Abstract
ABSTRACTTranscriptomes are dynamic, with cells, tissues, and body parts expressing particular sets of transcripts. Transposons are a known source of transcriptome diversity, however studies often focus on a particular type of chimeric transcript, analyze single body parts or cell types, or are based on incomplete transposon annotations from a single reference genome. In this work, we have implemented a method based onde novotranscriptome assembly that minimizes the potential sources of errors while identifying a comprehensive set of gene-TE chimeras. We applied this method to head, gut and ovary dissected from fiveDrosophila melanogaster natural populations, with individual reference genomes available. We found that 18.6% of body part specific transcripts are gene-TE chimeras. Overall, chimeric transcripts contribute a median of 38% to the total gene expression, and they provide both DNA binding and catalytic protein domains. Our comprehensive dataset is a rich resource for follow-up analysis. Moreover, because transposable elements are present in virtually all species sequenced to date, their relevant role in spatially restricted transcript expression is likely not exclusive to the species analyzed in this work.
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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