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Open AccessJournal ArticleDOI

NEAT1 Long Noncoding RNA and Paraspeckle Bodies Modulate HIV-1 Posttranscriptional Expression

TLDR
The knockdown of NEAT1 enhances virus production through increased nucleus-to-cytoplasm export of Rev-dependent instability element (INS)-containing HIV-1 mRNAs as well as identifying the nuclear paraspeckle body as another important subcellular organelle for HIV- 1 replication.
Abstract
Most of the human genome is transcribed into protein-noncoding RNAs (ncRNAs), including small ncRNAs and long ncRNAs (lncRNAs). Over the past decade, rapidly emerging evidence has increasingly supported the view that lncRNAs serve key regulatory and functional roles in mammal cells. HIV-1 replication relies on various cell functions. To date, while the involvement of host protein factors and microRNAs (miRNAs) in the HIV-1 life cycle has been extensively studied, the relationship between lncRNAs and HIV-1 remains uncharacterized. Here, we have profiled 83 disease-related lncRNAs in HIV-1-infected T cells. We found NEAT1 to be one of several lncRNAs whose expression is changed by HIV-1 infection, and we have characterized its role in HIV-1 replication. We In the abstract, added definition of INS OK, or should "cis-acting" be added?report here that the knockdown of NEAT1 enhances virus production through increased nucleus-to-cytoplasm export of Rev-dependent instability element (INS)-containing HIV-1 mRNAs. IMPORTANCE Long protein-noncoding RNAs (lncRNAs) play roles in regulating gene expression and modulating protein activities. There is emerging evidence that lncRNAs are involved in the replication of viruses. To our knowledge, this report is the first to characterize a role contributed by an lncRNA, NEAT1, to HIV-1 replication. NEAT1 is essential for the integrity of the nuclear paraspeckle substructure. Based on our findings from NEAT1 knockdown, we have identified the nuclear paraspeckle body as another important subcellular organelle for HIV-1 replication.

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Live cell imaging and proteomic profiling of endogenous NEAT1 lncRNA by CRISPR/Cas9-mediated knock-in.

TL;DR: The development of CERTIS (CRISPR-mediated Endogenous lncRNA Tracking and Immunoprecipitation System) to visualize and isolate endogenous lncRNAs, by precisely inserting a 24-repeat MS2 tag into the distal end of lnc RNA locus through the CRISPR/Cas9 technology is reported.
Journal ArticleDOI

LncRNA NEAT1: Shedding light on mechanisms and opportunities in liver diseases.

TL;DR: A review of relevant studies on the different casting of NEAT1 in liver diseases, especially focusing on its regulatory mechanisms and new opportunities for alcoholic liver disease.
Journal ArticleDOI

Arthropod viruses and small RNAs.

TL;DR: This review highlights recent research on the role of small RNAs in arthropod host-virus interactions with reference to other host-pathogen systems.
Journal ArticleDOI

STAT3‑regulated long non‑coding RNAs lnc‑7SK and lnc‑IGF2‑AS promote hepatitis C virus replication

TL;DR: Two new types of lncRNAs are identified, lnc-IGF2-AS and lNC-7SK, which can be upregulated by STAT3 and are involved in HCV replication by regulating PI4P.
Journal ArticleDOI

LncRNAs and immunity: watchdogs for host pathogen interactions

TL;DR: The functional developments and mechanism of action of lncRNAs, in immunity and defense of host against pathogens, and how they alter cell differentiation/function are summarized.
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Journal ArticleDOI

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