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Augmented annotation of the Schizosaccharomyces pombe genome revealsadditional genes required for growth and viability

  • Danny A. Bitton
  • , Valerie Wood
  • , Paul J. Scutt
  • , Agnes Grallert
  • , Tim Yates
  • , Duncan L. Smith
  • , Iain M. Hagan
  • , Crispin J. Miller

Research output: Contribution to journalArticlepeer-review

Abstract

Genome annotation is a synthesis of computational prediction and experimental evidence. Small genes are notoriously difficult to detect because the patterns used to identify them are often indistinguishable from chance occurrences, leading to an arbitrary cutoff threshold for the length of a protein-coding geneidentified solely by in silico analysis. We report a systematic reappraisal of the Schizosaccharomyces pombegenome that ignores thresholds. A complete six-frame translation was compared to a proteome data set, the Pfam domain database, and the genomes of six other fungi. Thirty-nine novel loci were identified. RTPCR and RNA-Seq confirmed transcription at 38 loci; 33 novel gene structures were delineated by 59 and39 RACE. Expression levels of 14 transcripts fluctuated during meiosis. Translational evidence for 10 genes, evolutionary conservation data supporting 35 predictions, and distinct phenotypes upon ORF deletion (one essential, four slow-growth, two delayed-division phenotypes) suggest that all 39 predictions encode functional proteins. The popularity of S. pombe as a model organism suggests that this augmented annotation will be of interest in diverse areas of molecular and cellular biology, while the generality of the approach suggests widespread applicability to other genomes. © 2011 by the Genetics Society of America.
Original languageEnglish
Pages (from-to)1207-1217
Number of pages10
JournalGenetics
Volume187
Issue number4
DOIs
Publication statusPublished - Apr 2011

Research Beacons, Institutes and Platforms

  • Manchester Cancer Research Centre

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