4.4 Article

Genome-wide analysis of poly(A) site selection in Schizosaccharomyces pombe

Journal

RNA
Volume 19, Issue 12, Pages 1617-1631

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.040675.113

Keywords

polyadenylation; transcription termination; RNA-Seq; genome-wide; fission yeast

Funding

  1. King Abdullah University of Science and Technology (KAUST) [KUK-C1-013-04]
  2. Engineering and Physical Sciences Research Council
  3. L'Oreal/UNESCO Woman in Science UK and Ireland award
  4. MRC Career Development Award
  5. Wellcome Trust Senior Investigator Award
  6. Wellcome Trust programme grant
  7. European Research Council [239870]
  8. Royal Society
  9. Brasenose College, University of Oxford
  10. Nicholas Kurti Junior Fellowship
  11. Leverhulme Trust Philip Leverhulme Prize
  12. European Research Council (ERC) [239870] Funding Source: European Research Council (ERC)
  13. Medical Research Council [MR/K006606/1] Funding Source: researchfish
  14. MRC [MR/K006606/1] Funding Source: UKRI

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Polyadenylation of pre-mRNAs, a critical step in eukaryotic gene expression, is mediated by cis elements collectively called the polyadenylation signal. Genome-wide analysis of such polyadenylation signals was missing in fission yeast, even though it is an important model organism. We demonstrate that the canonical AATAAA motif is the most frequent and functional polyadenylation signal in Schizosaccharomyces pombe. Using analysis of RNA-Seq data sets from cells grown under various physiological conditions, we identify 3' UTRs for nearly 90% of the yeast genes. Heterogeneity of cleavage sites is common, as is alternative polyadenylation within and between conditions. We validated the computationally identified sequence elements likely to promote polyadenylation by functional assays, including qRT-PCR and 3' RACE analysis. The biological importance of the AATAAA motif is underlined by functional analysis of the genes containing it. Furthermore, it has been shown that convergent genes require trans elements, like cohesin for efficient transcription termination. Here we show that convergent genes lacking cohesin (on chromosome 2) are generally associated with longer overlapping mRNA transcripts. Our bioinformatic and experimental genome-wide results are summarized and can be accessed and customized in a user-friendly database Pomb(A).

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