Deciphering HIV-1 transcription initiation and elongation from single-molecule imaging data
Peer-Reviewed Publication
Updates every hour. Last Updated: 12-Dec-2025 13:11 ET (12-Dec-2025 18:11 GMT/UTC)
Recently, professor Jiajun Zhang's team at Sun Yat-sen University, in collaboration with associate professor Xiyan Yang at Guangdong University of Finance, developed a dual-driven framework based on single-molecule imaging data and stochastic dynamic modeling to infer HIV-1 transcription dynamics. This work provides new insights and methodologies for understanding the latent regulation mechanism of HIV-1 and optimizing antiviral treatment strategies.
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In recent years, the regulatory role of the gut microbiota in the initiation and progression of colorectal cancer (CRC) has attracted growing attention. Among the key microbial contributors, Fusobacterium nucleatum (Fn) has been identified as a critical pathogenic factor in CRC. As an oral anaerobic commensal, Fn is rarely found in the lower gastrointestinal tract of healthy individuals. However, under pathological conditions, it can ectopically colonize the gastrointestinal tract. Once enriched in the colorectal environment, mounting evidence suggests that Fn is involved in multiple aspects of CRC pathogenesis, including initiation, progression, metastasis, and resistance to conventional therapies such as chemotherapy, radiotherapy, and immunotherapy. A recent review by Wei Wei and Diwei Zheng's team at the Institute of Process Engineering systematically outlines the pathogenic mechanisms of Fn in CRC and summarizes both current and emerging strategies for its therapeutic targeting. Furthermore, the authors propose potential approaches to overcome existing challenges in Fn modulation, aiming to facilitate more effective therapeutic interventions and improve clinical outcomes.
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