The yeast RNA methylation complex consists of conserved yet reconfigured components with m6A-dependent and independent roles

  1. The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK
  2. Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel
  3. Human Technopole, Viale Rita Levi-Montalcini, 1, 20157 Milan, Italy
  4. Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA
  5. Charité Universitätsmedizin Berlin, Department of Biochemistry, Germany

Peer review process

Not revised: This Reviewed Preprint includes the authors’ original preprint (without revision), an eLife assessment, and public reviews.

Read more about eLife’s peer review process.

Editors

  • Reviewing Editor
    Pablo Manavella
    Universidad Nacional del Litoral-CONICET, Santa Fe, Argentina
  • Senior Editor
    Benoit Kornmann
    University of Oxford, Oxford, United Kingdom

Reviewer #1 (Public Review):

Here, Ensinck et al. investigated the composition of the yeast mRNA m6A methyltransferase complex required for meiosis. This complex was known to contain three proteins but is much more complex in mammals, insects, and plants. Through IP-MS analysis, they identified three more proteins Kar4, Ygl036w, and Dyn2. Of these, Kar4 and Ygl036w are homologous to Mettl14 and Virma, respectively, and, like the previously described factors, are essential for m6A deposition, mating, and binding of the reader Pho92 to mRNA during meiosis by evidence acquired with appropriate methodology. Dyn2 is a novel factor not described for any m6A complex and is not essential for m6A deposition, mating, and binding of the reader Pho92 to mRNA during meiosis.

In addition, detailed analysis of the Slz1 revealed homology to the mammalian factor m6A complex member ZC3H13 to comprise a conserved complex of five proteins, Mettl3, Mettl14, Mum2/WTAP, Virma, and Slz/ZC3H13. When co-expressed in insect cells, they co-purify stoichiometrically, and the presence of Mum2 as a dimer is also indicated, as shown for WTAP.

Complementary to these data, they show that the stability of the individual complex members is affected in mutants supporting that they are stabilized through complex formation.
Furthermore, the authors then show that kar4 has additional roles in mating that are separable from its role through the m6A complex in meiosis.
The authors employ appropriate methodology throughout to address their aims and present convincing evidence for their claims. The evidence presented here reinforces that the m6A complex is evolutionary and highly conserved, with a broad scope for its functional analysis in humans and model organisms.

Reviewer #2 (Public Review):

N6-methyladenosine (m6A), the most abundant mRNA modification, is deposited by the m6A methyltransferase complexes (MTC). While MTC in mammals/flies/plants consists of at least six subunits, yeast MTC was known to contain only three proteins. Ensinck, Maman, et al. revisited this question using a proteomic approach and uncovered three new yeast MTC components, Kar4/Ygl036w/Dyn2. By applying sequence and structure comparisons, they identified Kar4, Ygl036w, and Slz1 as homologs of the mammalian METTL14, VIRMA. ZC3H13, respectively. While these proteins are essential for m6A deposition, the dynein light chain protein, Dyn2, is not involved in mRNA methylation. Interestingly, while mammalian and fly MTCs are configured as MAC (METTL3 and METTL14), and MACOM (other subunits) complexes, yeast MTC subunits appear to have different configurations. Finally, Kar4 has a different role as a transcription regulator in mating, which is not mediated by other MTC members. These data establish an important framework for the yeast MTC and also provide novel insights for those studying m6A deposition.

  1. Howard Hughes Medical Institute
  2. Wellcome Trust
  3. Max-Planck-Gesellschaft
  4. Knut and Alice Wallenberg Foundation