Novel molecular players of X chromosome inactivation: new technologies and new insights

Piotr Przanowski* , Urszula Waśko* , Sanchita Bhatnagar

Journal of Translational Genetics and Genomics ›› 2018, Vol. 2 ›› Issue (1) : 2

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Journal of Translational Genetics and Genomics ›› 2018, Vol. 2 ›› Issue (1) :2 DOI: 10.20517/jtgg.2017.03
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Novel molecular players of X chromosome inactivation: new technologies and new insights
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Abstract

The dosage compensation in placental mammals is achieved by silencing of one copy of the X chromosomes in a female cell by a process called X chromosome inactivation (XCI). XCI ensures equal gene dosage for X-linked genes between the two genders. Although the choice of X chromosome to be silenced is random, once the silencing of the X chromosome has been established, this process is highly regulated and maintained throughout subsequent cell divisions. A long non-coding RNA, Xist, and its interacting proteins execute this multistep process, but several of these regulatory proteins remain unidentified. Recent technological advances based on the genetic and proteomics screening have identified several new regulatory factors as well as dissected the molecular details of XCI regulation. Moreover, identification of regulators of XCI offers an opportunity to explore reactivation of the inactive X chromosome (Xi) as a potential therapeutic strategy to treat X-linked diseases, like Rett syndrome. Here, we summarize recent reports that identified new regulatory proteins and RNA species playing a crucial role in Xist localization and spreading, recruitment of silencing machinery to the Xi, Xist interaction with chromatin, and structural organization of the Xi in the nuclei.

Keywords

X chromosome inactivation / X chromosome reactivation / inactive X chromosome / X chromosome inactivation factor / Xist

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Piotr Przanowski*, Urszula Waśko*, Sanchita Bhatnagar. Novel molecular players of X chromosome inactivation: new technologies and new insights. Journal of Translational Genetics and Genomics, 2018, 2(1): 2 DOI:10.20517/jtgg.2017.03

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