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Chong-Lei Fu

Tsinghua University · CN
Area of research
Molecular Biology · Cellular and Molecular Neuroscience
Research interest
Research topics from publications: Zika virus NS5 protein inhibits type I interferon signaling via CRL3 E3 ubiquitin ligase-mediated degradation of STAT2. Representative work: The ZIKA virus (ZIKV) evades the host immune response by degrading STAT2 through its NS5 protein, thereby inhibiting type I interferon (IFN)-mediated antiviral immunity. However, the molecular mechanism underlying this process has remained elusive. In this study, we performed a genome-wide CRISPR/Cas9 screen, revealing that ZSWIM8 as the substrate receptor of Cullin3-RING E3 ligase is required for NS5-mediated STAT2 degradation. Genetic depletion of ZSWIM8 and CUL3 substantially impeded NS5-mediated STAT2 degradation. Biochemical analysis illuminated that NS5 enhances the interaction between STAT2 and the ZSWIM8-CUL3 E3 ligase complex, thereby facilitating STAT2 ubiquitination. Moreover, ZSW
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Recent publications

Zika virus NS5 protein inhibits type I interferon signaling via CRL3 E3 ubiquitin ligase-mediated degradation of STAT2
Proceedings of the National Academy of Sciences 2024cited by 37position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Xi Zhuo Jiang · Jilin University1 papers (2024–2024)Wenchun Fan · Jiangyin Traffic Planning Survey & Design Institute (China)1 papers (2024–2024)Jun Yao · Northwestern University1 papers (2024–2024)Qiang Ding · University of Alabama at Birmingham1 papers (2024–2024)Yu Zhang · Huaihua University1 papers (2024–2024)Zhuoyang Li · Anhui University1 papers (2024–2024)Xiaohui Ju · Tsinghua University1 papers (2024–2024)Mingli Gong · Tsinghua University1 papers (2024–2024)Wenlin Ren · Tsinghua University1 papers (2024–2024)