Retrotransposons and their recognition of pol II promoters: a comprehensive survey of the transposable elements from the complete genome sequence of Schizosaccharomyces pombe. Genome Res

Section on Eukaryotic Transposable Elements, Laboratory of Gene Regulation and Development, National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, Maryland 20892, USA.
Genome Research (Impact Factor: 14.63). 10/2003; 13(9):1984-97. DOI: 10.1101/gr.1191603
Source: PubMed

ABSTRACT The complete DNA sequence of the genome of Schizosaccharomyces pombe provides the opportunity to investigate the entire complement of transposable elements (TEs), their association with specific sequences, their chromosomal distribution, and their evolution. Using homology-based sequence identification, we found that the sequenced strain of S. pombe contained only one family of full-length transposons. This family, Tf2, consisted of 13 full-length copies of a long terminal repeat (LTR) retrotransposon. We found that LTR-LTR recombination of previously existing transposons had resulted in extensive populations of solo LTRs. These included 35 solo LTRs of Tf2, as well as 139 solo LTRs from other Tf families. Phylogenetic analysis of solo Tf LTRs reveals that Tf1 and Tf2 were the most recently active elements within the genome. The solo LTRs also served as footprints for previous insertion events by the Tf retrotransposons. Analysis of 186 genomic insertion events revealed a close association with RNA polymerase II promoters. These insertions clustered in the promoter-proximal regions of genes, upstream of protein coding regions by 100 to 400 nucleotides. The association of Tf insertions with pol II promoters was very similar to the preference previously observed for Tf1 integration. We found that the recently active Tf elements were absent from centromeres and pericentromeric regions of the genome containing tandem tRNA gene clusters. In addition, our analysis revealed that chromosome III has twice the density of insertion events compared to the other two chromosomes. Finally we describe a novel repetitive sequence, wtf, which was also preferentially located on chromosome III, and was often located near solo LTRs of Tf elements.

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Available from: Nathan J Bowen, Sep 28, 2015
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    • "(Fig 2A). Strikingly, transcripts from all 13 Tf2 retrotransposons and many solo LTRs dispersed throughout the three fission yeast chromosomes (Bowen et al, 2003) strongly accumulated in cay1Δ cells (Fig 2A; Supplementary Fig S2A and B). Tf2 transcript hybridization signals were increased most robustly at the flanking LTR sequences (Supplementary Fig S2A). "
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    ABSTRACT: The telomeric transcriptome comprises multiple long non-coding RNAs generated by transcription of linear chromosome ends. In a screening performed in Schizosaccharomyces pombe, we identified factors modulating the cellular levels of the telomeric transcriptome. Among these factors, Cay1 is the fission yeast member of the conserved family of Cactins, uncharacterized proteins crucial for cell growth and survival. In cay1∆ mutants, the cellular levels of the telomeric factor Rap1 are drastically diminished due to defects in rap1+ pre-mRNA splicing and Rap1 protein stability. cay1∆ cells accumulate histone H3 acetylated at lysine 9 at telomeres, which become transcriptionally desilenced, are over-elongated by telomerase and cause chromosomal aberrations in the cold. Overexpressing Rap1 in cay1+ deleted cells significantly reverts all telomeric defects. Additionally, cay1∆ mutants accumulate unprocessed Tf2 retrotransposon RNA through Rap1-independent mechanisms. Thus, Cay1 plays crucial roles in cells by ultimately harmonizing expression of transcripts originating from seemingly unrelated genomic loci.
    The EMBO Journal 11/2014; 34(1). DOI:10.15252/embj.201489559 · 10.43 Impact Factor
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    • "A fission yeast TE termed Tf1 is a retrotransposon prevailing in the specific yeast genome. Tf1 insertion predominantly occurs closer to the 5′ end of genes, in regions known to have relatively open chromatin [78,79]. These studies clearly argue for the relationships between open chromatin and preferential transposition sites. "
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    ABSTRACT: Transposable elements (TEs) are major structural components of eukaryotic genomes; however, mobilization of TEs generally has negative effects on the host genome. To counteract this threat, host cells have evolved genetic and epigenetic mechanisms that keep TEs silenced. One such mechanism involves the Piwi-piRNA complex, which represses TEs in animal gonads either by cleaving TE transcripts in the cytoplasm or by directing specific chromatin modifications at TE loci in the nucleus. Most Piwi-interacting RNAs (piRNAs) are derived from genomic piRNA clusters. There has been remarkable progress in our understanding of the mechanisms underlying piRNA biogenesis. However, little is known about how a specific locus in the genome is converted into a piRNA-producing site. In this review, we will discuss a possible link between chromatin boundaries and piRNA cluster formation.
    Mobile DNA 08/2014; 5(1):22. DOI:10.1186/1759-8753-5-22 · 2.11 Impact Factor
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    • "In compact genomes, TE insertions are usually highly targeted toward genomic regions where interference with endogenous functions is minimized. This is seen in fission yeast where LTR elements are preferentially inserted upstream of polymerase II transcribed genes (Bowen et al., 2003; Leem et al., 2008). Upon low oxygen levels, a specific transcription factor induces LTR transposition in fission yeast and in turn, transcription of downstream genes (Sehgal et al., 2007). "
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    ABSTRACT: Transposable elements (TEs) are ubiquitous in eukaryotic genomes. Barbara McClintock's famous notion of TEs acting as controlling elements modifying the genetic response of an organism upon exposure to stressful environments has since been solidly supported in a series of model organisms. This requires the TE activity response to possess an element of specificity and be targeted toward certain parts of the genome. We propose that a similar TE response is present in human cells, and that this stress response may drive the onset of human cancers. As such, TE-driven cancers may be viewed as an evolutionary by-product of organisms' abilities to genetically adapt to environmental stress.
    Frontiers in Genetics 05/2014; 5:156. DOI:10.3389/fgene.2014.00156
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