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Jpx RNA Activates Xist by Evicting CTCF
Author(s) -
Sha Sun,
Brian C. Del Rosario,
Attila Szántó,
Yuya Ogawa,
Yesu Jeon,
Jeannie T. Lee
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2013.05.028
Subject(s) - xist , ctcf , biology , x inactivation , rna , genetics , dosage compensation , rna binding protein , x chromosome , long non coding rna , non coding rna , transcription (linguistics) , microbiology and biotechnology , transcription factor , gene , enhancer , linguistics , philosophy
In mammals, dosage compensation between XX and XY individuals occurs through X chromosome inactivation (XCI). The noncoding Xist RNA is expressed and initiates XCI only when more than one X chromosome is present. Current models invoke a dependency on the X-to-autosome ratio (X:A), but molecular factors remain poorly defined. Here, we demonstrate that molecular titration between an X-encoded RNA and an autosomally encoded protein dictates Xist induction. In pre-XCI cells, CTCF protein represses Xist transcription. At the onset of XCI, Jpx RNA is upregulated, binds CTCF, and extricates CTCF from one Xist allele. We demonstrate that CTCF is an RNA-binding protein and is titrated away from the Xist promoter by Jpx RNA. Thus, Jpx activates Xist by evicting CTCF. The functional antagonism via molecular titration reveals a role for long noncoding RNA in epigenetic regulation.

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