Rrp6 Regulates Heterochromatic Gene Silencing via ncRNA RUF6 Decay in Malaria Parasites

Author:

Fan Yanting1,Shen Shijun2,Wei Guiying1,Tang Jianxia3,Zhao Yuemeng1,Wang Fei1,He Xiaohui1,Guo Gangqiang2,Shang Xiaomin1,Yu Xinyu3,Ma Zhenlin4,He Xiaoqin3,Liu Meng2,Zhu Qianshu2,Le Zhen1,Wei Gang4,Cao Jun356,Jiang Cizhong27,Zhang Qingfeng1

Affiliation:

1. Research Center for Translational Medicine, Key Laboratory of Arrhythmias of the Ministry of Education of China, East Hospital, Tongji University School of Medicine, Shanghai, China

2. Institute of Translational Research, Tongji Hospital, the School of Life Sciences and Technology, Shanghai Key Laboratory of Signaling and Disease Research, Tongji University, Shanghai, China

3. National Health Commission Key Laboratory of Parasitic Disease Control and Prevention, Jiangsu Provincial Key Laboratory on Parasite and Vector Control Technology, Jiangsu Institute of Parasitic Diseases, Wuxi, China

4. CAS Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China

5. Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, China

6. Public Health Research Center, Jiangnan University, Wuxi, China

7. The Research Center of Stem Cells and Ageing, Tsingtao Advanced Research Institute, Tongji University, Tsingtao, China

Abstract

Malaria remains a major public health and economic burden. The heterochromatin environment controls the silencing of genes associated with the fate of malaria parasites. Previous studies have demonstrated that a group of GC-rich ncRNAs (RUF6) is associated with the mutually exclusive expression of var genes, but the underlying mechanisms remain elusive. Here, through a series of genetic manipulation and genome-wide multiomics analysis, we have identified the plasmodial orthologue of RNA exosome-associated Rrp6 as an upstream regulator of RUF6 expression and revealed that the dysregulation of RUF6 upon Rrp6 knockdown triggered local chromatin alteration, thereby activating most heterochromatic genes via direct interaction of RUF6 and distal gene loci. This finding not only uncovered the in-depth mechanism of RUF6-mediated regulation of heterochromatic genes but also identified Rrp6 as a novel regulator of gene expression in human malaria parasites, which provides a new target for developing intervention strategies against malaria.

Funder

national key R&D program of China

Jiangsu provincial department of science and technology

National Natural Science Foundation of China

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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