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Long non-coding RNAs: new players in cell differentiation and development

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TLDR
The function of lncRNAs in developmental processes, such as in dosage compensation, genomic imprinting, cell differentiation and organogenesis, with a particular emphasis on mammalian development are described.
Abstract
Genomes of multicellular organisms are characterized by the pervasive expression of different types of non-coding RNAs (ncRNAs). Long ncRNAs (lncRNAs) belong to a novel heterogeneous class of ncRNAs that includes thousands of different species. lncRNAs have crucial roles in gene expression control during both developmental and differentiation processes, and the number of lncRNA species increases in genomes of developmentally complex organisms, which highlights the importance of RNA-based levels of control in the evolution of multicellular organisms. In this Review, we describe the function of lncRNAs in developmental processes, such as in dosage compensation, genomic imprinting, cell differentiation and organogenesis, with a particular emphasis on mammalian development.

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Gene regulation by long non-coding RNAs and its biological functions.

TL;DR: A review of the mechanisms of lncRNA biogenesis, localization and functions in transcriptional, post-transcriptional and other modes of gene regulation, and their potential therapeutic applications is presented in this article.
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Non-coding RNAs in Development and Disease: Background, Mechanisms, and Therapeutic Approaches

TL;DR: This review guides the reader through important aspects of non-coding RNA biology, including their biogenesis, mode of actions, physiological function, as well as their role in the disease context (such as in cancer or the cardiovascular system).
Journal ArticleDOI

LncRNA-mediated regulation of cell signaling in cancer.

TL;DR: The latest developments primarily in important cell signaling pathways regulated by lncRNAs in cancer are discussed, including changes in transcription, translation, protein modification and the formation of RNA–protein or protein–protein complexes.
Journal Article

A High-Resolution Map of Human Evolutionary Constraint Using 29 Mammals

TL;DR: The comparison of related genomes has emerged as a powerful lens for genome interpretation as mentioned in this paper, which reveals a small number of new coding exons, candidate stop codon readthrough events and over 10,000 regions of overlapping synonymous constraint within protein-coding exons.
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Transition from inflammation to proliferation: a critical step during wound healing

TL;DR: This review summarizes mechanisms regulating the inflammation–proliferation transition at cellular and molecular levels and proposes that identification of such mechanisms will reveal promising targets for development of more effective therapies.
References
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Journal ArticleDOI

Conserved long noncoding RNAs transcriptionally regulated by Oct4 and Nanog modulate pluripotency in mouse embryonic stem cells

TL;DR: It is demonstrated that these lncRNAs are not merely controlled by mESC transcription factors, but that they themselves regulate developmental state: knockdown and overexpression of these transcripts lead to robust changes in Oct4 and Nanog mRNA levels, in addition to alterations in cellular lineage-specific gene expression and in the pluripotency of mESCs.
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R-Loop Stabilization Represses Antisense Transcription at the Arabidopsis FLC Locus

TL;DR: A homeodomain protein, AtNDX, is identified that regulates COOLAIR, a set of antisense transcripts originating from the 3′ end of Arabidopsis FLOWERING LOCUS C (FLC), and R-loop stabilization mediated by AtNDx inhibits COOL AIR transcription, which in turn modifies FLC expression.
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The transcriptional activity of human Chromosome 22

TL;DR: A DNA microarray representing nearly all of the unique sequences of human Chromosome 22 was constructed and used to measure global-transcriptional activity in placental poly(A)(+) RNA and revealed twice as many transcribed bases as have been reported previously.
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Targeted Disruption of Hotair Leads to Homeotic Transformation and Gene Derepression

TL;DR: It is shown that targeted deletion of mouse Hotair lncRNA leads to derepression of hundreds of genes, resulting in homeotic transformation of the spine and malformation of metacarpal-carpal bones.
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