Small noncoding vault RNA modulates synapse formation by amplifying MAPK signaling

Author:

Wakatsuki Shuji1ORCID,Takahashi Yoko1,Shibata Megumi1,Adachi Naoki23,Numakawa Tadahiro24,Kunugi Hiroshi2,Araki Toshiyuki1ORCID

Affiliation:

1. Department of Peripheral Nervous System Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan

2. Department of Mental Disorder Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan

3. Department of Biomedical Chemistry, School of Science and Technology, Kwansei Gakuin University, Hyogo, Japan

4. Department of Cell Modulation, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan

Abstract

The small noncoding vault RNA (vtRNA) is a component of the vault complex, a ribonucleoprotein complex found in most eukaryotes. Emerging evidence suggests that vtRNAs may be involved in the regulation of a variety of cellular functions when unassociated with the vault complex. Here, we demonstrate a novel role for vtRNA in synaptogenesis. Using an in vitro synapse formation model, we show that murine vtRNA (mvtRNA) promotes synapse formation by modulating the MAPK signaling pathway. mvtRNA is transported to the distal region of neurites as part of the vault complex. Interestingly, mvtRNA is released from the vault complex in the neurite by a mitotic kinase Aurora-A–dependent phosphorylation of MVP, a major protein component of the vault complex. mvtRNA binds to and activates MEK1 and thereby enhances MEK1-mediated ERK activation in neurites. These results suggest the existence of a regulatory mechanism of the MAPK signaling pathway by vtRNAs as a new molecular basis for synapse formation.

Funder

Japan Society for the Promotion of Science

National Center of Neurology and Psychiatry

Takeda Science Foundation

Publisher

Rockefeller University Press

Subject

Cell Biology

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