Interactions between the 5′ UTR mRNA of the spe2 gene and spermidine regulate translation in S. pombe

  1. Alastair I.H. Murchie
  1. Fudan University Pudong Medical Center, Pudong and Key Laboratory of Medical Epigenetics and Metabolism, Institute of Biomedical Sciences, Shanghai Medical College, Fudan University, Shanghai 200032, China
  2. Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, School of Basic Medical Sciences, Fudan University, Shanghai 200032, China
  1. Corresponding authors: aihm{at}fudan.edu.cn, drchen{at}fudan.edu.cn
  1. 1 These authors contributed equally to this work.

Abstract

The 5′ untranslated regions (5′ UTR) of mRNAs play an important role in the eukaryotic translation initiation process. Additional levels of translational regulation may be mediated through interactions between structured mRNAs that can adopt interchangeable secondary or tertiary structures and the regulatory protein/RNA factors or components of the translational apparatus. Here we report a regulatory function of the 5′ UTR mRNA of the spe2 gene (SAM decarboxylase) in polyamine metabolism of the fission yeast Schizosaccharomyces pombe. Reporter assays, biochemical experiments, and mutational analysis demonstrate that this 5′ UTR mRNA of spe2 can bind to spermidine to regulate translation. A tertiary structure transition in the 5′ UTR RNA upon spermidine binding is essential for translation regulation. This study provides biochemical evidence for spermidine binding to regulate translation of the spe2 gene through interactions with the 5′ UTR mRNA. The identification of such a regulatory RNA that is directly associated with an essential eukaryotic metabolic process suggests that other ligand-binding RNAs may also contribute to eukaryotic gene regulation.

Keywords

  • Received August 22, 2019.
  • Accepted December 10, 2019.

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