Modulation of metabolic functions through Cas13d-mediated gene knockdown in liver

Bingbing He(Chinese Academy of Sciences), Wenbo Peng(Chinese Academy of Sciences), Jia Huang(Chinese Academy of Sciences), Hang Zhang(ShanghaiTech University), Yingsi Zhou(Chinese Academy of Sciences), Xiali Yang(Chinese Academy of Sciences), Jing Liu(Agricultural Genomics Institute at Shenzhen), Zhijie Li(ShanghaiTech University), Chunlong Xu(Chinese Academy of Sciences), Mingxing Xue(Chinese Academy of Sciences), Hui Yang(Chinese Academy of Sciences), Pengyu Huang(Chinese Academy of Sciences)
Protein & Cell
March 18, 2020
Cited by 103Open Access
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Abstract

In this study, the CasRx system was demonstrated to efficiently and functionally knock down genes related to metabolism functions, including Pten, Pcsk9 and lncLstr, in mouse hepatocytes. CasRx-mediated simultaneous knockdown of multiple genes was also achieved by sgRNA arrays, providing a useful strategy to modulate complex metabolism networks. Moreover, the AAV (adeno-associated virus)-mediated delivery of CasRx and Pcsk9 sgRNAs into mouse liver successfully decreased serum PCSK9, resulting in significant reduction of serum cholesterol levels. Importantly, CasRx-mediated knockdown of Pcsk9 is reversible and Pcsk9 could be repeatedly down-regulated, providing an effective strategy to reversibly modulate metabolic genes. The present work supplies a successful proof-of-concept trial that suggests efficient and regulatory knockdown of target metabolic genes for a designed metabolism modulation in the liver.


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