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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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Long Noncoding RNA NEAT1-Dependent SFPQ Relocation from Promoter Region to Paraspeckle Mediates IL8 Expression upon Immune Stimuli

TL;DR: Nuclear enriched abundant transcript 1 (NEAT1), an essential lncRNA for the formation of nuclear body paraspeckles, is induced by influenza virus and herpes simplex virus infection as well as by Toll-like receptor3-p38 pathway-triggered poly I:C stimulation, resulting in excess formation of paraspeakles.
Journal ArticleDOI

Long Non-Coding RNA in the Pathogenesis of Cancers.

TL;DR: The latest findings regarding the roles and mechanisms of some important lncRNAs in the pathogenesis of certain malignant cancers, including lung, breast, liver, and colorectal cancers, as well as hematological malignancies and neuroblastoma are discussed.
Journal ArticleDOI

Long non-coding RNAs and complex diseases: from experimental results to computational models

TL;DR: Some state-of-the-art computational models are introduced, which could be effectively used to identify disease-related lncRNAs on a large scale and select the most promising disease- related lnc RNAs for experimental validation and discussed the future directions of developing computational models for lncRNA research.
Journal ArticleDOI

Long Non-Coding RNAs in the Regulation of Gene Expression: Physiology and Disease

TL;DR: Key aspects of lncRNA biology are reviewed, focusing on their role as regulatory elements in gene expression modulation during physiological and disease processes, with implications in host and pathogens physiology, and their role in immune response modulation.
References
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Journal ArticleDOI

PSF and p54nrb/NonO – multi-functional nuclear proteins

TL;DR: This review describes the functions of the nuclear factors PSF (polypyrimidine tract‐binding protein‐associated splicing factor) and p54nrb/NonO and shows that these proteins exhibit multi‐functional characteristics in a variety of nuclear processes.
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Induction of incomplete autophagic response by hepatitis C virus via the unfolded protein response

TL;DR: It is demonstrated by a battery of morphological and biochemical assays that hepatitis C virus induces the accumulation of autophagosomes in cells without enhancing autophagic protein degradation, indicating a positive role of UPR and the incomplete Autophagic response in HCV replication.
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Human genome: end of the beginning.

TL;DR: Just over three years ago, it was announced that a first draft of the human genome sequence had been completed, but gaps and errors remained, and the job of fixing those problems is now largely done.
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Inactivation of the human immunodeficiency virus type 1 inhibitory elements allows Rev-independent expression of Gag and Gag/protease and particle formation.

TL;DR: It is shown that in addition to the previously identified INS1 within p17gag, several other INS elements exist within the gag/pol region of HIV-1 and these elements act independently of each other and were eliminated by mutagenesis after the introduction of multiple point mutations not affecting the coding region.
Journal ArticleDOI

Mutational inactivation of an inhibitory sequence in human immunodeficiency virus type 1 results in Rev-independent gag expression.

TL;DR: The results demonstrate the presence of a strong inhibitory element acting at the level of mRNA and provide a general method for the removal of such elements from mRNA coding regions, suggesting that cellular factors are responsible for this inhibition.
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