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Identification of RNA 3 ́ ends and termination sites in Haloferax volcanii

  • Sarah J. Berkemer
  • , Lisa Katharina Maier
  • , Fabian Amman
  • , Stephan H. Bernhart
  • , Julia Wörtz
  • , Pascal Märkle
  • , Friedhelm Pfeiffer
  • , Peter F. Stadler
  • , Anita Marchfelder
  • University of Leipzig
  • Max Planck Institute for Mathematics in the Sciences
  • Biologie II
  • University of Ulm
  • Institute for Theoretical Chemistry
  • University of Vienna
  • Division of Cell and Developmental Biology
  • Medical University of Vienna
  • Bioinformatics
  • Transcriptome Bioinformatics
  • Computational Biology Group
  • Max Planck Institute of Biochemistry
  • Facultad de Ciencias
  • Universidad Nacional de Colombia
  • Centre for Non-coding RNA in Technology and Health
  • University of Copenhagen
  • Santa Fe Institute
  • German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig
  • Competence Center for Scalable Data Services and Solutions Dresden/Leipzig

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11 Citations (Scopus)

Résumé

Archaeal genomes are densely packed; thus, correct transcription termination is an important factor for orchestrated gene expression. A systematic analysis of RNA 3´ termini, to identify transcription termination sites (TTS) using RNAseq data has hitherto only been performed in two archaea, Methanosarcina mazei and Sulfolobus acidocaldarius. In this study, only regions directly downstream of annotated genes were analysed, and thus, only part of the genome had been investigated. Here, we developed a novel algorithm (Internal Enrichment-Peak Calling) that allows an unbiased, genome-wide identification of RNA 3´ termini independent of annotation. In an RNA fraction enriched for primary transcripts by terminator exonuclease (TEX) treatment we identified 1,543 RNA 3´ termini. Approximately half of these were located in intergenic regions, and the remainder were found in coding regions. A strong sequence signature consistent with known termination events at intergenic loci indicates a clear enrichment for native TTS among them. Using these data we determined distinct putative termination motifs for intergenic (a T stretch) and coding regions (AGATC). In vivo reporter gene tests of selected TTS confirmed termination at these sites, which exemplify the different motifs. For several genes, more than one termination site was detected, resulting in transcripts with different lengths of the 3´ untranslated region (3´ UTR).

langue originaleAnglais
Pages (de - à)663-676
Nombre de pages14
journalRNA Biology
Volume17
Numéro de publication5
Les DOIs
étatPublié - 3 mai 2020
Modification externeOui

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