Abstract

The human genome must be tightly packaged in order to fit inside the nucleus of a cell. Genome organization is functional rather than random, which allows for the proper execution of gene expression programs and other biological processes. Recently, three-dimensional chromatin organization has emerged as an important transcriptional control mechanism. For example, enhancers were shown to regulate target genes by physically interacting with them regardless of their linear distance and even if located on different chromosomes. These chromatin contacts can be measured with the “chromosome conformation capture” (3C) technology and other 3C-related techniques. Given the recent innovation of 3C-derived approaches, it is not surprising that we still know very little about the structure of our genome at high-resolution. Even less well understood is whether there exist distinct types of chromatin contacts and importantly, what regulates them. A new form of regulation involving the expression of long non-coding RNAs (lncRNAs) was recently identified. lncRNAs are a very abundant class of non-coding RNAs that are often expressed in a tissue-specific manner. Although their different subcellular localizations point to their involvement in numerous cellular processes, it is clear that lncRNAs play an important role in regulating gene expression. How they control transcription however is mostly unknown. In this review, we provide an overview of known lncRNA transcription regulation activities. We also discuss potential mechanisms by which ncRNAs might exert three-dimensional transcriptional control and what recent studies have revealed about their role in shaping our genome.

Highlights

  • Organisms with large genomes face the interesting problem of having to contain their genetic material within very small cellular volumes

  • The discovery that long non-coding RNAs (lncRNAs) represent a very large portion of our transcriptome has uncovered a new level of gene expression regulation

  • We know very little about them, their sequence diversity, potential splice variants, and cellular distribution suggests an important role in many aspects of RNA transcription, processing, and metabolism

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Summary

INTRODUCTION

Organisms with large genomes face the interesting problem of having to contain their genetic material within very small cellular volumes. It was shown that chromatin contacts could be mediated by tissue-specific transcription factors Such is the case for the beta-globin cluster where DNA looping between the locus control region (LCR) and activated beta-globin genes was shown to require the GATA-1 transcription factor and co-factor FOG-1 [18]. Other chromatin-binding proteins such as the CCCTCbinding factor (CTCF) and cohesin appear to play critical roles in genome organization and gene expression [22, 23]. Mammalian CTCF is a DNA-binding protein associated with insulator sequences, boundary elements and imprinting control regions, all of which are thought to organize our genome into functional subdomains. Since cohesin does not bind DNA directly, this observation points to the existence of CTCF-independent cohesin recruitment and looping mechanisms One such mechanism could involve tissue-specific transcription factors. Tsix is thought to change the epigenetic chromatin state of Xist, thereby preventing Xist and RepA

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