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논문 기본 정보

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학술저널
저자정보
Niu Xianli (Department of Biochemistry and Molecular Biology Zunyi Medical University Zhuhai Guangdong 519041 P) Nong Shirong (Key Laboratory of Genetic Engineering and Medicine Key Laboratory of Viral Biology Jinan University) Gong Junyuan (Key Laboratory of Genetic Engineering and Medicine Key Laboratory of Viral Biology Jinan University) Zhang Xin (Key Laboratory of Genetic Engineering and Medicine Key Laboratory of Viral Biology Jinan University) Tang Hui (Key Laboratory of Genetic Engineering and Medicine Key Laboratory of Viral Biology Jinan University) Zhou Tianhong (Key Laboratory of Genetic Engineering and Medicine Key Laboratory of Viral Biology Jinan University) Li Wei (Key Laboratory of Genetic Engineering and Medicine Key Laboratory of Viral Biology Jinan University)
저널정보
한국미생물생명공학회 Journal of Microbiology and Biotechnology Journal of Microbiology and Biotechnology 제31권 제1호
발행연도
2021.1
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16 - 24 (9page)

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Hepatitis B virus (HBV) genome P-encoded protein HBV DNA polymerase (Pol) has long been known as a reverse transcriptase during HBV replication. In this study, we investigated the impact of HBV Pol on host cellular processes, mainly apoptosis, and the underlying mechanisms. We showed a marked reduction in apoptotic rates in the HBV Pol-expressed HepG2 cells compared to controls. Moreover, a series of assays, i.e., yeast two-hybrid, GST pull-down, co-immunoprecipitation, and confocal laser scanning microscopy, identified the host factor eEF1A2 to be associated with HBV Pol. Furthermore, knockdown of eEF1A2 gene by siRNA abrogated the HBV Pol-mediated anti-apoptotic effect with apoptosis induced by endoplasmatic reticulum (ER) stress-inducer thapsigargin (TG), thus suggesting that the host factor eEF1A2 is essential for HBV Pol’s anti-apoptosis properties. Our findings have revealed a novel role for HBV Pol in its modulation of apoptosis through integrating with eEF1A2.

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