Crystal structure of a tetrameric RNA G-quadruplex formed by hexanucleotide repeat expansions of C9orf72 in ALS/FTD

Author:

Geng Yanyan123,Liu Changdong24,Xu Naining24,Suen Monica Ching24,Miao Haitao2,Xie Yuanyuan3,Zhang Bingchang3,Chen Xueqin1,Song Yuanjian5,Wang Zhanxiang3,Cai Qixu6,Zhu Guang24ORCID

Affiliation:

1. Clinical Research Institute of the First Affiliated Hospital of Xiamen University, Fujian Key Laboratory of Brain Tumors Diagnosis and Precision Treatment, Xiamen Key Laboratory of Brain Center, the First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University , Xiamen , Fujian , China

2. Institute for Advanced Study and State Key Laboratory of Molecular Neuroscience, Division of Life Science, The Hong Kong University of Science and Technology , Clear Water Bay, Kowloon , Hong Kong SAR, China

3. Department of Neurosurgery and Department of Neuroscience, Fujian Key Laboratory of Brain Tumors Diagnosis and Precision Treatment, Xiamen Key Laboratory of Brain Center, the First Affiliated Hospital of Xiamen University, School of Medicine, Xiamen University , Xiamen , Fujian , China

4. HKUST Shenzhen Research Institute, Hi-Tech Park , Nanshan, Shenzhen , Guangdong , China

5. Jiangsu Key Laboratory of Brain Disease Bioinformation, Department of Genetics, Xuzhou Medical University , Xuzhou , Jiangsu , China

6. State Key Laboratory of Vaccines for Infectious Diseases, School of Public Health, Xiamen University , Xiamen , Fujian , China

Abstract

Abstract The abnormal GGGGCC hexanucleotide repeat expansions (HREs) in C9orf72 cause the fatal neurodegenerative diseases including amyotrophic lateral sclerosis and frontotemporal dementia. The transcribed RNA HREs, short for r(G4C2)n, can form toxic RNA foci which sequestrate RNA binding proteins and impair RNA processing, ultimately leading to neurodegeneration. Here, we determined the crystal structure of r(G4C2)2, which folds into a parallel tetrameric G-quadruplex composed of two four-layer dimeric G-quadruplex via 5′-to-5′ stacking in coordination with a K+ ion. Notably, the two C bases locate at 3′- end stack on the outer G-tetrad with the assistance of two additional K+ ions. The high-resolution structure reported here lays a foundation in understanding the mechanism of neurological toxicity of RNA HREs. Furthermore, the atomic details provide a structural basis for the development of potential therapeutic agents against the fatal neurodegenerative diseases ALS/FTD.

Funder

National Scientific Foundation of China

Research Grants Council of the Hong Kong Special Administrative Region

Hong Kong University of Science and Technology

Guangdong Basic and Applied Basic Research Foundation

Publisher

Oxford University Press (OUP)

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