Advances in understanding chromosome silencing by the long non-coding RNA Xist

Author:

Sado Takashi1,Brockdorff Neil2

Affiliation:

1. Division of Epigenomics, Medical Institute of Bioregulation, Kyushu University, 3-1-1, Maidashi, Higashi-ku, Fukuoka 812-8582, Japan

2. Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK

Abstract

In female mammals, one of the two X chromosomes becomes genetically silenced to compensate for dosage imbalance of X-linked genes between XX females and XY males. X chromosome inactivation (X-inactivation) is a classical model for epigenetic gene regulation in mammals and has been studied for half a century. In the last two decades, efforts have been focused on the X inactive-specific transcript (Xist) locus, discovered to be the master regulator of X-inactivation. TheXistgene produces a non-coding RNA that functions as the primary switch for X-inactivation, coating the X chromosome from which it is transcribedin cis. Significant progress has been made towards understanding howXistis regulated at the onset of X-inactivation, but our understanding of the molecular basis of silencing mediated by Xist RNA has progressed more slowly. A picture has, however, begun to emerge, and new tools and resources hold out the promise of further advances to come. Here, we provide an overview of the current state of our knowledge, what is known about Xist RNA and how it may trigger chromosome silencing.

Publisher

The Royal Society

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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