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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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Host-virus interactions mediated by long non-coding RNAs

Ashish Prasad, +1 more
- 23 Mar 2021 - 
TL;DR: A review of the recent developments in viral interactions of animals and plants is presented in this article, where both pro-and anti-viral lncRNAs have been reported and they show immense potential to be used as markers and in therapeutics.
Journal ArticleDOI

Exploration of the involvement of LncRNA in HIV-associated encephalitis using bioinformatics.

TL;DR: Re-annotation on the expression profiling from the HIVE study in the public database, identified the lncRNA that might be involved in HIVE, and explored the possible mechanism suggest that lncRNAs may beinvolved in the occurrence and development of HIVE.
Journal ArticleDOI

Analysis of lncRNA-miRNA-mRNA Interactions in Hyper-proliferative Human Pulmonary Arterial Smooth Muscle Cells.

TL;DR: The interactions between long noncoding RNAs, mRNAs and micro-RNAs are comprehensively understood to determine their role in smooth muscle hyperplasia and specific knock down of the selected lncRNAs highlighted the importance of non-codingRNAs in smooth Muscle Hyperplasia.
Journal ArticleDOI

Landscape of post-transcriptional gene regulation during hepatitis C virus infection.

TL;DR: The interplay of post-transcriptional mechanisms that affect host immune responses in the setting of HCV infection is discussed and the sophisticated mechanisms both host and virus have evolved in the race for superiority are highlighted.
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Journal ArticleDOI

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TL;DR: A unique cellular gene, CEM15, is described, whose transient or stable expression in cells that do not normally express Cem15 recreates this phenotype, but whose antiviral action is overcome by the presence of Vif.
Journal ArticleDOI

RNA Maps Reveal New RNA Classes and a Possible Function for Pervasive Transcription

TL;DR: Three potentially functional classes of RNAs have been identified, two of which are syntenically conserved and correlate with the expression state of protein-coding genes and support a highly interleaved organization of the human transcriptome.
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