soma, as has been previously described for the canonical (M-type-related) P element of D. melanogaster. In contrast, in S. pallida only repressor mRNA of M-type elements was detected in all tissues. In D. bifasciata, M-type IVS3, although activated both in the soma and the germline, is never completely excised. Instead, two alternative double-spliced variants occur in which two small introns are removed within the IVS3 region. One of these variants codes for a protein 12 aa longer than the regular transposase. Taking these findings together, transposase production and transpositional activity of M-type elements seem to be limited to D. helvetica and D. melanogaster, whereas M-type elements have become immobile in D. bifasciata and S. pallida. Unlike the M type, the splicing of O-type transcripts in D. bifasciata and S. pallida follows the classical rules of tissue-specific P element regulation: transposase mRNA is produced exclusively in the germline whereas repressor mRNA is formed in somatic cells. Thus O-type elements are thought to be still transpositionally active in both species. This finding is in accordance with the postulated recent transfer of O-type elements between the gene pools of D. bifasciata and S. pallida. In addition, we were able to show that the IVS3 double-spliced variants of both P element types are produced regularily in all species of the genus Drosophila investigated so far, but not in S. pallida.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/PL00006335
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  • 4
    Electronic Resource
    Electronic Resource
    Repetitive sequences in the genome ofAnemone blanda: Identification of tandem arrays and of dispersed repeats (1993)
    Springer
    Chromosoma 102 (1993), S. 312-324 
    Details
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract A tandemly repetitive sequence family (AbS1) and a repetitive sequence (Hd) forming part of a larger dispersed element (dorf-1) ofAnemone blanda were characterised. TheAbS1 satellite sequence family is located in all 4′,6-diamidino-2-phenylindole (DAPI) positive intercalary heterochromatic bands and in the DAPI positive heterochromatic terminal region of chromosome 3, while the dispersedHd homologous sequences are preferentially associated with euchromatic chromosome regions. The major component of theAbS1 satellite isAbS1-H1 with a basic repeat unit of 1640 bp; a minor fraction (AbS1-H5) consists of 320 bp units. A subsection of theAbS1-H1 repeat unit exhibits homologies to the 25S rRNA gene of flowering plants suggesting that the 1.64 kb satellite was generated by amplification of a precursor satellite and/or single copy sequence together with an rDNA fragment. The rDNA homologous region is considered to evolve at a rate similar to pseudogenes and thus the age of this satellite DNA fraction can be roughly estimated as about 27 million years. The dispersed repeated sequenceHd (about 1300 bp) is associated with the 8 kb elementdorf-1. A. blanda dorf-1 constitutes about 0.2% of the genome (3×104 copies), is bounded by identical long terminal repeats, and exhibits partial homology to theLilium gypsy-type elementdell, but has yet to be confirmed as a retrotransposon. In contrast to theAbS1 satellite sequence family,Hd homologous sequences were found not only inA. apennina, the closest relative ofA. blanda, but also inA. nemorosa andA. ranunculoides indicating that a progenitor sequence ofdorf-1 was present in a common ancestor before speciation ocurred.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00661274
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  • 5
    Electronic Resource
    Electronic Resource
    Two distinct P element subfamilies in the genome of Drosophila bifasciata (1994)
    Springer
    Molecular genetics and genomics 244 (1994), S. 168-175 
    Details
    ISSN: 1617-4623
    Keywords: P element ; Transposon phylogeny ; Horizontal transfer ; Inverted repeats ; Drosophila bifasciata
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The genome of Drosophila bifasciata harbours two distinct subfamilies of P-homologous sequences, designated M-type and O-type elements based on similarities to P element sequences from other species. Both subfamilies have some general features in common: they are of similar length (M-type: 2935 bp, O-type: 2986 bp), are flanked by direct repeats of 8 by (the presumptive target sequence), contain terminal inverted repeats, and have a coding region consisting of four exons. The splice sites are at homologous positions and the exons have the coding capacity for proteins of 753 amino acids (M-type) and 757 amino acids (O-type). It seems likely that both types of element represent functional transposons. The nucleotide divergence of the two P element subfamilies is high (31%). The main structural difference is observed in the terminal inverted repeats. Whereas the termini of M-type elements consist of 31 by inverted repeats, the inverted repeats of the O-type elements are interrupted by non-complementary stretches of DNA, 12 by at the 5′ end and 14 by at the 3′ end. This peculiarity is shared by all members of the O-type subfamily. Comparison with other P element sequences indicates incongruities between the phylogenies of the species and the P transposons. M-type and O-type elements apparently have no common origin in the D. bifasciata lineage. The M-type sequence seems to be most closely related to the P element from Scaptomyza pallida and thus could be considered as a more recent invader of the D. bifasciata gene pool. The origin of the O-type elements cannot be unequivocally deduced from the present data. The sequence comparison also provides new insights into conserved domains with possible implications for the function of P transposons.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00283519
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