AI Article Synopsis

  • 3' untranslated regions (UTRs) in eukaryotes are crucial for controlling gene expression after transcription, with their regulation occurring during the processing of pre-mRNA.
  • Using 3P-Seq technology, researchers analyzed the genome of Schmidtea mediterranea to pinpoint about 14,000 3'UTRs and enhance gene annotations.
  • The study revealed that around 40% of transcripts undergo alternative polyadenylation, affecting protein coding and expression patterns, which may be significant for understanding how planarians regenerate and manage stem cell functions.

Article Abstract

In eukaryotes, 3' untranslated regions (UTRs) play important roles in regulating posttranscriptional gene expression. The 3'UTR is defined by regulated cleavage/polyadenylation of the pre-mRNA. The advent of next-generation sequencing technology has now enabled us to identify these events on a genome-wide scale. In this study, we used poly(A)-position profiling by sequencing (3P-Seq) to capture all poly(A) sites across the genome of the freshwater planarian, Schmidtea mediterranea, an ideal model system for exploring the process of regeneration and stem cell function. We identified the 3'UTRs for ∼14,000 transcripts and thus improved the existing gene annotations. We found 97 transcripts, which are polyadenylated within an internal exon, resulting in the shrinking of the ORF and loss of a predicted protein domain. Around 40% of the transcripts in planaria were alternatively polyadenylated (ApA), resulting either in an altered 3'UTR or a change in coding sequence. We identified specific ApA transcript isoforms that were subjected to miRNA mediated gene regulation using degradome sequencing. In this study, we also confirmed a tissue-specific expression pattern for alternate polyadenylated transcripts. The insights from this study highlight the potential role of ApA in regulating the gene expression essential for planarian regeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5068929PMC
http://dx.doi.org/10.1534/g3.116.031120DOI Listing

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