1. Academic Validation
  2. Identification and characterization of long non-coding RNA Carip in modulating spatial learning and memory

Identification and characterization of long non-coding RNA Carip in modulating spatial learning and memory

  • Cell Rep. 2022 Feb 22;38(8):110398. doi: 10.1016/j.celrep.2022.110398.
Xiaoli Cui 1 Ruijin Zhang 1 Ye Yang 2 Erzhong Wu 1 Yiheng Tang 1 Zhihua Zhao 2 Chao Li 1 Lei Yang 1 Xueyi Teng 1 Yanzhen Ye 2 Ya Cui 3 Feng Xu 1 Zewen Su 1 Dongpeng Wang 3 Dongdong Zhang 3 Yan Yang 1 Jianyuan Sun 4 Jianjun Luo 5 Shuli Zhang 6 Runsheng Chen 7 Jianzhong Jeff Xi 8
Affiliations

Affiliations

  • 1 Key Laboratory of RNA Biology, State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
  • 2 Department of Biomedical Engineering, College of Future Technology, Peking University, Beijing 100871, China; State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100871, China.
  • 3 Key Laboratory of RNA Biology, State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.
  • 4 Key Laboratory of RNA Biology, State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China; University of Chinese Academy of Sciences, Beijing 100049, China.
  • 5 Key Laboratory of RNA Biology, State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address: [email protected].
  • 6 Key Laboratory of RNA Biology, State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address: [email protected].
  • 7 Key Laboratory of RNA Biology, State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China. Electronic address: [email protected].
  • 8 Department of Biomedical Engineering, College of Future Technology, Peking University, Beijing 100871, China; State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100871, China. Electronic address: [email protected].
Abstract

CaMKII has long been known to be a key effector for synaptic plasticity. Recent studies have shown that a variety of modulators interact with the subunits of CaMKII to regulate the long-term potentiation (LTP) of hippocampal neurons. However, whether long non-coding RNAs modulate the activity of CaMKII and affect synaptic plasticity is still elusive. Here, we identify a previously uncharacterized long non-coding RNA Carip that functions as a scaffold, specifically interacts with CaMKIIβ, and regulates the phosphorylation of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and N-methyl-d-aspartate (NMDA) receptor subunits in the hippocampus. The absence of Carip causes dysfunction of synaptic transmission and attenuates LTP in hippocampal CA3-CA1 synapses, which further leads to impairment of spatial learning and memory. In summary, our findings demonstrate that Carip modulates long-term synaptic plasticity by changing AMPA receptor and NMDA receptor activities, thereby affecting spatial learning and memory in mice.

Keywords

CaMKIIβ; Carip; LTP; hippocampal neurons; learning and memory.

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