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Open AccessJournal ArticleDOI

How do lncRNAs regulate transcription

TLDR
Recent progress in elucidating the molecular mechanisms by which lncRNAs modulate gene expression is reviewed, including the act of lnc RNA transcription rather than the lncRNA product that appears to be regulatory.
Abstract
It has recently become apparent that RNA, itself the product of transcription, is a major regulator of the transcriptional process. In particular, long noncoding RNAs (lncRNAs), which are so numerous in eukaryotes, function in many cases as transcriptional regulators. These RNAs function through binding to histone-modifying complexes, to DNA binding proteins (including transcription factors), and even to RNA polymerase II. In other cases, it is the act of lncRNA transcription rather than the lncRNA product that appears to be regulatory. We review recent progress in elucidating the molecular mechanisms by which lncRNAs modulate gene expression and future opportunities in this research field.

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Citations
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Journal ArticleDOI

RNA delivery by extracellular vesicles in mammalian cells and its applications.

TL;DR: This Review focuses on the current state of knowledge pertaining to packaging, transport and function of RNAs in extracellular vesicles and outlines the progress made thus far towards their clinical applications.
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.
Journal ArticleDOI

Non-Coding RNAs and their Integrated Networks.

TL;DR: This review discusses the distinct types of ncRNAs, including housekeeping n cRNAs and regulatory nc RNAs, their versatile functions and interactions, transcription, translation, and modification, and summarizes the integrated networks of n cRNA interactions, providing a comprehensive landscape of nCRNAs regulatory roles.
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Long non-coding RNA: Classification, biogenesis and functions in blood cells.

TL;DR: The current status of knowledge on lncRNAs classification, biogenesis and its role in blood cells is summarized.
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Emerging roles of lncRNAs in the post-transcriptional regulation in cancer.

TL;DR: In this paper, the authors discuss latest developments in lncRNA-meditated gene expression at the post-transcriptional level, including gene splicing, mRNA stability, protein stability and nuclear trafficking.
References
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Journal ArticleDOI

The CLAMP protein links the MSL complex to the X chromosome during Drosophila dosage compensation

TL;DR: It is demonstrated that a previously uncharacterized zinc finger protein, CLAMP (chromatin-linked adaptor for MSL proteins), functions as the first link between the MSL complex and the X chromosome, providing new insights into how subnuclear domains of coordinate gene regulation are formed within metazoan genomes.
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TERRA-Reinforced Association of LSD1 with MRE11 Promotes Processing of Uncapped Telomeres

TL;DR: It is shown that following TRF2 depletion, the levels of the long noncoding RNA TERRA increase and LSD1, which binds TERRA, is recruited to telomeres, and that recruitment of LSD1 to deprotected telomereres requires MRE11 and is promoted by TERRA.
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The structure of the core NuRD repression complex provides insights into its interaction with chromatin

TL;DR: Evidence is found that in this complex RBBP4 mediates interaction with histone H3 tails, but not hist one H4, suggesting a mechanism for recruitment of the NuRD complex to chromatin.
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Long non-coding RNA ROR decoys gene-specific histone methylation to promote tumorigenesis

TL;DR: It is shown that the lncRNA ROR occupies and activates the TESC promoter by repelling the histone G9A methyltransferase and promoting the release of histone H3K9 methylation, which significantly reduces tumor growth and metastasis.
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Chromatin dynamics and the role of G9a in gene regulation and enhancer silencing during early mouse development

TL;DR: It is shown that genome-wide accumulation of H3K9me2 is crucial for postimplantation development, and coincides with redistribution of enhancer of zeste homolog 2 (EZH2)-dependent histone H3 lysine 27 trimethylation (H3K27me3).
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