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Non-Coding RNA 2018, 4(4), 28; https://doi.org/10.3390/ncrna4040028

Local Tandem Repeat Expansion in Xist RNA as a Model for the Functionalisation of ncRNA

Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK
Received: 19 September 2018 / Revised: 15 October 2018 / Accepted: 16 October 2018 / Published: 19 October 2018
(This article belongs to the Special Issue Non-Coding RNAs, from an Evolutionary Perspective)
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Abstract

Xist, the master regulator of the X chromosome inactivation in mammals, is a 17 kb lncRNA that acts in cis to silence the majority of genes along the chromosome from which it is transcribed. The two key processes required for Xist RNA function, localisation in cis and recruitment of silencing factors, are genetically separable, at least in part. Recent studies have identified Xist RNA sequences and associated RNA-binding proteins (RBPs) that are important for these processes. Notably, several of the key Xist RNA elements correspond to local tandem repeats. In this review, I use examples to illustrate different modes whereby tandem repeat amplification has been exploited to allow orthodox RBPs to confer new functions for Xist-mediated chromosome inactivation. I further discuss the potential generality of tandem repeat expansion in the evolution of functional long non-coding RNAs (lncRNAs). View Full-Text
Keywords: X inactivation; Xist; lncRNA; tandem repeat X inactivation; Xist; lncRNA; tandem repeat
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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).
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Brockdorff, N. Local Tandem Repeat Expansion in Xist RNA as a Model for the Functionalisation of ncRNA. Non-Coding RNA 2018, 4, 28.

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