RNF220 is an E3 ubiquitin ligase for AMPA receptors to regulate synaptic transmission

Author:

Ma Pengcheng1ORCID,Wan Li Pear12ORCID,Li Yuwei12ORCID,He Chun-Hui3ORCID,Song Ning-Ning45ORCID,Zhao Shiping1,Wang Huishan12ORCID,Ding Yu-Qiang345ORCID,Mao Bingyu16ORCID,Sheng Nengyin16ORCID

Affiliation:

1. State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China.

2. Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming 650223, China.

3. Key Laboratory of Arrhythmias, Ministry of Education of China, East Hospital, and Department of Anatomy and Neurobiology, Tongji University School of Medicine, Shanghai 200092, China.

4. State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai 200032, China.

5. Department of Laboratory Animal Science, Fudan University, Shanghai 200032, China.

6. Center for Excellence in Animal Evolution and Genetics, Chinese Academy of Sciences, Kunming 650223, China

Abstract

The accurate expression of postsynaptic AMPA receptors (AMPARs) is critical for information processing in the brain, and ubiquitination is a key regulator for this biological process. However, the roles of E3 ubiquitin ligases in the regulation of AMPARs are poorly understood. Here, we find that RNF220 directly interacts with AMPARs to meditate their polyubiquitination, and RNF220 knockout specifically increases AMPAR protein levels, thereby enhancing basal synaptic activity while impairing synaptic plasticity. Moreover, depending on its E3 ubiquitin ligase activity, RNF220 represses AMPAR-mediated excitatory synaptic responses and their neuronal surface expression. Furthermore, learning and memory are altered in forebrain RNF220-deficient mice. In addition, two neuropathology-related RNF220 variants fail to repress excitatory synaptic activity because of the incapability to regulate AMPAR ubiquitination due to their attenuated interaction. Together, we identify RNF220 as an E3 ubiquitin ligase for AMPARs and establish its substantial role in excitatory synaptic transmission and brain function.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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