NF-κB-Interacting Long Noncoding RNA Regulates HIV-1 Replication and Latency by Repressing NF-κB Signaling

Author:

Wang Hong1,Liu Yue12,Huan Chen1,Yang Jing1,Li Zhaolong1,Zheng Baisong1,Wang Yingchao3,Zhang Wenyan1

Affiliation:

1. Institute of Virology and AIDS Research, The First Hospital of Jilin University, Changchun, People’s Republic of China

2. Department of Echocardiography, The First Hospital of Jilin University, Changchun, People’s Republic of China

3. Department of Hepatobiliary Pancreatic Surgery, The First Hospital of Jilin University, Changchun, People’s Republic of China

Abstract

The NF-κB pathway plays key roles in HIV-1 replication and reactivation of HIV-1 latency. A regulator inhibiting NF-κB activation may be a promising therapeutic strategy against HIV-1. Recently, NF-κB-interacting long noncoding RNA (NKILA) was identified to suppress the development of different human cancers by inhibiting IκB kinase (IKK)-induced IκB phosphorylation and NF-κB pathway activation, whereas the relationship between NKILA and HIV-1 replication is still unknown. Here, our results show that NKILA inhibits HIV-1 replication and reactivation by suppressing HIV-1 long terminal repeat (LTR)-driven transcription initiation. Moreover, NKILA inhibited the replication of HIV-1 clones with different coreceptor tropisms. This project may reveal a target for the development of novel anti-HIV drugs.

Funder

Science and Technology Department of Jilin Province

Key Laboratory of Molecular Virology, Jilin Province

China Postdoctoral Science Foundation

Ministry of Science and Technology of the People's Republic of China

JLU | Program for Jilin University Science and Technology Innovative Research Team

National Natural Science Foundation of China

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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