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Merck

HIV-1 resists MxB inhibition of viral Rev protein.

Emerging microbes & infections (2020-09-03)
Zhen Wang, Keli Chai, Qian Liu, Dong-Rong Yi, Qinghua Pan, Yu Huang, Juan Tan, Wentao Qiao, Fei Guo, Shan Cen, Chen Liang
要旨

The interferon-inducible myxovirus resistance B (MxB) protein has been reported to inhibit HIV-1 and herpesviruses by blocking the nuclear import of viral DNA. Here, we report a new antiviral mechanism in which MxB restricts the nuclear import of HIV-1 regulatory protein Rev, and as a result, diminishes Rev-dependent expression of HIV-1 Gag protein. Specifically, MxB disrupts the interaction of Rev with the nuclear transport receptor, transportin 1 (TNPO1). Supporting this, the TNPO1-independent Rev variants become less restricted by MxB. In addition, HIV-1 can overcome this inhibition by MxB through increasing the expression of multiply spliced viral RNA and hence Rev protein. Therefore, MxB exerts its anti-HIV-1 function through interfering with the nuclear import of both viral DNA and viral Rev protein.

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製品内容

Sigma-Aldrich
モノクローナル抗FLAG® M2抗体 マウス宿主抗体, 1 mg/mL, clone M2, affinity isolated antibody, buffered aqueous solution (50% glycerol, 10 mM sodium phosphate, and 150 mM NaCl, pH 7.4)
Sigma-Aldrich
レプトマイシンB 溶液 放線菌由来, ≥95% (HPLC), Supplied in methanol: water (7:3)
Sigma-Aldrich
チミジン5′-三リン酸 ナトリウム塩, ≥96%
Sigma-Aldrich
Anti-HIV-1 P24 antibody produced in rabbit, affinity isolated antibody
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Sigma-Aldrich
MISSION® esiRNA, targeting human KPNB1