Long noncoding RNA LRG modulates Drosophila locomotion by sequestering Synaptotagmin 1 protein

Author:

Cui Ming‐Yang12,Xu Meng‐Bo1,Wang Ying‐Xuan12,Bai Bao‐Yan3,Chen Run‐Sheng3,Liu Li1,Li Mei‐Xia1ORCID

Affiliation:

1. State Key Laboratory of Brain and Cognitive Science, Institute of Biophysics Chinese Academy of Sciences Beijing China

2. College of Life Sciences University of Chinese Academy of Sciences Beijing China

3. Key Laboratory of Noncoding RNA, Institute of Biophysics Chinese Academy of Sciences Beijing China

Abstract

AbstractApparently, the genomes of many organisms are pervasively transcribed, and long noncoding RNAs (lncRNAs) make up the majority of cellular transcripts. LncRNAs have been reported to play important roles in many biological processes; however, their effects on locomotion are poorly understood. Here, we presented a novel lncRNA, Locomotion Regulatory Gene (LRG), which participates in locomotion by sequestering Synaptotagmin 1 (SYT1). LRG deficiency resulted in higher locomotion speed which could be rescued by pan‐neuronal overexpression but not by limited ellipsoid body, motoneuron or muscle‐expression of LRG. At the molecular level, the synaptic vesicles (SVs) release and movement‐related SYT1 protein was recognized as LRG‐interacting protein candidate. Furthermore, LRG had no effects on SYT1 expression. Genetically, the behavioral defects in LRG mutant could be rescued by pan‐neuronal knock‐down of Syt1. Taken together, all the results suggested LRG exerts regulatory effects on locomotion via sequestering SYT1 thereby blocking its function without affecting its expression. Our work displays a new function of lncRNA and provides insights for revealing the pathogenesis of neurological diseases with motor disorders.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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