Gm14230 controls Tbc1d24 cytoophidia and neuronal cellular juvenescence

Author:

Morimune Takao,Tano Ayami,Tanaka Yuya,Yukiue Haruka,Yamamoto Takefumi,Tooyama Ikuo,Maruo Yoshihiro,Nishimura Masaki,Mori MasakiORCID

Abstract

It is not fully understood how enzymes are regulated in the tiny reaction field of a cell. Several enzymatic proteins form cytoophidia, a cellular macrostructure to titrate enzymatic activities. Here, we show that the epileptic encephalopathy-associated protein Tbc1d24 forms cytoophidia in neuronal cells both in vitro and in vivo. The Tbc1d24 cytoophidia are distinct from previously reported cytoophidia consisting of inosine monophosphate dehydrogenase (Impdh) or cytidine-5’-triphosphate synthase (Ctps). Tbc1d24 cytoophidia is induced by loss of cellular juvenescence caused by depletion of Gm14230, a juvenility-associated lncRNA (JALNC) and zeocin treatment. Cytoophidia formation is associated with impaired enzymatic activity of Tbc1d24. Thus, our findings reveal the property of Tbc1d24 to form cytoophidia to maintain neuronal cellular juvenescence.

Funder

Japan Society for the Promotion of Science

Morinaga Service Society

Kato Memorial Bioscience Foundation

Japan Epilepsy Research Foundation

Hoansha Foundation

MSD Life Science Foundation

Ichiro Kanehara Foundation for the Promotion of Medical Sciences and Medical Care

Japan Brain Foundation

Takeda Science Foundation

Japan Spina Bifida & Hydrocephalus Research Foundation

Japan Intractable Diseases (Nanbyo) Research Foundation

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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