scholarly journals Hepatitis C Virus NS5A Protein Modulates IRF-7-Mediated Interferon-α Signaling

2014 ◽  
Vol 34 (1) ◽  
pp. 16-21 ◽  
Author(s):  
Joydip Bhanja Chowdhury ◽  
Hangeun Kim ◽  
Ranjit Ray ◽  
Ratna B. Ray
2006 ◽  
Vol 196 (1) ◽  
pp. 11-21 ◽  
Author(s):  
Ankur Goyal ◽  
Wolf P. Hofmann ◽  
Eva Hermann ◽  
Stella Traver ◽  
Syed S. Hissar ◽  
...  

Hepatology ◽  
2007 ◽  
Vol 46 (4) ◽  
pp. 999-1008 ◽  
Author(s):  
Robert E. Lanford ◽  
Bernadette Guerra ◽  
Catherine B. Bigger ◽  
Helen Lee ◽  
Deborah Chavez ◽  
...  

2015 ◽  
Vol 90 (6) ◽  
pp. 2794-2805 ◽  
Author(s):  
Giao V. Q. Tran ◽  
Trang T. D. Luong ◽  
Eun-Mee Park ◽  
Jong-Wook Kim ◽  
Jae-Woong Choi ◽  
...  

ABSTRACTHepatitis C virus (HCV) is a major cause of chronic liver disease and is highly dependent on cellular proteins for virus propagation. To identify the cellular factors involved in HCV propagation, we recently performed protein microarray assays using the HCV nonstructural 5A (NS5A) protein as a probe. Of 90 cellular protein candidates, we selected the soluble resistance-related calcium-binding protein (sorcin) for further characterization. Sorcin is a calcium-binding protein and is highly expressed in certain cancer cells. We verified that NS5A interacted with sorcin through domain I of NS5A, and phosphorylation of the threonine residue 155 of sorcin played a crucial role in protein interaction. Small interfering RNA (siRNA)-mediated knockdown of sorcin impaired HCV propagation. Silencing of sorcin expression resulted in a decrease of HCV assembly without affecting HCV RNA and protein levels. We further demonstrated that polo-like kinase 1 (PLK1)-mediated phosphorylation of sorcin was increased by NS5A. We showed that both phosphorylation and calcium-binding activity of sorcin were required for HCV propagation. These data indicate that HCV modulates sorcin activity via NS5A protein for its own propagation.IMPORTANCESorcin is a calcium-binding protein and regulates intracellular calcium homeostasis. HCV NS5A interacts with sorcin, and phosphorylation of sorcin is required for protein interaction. Gene silencing of sorcin impaired HCV propagation at the assembly step of the HCV life cycle. Sorcin is phosphorylated by PLK1 via protein interaction. We showed that sorcin interacted with both NS5A and PLK1, and PLK1-mediated phosphorylation of sorcin was increased by NS5A. Moreover, calcium-binding activity of sorcin played a crucial role in HCV propagation. These data provide evidence that HCV regulates host calcium metabolism for virus propagation, and thus manipulation of sorcin activity may represent a novel therapeutic target for HCV.


2006 ◽  
Vol 131 (5) ◽  
pp. 1452-1462 ◽  
Author(s):  
Scot D. Henry ◽  
Herold J. Metselaar ◽  
Richard C.B. Lonsdale ◽  
Alice Kok ◽  
Bart L. Haagmans ◽  
...  

1997 ◽  
Vol 55 (1) ◽  
pp. 41-45 ◽  
Author(s):  
Lucile Musset ◽  
Pascale Ghillani ◽  
Françoise Lunel ◽  
Patrice Cacoub ◽  
Pascale Cresta ◽  
...  

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Shanshan Wang ◽  
Yongzhi Chen ◽  
Chunfeng Li ◽  
Yaoxing Wu ◽  
Lei Guo ◽  
...  

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