| Literature DB >> 33428246 |
Lina Worpenberg1, Chiara Paolantoni1, Sara Longhi2, Miriam M Mulorz3, Tina Lence3, Hans-Hermann Wessels4,5, Erik Dassi6, Giuseppe Aiello7, F X Reymond Sutandy3, Marion Scheibe3, Raghu R Edupuganti8, Anke Busch9, Martin M Möckel10, Michiel Vermeulen8, Falk Butter3, Julian König3, Michela Notarangelo2, Uwe Ohler4,5, Christoph Dieterich11,12, Alessandro Quattrone2, Alessia Soldano2, Jean-Yves Roignant1,13.
Abstract
N6-methyladenosine (m6 A) regulates a variety of physiological processes through modulation of RNA metabolism. This modification is particularly enriched in the nervous system of several species, and its dysregulation has been associated with neurodevelopmental defects and neural dysfunctions. In Drosophila, loss of m6 A alters fly behavior, albeit the underlying molecular mechanism and the role of m6 A during nervous system development have remained elusive. Here we find that impairment of the m6 A pathway leads to axonal overgrowth and misguidance at larval neuromuscular junctions as well as in the adult mushroom bodies. We identify Ythdf as the main m6 A reader in the nervous system, being required to limit axonal growth. Mechanistically, we show that the m6 A reader Ythdf directly interacts with Fmr1, the fly homolog of Fragile X mental retardation RNA binding protein (FMRP), to inhibit the translation of key transcripts involved in axonal growth regulation. Altogether, this study demonstrates that the m6 A pathway controls development of the nervous system and modulates Fmr1 target transcript selection.Entities:
Keywords: Fmr1; RNA modification; Ythdf; m6A; nervous system
Year: 2021 PMID: 33428246 DOI: 10.15252/embj.2020104975
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598